Key result
Clinical obesity linked to ~149% higher cardiovascular risk versus preclinical obesity.
Why the study?
The Lancet Diabetes & Endocrinology Commission proposed a new definition for clinical obesity, but its prognostic value remains unclear.
Does clinical obesity (by new criteria) increase the risk of cardiovascular outcomes and mortality compared to preclinical obesity or non-obesity?
Cohort
Yes
Does clinical obesity (by new criteria) increase the risk of cardiovascular outcomes and mortality compared to preclinical obesity or non-obesity?
The new Lancet Commission definition of clinical obesity effectively stratifies cardiovascular and mortality risk across diverse international cohorts.
Answers are grounded in this paper and cite their sources.
Clinical obesity per new criteria identifies higher-risk adults; observational cohorts leave open whether it refines risk stratification beyond BMI.
Objective The Lancet Diabetes & Endocrinology Commission proposed a new definition for clinical obesity. However, its prognostic value remains unclear. Methods Clinical obesity was defined using the Commission's criteria in the China Health and Retirement Longitudinal Study (CHARLS), the English Longitudinal Study of Aging (ELSA), and the National Health and Nutrition Examination Survey (NHANES). Prevalence estimation was conducted across four categories based on obesity and organ dysfunction status. Cox proportional hazards models were used to assess associations with clinical outcomes. Results The prevalence of clinical obesity was 2.50% (CHARLS), 6.18% (ELSA), and 9.08% (NHANES), respectively. Overall, older adults and men had lower prevalence, while older men in NHANES showed higher prevalence. Compared with non‐obesity without dysfunctions, clinical obesity and non‐obesity with dysfunctions showed higher risks of cardiovascular outcomes. Compared with preclinical obesity, clinical obesity elevated cardiovascular risk in CHARLS (HR = 2.49, 95% CI: 1.32–4.70) and ELSA (HR = 1.80, 95% CI: 1.02–3.17) and increased all‐cause (HR = 1.88, 95% CI: 1.23–2.87) and cardiovascular (HR = 3.11, 95% CI: 1.49–6.50) mortality risk in NHANES. Conclusions The prevalence of clinical obesity varied by age, sex, and country. Overall, the prevalence was lower among older adults and men. Clinical obesity was associated with increased cardiovascular event risk across cohorts and increased all‐cause mortality risk in NHANES, highlighting its value for risk stratification.
No takes yet. Share an insight, caveat, or question.
Li et al. (2026) conducted a cohort in Clinical obesity. Clinical obesity vs. Preclinical obesity was evaluated on Cardiovascular risk (CHARLS cohort) (HR 2.49, 95% CI 1.32-4.70). Compared with preclinical obesity, clinical obesity increased cardiovascular risk in CHARLS (HR 2.49) and ELSA (HR 1.80), and increased cardiovascular mortality in NHANES (HR 3.11).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: