Pituitary Disorders and Osteoporosis
Open accessAbstract
Various hormonal disorders can influence bone metabolism and cause secondary osteoporosis. The consequence of this is a significant increase of fracture risk. Among pituitary disorders such effects are observed in patients with Cushing’s disease, hyperprolactinemia, acromegaly, and hypopituitarism. Severe osteoporosis is the result of the coexistence of some of these disorders and hypogonadism at the same time, which is quite often.
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Written from the paper’s full text.
TL;DR
This narrative review examines how pituitary disorders — Cushing's disease, hyperprolactinemia, acromegaly, and hypopituitarism/GH deficiency — cause secondary osteoporosis and increase fracture risk, often through mechanisms beyond bone mineral density (BMD). It emphasizes that fractures frequently occur despite normal or only slightly reduced BMD, so bone quality assessment and early treatment of the underlying disease are central to management.
Key findings
- In Cushing's syndrome, glucocorticoid excess inhibits bone formation and enhances resorption; among 58 pituitary-dependent and 21 adrenal-dependent patients, 82% had osteopenia by WHO criteria, with lower lumbar spine than femoral neck BMD (difference not statistically significant). Vertebral fractures occur in up to 70% of patients with endogenous hypercortisolism, and osteoporosis/atraumatic fractures are more prevalent in adrenal than pituitary Cushing's syndrome.
- In hyperprolactinemia, a study of males found low lumbar spine BMD in 80% of patients versus reduced femoral neck BMD in only 30%; bone loss risk factors were disease duration and hypogonadism. Dopamine agonist therapy (bromocriptine, quinagolide, or cabergoline) over 18 months normalized PRL, osteocalcin, and gonadal function but did not fully restore lumbar spine or femoral neck BMD or normalize Ntx.
- In acromegaly, reported vertebral fracture prevalence varies between 39% and 59%; fractures are more frequent and more severe/multiple in men, and Claessen et al. found vertebral fractures progressed long-term in 20% of patients with biochemically controlled disease despite absence of osteoporosis or osteopenia. Bone turnover is increased, with elevated osteocalcin and resorption markers.
- In hypopituitarism/GHD, a meta-analysis found recombinant human GH significantly increased BMD in randomized/controlled studies longer than 12 months (doses 0.2–0.96 mg/day, higher in women and childhood-onset GHD); Holmer et al. found women with childhood-onset GHD had more than doubled risk for nonosteoporotic fractures, while adult-onset GHD men had significantly decreased fracture incidence.
Methods
- Narrative review of the literature on pituitary disorders and osteoporosis, covering Cushing's disease, hyperprolactinemia, acromegaly, and hypopituitarism/GH deficiency.
- Summarizes mechanisms of hormone effects on bone (Table 1) and their influence on bone turnover, bone density, and fracture risk (Table 2), drawing on cited studies including DXA, trabecular bone score (TBS), quantitative ultrasound, and HR-pQCT.
- No primary data collection or systematic search methodology is described.
Limitations
- Not stated in the paper: the review does not include a limitations section or describe its search strategy, inclusion criteria, or risk of bias.
- Evident from the text: the authors repeatedly note conflicting BMD findings in acromegaly, attributing variation to gonadal status, skeletal site, technique, gender, age, and disease activity, which limits firm conclusions.
- Evident from the text: several cited studies are small (e.g., 58 pituitary-dependent and 21 adrenal-dependent Cushing's patients), and the review relies on heterogeneous observational designs.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
15 of 219 cited sources checked · 10 supported · 0 flagged · accuracy not yet measured
- Premisecitation
Some pituitary diseases can influence bone mineral density and bone turnover, causing osteopenia, osteoporosis, and fractures.
“Some pituitary diseases may influence bone mineral density (BMD) and bone turnover causing osteopenia, osteoporosis, and fractures [2].”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [2] source
- Premisecitation
The trabecular bone score has been introduced as a method of bone quality estimation in glucocorticoid-induced osteoporosis.
“The trabecular bone score (TBS) has been recently introduced as a method of bone quality estimation in GIO [10, 15].”
Quote in the paperSubstantial claim1 of 2 sources checked - Premisecitation
The prevalence of osteoporosis and atraumatic fractures is higher in adrenal Cushing's syndrome than in pituitary Cushing's syndrome.
“The prevalence of osteoporosis and atraumatic fractures is higher in adrenal Cushing's syndrome than in pituitary Cushing's syndrome [11].”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [11] source
- Interpretationcitation
Conflicting data on bone mineral density in acromegaly might be related to gonadal status, different skeletal sites measured, various techniques employed, subject's gender, age, and activity of the disease.
“Conflicting data on bone mineral density might be related to gonadal status, different skeletal sites being measured, various techniques employed, subject's gender, age, and activity of the disease [28, 36, 38].”
Quote in the paperSubstantial claim1 of 3 sources checked- cites [28] source
- cites [36] source
The Abstract and Discussion attribute conflicting BMD findings to differences in gonadal status, disease activity, gender-related stratification, and skeletal site. The Measurements section accounts for patients’ ages and different devices, but the paper does not identify age or measurement techniques as reasons previous studies conflicted. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [38] source
- Premisecitation
In patients with acromegaly, changes in bone size and density and arthropathy are common problems.
“In patients with acromegaly changes in bone size and density and arthropathy are common problems [31–33].”
Quote in the paperNot a substantial claim1 of 3 sources checked- cites [31] source
The Acromegalic Arthropathy section (page not available in our copy) calls arthropathy one of the most frequent complications of acromegaly and reports joint involvement in many patients. It describes cartilage growth and osteophyte formation, but does not establish that changes in bone size and density are common problems. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [32] source
- cites [33] source
- Interpretationreasoning
GH may play a role in the achievement of peak bone mass.
“which may present the potential role of GH in the achievement of peak bone mass [44–49].”
Quote in the paperSubstantial claim1 of 6 sources checked- cites [44] source
- cites [45] source
- cites [46] 1997, Journal of Clinical Endocrinology and Metabolism
Not checked in the free run.
- cites [47] source
The introductory passage says GH affects bone directly and through IGF-I, and the Discussion describes an important role for GH in bone strength (page numbers unavailable). But the study examines bone density in adults with adult-onset GH deficiency; it does not address GH’s role in achieving peak bone mass. (LLM, conf=0.82)
Experimental — accuracy not yet measured - cites [48] source
- cites [49] 1999, The Journal of Clinical Endocrinology and Metabolism
Not checked in the free run.
- Premisecitation
The mechanisms underlying the association between ACTH or TSH deficiency and lower BMD are not clarified.
“The mechanisms underlying the association between either ACTH or TSH deficiency and lower BMD are not clarified”
Quote in the paperNot a substantial claim1 of 3 sources checked - Premisecitation
BMD in patients with hypopituitarism and untreated GHD might be affected by age at onset, gender, body mass index, gonadal status, and severity of GHD.
“According to the literature BMD might be affected by many factors such as age at onset, gender, body mass index, gonadal status, and the severity of growth hormone deficiency [47, 49, 51].”
Quote in the paperNot a substantial claim1 of 3 sources checked - Premisecitation
In patients with childhood onset GHD, there is a clear reduction in BMD.
“In patients with childhood onset (CO) GHD there seems to be a clear reduction in BMD, which may present the potential role of GH in the achievement of peak bone mass [44–49].”
Quote in the paperSubstantial claim1 of 6 sources checked- cites [44] source
- cites [45] source
- cites [46] 1997, Journal of Clinical Endocrinology and Metabolism
Not checked in the free run.
- cites [47] source
The paper states that GHD is associated with low BMD (opening background passage, labeled Abstract in our copy). But its study population comprised adults with adult-onset GHD (Abstract; Results), so it does not establish a clear BMD reduction specifically in patients with childhood-onset GHD. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [48] source
- cites [49] 1999, The Journal of Clinical Endocrinology and Metabolism
Not checked in the free run.
- Premisecitation
Pituitary hormone deficiencies causing hypogonadism, hypothyroidism, or hypoadrenalism may contribute to bone loss.
“Pituitary hormone deficiencies causing hypogonadism, hypothyroidism, or hypoadrenalism may also contribute to bone loss.”
Quote in the paperSubstantial claim1 of 3 sources checked - Premisecitation
GH replacement therapy may reduce the risk of fracture in patients with hypopituitarism and GHD.
“Some studies suggest that GH replacement therapy may reduce the risk of fracture in patients with hypopituitarism and GHD [51, 59].”
Quote in the paperNot a substantial claim1 of 2 sources checked - Premisecitation
Hypercorticism affects bone metabolism through a variety of mechanisms.
“Hypercorticism affects bone metabolism in a variety of mechanisms [3].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [3] source
- Premisecitation
Glucocorticoids inhibit bone formation directly and indirectly by regulating the synthesis of factors present in the bone microenvironment.
“The most significant influences of glucocorticoids (GCs) are their inhibitory effects on bone formation, acting directly and indirectly by regulating the synthesis of factors present in the bone microenvironment [4].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [4] source
- Premisecitation
Glucocorticoids inhibit synthesis of type I collagen, decreasing bone matrix available for mineralization.
“GCs also exert effects on their function by inhibiting the synthesis of type I collagen, the major component of bone extracellular matrix, with a consequent decrease in bone matrix available for mineralization.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [4] source
- Premisecitation
In males and females with Cushing's syndrome, there was a positive correlation between age and Z-score at both the lumbar spine and the femoral neck.
“In males as well as in females, there was positive correlation between age and Z-score at both the lumbar spine and the femoral neck [7].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [7] 2007, Netherlands Journal of Medicine
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Patients with subclinical hypercortisolism showed higher fracture incidence despite stable BMD throughout observation.
“Patients with SH showed higher fracture incidence in spite of stable BMD throughout the observation [13].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [13] source
- Premisecitation
Glucocorticoids prolong the life span of mature osteoclasts directly or through increased expression of macrophage colony-stimulating factor.
“GCs prolong the life span of mature osteoclasts by acting directly or through the increased expression of macrophage colony-stimulating factor (M-CSF) [3].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [3] source
- Premisecitation
In a study of 58 patients with pituitary-dependent and 21 patients with adrenal-dependent Cushing's syndrome, mean BMD before treatment was low.
“A study on 58 patients with pituitary-dependent and 21 patients with adrenal-dependent Cushing's syndrome showed low mean BMD before treatment.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [7] 2007, Netherlands Journal of Medicine
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
In endogenous or exogenous hypercortisolism, bone loss is more severe in trabecular bone than in cortical bone.
“In patients with endogenous or exogenous hypercortisolism bone loss is more severe in trabecular bone than in cortical bone.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [7] 2007, Netherlands Journal of Medicine
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
In both endogenous and exogenous hypercortisolism, fractures may be asymptomatic and occur in patients with normal or only slightly decreased BMD values.
“In both endogenous and exogenous hypercortisolism fractures might be asymptomatic and occur in patients with normal or only slightly decreased BMD values [3, 10, 12].”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation
Treatment of growth hormone deficiency protects the skeleton from the adverse effects of glucocorticoid overtreatment in hypopituitary patients.
“It seems that treatment of GHD protects the skeleton from the adverse effects of glucocorticoid overtreatment in hypopituitary patients [3, 17].”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
In patients with endogenous Cushing's syndrome, fractures occur most commonly at the thoracic and lumbar vertebrae, hip, ribs, and pelvis, often spontaneously or after low-energy trauma.
“In patients with endogenous Cushing's syndrome fractures occur most commonly at the thoracic and lumbar vertebrae, hip, ribs, and pelvis, not infrequently developing spontaneously or after low-energy trauma [10].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [10] 2013, Clinical Endocrinology source
- Premiseown data
The prevalence of osteopenia and osteoporosis in Cushing's syndrome was independent of age.
“Interestingly, the prevalence of osteopenia and osteoporosis was independent of age.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [7] 2007, Netherlands Journal of Medicine
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Patients with low BMD and low TBS are more likely to present fractures than patients with low BMD and high TBS.
“The patients with low BMD and low TBS will present fractures more likely than patients with low BMD and high TBS [16].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [16] source
- Premisecitation
The effects of estrogen deficiency on bone include an acceleration of bone turnover with higher resorption than formation.
“The effects of estrogen deficiency on bone include an acceleration of bone turnover with higher resorption than formation [19].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [19] 1999, The Journal of Clinical Endocrinology and Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationcitation
Factors other than BMD, such as bone quality, are associated with increased risk of fracture.
“This suggests that factors other than BMD, such as bone quality, are associated with increased risk of fracture [7, 13].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [7] 2007, Netherlands Journal of Medicine
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [13] source
- Premisecitation
Catabolic effects of glucocorticoids on muscle could contribute to fracture risk because muscle weakness increases the incidence of falls.
“The catabolic effects of GCs on muscle could contribute to the fracture risk because muscle weakness increases the incidence of falls.”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
Administration of alendronate or clodronate provides faster BMD recovery in comparison with untreated patients.
“Administration of alendronate or clodronate provides faster BMD recovery in comparison with untreated patients [3].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [3] source
- Premisecitation
According to WHO criteria, 82% of patients in that Cushing's syndrome study were diagnosed with osteopenia.
“According to World Health Organization (WHO) criteria 82% patients were diagnosed with osteopenia.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [7] 2007, Netherlands Journal of Medicine
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
The presence of subclinical hypercortisolism was related to worsening of spinal deformity index and occurrence of a new vertebral fracture or progression of a preexisting vertebral deformity, regardless of age, gender, BMI, years since menopause, lumbar spine BMD, and basal SDI.
“The presence of SH was related with worsening of SDI and occurrence of a new vertebral fracture or the progression of the grade of a preexisting vertebral deformity regardless of age, gender, BMI, years since menopause, lumbar spine BMD, and basal SDI.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [13] source
- Premisecitation
Higher prevalence of radiological vertebral fractures occurs in women and men with PRL-secreting adenomas compared to controls.
“Mazziotti et al. have shown that higher prevalence of radiological vertebral fractures (VFs) occurs in women and men with PRL-secreting adenomas compared to controls [18, 24].”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
Patients with a longer duration of hypogonadism are likely to have lower bone density.
“In addition, patients with a longer duration of hypogonadism are likely to have lower bone density [19, 22].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [19] 1999, The Journal of Clinical Endocrinology and Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [22] source
- Premisecitation
Fractures were more frequent in patients with untreated hyperprolactinemia in comparison with patients treated with cabergoline.
“Fractures were more frequent in patients with untreated hyperprolactinemia in comparison with patients treated with cabergoline [18, 24].”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
Untreated prolactinomas are associated with a significant increase in fracture risk attributed to gonadotropins and sex steroids deficiency or hyperprolactinemia per se.
“Untreated prolactinomas were associated with a significant increase in fracture risk attributed to gonadotropins and sex steroids deficiency or hyperprolactinemia per se [17].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [17] source
- Premisecitation
In female patients, prevalence of vertebral fractures was associated with duration of disease independently of hypopituitarism, age, BMD, serum PRL levels, and treatment with dopaminergic drugs.
“In female patients prevalence of VFs was associated with the duration of the disease independently of the effects of hypopituitarism, age, BMD, serum PRL levels, and treatment with dopaminergic drugs [24].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [24] source
- Premisecitation
Hypogonadal patients with acromegaly are at higher risk of osteoporosis, particularly at sites composed predominantly of trabecular bone.
“Hypogonadal patients with acromegaly are at higher risk of osteoporosis, particularly at sites composed predominantly of trabecular bone, which has more intimate contact with the circulation and is influenced by sex steroids to a greater extent [34, 39, 40].”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
Patients who developed hyperprolactinemia in childhood or adolescence have more severe bone impairment than subjects who developed hyperprolactinemia in adulthood.
“Patients who developed hyperprolactinemia in childhood or adolescence have more severe bone impairment than subjects who developed hyperprolactinemia in adulthood [20, 22].”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
Acromegaly is known to be a secondary cause of osteoporosis.
“Acromegaly is known to be a secondary cause of osteoporosis [27].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [27] 2011, Clinical Cases in Mineral and Bone Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
In men with prolactinoma, the absence of detectable levels of estradiol is correlated with lower BMD in all analyzed sites.
“In men with prolactinoma the absence of detectable levels of estradiol was correlated with lower BMD in all analyzed sites.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [22] source
- Premisecitation
Hypogonadism occurs frequently in patients with acromegaly as a consequence of PRL and GH hypersecretion or hypopituitarism due to local mass effects.
“Hypogonadism occurs frequently in patients with acromegaly as a consequence of PRL and GH hypersecretion or hypopituitarism due to local mass effects [25].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [25] source
- Premisecitation
History of amenorrhea may be a cause of increased fracture risk despite resumption of menses.
“History of amenorrhea may be a cause of an increased fracture risk despite resumption of menses [19].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [19] 1999, The Journal of Clinical Endocrinology and Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
DXA and QUS methods are not sufficient for identifying patients at risk for fracture, due to possible interferences including bone deformities, osteoarthritis, joint rigidity, and soft tissue thickening.
“However, DXA and QUS methods are not sufficient for identifying patients at risk for fracture, due to the many possible interferences including bone deformities, osteoarthritis, joint rigidity, and soft tissue thickening [26, 27].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [26] source
- cites [27] 2011, Clinical Cases in Mineral and Bone Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Osteocalcin, a specific marker of bone formation, is elevated in subjects with active acromegaly.
“A specific marker of bone formation, osteocalcin, is elevated in subjects with active disease [28, 29, 35, 40, 43].”
Quote in the paperNot a substantial claim0 of 5 sources checked - Premisecitation
Vertebral fractures tend to progress in the long term in 20% of patients with biochemically controlled acromegaly in the absence of osteoporosis or osteopenia.
“Claessen et al. showed that VFs tend to progress in the long term in 20% of patients with biochemically controlled acromegaly in the absence of osteoporosis or osteopenia.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Claessen et al.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
In patients with acromegaly, bone turnover is increased.
“It is well known that in patients with acromegaly bone turnover is increased [28, 29, 35].”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation
Serum calcium and phosphate values and 24-hour urinary calcium are elevated in patients with active acromegaly.
“Additionally, serum calcium and phosphate values and 24-hour urinary calcium are elevated in patients with active disease [27, 29, 34, 35, 41].”
Quote in the paperNot a substantial claim0 of 5 sources checked- cites [27] 2011, Clinical Cases in Mineral and Bone Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [29] 1993, Journal of Clinical Endocrinology and Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [34] source
- cites [35] 1993, Journal of Bone and Mineral Research source
- cites [41] source
- Interpretationreasoning
BMD is a poor predictor of vertebral fractures in acromegaly.
“which makes BMD a poor fracture predictor [27, 30, 39, 42].”
Quote in the paperSubstantial claim0 of 4 sources checked - Premisecitation
Fractures occur more frequently in men than women in acromegaly.
“Fractures occur more frequently in men than women.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [27] 2011, Clinical Cases in Mineral and Bone Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [42] source
- Premisecitation
Impaired gonadal status including hypogonadism and hyperprolactinemia is thought to be a cause of BMD decline in acromegaly.
“Impaired gonadal status including hypogonadism and hyperprolactinemia is thought to be a cause of BMD decline [28, 34].”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
The reported prevalence of vertebral fractures in acromegaly varies between 39% and 59%.
“The reported prevalence of VFs varies between 39% and 59% [27, 42].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [27] 2011, Clinical Cases in Mineral and Bone Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [42] source
- Premisecitation
Bone quality depends not only on bone density and bone turnover but also on collagen integrity and the macrostructure and microstructure of bone.
“Bone quality depends not only on bone density and bone turnover but also on collagen integrity and the macrostructure and microstructure of bone [26].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [26] source
- Premisecitation
Indicators of bone resorption such as urinary hydroxyproline/creatinine, urinary type I collagen cross-linked N-telopeptide, and serum C-terminal collagen type I cross-links are in higher concentrations in acromegaly than in controls.
“Indicators of bone resorption such as urinary hydroxyproline/creatinine, urinary type I collagen cross-linked N-telopeptide, and serum C-terminal collagen type I cross-links are in higher concentrations than in controls [28, 29, 35, 40, 43].”
Quote in the paperNot a substantial claim0 of 5 sources checked - Premisecitation
In a prospective study, the incidence of vertebral fractures was significantly higher in patients with active acromegaly compared with those who had controlled or cured acromegaly at the beginning of the study.
“In a prospective study the incidence of VFs was significantly higher in patients with active disease as compared with those who had controlled/cured acromegaly at the beginning of the study [38].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [38] source
- Premisecitation
Vertebral fractures may be present in patients with normal or slightly decreased BMD.
“Vertebral fractures may be present in patients with normal or slightly decreased BMD, which makes BMD a poor fracture predictor [27, 30, 39, 42].”
Quote in the paperSubstantial claim0 of 4 sources checked - Premisecitation
Administration of recombinant human growth hormone (rhGH) resulted in a significant increase in BMD in randomized/controlled studies of more than 12 months.
“Recent meta-analysis revealed that administration of recombinant human growth hormone (rhGH) resulted in a significant increase in BMD in randomized/controlled studies of more than 12 months.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [57] source
- Premisecitation
In adult onset GHD men on complete hormone replacement therapy, a significantly decreased incidence of fractures was observed.
“In contrast, a significantly decreased incidence of fractures was observed in AO GHD men.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [44] source
- Premisecitation
Women with childhood onset GHD on complete hormone replacement therapy had more than doubled risk for nonosteoporotic fractures.
“They demonstrated that women with CO GHD had more than doubled risk for nonosteoporotic fractures.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [44] source
- Premisecitation
In hypopituitary adult males with untreated GH deficiency, vertebral fractures occurred more frequently in patients who received higher cumulative and current doses of cortisone than in patients who received lower doses.
“In hypopituitary adult males with untreated GH deficiency vertebral fractures occurred more frequently in patients who received higher cumulative and current doses of cortisone than in patients who received lower doses [54].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [54] source
- Interpretationcitation
There is a direct relation between GHD and decreased bone mass in hypopituitarism.
“A direct relation between GHD and decreased bone mass in hypopituitarism is supported by the fact that GH replacement therapy improves BMD values [51, 52].”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
GH replacement promotes bone turnover by stimulating both bone formation and bone resorption, which is prominent during the first phase of GH treatment.
“GH replacement promotes bone turnover by stimulating both bone formation and bone resorption, which is prominent during the first phase of GH treatment.”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
GHD itself is crucial for the development of osteopenia in hypopituitary patients.
“Studies have shown that GHD itself is crucial for the development of osteopenia in hypopituitary patients [44, 49, 51].”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
During rhGH treatment, BMD decreases within the first months and then increases after at least one year of therapy.
“BMD within the first months of treatment decreased which was followed by a subsequent increase after at least one year of therapy.”
Quote in the paperNot a substantial claim0 of 3 sources checked - Interpretationcitation
The increased fracture risk in adult onset GHD females is explained by a reduced percentage of properly treated females with hypogonadism compared to men.
“This was explained by a reduced percentage of properly treated females with hypogonadism compared to men [56].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [56] source
- Interpretationcitation
Fracture rate is rather attributable to GHD alone than other pituitary hormone deficiencies or their replacement therapy.
“Studies suggest that fracture rate is rather attributable to GHD alone than other pituitary hormone deficiencies or their replacement therapy [51].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [51] source
- Interpretationreasoning
Hypopituitarism might also be a cause of bone loss due to deficiencies of several pituitary hormones, especially growth hormone or excessive replacement therapy.
“Hypopituitarism might also be a cause of bone loss due to deficiencies of several pituitary hormones, especially growth hormone or excessive replacement therapy.”
Quote in the paperNot a substantial claim
- May combine two claims. 48
- Classified as probably not a substantial claim. 2
- The quote only partly states this claim. 1
May combine two claims.
PremisecitationInformation about the influence of GH excess on BMD varies in the literature: in some studies BMD was increased or within reference ranges, while in other papers it was decreased.
“Information about the influence of GH excess on BMD varies in the literature. In some studies BMD was reported to be increased or within the reference ranges, while in other papers it was decreased [17, 26, 34–37].”
Quote in the paperNot a substantial claim1 of 6 sources checkedMay combine two claims.
PremisecitationPatients with isolated GH deficiency and with multiple pituitary deficiencies usually have low BMD.
“Patients with isolated GH deficiency (GHD) and with multiple pituitary deficiencies usually have low BMD.”
Quote in the paperSubstantial claim1 of 6 sources checked- cites [44] source
- cites [45] source
- cites [46] 1997, Journal of Clinical Endocrinology and Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [47] source
The Abstract (page unavailable) says GHD is associated with low BMD, and the Discussion (page unavailable) identifies additional pituitary hormone deficiencies as possible predictors of lower BMD. The passages do not establish that patients in both the isolated-GHD and multiple-deficiency groups usually have low BMD; in particular, they provide no prevalence for either group. (LLM, conf=0.82)
Experimental — accuracy not yet measured - cites [48] source
- cites [49] 1999, The Journal of Clinical Endocrinology and Metabolism
Not checked in the free run.
May combine two claims.
PremisecitationScillitani et al. reported that the anabolic effect of GH excess on bone in acromegalic patients is gender independent, evident only at the spine in eugonadal patients regardless of disease activity, and present only at the femoral neck during active disease regardless of gonadal status.
“Scillitani et al. reported that the anabolic effect of GH excess on bone in acromegalic patients is gender independent, evident only at the spine in eugonadal patients regardless of disease activity and present only at femoral neck during active disease regardless of gonadal status [36].”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [36] source
May combine two claims.
InterpretationcitationThe association between ACTH or TSH deficiency and lower BMD might be a consequence of either deficiencies of pituitary hormones or excessive hormone replacement.
“might be a consequence of either deficiencies of pituitary hormones or excessive hormone replacement [47, 53, 54].”
Quote in the paperNot a substantial claim1 of 3 sources checkedMay combine two claims.
PremisecitationGlucocorticoids reduce replication and prevent terminal differentiation of bone-forming cells and promote apoptosis of osteoblasts and osteocytes by activating caspase 3.
“GCs reduce replication and prevent the terminal differentiation of bone forming cells and additionally promote apoptosis of osteoblasts and osteocytes by activating caspase 3.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [4] source
May combine two claims.
PremisecitationGlucocorticoid-induced osteoporosis occurs in two phases: a rapid early phase in which BMD is reduced by bone resorption, followed by a slower progressive phase in which BMD declines because of impaired bone formation.
“GIO occurs in two phases, a rapid early phase in which BMD is reduced as a result of bone resorption, followed by a slower, progressive phase in which BMD declines because of impaired bone formation [3].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [3] source
May combine two claims.
PremisecitationPatients with Cushing's syndrome may have lower BMD and increased osteoporotic fracture risk.
“It is well known that patients with Cushing's syndrome may have lower BMD and increased osteoporotic fracture risk [6, 7, 9].”
Quote in the paperSubstantial claim0 of 3 sources checkedMay combine two claims.
PremisecitationType of Cushing's syndrome, mean 24-hour serum cortisol level, and duration of symptomatic glucocorticoid overproduction had no influence on Z-scores.
“Factors such as type of Cushing's syndrome, mean 24-hour serum level of cortisol, and duration of symptomatic glucocorticoid overproduction had no influence on Z-scores.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [7] 2007, Netherlands Journal of Medicine
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationFactors associated with fracture risk in Cushing's syndrome include age at onset, span and severity of disease, and individual susceptibility to glucocorticoids.
“Factors associated with fracture risk include age at the onset, span and severity of the disease, and individual susceptibility to GCs [3].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [3] source
May combine two claims.
PremisecitationDXA is considered a gold-standard measurement of BMD, but it cannot assess bone microarchitecture, the most important factor in determining bone quality.
“Although dual-energy X-ray absorptiometry (DXA) is considered a gold-standard measurement of BMD, it cannot be employed to assess bone microarchitecture, the most important factor in determining bone quality [10, 14].”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationIn adrenal incidentaloma patients with subclinical hypercortisolism, TBS is reduced and correlates with the number and severity of vertebral fractures and with the degree of cortisol excess.
“Eller-Vainicher et al. showed that, in AI patients with subclinical hypercortisolism, TBS is reduced and correlates with the number and severity of vertebral fractures and with the degree of cortisol excess [16].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [16] source
May combine two claims.
PremisecitationIn adrenal incidentaloma patients, BMD was comparable between subjects with and without subclinical hypercortisolism, but the prevalence of vertebral fracture and spinal deformity index were significantly higher in those with subclinical hypercortisolism.
“BMD in subjects with and without SH was comparable; however the prevalence of vertebral fracture and spinal deformity index (SDI) were significantly higher in SH subjects than in the group of patients without SH.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [13] source
May combine two claims.
PremisecitationBMI and menstrual status did not show a correlation with Z-score in patients with Cushing's syndrome.
“Body mass index (BMI) and menstrual status did not show a correlation with Z-score.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [7] 2007, Netherlands Journal of Medicine
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationThere was no significant difference in BMD between patients with Cushing's syndrome of different origins, neither in the whole group nor in male or female patients separately.
“There was no significant difference in BMD between patients with Cushing's syndrome of different origins, neither in the whole group nor in male or female patients separately.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [7] 2007, Netherlands Journal of Medicine
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationIn that study, BMD values were lower in the lumbar spine than in the femoral neck, although the difference was not statistically significant.
“BMD values were lower in the lumbar spine than in the femoral neck, although the difference was not statistically significant.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [7] 2007, Netherlands Journal of Medicine
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationSubclinical hypercortisolism might cause osteoporosis and increased risk of vertebral fractures.
“It is thought that even subclinical hypercortisolism (SH) might be the cause of osteoporosis and increased risk of vertebral fractures [3, 13].”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationIn functional GnRH deficiency, the pattern of GnRH secretion is altered, involving reduced frequency of pulsations and decreased pulse amplitude.
“In cases of functional GnRH deficiency the pattern of GnRH secretion is altered, involving reduced frequency of pulsations and decreased pulse amplitude [4, 5].”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationHyperprolactinemia causes secondary hypogonadism and may have sex hormone-independent effects on bone metabolism.
“Hyperprolactinemia causes secondary hypogonadism and may have sex hormone-independent effects on bone metabolism [17, 18].”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationEndogenous hypercortisolism changes bone structure and causes vertebral fractures in up to 70% of patients.
“Endogenous hypercortisolism changes bone structure and causes vertebral fractures in up to 70% of patients.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [3] source
May combine two claims.
PremisecitationGlucocorticoids indirectly decrease production of insulin-like growth factors and shift transforming growth factor-beta binding.
“Indirect actions of GCs involve decreased production of insulin-like growth factors (IGFs) and shifting transforming growth factor-β (TGF-β) binding [4, 5].”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationGlucocorticoids decrease release of growth hormone and gonadotropins, which may play a role in bone turnover.
“In addition, GCs decrease the release of growth hormone and gonadotropins which may also play a role in bone turnover [7].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [7] 2007, Netherlands Journal of Medicine
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationNormal or increased bone mass in acromegaly is attributable to the anabolic effect of GH, although BMD measurements may be overestimated due to structural modification of the spine.
“Normal or increased bone mass is attributable to anabolic effect of GH, although BMD measurements may be overestimated due to structural modification of the spine [27].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [27] 2011, Clinical Cases in Mineral and Bone Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationDopamine agonist therapy restores gonadal function and increases vertebral BMD in most hyperprolactinemic women.
“Dopamine agonist therapy restores gonadal function and increases vertebral BMD in most hyperprolactinemic women [19, 20].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [19] 1999, The Journal of Clinical Endocrinology and Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [20] source
May combine two claims.
PremisecitationPatients with prolactinomas present with osteopenia or osteoporosis, and the risk factors for bone loss are disease duration and hypogonadism.
“Authors reported that the patients with prolactinomas also presented with osteopenia or osteoporosis and the risk factors of bone loss were disease duration and hypogonadism [21].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [21] source
May combine two claims.
PremisecitationAcromegaly is characterized by excessive growth hormone secretion and in most cases is caused by a somatotroph tumor of the pituitary gland.
“Acromegaly is characterized by growth hormone (GH) excessive secretion and in most cases is caused by the presence of a somatotroph tumor of the pituitary gland [25, 26].”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationAfter 6, 12, and 18 months of treatment, serum osteocalcin levels significantly increased and Ntx levels significantly decreased in the three groups of patients.
“A progressive significant increase in serum OC levels and a significant decrease in Ntx levels were noted after 6, 12, and 18 months of treatment in the 3 groups of patients.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [20] source
May combine two claims.
Premisecitation18-month treatment with bromocriptine, quinagolide, or cabergoline normalized serum PRL and osteocalcin levels and gonadal function, although it was unable to completely restore lumbar spine and femoral neck BMD and normalize Ntx levels.
“18-month treatment with one of the dopamine agonists (bromocriptine, quinagolide, or cabergoline) normalized serum PRL and OC levels and gonadal function, although it was unable to completely restore lumbar spine and femoral neck BMD and normalize Ntx levels [20].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [20] source
May combine two claims.
PremisecitationIncrease in bone resorption and low BMD occur in males and females with hyperprolactinemia.
“Increase in bone resorption and low BMD occur in males and females with hyperprolactinemia [18, 20–23].”
Quote in the paperSubstantial claim0 of 5 sources checkedMay combine two claims.
PremisecitationLumbar spine and femoral neck BMD values are negatively correlated with prolactin levels and disease duration in hyperprolactinemia.
“A significant negative correlation was found between lumbar spine and femoral neck BMD values and both prolactin (PRL) levels and disease duration, which suggests that the duration of the disease is strongly correlated with the severity of bone loss [20, 22].”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
PremisecitationIn the prepubertal period, the anabolic action of GH is responsible for longitudinal bone growth; during adolescence and early adulthood it induces skeletal maturation until peak bone mass is achieved; in adulthood GH regulates bone turnover, maintaining bone mass.
“In prepubertal period anabolic action of GH is responsible for longitudinal bone growth, whereas during the adolescence and early adulthood it induces skeletal maturation until the achievement of peak bone mass. In adulthood GH regulates bone turnover, thus maintaining bone mass [27].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [27] 2011, Clinical Cases in Mineral and Bone Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationIn hyperprolactinemic males, low BMD at the lumbar spine was found in 80% of patients, whereas only 30% had reduced BMD at the femoral neck; a similar finding was reported in women.
“A study on hyperprolactinemic males showed low BMD at the lumbar spine in 80% of patients, whereas only 30% subjects had a reduced BMD at the femoral neck. Similar finding was reported in women [20].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [20] source
May combine two claims.
PremisecitationGH and IGF-1 stimulate proliferation, differentiation, and extracellular matrix production in osteoblastic cells, and also promote osteoclast recruitment and bone resorption activity.
“GH and its main peripheral mediator insulin-like growth factor-1 (IGF-1) stimulate proliferation, differentiation, and extracellular matrix production in osteoblastic cells. GH and IGF-1 also promote osteoclast recruitment and bone resorption activity [27–30].”
Quote in the paperSubstantial claim0 of 4 sources checkedMay combine two claims.
PremisecitationMales with prolactinomas who suffered fractures had lower BMD T-score and longer duration of disease, independently of age, serum IGF-1 and PRL values, frequency of macroadenomas, adrenal insufficiency, hypothyroidism, diabetes insipidus, parental history of fractures, cigarette smoking, and excessive alcohol consumption.
“Males with prolactinomas who suffered fractures had lower BMD T-score and longer duration of the disease, independently of the effects of age, serum IGF-1 and PRL values, frequency of macroadenomas, adrenal insufficiency, hypothyroidism, diabetes insipidus, parental history of fractures, cigarette smoking, and excessive alcohol consumption [18].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [18] source
May combine two claims.
PremisecitationIn one study, all patients had significantly lower osteocalcin levels and significantly higher urinary Ntx levels, but BMD values were in normal ranges in 20% of the patients.
“In one study, in all patients, osteocalcin (OC) levels were significantly lower and urinary cross-linked N-telopeptide of type I collagen (Ntx) levels were significantly higher; however BMD values were in normal ranges in 20% of the patients [20].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [20] source
May combine two claims.
PremisecitationPatients with acromegaly generally demonstrate increased cortical bone mass, whereas trabecular BMD is more variable.
“Patients with acromegaly generally demonstrate increased cortical bone mass, whereas trabecular BMD is more variable [23, 35, 41, 42].”
Quote in the paperNot a substantial claim0 of 4 sources checkedMay combine two claims.
PremisecitationFractures are more severe and often multiple in men with acromegaly.
“They are also more severe and often multiple in men [27, 42].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [27] 2011, Clinical Cases in Mineral and Bone Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [42] source
May combine two claims.
InterpretationcitationThe rise in serum calcium levels in active acromegaly may be caused by increased intestinal calcium absorption, while high serum phosphate levels may be due to GH-mediated increased intestinal and renal absorption.
“Rise in serum calcium levels may be caused by increased intestinal calcium absorption, while high serum phosphate levels may be due to GH-mediated increased intestinal and renal absorption [27].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [27] 2011, Clinical Cases in Mineral and Bone Metabolism
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationPatients with acromegaly have an increased risk of fractures, which might be correlated with insufficient quality of bone.
“Patients with acromegaly have an increased risk of fractures, which might be correlated with insufficient quality of bone [26, 27, 39, 42].”
Quote in the paperSubstantial claim0 of 4 sources checkedMay combine two claims.
InterpretationcitationAbnormal bone quality persists after remission in biochemically controlled acromegaly, possibly due to pretreatment long-term exposure to high circulating levels of GH.
“This is suggestive of an abnormal bone quality persisting after remission, possibly due to pretreatment long-term exposure to high circulating levels of GH [30].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [30] source
May combine two claims.
PremisecitationIn one study, forearm and vertebral BMD values changed in opposite directions; forearm BMD was increased because of GH and IGF-1 action and vertebral BMD was low due to hypogonadism.
“In one study, forearm and vertebral BMD values changed in opposite directions. It seems that forearm BMD was increased because of GH and IGF-1 action and vertebral BMD was low due to hypogonadism [41].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [41] source
May combine two claims.
PremisecitationThe axial skeleton is composed of 70% trabecular bone, while the appendicular skeleton is composed of 90% cortical bone.
“Axial skeleton is composed of 70% trabecular bone, while appendicular skeleton of 90% cortical bone [40].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [40] source
May combine two claims.
PremisecitationAfter the first phase of GH treatment, bone turnover slows down and bone mass increases.
“After this period bone turnover slows down and bone mass increases [48, 57, 58].”
Quote in the paperSubstantial claim0 of 3 sources checkedMay combine two claims.
PremisecitationIn a nationwide study of patients with GHD, the risk of fracture was significantly increased in adult onset GHD females, but not in males.
“In one nationwide study of patients suffering from GHD the risk of fracture was significantly increased in adult onset (AO) GHD females, but not in males.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [56] source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationThe doses of rhGH used in studies varied from 0.2 to 0.96 mg/daily, with higher doses prescribed to women and patients with CO GHD.
“The doses used in studies varied from 0.2 to 0.96 mg/daily with higher doses prescribed to women and patients with CO GHD [57].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [57] source
May combine two claims.
PremisecitationThe beneficial effect of rhGH replacement therapy on BMD is affected by gender, age, and treatment duration.
“This beneficial effect of rhGH replacement therapy is affected by gender, age, and treatment duration.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [57] source
May combine two claims.
InterpretationcitationThe findings on fracture incidence in GHD patients on complete hormone replacement therapy are justified by the interaction between oral estrogen and the GH-IGF-1 axis in women and by the adequate substitution of testosterone and GH in men.
“These findings were justified by the interaction between oral estrogen and the GH-IGF-1 axis in women and by the adequate substitution of testosterone and GH in men [44].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [44] source
May combine two claims.
PremisecitationGHD and hypopituitarism are associated with increased fracture risk.
“It has been reported that GHD and hypopituitarism are associated with increased fracture risk [17, 44, 51, 55].”
Quote in the paperSubstantial claim0 of 4 sources checkedThe quote only partly states this claim.
PremisecitationSimilar outcomes (significant increase in BMD) were observed in prospective studies of rhGH administration.
“Similar outcomes were observed in prospective studies.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [57] source
Probably not a substantial claim: may not pass S4 (based). May combine two claims.
Interpretationnone givenSecondary osteoporosis and fragility fractures can be a result of Cushing's syndrome, hyperprolactinemia, acromegaly, and reduced production of sex steroids (hypogonadism).
“Secondary osteoporosis and fragility fractures can be a result of Cushing's syndrome, hyperprolactinemia, acromegaly, and reduced production of sex steroids (hypogonadism).”
Quote in the paperNot a substantial claim
The paper relies on this without support.
The final bone effects of pituitary-dependent and adrenal-dependent Cushing's syndrome are caused by hypercorticism.
“In current review we discuss both pituitary-dependent Cushing's syndrome (Cushing's disease) and adrenal-dependent Cushing's syndrome, since the final bone effects of both are caused by hypercorticism.”
The paper relies on this without support.
Glucocorticoid-induced osteoporosis is the most common cause of secondary osteoporosis.
“Glucocorticoid-induced osteoporosis (GIO) is the most common cause of secondary osteoporosis.”
The paper relies on this without support.
Vertebral fractures are often asymptomatic and are largely underdiagnosed.
“VFs are often asymptomatic and are largely underdiagnosed.”
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Tóth, M., & Grossman, A. (2013) · Clinical Endocrinology · doi:10.1111/cen.12189 · Cited by 81 · see citing works
Osteoporosis Is More Prevalent in Adrenal than in Pituitary Cushing's Syndrome.
OHMORI, N., NOMURA, K., OHMORI, K., KATO, Y., ITOH, T., & TAKANO, K. (2003) · Endocrine Journal · doi:10.1507/endocrj.50.1 · Cited by 81 · see citing works
Osteopenia occurs in a minority of patients with acromegaly and is predominant in the spine
Kayath, M. J., & Vieira, J. G. H. (1997) · Osteoporosis International · doi:10.1007/bf01622293 · Cited by 75 · see citing works
Bolanowski, M., Daroszewski, J., Mędraś, M., & Zadrożna-Śliwka, B. (2005) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-005-0649-9 · Cited by 74 · see citing works
Self-citationSkeletal Diseases in Cushing’s Syndrome: Osteoporosis versus Arthropathy
Kaltsas, G., & Makras, P. (2010) · Neuroendocrinology · doi:10.1159/000314298 · Cited by 71 · see citing works
Ueland, T., Fougner, S. L., Godang, K., Schreiner, T., & Bollerslev, J. (2006) · European Journal of Endocrinology · doi:10.1530/eje.1.02285 · Cited by 69 · see citing works
Mazziotti, G., Porcelli, T., Bianchi, A., Cimino, V, Patelli, I., Mejia, C., Fusco, A., Giampietro, A., De Marinis, L., & Giustina, A. (2010) · European Journal of Endocrinology · doi:10.1530/eje-10-0125 · Cited by 68 · see citing works
Fracture Incidence in GH-Deficient Patients on Complete Hormone Replacement Including GH
Holmer, H., Svensson, J., Rylander, L., Johannsson, G., Rosén, T., Bengtsson, B.-Å., Thorén, M., Höybye, C., Degerblad, M., Bramnert, M., et al. (2007) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.070811 · Cited by 66 · see citing works
Bone mineral density in acromegaly: the effect of gender, disease activity and gonadal status
Scillitani, A., Battista, C., Chiodini, I., Carnevale, V., Fusilli, S., Ciccarelli, E., Terzolo, M., Oppizzi, G., Arosio, M., Gasperi, M., et al. (2003) · Clinical Endocrinology · doi:10.1046/j.1365-2265.2003.01777.x · Cited by 63 · see citing works
Treatment of skeletal impairment in patients with endogenous hypercortisolism: when and how?
On behalf of ABC Group, Scillitani, A., Mazziotti, G., Di Somma, C., Moretti, S., Stigliano, A., Pivonello, R., Giustina, A., & Colao, A. (2014) · Osteoporosis International · doi:10.1007/s00198-013-2588-y · Cited by 62 · see citing works
Prevalence of osteopenia in men with prolactinoma
Naliato, E. C. O., Farias, M. L. F., Braucks, G. R., Costa, F. S. R., Zylberberg, D., & Violante, A. H. D. (2005) · Journal of Endocrinological Investigation · doi:10.1007/bf03345523 · Cited by 62 · see citing works
Prevalence of osteoporosis and vertebral fractures in acromegalic patients.
Padova, G., Borzì, G., Incorvaia, L., Siciliano, G., Migliorino, V., Vetri, M. G., & Tita, P. (2011) · PubMed Central · Cited by 60 · see citing works
Filipsson, H., & Johannsson, G. (2009) · European Journal of Endocrinology · doi:10.1530/eje-09-0319 · Cited by 50 · see citing works
Morbidity and GH deficiency: a nationwide study.
Stochholm, K., Laursen, T., Green, A., Laurberg, P., Andersen, M., Kristensen, L. Ø., Feldt-Rasmussen, U., Christiansen, J. S., Frydenberg, M., & Gravholt, C. H. (2008) · European Journal of Endocrinology · doi:10.1530/eje-07-0523 · Cited by 44 · see citing works
Effects of 6 years of growth hormone (GH) treatment on bone mineral density in GH‐deficient adults
Clanget, C., Seck, T., Hinke, V., Wüster, C., Ziegler, R., & Pfeilschifter, J. (2001) · Clinical Endocrinology · doi:10.1046/j.1365-2265.2001.01284.x · Cited by 42 · see citing works
Tritos, N. A., Greenspan, S. L., King, D., Hamrahian, A., Cook, D. M., Jönsson, P. J., Wajnrajch, M. P., Koltowska-Häggstrom, M., & Biller, B. M. K. (2011) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2010-2662 · Cited by 40 · see citing works
Cushing's syndrome and bone mineral density: lowest Z scores in young patients.
van der Eerden, A. W., den Heijer, M., Oyen, W. J. G., & Hermus, A. R. M. M. (2007) · PubMed · Cited by 39 · see citing works
Gómez, J., Gómez, N., Fiter, J., & Soler, J. (2000) · Hormone and Metabolic Research · doi:10.1055/s-2007-978591 · Cited by 39 · see citing works
Lekva, T., Ueland, T., Bøyum, H., Evang, J. A., Godang, K., & Bollerslev, J. (2012) · European Journal of Endocrinology · doi:10.1530/eje-11-1082 · Cited by 32 · see citing works
Barkan, A. L. (2001) · Pituitary · doi:10.1023/a:1020754615863 · Cited by 32 · see citing works
Axial bone mineral density in patients with acromegaly
Bolanowski, M., Wielgus, W., Milewicz, A., & Marciniak, R. (2000) · Academic Radiology · doi:10.1016/s1076-6332(00)80573-5 · Cited by 25 · see citing works
Self-citationRota, F., Savanelli, M. C., Tauchmanova, L., Savastano, S., Lombardi, G., Colao, A., & Di Somma, C. (2008) · Journal of Endocrinological Investigation · doi:10.1007/bf03345574 · Cited by 25 · see citing works
Quantitative Ultrasound of the Heel and Some Parameters of Bone Turnover in Patients with Acromegaly
Bolanowski, M., Jędrzejuk, D., Milewicz, A., & Arkowska, A. (2002) · Osteoporosis International · doi:10.1007/s001980200030 · Cited by 21 · see citing works
Self-citationVarious risks of osteoporosis in patients with pituitary adenomas
Matsuyama, J., Eshima, N., Fukunaga, T., Hori, S., Kobayashi, H., & Isono, M. (2003) · Journal of Bone and Mineral Metabolism · doi:10.1007/s007740300015 · Cited by 14 · see citing works
Quantitative ultrasound at the hand phalanges in patients with acromegaly
Bolanowski, M., Pluskiewicz, W., Adamczyk, P., & Daroszewski, J. (2006) · Ultrasound in Medicine & Biology · doi:10.1016/j.ultrasmedbio.2005.10.003 · Cited by 12 · see citing works
Self-citationThe risk of osteopenia in premenopausal women with various sellar tumors
Zhao, Y., Gan, X., Luo, P., He, Q., Guo, Q., Zhang, L., Zhang, X., Zhang, X., & Fei, Z. (2012) · Gynecological Endocrinology · doi:10.3109/09513590.2012.683080 · Cited by 10 · see citing works
Flagged first, then by citations
2 of the 62 references couldn’t be matched to a known paper.
Research works printed but not linked: 6
- 2007, Netherlands Journal of Medicine, 65, 137
- 1999, The Journal of Clinical Endocrinology and Metabolism, 84, 1775
- 2011, Clinical Cases in Mineral and Bone Metabolism, 8, 37
- 1993, Journal of Clinical Endocrinology and Metabolism, 76, 1452
- 1997, Journal of Clinical Endocrinology and Metabolism, 82, 1462
- 1999, The Journal of Clinical Endocrinology and Metabolism, 84, 1919
Cited by
Sorted by citations
Morbidity and mortality in patients with hyperprolactinaemia: the PROLEARS study
Soto‐Pedre, E., Newey, P. J., Bevan, J. S., & Leese, G. (2017) · Endocrine Connections · doi:10.1530/ec-17-0171 · Cited by 55 · see citing works
Sarcopenia – Endocrinological and Neurological Aspects
Stangl, M. K., Böcker, W., Chubanov, V., Ferrari, U., Fischereder, M., Gudermann, T. W., Hesse, E., Meinke, P., Reincke, M., Reisch, N., et al. (2018) · Experimental and Clinical Endocrinology & Diabetes · doi:10.1055/a-0672-1007 · Cited by 54 · see citing works
Elabd, S., & Sabry, I. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00121 · Cited by 46 · see citing works
Heterogeneity and Dynamics of Vasculature in the Endocrine System During Aging and Disease
Stücker, S., Angelis, J. E. D., & Kusumbe, A. P. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.624928 · Cited by 32 · see citing works
Acromegaly and the long-term fracture risk of the vertebra and hip: a national cohort study
Kwon, H., Han, K., Kim, B., Moon, S. J., Park, S. E., Rhee, E., & Lee, W. (2023) · Osteoporosis International · doi:10.1007/s00198-023-06800-z · Cited by 15 · see citing works
A comprehensive review and advanced biomolecule-based therapies for osteoporosis
Ali, M., & Kim, Y. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.05.024 · Cited by 14 · see citing works
Association Between Antipsychotics and Osteoporosis Based on Real-World Data
Yokoyama, S., Wakamoto, S., Tanaka, Y., NAKAGAWA, C., Hosomi, K., & Takada, M. (2020) · Annals of Pharmacotherapy · doi:10.1177/1060028020913974 · Cited by 14 · see citing works
Cavalcante, D. D. S., Castro, M. G., Quidute, A. R. P., et al. (2019) · Osteoporosis International · doi:10.1007/s00198-019-05086-4 · Cited by 11 · see citing works
Approaches to osteoporosis in paleopathology: How did methodology shape bone loss research?
van Spelde, A.-M., Schroeder, H., Kjellström, A., & Lidén, K. (2021) · International Journal of Paleopathology · doi:10.1016/j.ijpp.2021.05.001 · Cited by 11 · see citing works
Simultaneous bilateral neck of femur fractures in an adolescent secondary to hypocalcaemic seizure
Chandankere, V., Mulpur, P., Maryada, V. R., et al. (2018) · Journal of Pediatric Orthopaedics B · doi:10.1097/bpb.0000000000000560 · Cited by 10 · see citing works
Jawiarczyk-Przybyłowska, A., Halupczok-Żyła, J., Syrycka, J., Zembska, A., Kuliczkowska-Płaksej, J., & Bolanowski, M. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.862845 · Cited by 8 · see citing works
Self-citationYi, H., Kim, J. M., Ju, S. H., Lee, Y., Kim, H. J., & Kim, K. S. (2016) · Journal of Bone Metabolism · doi:10.11005/jbm.2016.23.1.40 · Cited by 8 · see citing works
Ságová, I., Mokáň, M., Tonhajzerová, I., Rončáková, M., & Vaňuga, P. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1197725 · Cited by 7 · see citing works
Diagnosis and therapeutic approach to bone health in patients with hypopituitarism
Kuliczkowska-Płaksej, J., Zdrojowy-Wełna, A., Jawiarczyk-Przybyłowska, A., Gojny, Ł., & Bolanowski, M. (2024) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-024-09878-w · Cited by 6 · see citing works
Self-citationMultiple Endocrine Neoplasia Syndromes
Newey, P. J., & Thakker, R. V. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804182-6.00038-1 · Cited by 5 · see citing works
Differential diagnosis and management of abnormal uterine bleeding due to hyperprolactinemia
Adra, A. M., Zibdeh, M., Malek, A. M. M. A., Hamrahian, A. H., Abdelhamid, A. M. S., Colao, A., Anastasiades, E., Ahmed, E. M. A. F., EZEDDINE, J., Sattar, M. I. A. E., et al. (2016) · Middle East Fertility Society Journal · doi:10.1016/j.mefs.2016.02.001 · Cited by 4 · see citing works
di Filippo, L., Acanfora, M., Bolamperti, S., Terenzi, U., Bonomo, M., & Giustina, A. (2026) · Pituitary · doi:10.1007/s11102-026-01667-9 · Cited by 4 · see citing works
Osteoporosis: definition, diagnosis, and considerations prior to starting treatment
Vidal, M., & Lane, N. E. (2026) · Exploration of Endocrine and Metabolic Diseases · doi:10.37349/eemd.2026.101456 · Cited by 2 · see citing works
Costanza, F., Giampietro, A., Marinis, L. D., Bianchi, A., Chiloiro, S., & Pontecorvi, A. (2025) · Targets · doi:10.3390/targets3030026 · Cited by 1 · see citing works
An Aggressive Plurihormonal Pituitary Adenoma With Thyrotropin, Growth Hormone, and Prolactin Excess
Goh, Q., Nee, L. Y., Rani, N. H. A., et al. (2023) · JCEM Case Reports · doi:10.1210/jcemcr/luad016 · Cited by 1 · see citing works
Rocha, D. R., Nery, J. F., Furini, L. N., et al. (2020) · Lasers in Medical Science · doi:10.1007/s10103-020-02961-z · Cited by 1 · see citing works
Oyibo, S. O. (2020) · Cureus · doi:10.7759/cureus.7817 · Cited by 1 · see citing works
Cid, A. M. P. L., Quidute, A. R. P., Martins, M. R. A., et al. (2021) · Research Society and Development · doi:10.33448/rsd-v10i5.15316
Evaluation of Bone Mineral Densitometry Measurements in Newly Diagnosed Acromegaly Patients
Çalapkulu, M., Sencar, M. E., Ünsal, İ. Ö., Sakız, D., Bostan, H., Düğer, H., Özbek, M., & Çakal, E. (2022) · Turkish Journal of Osteoporosis · doi:10.4274/tod.galenos.2021.59489
Multiple endocrine neoplasia syndromes
Newey, P. J., & Thakker, R. V. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-13683-2.00033-5
Diagnostic delay of prolactinoma: Focus on clinical manifestations
Bauer, M. J., Pelsma, I. C. M., Geer, E. B., & Biermasz, N. R. (2026) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2026.102106
- Authors
- Bolanowski, M., Halupczok, J., & Jawiarczyk-Przybyłowska, A.
- Affiliations
- Wroclaw Medical University (PL)
- Department of Endocrinology, Diabetes and Isotope Therapy, Wroclaw Medical University, Pasteura 4, 50-367 Wroclaw, Poland
- Corresponding author
- Bolanowski, Marek
- Venue
- International Journal of Endocrinology
- Publisher
- Wiley
- Published
- 2015
- Volume
- 2015
- Pages
- 1-7
- ISSN
- 1687-8337 (ISSN-L)
- 1687-8345
- PMC
- PMC4383139
- OpenAlex
- W2001678032
- Cited by
- 27
- References
- 62
- Citations by year
- 2026: 4 · 2025: 1 · 2024: 2 · 2023: 4 · 2022: 2 · 2021: 3 · 2020: 3 · 2019: 1 · 2018: 2 · 2017: 2 · 2016: 2 · 2015: 1
- FWCI
- 2.17
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- International Journal of Endocrinology (publishedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pituitary Gland Disorders and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Keywords
- pituitary disorders, secondary osteoporosis, bone metabolism, fracture risk, Cushing's disease, hyperprolactinemia, acromegaly, hypopituitarism, hypogonadism
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.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-14.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-14.
Cited sources are checked by gpt-6-sol.
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.
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