The DOI matches its Crossref record; 94 of the 98 references it cites were found in a registry or an index; none of the 95 sources its claims cite is checked for support yet.
Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight
Open accessAbstract
Maintenance of a reduced body weight is accompanied by decreased energy expenditure that is due largely to increased skeletal muscle work efficiency. In addition, decreased sympathetic nervous system tone and circulating concentrations of leptin, thyroxine, and triiodothyronine act coordinately to favor weight regain. These "weight-reduced" phenotypes are similar to those of leptin-deficient humans and rodents. We examined metabolic, autonomic, and neuroendocrine phenotypes in 10 inpatient subjects (5 males, 5 females [3 never-obese, 7 obese]) under 3 sets of experimental conditions: (a) maintaining usual weight by ingesting a liquid formula diet; (b) maintaining a 10% reduced weight by ingesting a liquid formula diet; and (c) receiving twice-daily subcutaneous doses of leptin sufficient to restore 8 am circulating leptin concentrations to pre-weight-loss levels and remaining on the same liquid formula diet required to maintain a 10% reduced weight. During leptin administration, energy expenditure, skeletal muscle work efficiency, sympathetic nervous system tone, and circulating concentrations of thyroxine and triiodothyronine returned to pre-weight-loss levels. These responses suggest that the weight-reduced state may be regarded as a condition of relative leptin insufficiency. Prevention of weight regain might be achievable by strategies relevant to reversing this leptin-insufficient state.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
In 10 inpatient subjects, maintenance of a 10% reduced body weight produced coordinated declines in energy expenditure, skeletal muscle efficiency, sympathetic tone, and thyroid hormones. Low-dose leptin, titrated to restore 8 am leptin concentrations to pre-weight-loss levels, reversed many of these weight-reduced adaptations, suggesting the state is one of relative leptin insufficiency.
Key findings
- At Wt−10%, 24-hour energy expenditure (TEE) and nonresting energy expenditure (NREE) fell out of proportion to body-composition changes; skeletal muscle gross mechanical efficiency at 10 W was approximately 23% higher than at Wtinitial, and glucose oxidation at 10 W fell by approximately 12%.
- Leptin administration at Wt−10%lep restored TEE, NREE, skeletal muscle work efficiency, fuel utilization, sympathetic nervous system activity, urinary epinephrine, and circulating T4/T3 to pre-weight-loss levels; it did not significantly alter TSH, 24-hour urinary norepinephrine, parasympathetic activity, or intrinsic heart rate.
- Mean total daily leptin dose was 0.068 ± 0.01 mg/kg (range 0.019–0.121 mg/kg/d) divided q12 hours; 8 am plasma leptin at Wt−10%lep was not significantly different from Wtinitial.
- During leptin administration on an isocaloric diet, body weight and fat mass declined further; fat mass accounted for 67.2% ± 8.5% of weight lost during leptin, versus 71% ± 6.7% during the initial 800-kcal/d weight loss. No significant gender or initial somatotype effects were noted, except lean subjects lost 10% of weight faster (mean 6 weeks) than obese subjects (mean 9 weeks).
Methods
- Ten subjects (5 male, 5 female; 3 never-obese, 7 obese; mean ± SEM age 32.2 ± 2.9 years) were studied as inpatients at three weight plateaus: usual weight (Wtinitial), 10% reduced weight (Wt−10%), and 10% reduced weight during 5 weeks of twice-daily subcutaneous recombinant human leptin (A-100; Amgen) titrated to restore 8 am leptin to Wtinitial levels (Wt−10%lep).
- Measurements included body composition by DXA; energy expenditure by weight-maintenance caloric titration, indirect calorimetry, and calculated NREE; skeletal muscle work efficiency by graded bicycle ergometry; autonomic function by heart-rate analysis during pharmacological blockade and 24-hour urinary catecholamines; and neuroendocrine measures by ELISA/RIA.
- Intragroup comparisons used repeated-measures ANOVA; between-group comparisons used ANOVA; significance was prospectively defined as P < 0.05.
Limitations
- Stated in the paper: twice-daily exogenous leptin does not mimic normal leptin pulsatility, and effects of weight reduction or exogenous leptin on leptin pulsatility in humans had not been reported; therefore 8 am leptin concentrations may not reflect total daily leptin or pulsatility.
- Stated in the paper: organ-specific autonomic measures do not necessarily reflect systemic autonomic nervous system tone; longer studies are needed to determine whether chronic leptin-axis reactivation helps maintain reduced body weight.
- Evident from the text: the study had only 10 subjects, some energy-expenditure and thyroid data from 4 subjects had been reported previously, and the leptin phase lasted 5 weeks, limiting generalizability and long-term inference.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
53 Not checked yet · 35 Own result · 14 Own interpretation · 6 Own method · 1 No basis given
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“No significant effects of weight loss or leptin administration on resting energy expenditure (REE) or the thermic effect of feeding (TEF) beyond those predicted by changes in body composition were noted.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Body composition.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“At Wt -10% , circulating concentrations of T3 and T4 were reduced compared with Wt initial .”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The relationships among TEE, NREE, and body composition were restored at Wt -10%lep to levels present at Wt initial (Figure 4).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Body composition.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
In the paper
“Extrapolating from RQ data (31), at Wt -10% there was an approximate 12% decrease -compared with Wt initial -in the percentage of calories derived from the oxidation of glucose during bicycling to generate 10 W of power.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
What the sources say
- Not checked yetcites [31]
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Administration of leptin to subjects ingesting the same number of calories required to maintain their weight at Wt -10% resulted in further reduction in body weight.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Body composition.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“At all study periods, the respiratory quotient (RQ) at rest was not significantly different from the diet formula quotient (by bomb calorimetry) of 0.85.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Body composition.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“At Wt -10% and Wt -10%lep , circulating thyroid-stimulating hormone (TSH) concentrations were significantly reduced compared with Wt initial values; no significant effects of leptin administration on circulating TSH concentrations were noted (Figure 5).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“During leptin administration, energy expenditure, skeletal muscle work efficiency, sympathetic nervous system tone, and circulating concentrations of thyroxine and triiodothyronine returned to pre-weight-loss levels.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Abstract
plaindirectn = 10- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“At Wt -10% , 24-hour energy expenditure (TEE) and nonresting energy expenditure (NREE; energy expended in physical activity above resting) were decreased out of proportion to changes in body composition from Wt initial .”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Body composition.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“During leptin administration, energy expenditure, skeletal muscle work efficiency, sympathetic nervous system tone, and circulating concentrations of thyroxine and triiodothyronine returned to pre-weight-loss levels.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Abstract
plaindirectn = 10- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- It may state two separate claims as one. 32
- Probably not a substantial claim. 22
- The quote only partly states this claim. 1
In the paper
“At Wt -10% , skeletal muscle work efficiency was increased and RQ was decreased at low levels of work (pedaling a bicycle ergometer to generate 10 W of power) compared with sub- jects at Wt initial , similar to our previous observations (3).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
What the sources say
- Not checked yetcites [3]
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“No significant effects of gender or initial somatotype were noted on any results, except that lean subjects consistently required less time (mean 6 weeks) to lose 10% of their weight than obese subjects (mean 9 weeks).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Results
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“At Wt -10%lep , circulating T4 and T3 concentrations were, respectively, similar to and higher than those at Wt initial .”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“At Wt -10% , the gross mechanical efficiency (GME) of skeletal muscle while bicycling to generate 10 W of power was approximately 23% higher than at Wt initial and was fully reversed during leptin administration at Wt -10%lep .”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“No significant effects of gender or initial somatotype were noted on any results, except that lean subjects consistently required less time (mean 6 weeks) to lose 10% of their weight than obese subjects (mean 9 weeks).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Results
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Loss of fat mass accounted for 67.2% ± 8.5% of the weight lost during leptin administration, similar to 71% ± 6.7% of weight lost as fat observed during weight loss on an 800-kcal/d diet from Wt initial to Wt -10% (Figure 3).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Body composition.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“When subjects who had lost 10% (Wt -10% ) of their initial body weight (Wt initial ) received subcutaneous leptin (Wt -10%lep ), plasma leptin concentrations at 8 am were significantly higher than those values observed at Wt -10% and not significantly different from those observed at Wt initial (Figure 2).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Results
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Maintenance of a 10% reduced body weight was associated with decreased SNS activity (measured by heart rate analysis and by urinary catecholamine excretion) and increased PNS activity (measured by heart rate analysis).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Autonomic function.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In the present study, mean ± SEM total daily leptin doses relative to body mass at Wt -10% were 0.068 ± 0.01 mg/kg (range 0.019-0.121mg/kg/d) divided q12 hours (8 am and 8 pm)”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Results
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Administration of leptin to weight-reduced subjects reversed the decline in SNS activity and 24-hour urinary epinephrine excretion but did not significantly alter the decline in 24-hour urinary norepinephrine excretion or the increase in PNS activity (Figure 6).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Autonomic function.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Administration of leptin to leptindeficient rodents in doses that restore circulating leptin concentrations to their physiological range increases energy expenditure, decreases energy intake, increases SNS output (18,19), and normalizes hypothalamic-pituitary-adrenal, thyroid, and gonadal function (20)(21)(22)(23).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Introduction
What the sources say
- Not checked yetcites [18]
- Not checked yetcites [19]
- Not checked yetcites (20)(21)(22)(23)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“It should be noted that twice-daily administration of exogenous leptin does not mimic the normal pulsatility of leptin secretion (27)(28)(29)(30)”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Results
What the sources say
- Not checked yetcites (27)(28)(29)(30)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“no such effects were detected when leptin was administered in similar doses to eumenorrheic women without reduced fat mass.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Introduction
What the sources say
- Not checked yetcites [26]
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
In the paper
“Similarly, Welt et al. (26) reported that leptin administration (0.08 mg/kg/d) to women with secondary hypothalamic amenorrhea due to reduced fat mass reversed the decline in hypothalamic-pituitary-gonadal axis function and raised circulating concentrations of triiodothyronine (T3) and thyroxine (T4); no such effects were detected when leptin was administered in similar doses to eumenorrheic women”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Introduction
What the sources say
- Not checked yetcites [26]
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Leptin administration to leptin-deficient humans decreases energy intake and increases activity of the hypothalamic-pituitary-thyroid axis (15,24).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Introduction
What the sources say
- Not checked yetcites [15]
- Not checked yetcites [24]
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“In such subjects, sympathetic nervous system (SNS) tone and circulating concentrations of leptin and bioactive thyroid hormones are reduced, while parasympathetic nervous system (PNS) tone is increased (2)(3)(4)(5)(6)(7)(8)(9).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Introduction
What the sources say
- Not checked yetcites (2)(3)(4)(5)(6)(7)(8)(9)
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The metabolic phenotypes of weight-reduced humans, leptindeficient humans, and leptin-deficient rodents are similar but not identical (13)(14)(15).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Introduction
What the sources say
- Not checked yetcites (13)(14)(15)
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These in vivo responses of weight-reduced humans to leptin are concordant with in vitro and in vivo studies of leptin effects on skeletal muscle, autonomic nervous system activity, and neuroendocrine axes and demonstrate that leptin administration to weight-reduced subjects reverses many of the metabolic phenotypes that characterize the weight-reduced state.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Both systemic and intracerebroventricular leptin administration increase insulin-mediated glucose uptake in rat skeletal muscle (36)(37)(38), and leptin increases both glucose and fatty acid oxidation in rodent skeletal muscle in vitro (34,36,(39)(40)(41)(42).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites (36)(37)(38)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Physiological responses to concentrations of leptin below and above this threshold are very asymmetrical: decreased concentrations of leptin trigger full-strength counterregulation to what is “perceived” as a threat to survival; concentrations of leptin above the threshold -signaling “sufficient” or excess fat stores -are not responded to vigorously, or at all (74).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites [74]
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Leptin could affect skeletal muscle function via direct interaction with muscle cells and/or by engaging hypothalamic/brain stem pathways regulating autonomic and neuroendocrine function.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: fails — The paper may give no reason why it holds.
Probably not a substantial claim. The paper may give no reason why it holds. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These organ-specific measures of autonomic activity do not necessarily reflect systemic autonomic nervous system tone.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: fails — The paper may give no reason why it holds.
Probably not a substantial claim. The paper may give no reason why it holds.
In the paper
“Skeletal muscle expresses the short and long isoforms of the leptin receptor (34), and incubation of skeletal muscle from lean mice with leptin stimulates oxygen consumption (35).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites [34]
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Skeletal muscle expresses the short and long isoforms of the leptin receptor (34), and incubation of skeletal muscle from lean mice with leptin stimulates oxygen consumption (35).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites [35]
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Similar doses of leptin decrease hunger and increase satiety in individuals who are hypoleptinemic by virtue of lipodystrophy (70).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites [70]
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Both systemic and intracerebroventricular leptin administration increase insulin-mediated glucose uptake in rat skeletal muscle (36)(37)(38), and leptin increases both glucose and fatty acid oxidation in rodent skeletal muscle in vitro (34,36,(39)(40)(41)(42).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites (34,36,(39)(40)(41)(42)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These data suggest that that changes in SNS, but not PNS, activity following weight loss are due to decreased circulating leptin concentrations.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“These inferences are supported by direct effects of leptin on epinephrine release from porcine adrenal medullary cells (50) and the increases in circulating concentrations of epinephrine and norepinephrine, renal sympathetic nerve activity, heart rate, arterial pressure, and sympathoexcitation of brown adipose tissue (51-54) following systemic leptin infusion, or”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites [50]
- Not checked yetcites [51]
- Not checked yetcites [52]
- Not checked yetcites [53]
- Not checked yetcites [54]
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Increased TRH secretion increases TSH bioactivity in vitro and in vitro by apparent effects on sialation of TSH (63), and TSH bioactivity is decreased in low-TRH states (analogous to the low-TRH state of weight-reduced humans) (64)(65)(66)(67).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites (64)(65)(66)(67)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“In rats, the thyroid gland expresses the long isoform of the leptin receptor, and administration of leptin to euthyroid, leptin-sufficient animals increases circulating concentrations of T3 and T4, thyroid gland weight, and volume of the thyroid follicle epithelium without affecting circulating concentrations of TSH (61,62).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites [61]
- Not checked yetcites [62]
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Leptin-stimulated TRH release alone would not account for our observation that 5 weeks of leptin administration to weightreduced subjects raised circulating concentrations of T3 and T4 but not TSH, nor the observation of Farooqi et al. (15) that 1-6 months of leptin administration to humans with congenital leptin deficiency raised circulating concentrations of bioactive thyroid hormones but not”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites [15]
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“This asymmetry permits the deposition of additional fat stores in environmental circumstances when this is possible, conveying survival advantage in most instances.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: fails — It may be too vague to check against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. It may be too vague to check against evidence. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Leptin-mediated SNS effects probably reflect both the peripheral stimulatory effects of leptin on adrenal epinephrine release and centrally mediated increases in sympathetic outflow.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Leptin deficiency is associated with decreased SNS tone as measured by blood pressure changes during a cold pressor test in humans (46) and a leptin-reversible decline in brown adipose tissue thermogenesis in mice (47).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites [46]
- Not checked yetcites [47]
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Pharmacologic and other strategies designed to maintain lost body weight may, for these reasons, be more effective than those designed to induce weight loss (74).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
What the sources say
- Not checked yetcites [74]
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“The intraassay coefficients of variation for these assays are less than 5%.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. The quote only partly states this claim.
In the paper
“SNS activity measured by pharmacological blockade reflects the action of catecholamines (predominantly norepinephrine) released at nerve endings and from the adrenal gland (predominantly epinephrine), as well as the sensitivity, number, and relative proportion of cardiac αand β-adrenoreceptors (84).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
What the sources say
- Not checked yetcites [84]
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
In the paper
“To correct for the non-zero intercept of regressions relating energy expenditure to body composition (83), residual values of REE, TEE, and NREE were calculated for subjects at Wt-10% and Wt-10%lep as the difference between measured energy expenditures and values predicted from the regression equations relating energy expenditure to fat mass and fat-free mass at Wtinitial (83).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Subjects.
What the sources say
- Not checked yetcites [83]
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“The interassay coefficients of variation for assays of dopamine, epinephrine, and norepinephrine are, respectively, 6.2%, 5.7%, and 7.1%.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In this model, the experiments described here are examples of restoration of circulating leptin concentrations to points above each subject's threshold with resultant reversal of leptin-insufficient/weight-reduced phenotypes.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Discussion
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- The authors state this as an assumption: The threshold for determination of leptin sufficiency is determined by anatomic and functional characteristics of the hypothalamus and other parts of the brain that are, in turn, determined by genetic and developmental factors.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“All women were in the follicular phase of their menstrual cycle at the start of testing.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“In larger study groups, we have not found a significant effect of the order of testing or of duration of time spent at reduced weight on any of these parameters (2).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
What the sources say
- Not checked yetcites [2]
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Circulating leptin concentrations at 8 am were measured weekly in subjects receiving leptin, and dosages were adjusted until circulating leptin concentrations were similar to those measured at 8 am at Wtinitial.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Subjects.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“The intra-and interassay coefficients of variation for each of these assays are less than 5%.”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“To prevent changes in physical fitness as a result of the 6-7 months in-patient stay, and to insure that subjects did not substantially vary their in-patient physical activity levels during the study, either of which might affect skeletal muscle metabolism/performance, each subject's aerobic fitness was measured by bicycle ergometry upon admission and was then maintained at that level throughout”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Subjects.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. It may state two separate claims as one.
In the paper
“Chemical energy content was assigned as 9.4 kcal/g wet weight of fat mass and 0.91 kcal/g wet weight of fat-free mass excluding bone (82).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Subjects.
What the sources say
- Not checked yetcites [82]
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. It may state two separate claims as one.
The authors state this as an assumption.
The threshold for determination of leptin sufficiency is determined by anatomic and functional characteristics of the hypothalamus and other parts of the brain that are, in turn, determined by genetic and developmental factors.
“The threshold for determination of leptin sufficiency in this context is determined by anatomic and functional characteristics of the hypothalamus and other parts of the brain that are, in turn, determined by genetic and developmental factors.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In fact, replacing leptin during maintenance of reduced weight reversed two-thirds of the fall in TEE and AEE while increasing work efficiency in skeletal muscle [64, 65•].”
From Changes in energy expenditure with weight gain and weight loss in humans (2016) · cites this paper as [64]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Taken together, there was no thermogenic effect of leptin in subjects at usual weight and during weight loss.”
From Changes in energy expenditure with weight gain and weight loss in humans (2016) · cites this paper as [64]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“It should be mentioned that controlling body weight after gradual weight loss (as done in ref) [17, 64, 65•] does not follow a physiological response but may interfere with biology.”
From Changes in energy expenditure with weight gain and weight loss in humans (2016) · cites this paper as [64]
The cited source says what the claim attributes to it.
In the citing paper
“By contrast, an effect of exogenous leptin administration was seen in weight-stable-weight-reduced subjects only [64, 75•].”
From Changes in energy expenditure with weight gain and weight loss in humans (2016) · cites this paper as [64]
In the citing paper
“In addition, leptin, released by white adipocytes, regulates energy balance by effects on the hypothalamus that lead to inhibition of food intake and increased thermogenesis via activation of the SNS, though to date there is limited evidence that leptin mediates thermogenesis via the SNS in humans 66–70.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [70]
In the citing paper
“In addition, leptin, released by white adipocytes, regulates energy balance by effects on the hypothalamus that lead to inhibition of food intake and increased thermogenesis via activation of the SNS, though to date there is limited evidence that leptin mediates thermogenesis via the SNS in humans 66–70.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [70]
In the citing paper
“In humans subjected to weight loss due to energy restriction, administration of leptin at doses that maintain pre-weight loss plasma levels blocks the reduction of sympathetic nervous system (SNS) activity and metabolic rate characteristic of the weight-reduced state (151).”
From Leptin and the Central Nervous System Control of Glucose Metabolism (2011) · cites this paper as [151]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Rated minor: it would not touch a result — a value no result rests on, a p-value that stays on the same side of the significance level, or a conflict that is clerical, resolved elsewhere in the paper, or outside its own findings.
In the paper
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Skeletal muscle.
“Skeletal muscle work efficiency was expressed as gross mechanical efficiency (GME): the ratio of power generated in kcal/ min to change in energy expenditure above REE in kcal/min at power outputs of 10 W and 25 W (3).”
§ Low-dose leptin reverses skeletal muscle, autonomic, and neuroendocrine adaptations to maintenance of reduced weight > Statistics.
“Effects of weight loss and exogenous leptin on skeletal muscle gross mechanical work efficiency (kcal/min energy expended above resting per kcal/min work generated) and fuel utilization (derived from RQ; ref. 87) were only evident at low levels of work (bicycling to generate 10 W of power).”
Citations
Cites
The Metabolic and Molecular Bases of Inherited Disease
Scriver, R. C. (1995) · Medical Entomology and Zoology · Cited by 12,101
(1998) · PsycEXTRA Dataset · doi:10.1037/e565682010-001 · Cited by 9,453
The metabolic and molecular bases of inherited disease
Chen, Y.-T. (2001) · Medical Entomology and Zoology · Cited by 6,928
Campfield, L. A., Smith, F. J., Guisez, Y., Devos, R., & Burn, P. (1995) · Science · doi:10.1126/science.7624778 · Cited by 3,243
Role of leptin in the neuroendocrine response to fasting
Ahima, R. S., Prabakaran, D., Mantzoros, C., Qu, D., Lowell, B., Maratos-Flier, E., & Flier, J. S. (1996) · Nature · doi:10.1038/382250a0 · Cited by 3,117
Congenital leptin deficiency is associated with severe early-onset obesity in humans
Montague, C. T., Farooqi, I. S., Whitehead, J. P., Soos, M. A., Rau, H., Wareham, N. J., Sewter, C. P., Digby, J. E., Mohammed, S. N., Hurst, J. A., et al. (1997) · Nature · doi:10.1038/43185 · Cited by 2,936
(1998) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/68.4.899 · Cited by 2,722
Leptin stimulates fatty-acid oxidation by activating AMP-activated protein kinase
Minokoshi, Y., Kim, Y.-B., Peroni, O. D., Fryer, L. G. D., Müller, C., Carling, D., & Kahn, B. B. (2002) · Nature · doi:10.1038/415339a · Cited by 2,053
Changes in Energy Expenditure Resulting from Altered Body Weight
Leibel, R. L., Rosenbaum, M., & Hirsch, J. (1995) · New England Journal of Medicine · doi:10.1056/nejm199503093321001 · Cited by 2,012
Self-citationEffects of Recombinant Leptin Therapy in a Child with Congenital Leptin Deficiency
Farooqi, I. S., Jebb, S. A., Langmack, G., Lawrence, E., Cheetham, C. H., Prentice, A. M., Hughes, I. A., McCamish, M. A., & O'Rahilly, S. (1999) · New England Journal of Medicine · doi:10.1056/nejm199909163411204 · Cited by 1,998
Research works printed but not linked: 2
- Keesey, R.E. 1980. A set-point analysis of the regu- lation of body weight. In Obesity. A.J. Stunkard, editor. W.B. Saunders. Philadelphia, Pennsylvania, USA. 144-165.
- Miles, L. 1977. Chapter 4. In Handbook of radioimmu- noassay. G. Abraham, editor. Marcel Dekker. New York, New York, USA. 679-680.
Cited by
Sorted by citations
Garvey, W. T., Mechanick, J. I., Brett, E. M., Garber, A. J., Hurley, D. L., Jastreboff, A. M., Nadolsky, K., Pessah-Pollack, R., & Plodkowski, R. (2016) · Endocrine Practice · doi:10.4158/ep161365.gl · Cited by 1,914
The role of leptin and ghrelin in the regulation of food intake and body weight in humans: a review
Klok, M. D., Jakobsdottir, S., & Drent, M. L. (2007) · Obesity Reviews · doi:10.1111/j.1467-789x.2006.00270.x · Cited by 1,442
Pharmacological Management of Obesity: An Endocrine Society Clinical Practice Guideline
Apovian, C. M., Aronne, L. J., Bessesen, D. H., McDonnell, M. E., Murad, M. H., Pagotto, U., Ryan, D. H., & Still, C. D. (2015) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-3415 · Cited by 1,347
Leptin and Obesity: Role and clinical implication.
Obradovic, M., Sudar-Milovanovic, E., Soskic, S., Essack, M., Arya, S., Stewart, A. J., Gojobori, T., & Isenovic, E. R. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.585887 · Cited by 1,121
Stern, J. H., Rutkowski, J. M., & Scherer, P. E. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.04.011 · Cited by 1,031
Obesity Pathogenesis: An Endocrine Society Scientific Statement
Schwartz, M. W., Seeley, R. J., Zeltser, L. M., Drewnowski, A., Ravussin, E., Redman, L. M., & Leibel, R. L. (2017) · Endocrine Reviews · doi:10.1210/er.2017-00111 · Cited by 727
Physiology of leptin: energy homeostasis, neuroendocrine function and metabolism
Park, H. K., & Ahima, R. S. (2014) · Metabolism · doi:10.1016/j.metabol.2014.08.004 · Cited by 710
Narrative Review: The Role of Leptin in Human Physiology: Emerging Clinical Applications
Kelesidis, T., Kelesidis, I., Chou, S. H.-H., & Mantzoros, C. S. (2010) · Annals of Internal Medicine · doi:10.7326/0003-4819-152-2-201001190-00008 · Cited by 693
Leptin and the endocrine control of energy balance
Friedman, J. M. (2019) · Nature Metabolism · doi:10.1038/s42255-019-0095-y · Cited by 661
Role of leptin and adiponectin in insulin resistance
Yadav, A., Kataria, M. A., Saini, V., & Yadav, A. (2012) · Clinica Chimica Acta · doi:10.1016/j.cca.2012.12.007 · Cited by 657
Adipose Tissue as an Endocrine Organ
Ahima, R. S. (2006) · Obesity · doi:10.1038/oby.2006.317 · Cited by 646
Leptin in Human Physiology and Pathophysiology
Mantzoros, C. S., Magkos, F., Brinkoetter, M., Sienkiewicz, E., Dardeno, T. A., Kim, S.-Y., Hamnvik, O.-P. R., & Koniaris, A. (2011) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00315.2011 · Cited by 593
Cellular bioenergetics as a target for obesity therapy
Tseng, Y.-H., Cypess, A. M., & Kahn, C. R. (2010) · Nature Reviews Drug Discovery · doi:10.1038/nrd3138 · Cited by 591
Understanding and Addressing the Epidemic of Obesity: An Energy Balance Perspective
Hill, J. O. (2006) · Endocrine Reviews · doi:10.1210/er.2006-0032 · Cited by 610
Lifestyle Modification for Obesity
Wadden, T. A., Webb, V. L., Moran, C. H., & Bailer, B. A. (2012) · Circulation · doi:10.1161/circulationaha.111.039453 · Cited by 613
NIH working group report: Innovative research to improve maintenance of weight loss
MacLean, P. S., Wing, R. R., Davidson, T. L., Epstein, L. H., Goodpaster, B. H., Hall, K. D., Levin, B. E., Perri, M. G., Rolls, B. J., ROSENBAUM, M. S., et al. (2014) · Obesity · doi:10.1002/oby.20967 · Cited by 576
Self-citationDiet-Induced Obesity Causes Severe but Reversible Leptin Resistance in Arcuate Melanocortin Neurons
Enriori, P. J., Evans, A. E., Sinnayah, P., Jobst, E. E., Tonelli-Lemos, L., Billes, S. K., Glavas, M. M., Grayson, B. E., Perello, M., Nillni, E. A., et al. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.02.004 · Cited by 552
Zhang, Y., Guo, K., LeBlanc, R. E., Loh, D., Schwartz, G. J., & Yu, Y. (2007) · Diabetes · doi:10.2337/db07-0123 · Cited by 545
Modulation of Blood Pressure by Central Melanocortinergic Pathways
Greenfield, J. R., Miller, J. W., Keogh, J. M., Henning, E., Satterwhite, J. H., Cameron, G. S., Astruc, B., Mayer, J. P., Brage, S., See, T. C., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0803085 · Cited by 477
Redman, L. M., Smith, S. R., Burton, J. H., Martin, C. K., Il'yasova, D., & Ravussin, E. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.02.019 · Cited by 472
The Human Microbiome and Obesity: Moving beyond Associations
Maruvada, P., Leone, V., Kaplan, L. M., & Chang, E. B. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.10.005 · Cited by 476
Obesity as a multisystem disease: Trends in obesity rates and obesity‐related complications
Sarma, S., Sockalingam, S., & Dash, S. (2021) · Diabetes Obesity and Metabolism · doi:10.1111/dom.14290 · Cited by 485
Structure, production and signaling of leptin
Münzberg, H., & Morrison, C. D. (2014) · Metabolism · doi:10.1016/j.metabol.2014.09.010 · Cited by 486
Biology's response to dieting: the impetus for weight regain
MacLean, P. S., Bergouignan, A., Cornier, M., & Jackman, M. R. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00755.2010 · Cited by 471
Rosenbaum, M., Hirsch, J., Gallagher, D. A., & Leibel, R. L. (2008) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/88.4.906 · Cited by 444
Self-citationMechanisms of Sympathetic Activation in Obesity-Related Hypertension
Esler, M., Straznicky, N., Eikelis, N., Masuo, K., Lambert, G., & Lambert, E. (2006) · Hypertension · doi:10.1161/01.hyp.0000242642.42177.49 · Cited by 443
Effects of Dietary Composition on Energy Expenditure During Weight-Loss Maintenance
Ebbeling, C. B., Swain, J. F., Feldman, H. A., Wong, W. W., Hachey, D. L., Garcia-Lago, E., & Ludwig, D. S. (2012) · JAMA · doi:10.1001/jama.2012.6607 · Cited by 431
Long-Term Impact of Bariatric Surgery on Body Weight, Comorbidities, and Nutritional Status
Shah, M., Simha, V., & Garg, A. (2006) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2006-0557 · Cited by 425
ROSENBAUM, M. S., Sy, M., Pavlovich, K. H., Leibel, R. L., & Joy Hirsch, C. (2008) · Journal of Clinical Investigation · doi:10.1172/jci35055 · Cited by 408
Self-citationInsufficient Sleep Undermines Dietary Efforts to Reduce Adiposity
Nedeltcheva, A. V., Kilkus, J. M., Imperial, J., Schoeller, D. A., & Penev, P. D. (2010) · Annals of Internal Medicine · doi:10.7326/0003-4819-153-7-201010050-00006 · Cited by 397
The Hunger Genes: Pathways to Obesity
van der Klaauw, A. A., & Farooqi, I. S. (2015) · Cell · doi:10.1016/j.cell.2015.03.008 · Cited by 414
Brennan, A. M., & Mantzoros, C. S. (2006) · Nature Clinical Practice Endocrinology & Metabolism · doi:10.1038/ncpendmet0196 · Cited by 374
Obesity energetics: body weight regulation and the effects of diet composition
Hall, K. D., & Guo, J. (2017) · Gastroenterology · doi:10.1053/j.gastro.2017.01.052 · Cited by 367
Sixteen years and counting: an update on leptin in energy balance
Gautron, L., & Elmquist, J. K. (2011) · Journal of Clinical Investigation · doi:10.1172/jci45888 · Cited by 367
Disinhibition: its effects on appetite and weight regulation
Bryant, E. J., King, N. A., & Blundell, J. E. (2008) · Obesity Reviews · doi:10.1111/j.1467-789x.2007.00426.x · Cited by 380
Adaptive thermogenesis in humans
Rosenbaum, M., & Leibel, R. L. (2010) · International Journal of Obesity · doi:10.1038/ijo.2010.184 · Cited by 349
Self-citationLeptin Mediates the Increase in Blood Pressure Associated with Obesity
Simonds, S. E., Pryor, J. T., Ravussin, É., Greenway, F. L., Dileone, R., Allen, A. M., Bassi, J. K., Elmquist, J. K., Keogh, J. M., Henning, E., et al. (2014) · Cell · doi:10.1016/j.cell.2014.10.058 · Cited by 352
Leptin and the maintenance of elevated body weight
Pan, W. W., & Myers, M. G. (2018) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.168 · Cited by 344
Korner, J., Inabnet, W., Febres, G., Conwell, I. M., McMahon, D. J., Salas, R., Taveras, C., Schrope, B., & Bessler, M. (2009) · International Journal of Obesity · doi:10.1038/ijo.2009.79 · Cited by 338
Leptin and the Central Nervous System Control of Glucose Metabolism
Morton, G. J., & Schwartz, M. W. (2011) · Physiological Reviews · doi:10.1152/physrev.00007.2010 · Cited by 338
“In humans subjected to weight loss due to energy restriction, administration of leptin at doses that maintain preweight loss plasma levels blocks the reduction of sympathetic nervous system (SNS) activity and metabolic rate characteristic of the weight-reduced state (151).”
BackgroundRavussin, É., Smith, S. R., Mitchell, J. A., Shringarpure, R., Shan, K., Maier, H., Koda, J. E., & Weyer, C. (2009) · Obesity · doi:10.1038/oby.2009.184 · Cited by 335
Leptin: a pivotal regulator of human energy homeostasis
Farooqi, I. S., & O’Rahilly, S. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2008.26788c · Cited by 341
Adipokines and the Peripheral and Neural Control of Energy Balance
Ahima, R. S., & Lazar, M. A. (2008) · Molecular Endocrinology · doi:10.1210/me.2007-0529 · Cited by 324
Abete, I., Astrup, A. V., Martínez, J. A., Þórsdóttir, I., & Zulet, M. Á. (2010) · Nutrition Reviews · doi:10.1111/j.1753-4887.2010.00280.x · Cited by 328
The defence of body weight: a physiological basis for weight regain after weight loss
Sumithran, P., & Proietto, J. (2013) · Clinical Science · doi:10.1042/cs20120223 · Cited by 310
Partial Leptin Reduction as an Insulin Sensitization and Weight Loss Strategy
Zhao, S., Zhu, Y., Schultz, R. D., Li, N., He, Z., Zhang, Z., Caron, A., Zhu, Q., Sun, K., Xiong, W., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.08.005 · Cited by 299
Leptin in human physiology and therapeutics
Dardeno, T. A., Chou, S. H.-H., Moon, H., Chamberland, J. P., Fiorenza, C. G., & Mantzoros, C. S. (2010) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.06.002 · Cited by 297
Enriori, P. J., Evans, A. E., Sinnayah, P., & Cowley, M. A. (2006) · Obesity · doi:10.1038/oby.2006.319 · Cited by 281
Guyenet, S. J., & Schwartz, M. W. (2012) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2011-2525 · Cited by 293
20 YEARS OF LEPTIN: Human disorders of leptin action
Farooqi, I. S., & O'Rahilly, S. (2014) · Journal of Endocrinology · doi:10.1530/joe-14-0480 · Cited by 280
Ebbeling, C. B., Feldman, H. A., Klein, G. L., Wong, J. M. W., Bielak, L., Steltz, S. K., Luoto, P. K., Wolfe, R. R., Wong, W. W., & Ludwig, D. S. (2018) · BMJ · doi:10.1136/bmj.k4583 · Cited by 274
Müller, M. J., Enderle, J., Pourhassan, M., Braun, W., Eggeling, B., Lagerpusch, M., Glüer, C.-C., Kehayias, J. J., Kiosz, D., & Bosy-Westphal, A. (2015) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.115.109173 · Cited by 254
Leptin Function and Regulation
Zhang, Y., & Chua, S. C. (2017) · Comprehensive physiology · doi:10.1002/cphy.c160041 · Cited by 284
Changes in energy expenditure with weight gain and weight loss in humans
Müller, M. J., Enderle, J., & Bosy-Westphal, A. (2016) · Current Obesity Reports · doi:10.1007/s13679-016-0237-4 · Cited by 267
Recinella, L., Orlando, G., Ferrante, C., Chiavaroli, A., Brunetti, L., & Leone, S. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.578966 · Cited by 261
Leptin's Role in Lipodystrophic and Nonlipodystrophic Insulin-Resistant and Diabetic Individuals
Moon, H., Dalamaga, Μ., Kim, S. Y., Pοlyzos, S. A., Hamnvik, O. R., Magkos, F., Paruthi, J., & Mantzoros, C. S. (2013) · Endocrine Reviews · doi:10.1210/er.2012-1053 · Cited by 265
20 YEARS OF LEPTIN: Role of leptin in energy homeostasis in humans
ROSENBAUM, M. S., & Leibel, R. L. (2014) · Journal of Endocrinology · doi:10.1530/joe-14-0358 · Cited by 264
Self-citationThyroid hormone signaling in energy homeostasis and energy metabolism
McAninch, E. A., & Bianco, A. C. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12374 · Cited by 245
Santini, F., Marzullo, P., Rotondi, M., Ceccarini, G., Pagano, L., Ippolito, S., Chiovato, L., & Biondi, B. (2014) · European Journal of Endocrinology · doi:10.1530/eje-14-0067 · Cited by 240
Leptin applications in 2015: what have we learned about leptin and obesity?
Farr, O. M., Gavrieli, A., & Mantzoros, C. S. (2015) · Current Opinion in Endocrinology, Diabetes & Obesity · doi:10.1097/med.0000000000000184 · Cited by 233
Growth hormone regulates neuroendocrine responses to weight loss via AgRP neurons
Furigo, I. C., Teixeira, P. D. S., de Souza, G. O., Couto, G. C. L., Romero, G. G., Perelló, M., Frazão, R., Elias, L. L. K., Metzger, M., List, E. O., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08607-1 · Cited by 230
Sympathetic nervous system in obesity-related hypertension: mechanisms and clinical implications
Kalil, G. Z., & Haynes, W. G. (2011) · Hypertension Research · doi:10.1038/hr.2011.173 · Cited by 234
Type 1 iodothyronine deiodinase in human physiology and disease
Maia, A. L., Goemann, I. M., Meyer, E. L. D. S., & Wajner, S. M. (2011) · Journal of Endocrinology · doi:10.1530/joe-10-0481 · Cited by 229
Leptin signaling in brain: A link between nutrition and cognition?
Morrison, C. D. (2008) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2008.12.004 · Cited by 229
Leptin in Leanness and Obesity
Perakakis, N., Farr, O. M., & Mantzoros, C. S. (2021) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2020.11.069 · Cited by 230
Peripheral oxytocin suppresses food intake and causes weight loss in diet-induced obese rats
Morton, G. J., Thatcher, B. S., Reidelberger, R. D., Ogimoto, K., Wolden-Hanson, T., Baskin, D. G., Schwartz, M. W., & Blevins, J. E. (2012) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00296.2011 · Cited by 213
Energy balance, body composition, sedentariness and appetite regulation: pathways to obesity
Hopkins, M., & Blundell, J. E. (2016) · Clinical Science · doi:10.1042/cs20160006 · Cited by 227
The role for adipose tissue in weight regain after weight loss
MacLean, P. S., HIGGINS, J. A., Giles, E. D., Sherk, V. D., & Jackman, M. R. (2015) · Obesity Reviews · doi:10.1111/obr.12255 · Cited by 221
Stubbs, R. J., Whybrow, S., Teixeira, P. J., Blundell, J. E., Lawton, C. L., Westenhöfer, J., Engel, D., Shepherd, R., McConnon, Á., Gilbert, P., et al. (2011) · Obesity Reviews · doi:10.1111/j.1467-789x.2011.00883.x · Cited by 225
O'Rahilly, S., & Farooqi, I. S. (2008) · Diabetes · doi:10.2337/db08-0210 · Cited by 205
Autonomic imbalance: prophet of doom or scope for hope?
Vinik, A. I., Maser, R. E., & Ziegler, D. (2010) · Diabetic Medicine · doi:10.1111/j.1464-5491.2010.03184.x · Cited by 209
Revisiting leptin’s role in obesity and weight loss
Ahima, R. S. (2008) · Journal of Clinical Investigation · doi:10.1172/jci36284 · Cited by 209
Brown Adipose Tissue—A Translational Perspective
Carpentier, A. C., Blondin, D. P., Haman, F., & Richard, D. (2022) · Endocrine Reviews · doi:10.1210/endrev/bnac015 · Cited by 218
The role of leptin in anorexia nervosa: clinical implications
Hebebrand, J., Müller, T. D., Holtkamp, K., & Herpertz‐Dahlmann, B. (2006) · Molecular Psychiatry · doi:10.1038/sj.mp.4001909 · Cited by 209
Genetic approaches to understanding human obesity
Ramachandrappa, S., & Farooqi, I. S. (2011) · Journal of Clinical Investigation · doi:10.1172/jci46044 · Cited by 199
Exercise Induced Adipokine Changes and the Metabolic Syndrome
Golbidi, S., & Laher, I. (2014) · Journal of Diabetes Research · doi:10.1155/2014/726861 · Cited by 202
Rezai-Zadeh, K. P., Yu, S., Jiang, Y., Laque, A., Schwartzenburg, C., Morrison, C. D., Derbenev, A. V., Zsombok, A., & Münzberg, H. (2014) · Molecular Metabolism · doi:10.1016/j.molmet.2014.07.008 · Cited by 201
Dalamaga, Μ., Chou, S. H.-H., Shields, K. S., Papageorgiou, P., Pοlyzos, S. A., & Mantzoros, C. S. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.05.010 · Cited by 199
Biological mechanisms that promote weight regain following weight loss in obese humans
Ochner, C. N., M.S, D. M. B., Lee, C. D., & Pi-Sunyer, X. (2013) · Physiology & Behavior · doi:10.1016/j.physbeh.2013.07.009 · Cited by 196
Adaptive thermogenesis with weight loss in humans
Müller, M. J., & Bosy‐Westphal, A. (2013) · Obesity · doi:10.1002/oby.20027 · Cited by 181
The fundamental drivers of the obesity epidemic
James, W. P. T. (2008) · Obesity Reviews · doi:10.1111/j.1467-789x.2007.00432.x · Cited by 179
Metabolic adaptation to weight loss: implications for the athlete
Trexler, E. T., Smith‐Ryan, A. E., & Norton, L. E. (2014) · Journal of the International Society of Sports Nutrition · doi:10.1186/1550-2783-11-7 · Cited by 205
Plum, L., Lin, H. V., Dutia, R., Tanaka, J., Aizawa, K. S., Matsumoto, M., Kim, A. J., Cawley, N. X., Paik, J.-H., Loh, Y. P., et al. (2009) · Nature Medicine · doi:10.1038/nm.2026 · Cited by 176
Cannon, B., & Nedergaard, J. (2010) · International Journal of Obesity · doi:10.1038/ijo.2010.177 · Cited by 176
Goldsmith, R., Joanisse, D. R., Gallagher, D., Pavlovich, K., Shamoon, E., Leibel, R. L., & Rosenbaum, M. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00053.2009 · Cited by 171
Self-citationBowels control brain: gut hormones and obesity
Field, B. C. T., Chaudhri, O. B., & Bloom, S. R. (2010) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2010.93 · Cited by 172
Role of leptin in energy expenditure: the hypothalamic perspective
Pandit, R., Beerens, S., & Adan, R. A. H. (2017) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00045.2016 · Cited by 170
Identification of Body Fat Mass as a Major Determinant of Metabolic Rate in Mice
Kaiyala, K. J., Morton, G. J., Leroux, B. G., Ogimoto, K., Wisse, B. E., & Schwartz, M. W. (2010) · Diabetes · doi:10.2337/db09-1582 · Cited by 166
Leptin's Physiologic Role: Does the Emperor of Energy Balance Have No Clothes?
Flier, J. S., & Maratos–Flier, E. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.05.013 · Cited by 160
Selective leptin resistance revisited
Mark, A. L. (2013) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00180.2013 · Cited by 162
Brain Adipocytokine Action and Metabolic Regulation
Ahima, R. S., Qi, Y., Singhal, N. S., Jackson, M. B., & Scherer, P. E. (2006) · Diabetes · doi:10.2337/db06-s018 · Cited by 150
Trevaskis, J. L., Coffey, T. S., Cole, R. L., Lei, C., Wittmer, C., Walsh, B., Weyer, C., Koda, J. E., Baron, A., Parkes, D. G., et al. (2008) · Endocrinology · doi:10.1210/en.2008-0770 · Cited by 151
The role of leptin in glucose homeostasis
Denroche, H. C., Huynh, F. K., & Kieffer, T. J. (2012) · Journal of Diabetes Investigation · doi:10.1111/j.2040-1124.2012.00203.x · Cited by 153
Knuth, N. D., Johannsen, D. L., Tamboli, R. A., Marks–Shulman, P. A., Huizenga, R., Chen, K. Y., Abumrad, N. N., Ravussin, É., & Hall, K. D. (2014) · Obesity · doi:10.1002/oby.20900 · Cited by 150
Weight loss, weight maintenance, and adaptive thermogenesis
Camps, S. G., Verhoef, S. P. M., & Westerterp, K. R. (2013) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.112.050310 · Cited by 148
Pharmacological management of appetite expression in obesity
Halford, J. C. G., Boyland, E. J., Blundell, J. E., Kirkham, T. C., & Harrold, J. A. (2010) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2010.19 · Cited by 142
Energy intake in weight-reduced humans
Rosenbaum, M., Kissileff, H. R., Mayer, L. E. S., Hirsch, J., & Leibel, R. L. (2010) · Brain Research · doi:10.1016/j.brainres.2010.05.062 · Cited by 142
Self-citationIntegration of hormonal and nutrient signals that regulate leptin synthesis and secretion
Lee, M., & Fried, S. K. (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.90927.2008 · Cited by 144
Emerging Therapeutic Strategies for Obesity
Foster‐Schubert, K. E., & Cummings, D. E. (2006) · Endocrine Reviews · doi:10.1210/er.2006-0041 · Cited by 140
Pathophysiology of Resistant Hypertension: The Role of Sympathetic Nervous System
Tsioufis, C. P., Kordalis, A., Flessas, D., Anastasopoulos, I., Tsiachris, D., Papademetriou, V., & Stefanadis, C. (2011) · International Journal of Hypertension · doi:10.4061/2011/642416 · Cited by 140
Metadata
- Authors
- Rosenbaum, M.
- Affiliations
- Columbia University Irving Medical Center (US)
- Corresponding author
- Rosenbaum, M.
- ORCID
- Rosenbaum, M.
- Venue
- Journal of Clinical Investigation
- Published
- 2005-12-01
- Volume
- 115
- Issue
- 12
- Pages
- 3579-3586
- ISSN
- 0021-9738 (ISSN-L)
- PMC
- PMC1297250
- OpenAlex
- W2109742508
- Semantic Scholar
- 126ea46d72a14873cc23d560a0eb4e0c3b639c19
- Cited by
- 575
- References
- 98
- Citations by year
- 2026: 12 · 2025: 18 · 2024: 14 · 2023: 21 · 2022: 14 · 2021: 22 · 2020: 14 · 2019: 27 · 2018: 26 · 2017: 30 · 2016: 34 · 2015: 38 · 2014: 45 · 2013: 32 · 2012: 33
- FWCI
- 9.17
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Clinical Investigation (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Amgen
- National Institutes of Health (DK26687, RR-00645)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30 DK-26687, R01DK064773, DK64773, P30DK026687)
- National Center for Research Resources (RR 00645, M01RR000645)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
- Keywords
- leptin, weight maintenance, weight loss, weight regain, energy expenditure, sympathetic tone, thyroxine, triiodothyronine, neuroendocrine adaptation, leptin deficiency, obesity, liquid formula diet
- MeSH terms
- Adult, Body Composition, Body Weight, Energy Intake, Calorimetry, Diet, Reducing, Energy Metabolism, Female, Humans, Male, Neurosecretory Systems, Obesity, Phenotype, Thyroxine, Time Factors, Triiodothyronine, Weight Loss, Body Mass Index, Muscle, Skeletal, Leptin
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
A language model drew the claims from the paper on 2026-10-09, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-09 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
