Cardiometabolic characteristics of people with metabolically healthy and unhealthy obesity
Open accessAbstract
There is considerable heterogeneity in the cardiometabolic abnormalities associated with obesity. We evaluated multi-organ system metabolic function in 20 adults with metabolically healthy obesity (MHO; normal fasting glucose and triglycerides, oral glucose tolerance, intrahepatic triglyceride content, and whole-body insulin sensitivity), 20 adults with metabolically unhealthy obesity (MUO; prediabetes, hepatic steatosis, and whole-body insulin resistance), and 15 adults who were metabolically healthy lean. Compared with MUO, people with MHO had (1) altered skeletal muscle biology (decreased ceramide content and increased expression of genes involved in BCAA catabolism and mitochondrial structure/function); (2) altered adipose tissue biology (decreased expression of genes involved in inflammation and extracellular matrix remodeling and increased expression of genes involved in lipogenesis); (3) lower 24-h plasma glucose, insulin, non-esterified fatty acids, and triglycerides; (4) higher plasma adiponectin and lower plasma PAI-1 concentrations; and (5) decreased oxidative stress. These findings provide a framework of potential mechanisms responsible for MHO and the metabolic heterogeneity of obesity. This study was registered at ClinicalTrials.gov (NCT02706262).
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Klein et al. (2024) found shared pathophysiological alterations across metabolically healthy obese (MHO) and metabolically unhealthy obese (MUO) groups, including insulin resistance in skeletal muscle, subclinical inflammation, altered lipid turnover, oxidative stress, and cardiac structural changes.
“In a comprehensive multi-organ metabolic profiling study of people rigorously categorized as Metabolically Healthy Obese (MHO) versus Metabolically Unhealthy Obese (MUO), the authors found shared pathophysiological alterations across groups, including insulin resistance in skeletal muscle, subclinical inflammation, altered lipid turnover, oxidative stress, and cardiac structural changes.”
From Precision obesity medicine: A phenotype-guided framework for pharmacologic therapy across the lifespan (2025) · cites this paper as [96]
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References 99 · Cited by 149
- Authors
- Petersen, M. C., Smith, G. I., Palacios, H. H., Farabi, S. S., Yoshino, M., Yoshino, J., Cho, K., Davila-Roman, V. G., Shankaran, M., Barve, R. A., Yu, J., Stern, J. H., Patterson, B. W., Hellerstein, M. K., Shulman, G. I., Patti, G. J., & Klein, S.
- Affiliations
- Washington University in St. Louis (US)
- Keio University (JP)
- University of California, Berkeley (US)
- University of Arizona (US)
- Yale University (US)
- Corresponding author
- Klein, Samuel
- ORCID
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2024-04
- Volume
- 36
- Issue
- 4
- Pages
- 745-761.e5
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC11025492
- OpenAlex
- W4393535636
- Cited by
- 149
- References
- 99
- Citations by year
- 2026: 54 · 2025: 69 · 2024: 26
- FWCI
- 45.47
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Digital Commons@Becker (Washington University School of Medicine) (submittedVersion, cc-by-nc)
- Funders
- National Institutes of Health
- Foundation for Barnes-Jewish Hospital
- Endocrine Fellows Foundation
- Topics
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Disease and Adiposity
- Keywords
- metabolically healthy obesity, metabolically unhealthy obesity, skeletal muscle, adipose tissue, ceramide, branched-chain amino acid catabolism, mitochondrial function, lipogenesis, adiponectin, plasminogen activator inhibitor-1, oxidative stress, insulin resistance, hepatic steatosis, prediabetes, insulin sensitivity
- MeSH terms
- Obesity, Metabolically Benign, Adult, Cardiovascular Diseases, Humans, Insulin Resistance, Obesity, Risk Factors, Triglycerides, Body Mass Index, Metabolic Syndrome
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