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Brown adipose tissue is associated with cardiometabolic health
Open accessAbstract
White fat stores excess energy, whereas brown and beige fat are thermogenic and dissipate energy as heat. Thermogenic adipose tissues markedly improve glucose and lipid homeostasis in mouse models, although the extent to which brown adipose tissue (BAT) influences metabolic and cardiovascular disease in humans is unclear 1,2. Here we retrospectively categorized 134,529 18 F-fluorodeoxyglucose positron emission tomography-computed tomography scans from 52,487 patients, by presence or absence of BAT, and used propensity score matching to assemble a study cohort. Scans in the study population were initially conducted for indications related to cancer diagnosis, treatment or surveillance, without previous stimulation. We report that individuals with BAT had lower prevalences of cardiometabolic diseases, and the presence of BAT was independently correlated with lower odds of type 2 diabetes, dyslipidemia, coronary artery disease, cerebrovascular disease, congestive heart failure and hypertension. These findings were supported by improved blood glucose, triglyceride and high-density lipoprotein values. The beneficial effects of BAT were more pronounced in individuals with overweight or obesity, indicating that BAT might play a role in mitigating the deleterious effects of obesity. Taken together, our findings highlight a potential role for BAT in promoting cardiometabolic health.
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Whether exercise can brown WAT in humans, especially through an irisin-mediated pathway, remains controversial.
“Thus, whether exercise can brown WAT in humans, especially through an irisin-mediated pathway, remains controversial55,83,84,90.”
From Exerkines in health, resilience and disease (2022) · cites this paper as [83]
Individuals with PET-CT-defined brown adipose tissue have a lower prevalence of cardiometabolic disease, particularly if they have overweight or obesity.
“individuals with PET-CT-defined BAT had a decreased prevalence of cardiometabolic disease, particularly if they had overweight or obesity83.”
From Exerkines in health, resilience and disease (2022) · cites this paper as [83]
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Metadata
- Authors
- Becher, T., Palanisamy, S., Kramer, D. J., Eljalby, M., Marx, S. J., Wibmer, A. G., Butler, S. D., Jiang, C. S., Vaughan, R., Schöder, H., Mark, A., & Cohen, P.
- Affiliations
- German Centre for Cardiovascular Research (DE)
- Weill Cornell Medicine (US)
- Rockefeller University (US)
- Memorial Sloan Kettering Cancer Center (US)
- Cornell University (US)
- University of Iowa (US)
- Corresponding author
- Cohen, Paul
- ORCID
- Venue
- Nature Medicine
- Published
- 2021-01
- Volume
- 27
- Issue
- 1
- Pages
- 58-65
- ISSN
- 1078-8956 (ISSN-L)
- 1546-170X
- PMC
- PMC8461455
- OpenAlex
- W3120832178
- Cited by
- 743
- References
- 42
- Citations by year
- 2026: 119 · 2025: 145 · 2024: 151 · 2023: 125 · 2022: 124 · 2021: 76
- FWCI
- 74.94
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Nature Medicine (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- American Diabetes Association (1-17-ACE-17)
- Sinsheimer Foundation
- U.S. Department of Health & Human Services | NIH | National Center for Advancing Translational Sciences (UL1TR001866)
- 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, cardiometabolic health, type 2 diabetes, dyslipidemia, coronary artery disease, cerebrovascular disease, congestive heart failure, hypertension, obesity, thermogenesis, 18F-FDG PET/CT, glucose homeostasis, lipid homeostasis
- MeSH terms
- Positron Emission Tomography Computed Tomography, Blood Glucose, Adipose Tissue, Brown, Cardiovascular Diseases, Diabetes Mellitus, Type 2, Humans, Retrospective Studies, Fluorodeoxyglucose F18, Dyslipidemias
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