The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.
Identification and Importance of Brown Adipose Tissue in Adult Humans
Open accessAbstract
BACKGROUND: Obesity results from an imbalance between energy intake and expenditure. In rodents and newborn humans, brown adipose tissue helps regulate energy expenditure by thermogenesis mediated by the expression of uncoupling protein 1 (UCP1), but brown adipose tissue has been considered to have no physiologic relevance in adult humans. METHODS: We analyzed 3640 consecutive (18)F-fluorodeoxyglucose ((18)F-FDG) positron-emission tomographic and computed tomographic (PET-CT) scans performed for various diagnostic reasons in 1972 patients for the presence of substantial depots of putative brown adipose tissue. Such depots were defined as collections of tissue that were more than 4 mm in diameter, had the density of adipose tissue according to CT, and had maximal standardized uptake values of (18)F-FDG of at least 2.0 g per milliliter, indicating high metabolic activity. Clinical indexes were recorded and compared with those of date-matched controls. Immunostaining for UCP1 was performed on biopsy specimens from the neck and supraclavicular regions in patients undergoing surgery. RESULTS: Substantial depots of brown adipose tissue were identified by PET-CT in a region extending from the anterior neck to the thorax. Tissue from this region had UCP1-immunopositive, multilocular adipocytes indicating brown adipose tissue. Positive scans were seen in 76 of 1013 women (7.5%) and 30 of 959 men (3.1%), corresponding to a female:male ratio greater than 2:1 (P<0.001). Women also had a greater mass of brown adipose tissue and higher (18)F-FDG uptake activity. The probability of the detection of brown adipose tissue was inversely correlated with years of age (P<0.001), outdoor temperature at the time of the scan (P=0.02), beta-blocker use (P<0.001), and among older patients, body-mass index (P=0.007). CONCLUSIONS: Defined regions of functionally active brown adipose tissue are present in adult humans, are more frequent in women than in men, and may be quantified noninvasively with the use of (18)F-FDG PET-CT. Most important, the amount of brown adipose tissue is inversely correlated with body-mass index, especially in older people, suggesting a potential role of brown adipose tissue in adult human metabolism.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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
“Contrastingly, larger species, like rabbits, sheep, cows, and humans are born with BAT stores, but most of these are gradually replaced by WAT after birth [13, 45, 46].”
From Developmental programming of offspring adipose tissue biology and obesity risk (2021) · cites this paper as [13]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Cypess et al. found that not only were women twice as likely as men to have brown adipose tissue signal, they also had a greater mass of brown adipose tissue with higher metabolic activity [12].”
From Sex differences in metabolic homeostasis, diabetes, and obesity (2015) · cites this paper as [12]
The cited source says what the claim attributes to it.
In the citing paper
“This thermogenic effect is mediated by the expression of decoupling protein-1 (UCP1; Cypess et al., 2009).”
From Physical Exercise-Induced Myokines and Muscle-Adipose Tissue Crosstalk: A Review of Current Knowledge and the Implications for Health and Metabolic Diseases (2018) · cites this paper as Cypess et al., 2009
In the citing paper
“recent reports revealing significant amounts of metabolically active BAT in adults (146, 147)”
From Altered mitochondrial function in insulin-deficient and insulin-resistant states (2018) · cites this paper as [147]
In the citing paper
“adult humans maintain active depots of BAT [54, 55]”
From Regulation of obesity and insulin resistance by nitric oxide (2014) · cites this paper as [54]
In the citing paper
“All the groups showed major depots of metabolically active fat in the cervical–supraclavicular region, a slightly different site from that in rodents and children, where BAT is found mainly situated in the interscapular area.”
From Mitochondrial fatty acid oxidation in obesity (2013) · cites this paper as [30]
In the citing paper
“However, the real breakthrough arrived in 2009 when five independent groups used PET-CT to identify the presence and study the relevance of BAT in adult humans ([30](#B30), [143](#B143), [165](#B165), [168](#B168), [181](#B181)).”
From Mitochondrial fatty acid oxidation in obesity (2013) · cites this paper as [30]
In the citing paper
“The expression of UCP1, DIO2, and the β3-adrenergic receptor was also reported, thereby indicating the potential responsiveness of human BAT to both hormonal and pharmacological stimuli.”
From Mitochondrial fatty acid oxidation in obesity (2013) · cites this paper as [30]
In the citing paper
“Interestingly, human studies showed that BAT is reduced in obese and diabetic patients, thus indicating that this tissue participates in both cold-induced and diet-induced thermogenesis ([30](#B30)).”
From Mitochondrial fatty acid oxidation in obesity (2013) · cites this paper as [30]
In the citing paper
“Second, recent studies have shown that adult humans maintain potentially active brown adipose tissue, making this high energetic tissue a real therapeutic target 13–17.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [13]
In the citing paper
“Humans are quite different from rats, with much greater body mass (~200X), only moderately greater BAT mass (~10X), and much lower basal metabolic rate (~0.15X) 13,37,36.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [13]
In the citing paper
“However, it was only during the past year PET/CT imaging was used to prove conclusively that adult humans possess physiologically active UCP1-positive BAT,13–17.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [13]
In the citing paper
“More importantly, BAT activity correlates inversely with BMI13,14 and percentage body fat 13,14, suggesting a role in energy balance.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [13]
In the citing paper
“Retrospective case series using 18F-FDG PET/CT report this to be less than 10% 13,83.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [13]
In the citing paper
“PET/CT positivity shows seasonal variation 13,16,88, indicating a role of BAT in normal adaptation to cold.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [13]
In the citing paper
“Functional BAT also decreases with age, and is rarely observed in non-stimulated [i.e. no investigator-controlled stimulation such as cold or pharmacological interventions], overweight adults over 64 years-old 13, suggesting a possible role of decreased BAT activity in the development of age-related obesity.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [13]
In the citing paper
“Although it has only recently been proven that adult human BAT is functional and may be involved in protecting against weight loss 13–17, attempts to exploit BAT energy expenditure for treating obesity have been around for decades.”
From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [13]
In the citing paper
“This now needs to be reconsidered since very recent findings indicate that humans do express BAT in the neck region (78, 278, 318, 323) and the amount of BAT correlates inversely with body-mass index (78).”
From Mitochondrial Dysfunction in Diabetes: From Molecular Mechanisms to Functional Significance and Therapeutic Opportunities (2010) · cites this paper as [78]
In the citing paper
“This now needs to be reconsidered since very recent findings indicate that humans do express BAT in the neck region (78, 278, 318, 323) and the amount of BAT correlates inversely with body-mass index (78).”
From Mitochondrial Dysfunction in Diabetes: From Molecular Mechanisms to Functional Significance and Therapeutic Opportunities (2010) · cites this paper as [78]
In the citing paper
“Such depots appear to be less active as a function of aging and/or obesity (151, 164 -167).”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [151]
In the citing paper
“The role of adipose tissue mitochondria is most apparent in brown adipose tissue, where flux through the ETC generates heat in the process of thermogenesis, a potentially important mechanism regulating systemic metabolism even in adult humans (149 -152).”
From The role of mitochondria in the pathogenesis of type 2 diabetes (2010) · cites this paper as [151]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Brown Adipose Tissue: Function and Physiological Significance
CANNON, B., & NEDERGAARD, J. (2004) · Physiological Reviews · doi:10.1152/physrev.00015.2003 · Cited by 6,433
Obesity and Diabetes in the Developing World — A Growing Challenge
Hossain, P., Kawar, B., & El Nahas, M. (2007) · New England Journal of Medicine · doi:10.1056/nejmp068177 · Cited by 2,200
Adipocytes as regulators of energy balance and glucose homeostasis
Rosen, E. D., & Spiegelman, B. M. (2006) · Nature · doi:10.1038/nature05483 · Cited by 2,170
Transcriptional control of adipocyte formation
Farmer, S. R. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.07.001 · Cited by 1,836
Unexpected evidence for active brown adipose tissue in adult humans
Nedergaard, J., Bengtsson, T., & Cannon, B. (2007) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00691.2006 · Cited by 1,824
A role for brown adipose tissue in diet-induced thermogenesis
Rothwell, N. J., & Stock, M. J. (1979) · Nature · doi:10.1038/281031a0 · Cited by 1,606
Developmental Origin of Fat: Tracking Obesity to Its Source
Gesta, S., Tseng, Y.-H., & Kahn, C. R. (2007) · Cell · doi:10.1016/j.cell.2007.10.004 · Cited by 1,508
Self-citationDevelopment of obesity in transgenic mice after genetic ablation of brown adipose tissue
Lowell, B. B., S-Susulic, V., Hamann, A., Lawitts, J. A., Himms-Hagen, J., Boyer, B. B., Kozak, L. P., & Flier, J. S. (1993) · Nature · doi:10.1038/366740a0 · Cited by 1,075
The endocrine function of adipose tissue: an update
Ronti, T., Lupattelli, G., & Mannarino, E. (2006) · Clinical Endocrinology · doi:10.1111/j.1365-2265.2006.02474.x · Cited by 920
Cinti, S. (2005) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2005.04.010 · Cited by 720
Flagged first, then by citations
Research works printed but not linked: 8
- Cohade C, 2003, J Nucl Med, 44, 170
- Cohade C, 2003, J Nucl Med, 44, 1267
- Dobert N, 2004, Q J Nucl Med Mol Imaging, 48, 33
- Yeung HW, 2003, J Nucl Med, 44, 1789
- Heaton JM, 1972, J Anat, 112, 35
- Himms-Hagen J, 1979, Can Med Assoc J, 121, 1361
- Garruti G, 1992, Int J Obes Relat Metab Disord, 16, 383
- Tatsumi M, 2004, J Nucl Med, 45, 1189
Cited by
Sorted by citations
Items 101–173 of 173
‘Browning’ the cardiac and peri-vascular adipose tissues to modulate cardiovascular risk
Aldiss, P., Davies, G., Woods, R., Budge, H., Sacks, H. S., & Symonds, M. E. (2017) · International Journal of Cardiology · doi:10.1016/j.ijcard.2016.11.074 · Cited by 148
Glucagon Regulation of Energy Expenditure
Kleinert, M., Sachs, S., Habegger, K. M., Hofmann, S. M., & Müller, T. D. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20215407 · Cited by 147
Boucher, J., Mori, M. A., Lee, K. Y., Smyth, G., Liew, C. W., Macotela, Y., Rourk, M., Bluher, M., Russell, S. J., & Kahn, C. R. (2012) · Nature Communications · doi:10.1038/ncomms1905 · Cited by 142
Self-citationBrown Adipose Tissue as a Regulator of Energy Expenditure and Body Fat in Humans
Saito, M. (2013) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2013.37.1.22 · Cited by 146
Christoffersen, B. Ø., Sanchez‐Delgado, G., John, L. M., Ryan, D. H., Raun, K., & Ravussin, E. (2022) · Obesity · doi:10.1002/oby.23374 · Cited by 142
“The variable amount of BAT and the overall modest contribution of BAT to daily energy expenditure is challenging for activation of the existing BAT as an effective therapeutic concept (61,137).”
BackgroundGeerling, J. J., Boon, M. R., Kooijman, S., Parlevliet, E. T., Havekes, L. M., Romijn, J. A., Meurs, I. M., & Rensen, P. C. N. (2014) · Journal of Lipid Research · doi:10.1194/jlr.r045013 · Cited by 137
de Jong, J. M. A., Sun, W., Pires, N. D., Frontini, A., Balaz, M., Jespersen, N. Z., Feizi, A., Petrovic, K., Fischer, A. W., Bokhari, M. H., et al. (2019) · Nature Metabolism · doi:10.1038/s42255-019-0101-4 · Cited by 137
Mechanisms of Weight Loss After Obesity Surgery
Akalestou, E., Miras, A. D., Rutter, G. A., & le Roux, C. W. (2022) · Endocrine Reviews · doi:10.1210/endrev/bnab022 · Cited by 136
Jiang, Y., Berry, D. C., & Graff, J. M. (2017) · eLife · doi:10.7554/elife.30329 · Cited by 135
Psychogenic fever: how psychological stress affects body temperature in the clinical population
Oka, T. (2015) · Temperature · doi:10.1080/23328940.2015.1056907 · Cited by 127
A Functional Link between AMPK and Orexin Mediates the Effect of BMP8B on Energy Balance
Martins, L., Seoane-Collazo, P., Contreras, C., González-García, I., Martínez-Sánchez, N., González, F., Zalvide, J., Gallego, R., Diéguez, C., Nogueiras, R., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.07.045 · Cited by 154
Yepuru, M., Eswaraka, J., Kearbey, J. D., Barrett, C. M., Raghow, S., Veverka, K. A., Miller, D. D., Dalton, J. T., & Narayanan, R. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.147850 · Cited by 125
Zuriaga, M. A., Fuster, J. J., Gokce, N., & Walsh, K. (2017) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2017.00027 · Cited by 122
Obesity: A neuroimmunometabolic perspective
Larabee, C. M., Neely, O. C., & Domingos, A. I. (2020) · Nature Reviews Endocrinology · doi:10.1038/s41574-019-0283-6 · Cited by 123
Programming and regulation of metabolic homeostasis by HDAC11
Sun, L., Marin de Evsikova, C., Bian, K., Achille, A., Telles, E., Pei, H., & Seto, E. (2018) · EBioMedicine · doi:10.1016/j.ebiom.2018.06.025 · Cited by 125
Brown Adipose Tissue: Mechanisms and Potential Therapeutic Targets
Tam, C. S., Lecoultre, V., & Ravussin, E. (2012) · Circulation · doi:10.1161/circulationaha.111.042929 · Cited by 116
Thyroid Hormone Signaling and Homeostasis During Aging
Bowers, J., Terrien, J., Clerget-Froidevaux, M. S., Gothié, J. D., Rozing, M. P., Westendorp, R. G. J., van Heemst, D., & Demeneix, B. A. (2013) · Endocrine Reviews · doi:10.1210/er.2012-1056 · Cited by 117
Xu, Y., Yu, T., Ma, G., Zheng, L., Jiang, X., Yang, F., Wang, Z., Li, N., He, Z., Song, X., et al. (2021) · International Journal of Biological Sciences · doi:10.7150/ijbs.62556 · Cited by 110
Gamas, L., Matafome, P., & Seiça, R. (2015) · Journal of Diabetes Research · doi:10.1155/2015/359159 · Cited by 114
Zhang, X., Lam, K. S. L., Ye, H., Chung, S. K., Zhou, M., Wang, Y., & Xu, A. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.135509 · Cited by 112
Exercise induces white adipose tissue browning across the weight spectrum in humans
Otero-Díaz, B., Rodríguez-Flores, M., Sánchez-Muñoz, V., Monraz-Preciado, F., Ordoñez-Ortega, S., Becerril-Elias, V., Baay-Guzmán, G., Obando-Monge, R., García-García, E., Palacios-González, B., et al. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01781 · Cited by 110
Adaptive thermogenesis can make a difference in the ability of obese individuals to lose body weight
Tremblay, A., Royer, M.-M., Chaput, J.-P., & Doucet, É. (2013) · International Journal of Obesity · doi:10.1038/ijo.2012.124 · Cited by 108
Mechanisms of impaired brown adipose tissue recruitment in obesity
Alcalá, M., Calderon-Dominguez, M., Serra, D., Herrero, L., & Viana, M. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00094 · Cited by 106
Pessentheiner, A. R., Pelzmann, H. J., Walenta, E., Schweiger, M., Groschner, L. N., Graier, W. F., Kolb, D., Uno, K., Miyazaki, T., Nitta, A., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.491324 · Cited by 105
Zhu, Y., Gao, Y., Tao, C., Shao, M., Zhao, S., Huang, W., Yao, T., Johnson, J. A., Liu, T., Cypess, A. M., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.08.005 · Cited by 100
Self-citationLiu, X., Zhang, Z., Song, Y., Xie, H., & Dong, M. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1065263 · Cited by 102
Gut microbiota modulate the metabolism of brown adipose tissue in mice
Mestdagh, R., Dumas, M.-E., Rezzi, S., Kochhar, S., Holmes, E., Claus, S. P., & Nicholson, J. K. (2012) · Journal of Proteome Research · doi:10.1021/pr200938v · Cited by 97
Okla, M., Zaher, W., Alfayez, M., & Chung, S. (2018) · Inflammation · doi:10.1007/s10753-017-0718-y · Cited by 96
New insights into adipose tissue VEGF-A actions in the control of obesity and insulin resistance
Elias, I., Franckhauser, S., & Bosch, F. (2013) · Adipocyte · doi:10.4161/adip.22880 · Cited by 92
Bimagrumab improves body composition and insulin sensitivity in insulin‐resistant individuals
Garito, T., Roubenoff, R., Hompesch, M., Morrow, L., Gomez, K., Rooks, D., Meyers, C., Buchsbaum, M. S., Neelakantham, S., Swan, T., et al. (2018) · Diabetes, Obesity and Metabolism · doi:10.1111/dom.13042 · Cited by 88
Molecular Nutrition Research—The Modern Way Of Performing Nutritional Science
Norheim, F., Gjelstad, I., Hjorth, M., Vinknes, K., Langleite, T., Holen, T., Jensen, J., Dalen, K., Karlsen, A., Kielland, A., et al. (2012) · Nutrients · doi:10.3390/nu4121898 · Cited by 83
Blouet, C., & Schwartz, G. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051898 · Cited by 81
Role of bile acids in the regulation of the metabolic pathways
Taoka, H., Yokoyama, Y., Morimoto, K., Kitamura, N., Tanigaki, T., Takashina, Y., Tsubota, K., & Watanabe, M. (2016) · World Journal of Diabetes · doi:10.4239/wjd.v7.i13.260 · Cited by 80
FGF21-Mediated Improvements in Glucose Clearance Require Uncoupling Protein 1
Kwon, M. M., O’Dwyer, S. M., Baker, R. K., Covey, S. D., & Kieffer, T. J. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.10.021 · Cited by 77
Interleukin-6 released from differentiating human beige adipocytes improves browning
Kristóf, E., Klusóczki, Á., Veress, R., Shaw, A., Combi, Z. S., Varga, K., Győry, F., Balajthy, Z., Bai, P., Bacso, Z., et al. (2019) · Experimental Cell Research · doi:10.1016/j.yexcr.2019.02.015 · Cited by 77
Mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge
Lu, Y., Fujioka, H., Joshi, D., Li, Q., Sangwung, P., Hsieh, P., Zhu, J., Torio, J., Sweet, D., Wang, L., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-26394-5 · Cited by 76
Vasan, S. K., Noordam, R., Gowri, M. S., Neville, M. J., Karpe, F., & Christodoulides, C. (2019) · Diabetologia · doi:10.1007/s00125-019-4947-5 · Cited by 76
No evidence of white adipocyte browning after endurance exercise training in obese men
Tsiloulis, T., Carey, A. L., Bayliss, J., Canny, B., Meex, R. C. R., & Watt, M. J. (2018) · International Journal of Obesity · doi:10.1038/ijo.2017.295 · Cited by 70
JAK-STAT in Lipid Metabolism of Adipocytes
Xu, D., Yin, C., Wang, S., & Xiao, Y. (2013) · JAK-STAT · doi:10.4161/jkst.27203 · Cited by 69
Jiang, N., Yang, M., Han, Y., Zhao, H., & Sun, L. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.870250 · Cited by 68
Tiosano, D., Vlodavsky, E., Filmar, S., Weiner, Z., Goldsher, D., & Bar-Shalom, R. (2010) · Hormone Research in Paediatrics · doi:10.1159/000295722 · Cited by 65
A Hypothalamic Phosphatase Switch Coordinates Energy Expenditure with Feeding
Dodd, G. T., Andrews, Z. B., Simonds, S. E., Michael, N. J., DeVeer, M., Brüning, J. C., Spanswick, D., Cowley, M. A., & Tiganis, T. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.07.013 · Cited by 66
You, Y., Han, X., Guo, J., Guo, Y., Yin, M., Liu, G., Huang, W., & Zhan, J. (2018) · Journal of Functional Foods · doi:10.1016/j.jff.2017.12.025 · Cited by 65
The new era of drug therapy for obesity: the evidence and the expectations
Jones, B. J., & Bloom, S. R. (2015) · Drugs · doi:10.1007/s40265-015-0410-1 · Cited by 58
Paulo, E., Wu, D., Wang, Y., Zhang, Y., Wu, Y., Swaney, D. L., Soucheray, M., Jimenez-Morales, D., Chawla, A., Krogan, N. J., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-29333-6 · Cited by 59
Developmental programming of offspring adipose tissue biology and obesity risk
Rodgers, A., & Sferruzzi-Perri, A. N. (2021) · International Journal of Obesity · doi:10.1038/s41366-021-00790-w · Cited by 57
van Eyk, H. J., Paiman, E. H. M., Bizino, M. B., IJzermans, S. L., Kleiburg, F., Boers, T. G. W., Rappel, E. J., Burakiewicz, J., Kan, H. E., Smit, J. W. A., et al. (2020) · Nutrition, Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2019.12.005 · Cited by 54
Adipose Tissue CLK2 Promotes Energy Expenditure during High-Fat Diet Intermittent Fasting
Hatting, M., Rines, A. K., Luo, C., Tabata, M., Sharabi, K., Hall, J. A., Verdeguer, F., Trautwein, C., & Puigserver, P. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2016.12.007 · Cited by 54
MicroRNAs in brown and beige fat
Goody, D., & Pfeifer, A. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2018.05.003 · Cited by 54
The role of autophagy in brown and beige adipose tissue plasticity
Cairó, M., & Villarroya, J. (2020) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-019-00708-1 · Cited by 53
Glucagon, GLP-1 and Thermogenesis
González-García, I., Milbank, E., Diéguez, C., López, M., & Contreras, C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20143445 · Cited by 49
Building muscle, browning fat and preventing obesity by inhibiting myostatin
LeBrasseur, N. K. (2012) · Diabetologia · doi:10.1007/s00125-011-2361-8 · Cited by 46
Fang, C., Kim, H., Noratto, G., Sun, Y., Talcott, S. T., & Mertens-Talcott, S. U. (2018) · Journal of Functional Foods · doi:10.1016/j.jff.2018.04.043 · Cited by 46
Augmenting energy expenditure by mitochondrial uncoupling: A role of AMP-activated protein kinase
Klaus, S., Keipert, S., Rossmeisl, M., & Kopecky, J. (2012) · Genes & Nutrition · doi:10.1007/s12263-011-0260-8 · Cited by 44
Looking on the “brite” side exercise-induced browning of white adipose tissue
Townsend, L. K., & Wright, D. C. (2019) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-018-2177-1 · Cited by 44
Pervin, S., Reddy, S. T., & Singh, R. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.653179 · Cited by 42
Liu, T., Ji, R.-L., & Tao, Y.-X. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.108044 · Cited by 34
A metabolomic study of adipose tissue in mice with a disruption of the circadian system
Castro, C., Briggs, W., Paschos, G. K., FitzGerald, G. A., & Griffin, J. L. (2015) · Molecular BioSystems · doi:10.1039/c5mb00032g · Cited by 33
Nikolic, D. M., Li, Y., Liu, S., & Wang, S. (2011) · Obesity · doi:10.1038/oby.2010.223 · Cited by 30
“More recently, functionally active BAT has been identified in human adults and a potential role of BAT in human metabolism has been suggested (2).”
BackgroundMathew, D., Zhou, P., Pywell, C. M., van der Veen, D. R., Shao, J., Xi, Y., Bonar, N. A., Hummel, A. D., Chapman, S., Leevy, W. M., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073064 · Cited by 30
Pardo, R., Vilà, M., Cervela, L., de Marco, M., Gama-Pérez, P., González-Franquesa, A., Statuto, L., Vilallonga, R., Simó, R., Garcia-Roves, P. M., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201800310r · Cited by 27
Pyrżak, B., Demkow, U., & Kucharska, A. M. (2015) · Advances in experimental medicine and biology · doi:10.1007/5584_2015_149 · Cited by 26
Hypothalamic control of adipose tissue
Stefanidis, A., Wiedmann, N. M., Adler, E. S., & Oldfield, B. J. (2014) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2014.08.001 · Cited by 22
Michael, N. J., Simonds, S. E., van den Top, M., Cowley, M. A., & Spanswick, D. (2017) · Molecular Metabolism · doi:10.1016/j.molmet.2017.07.002 · Cited by 21
Sellayah, D. (2019) · Journal of the Endocrine Society · doi:10.1210/js.2018-00363 · Cited by 21
Targeting skeletal muscle mitochondrial health in obesity
Pileggi, C. A., Hooks, B. G., McPherson, R., Dent, R. R. M., & Harper, M.-E. (2022) · Clinical Science · doi:10.1042/cs20210506 · Cited by 21
Obesity and Exercise: New Insights and Perspectives
James, N. M., & Stanford, K. I. (2025) · Endocrine Reviews · doi:10.1210/endrev/bnaf017 · Cited by 20
Mendes, C., Gomes, G., Belpiede, L. T., do Carmo Buonfiglio, D., Motta-Teixeira, L. C., Amaral, F. G., & Cipolla-Neto, J. (2021) · Life Sciences · doi:10.1016/j.lfs.2020.118769 · Cited by 17
EID1-induces brown-like adipocyte traits in white 3T3-L1 pre-adipocytes
Lizcano, F., & Vargas, D. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.06.034 · Cited by 15
Hirata, Y., Fukuoka, H., Iguchi, G., Iwahashi, Y., Fujita, Y., Hari, Y., Iga, M., Nakajima, S., Nishimoto, Y., Mukai, M., et al. (2015) · European Journal of Endocrinology · doi:10.1530/eje-15-0130 · Cited by 14
Kou, G., Hu, Y., Jiang, Z., Li, Z., Li, P., Song, H., Chen, Q., Zhou, Z., & Lyu, Q. (2020) · Journal of Functional Foods · doi:10.1016/j.jff.2020.103860 · Cited by 14
Regulation of p27 and Cdk2 Expression in Different Adipose Tissue Depots in Aging and Obesity
Colón-Mesa, I., Fernández-Galilea, M., Sáinz, N., Lopez-Yus, M., Artigas, J. M., Arbonés-Mainar, J. M., Félix-Soriano, E., Escoté, X., & Moreno-Aliaga, M. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111745 · Cited by 9
Kim, N., Kim, J., Yoo, C., Lim, K., Akimoto, T., & Park, J. (2018) · Journal of Exercise Nutrition & Biochemistry · doi:10.20463/jenb.2018.0003 · Cited by 7
Metadata
- Authors
- Cypess, A. M., Lehman, S., Williams, G., Tal, I., Rodman, D., Goldfine, A. B., Kuo, F. C., Palmer, E. L., Tseng, Y.-H., Doria, A., Kolodny, G. M., & Kahn, C. R.
- Affiliations
- Joslin Diabetes Center (US)
- Beth Israel Deaconess Medical Center (US)
- Brigham and Women's Hospital (US)
- Harvard University (US)
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2009-04-09
- Volume
- 360
- Issue
- 15
- Pages
- 1509-1517
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- PMC
- PMC2859951
- OpenAlex
- W1965079305
- Cited by
- 4,399
- References
- 41
- Citations by year
- 2026: 146 · 2025: 194 · 2024: 214 · 2023: 224 · 2022: 264 · 2021: 305 · 2020: 331 · 2019: 307 · 2018: 295 · 2017: 313 · 2016: 315 · 2015: 309 · 2014: 250 · 2013: 284 · 2012: 223
- FWCI
- 139.97
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK055545, DK 33201, DK070722, R21DK070722, P30DK046200, R01DK056690, DK046200-16, R01DK033201, DK55545, T32DK007260, P30DK040561)
- National Center for Research Resources (UL1RR025758, KL2RR025757)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Disease and Adiposity
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Keywords
- brown adipose tissue, adults, thermogenesis, UCP1, body mass index, obesity, sex differences, age-related decline, beta-blocker use, outdoor temperature, energy expenditure, non-invasive measurement, immunostaining
- MeSH terms
- Adrenergic beta-Antagonists, Adult, Age Factors, Aged, Blood Glucose, Adipose Tissue, Brown, Energy Metabolism, Female, Humans, Immunohistochemistry, Male, Middle Aged, Neck, Sex Characteristics, Temperature, Body Mass Index, Multivariate Analysis, Logistic Models, Statistics, Nonparametric, Radiopharmaceuticals, Fluorodeoxyglucose F18, Positron-Emission Tomography, Adiposity, Adipocytes, Brown, Young Adult
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.
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