Genetics
GWAS of 49,915 Koreans finds CETP among the lipid genes shared by metabolically unhealthy normal-weight and obese phenotypes (Sci Rep 2021)
Original title: Understanding the genetic architecture of the metabolically unhealthy normal weight and metabolically healthy obese phenotypes in a Korean population
A Korean cohort of 49,915 people, classified into metabolically healthy normal weight, metabolically unhealthy normal weight (MUHNW), metabolically healthy obese (MHO), and metabolically unhealthy obese phenotypes, underwent genome-wide association studies comparing normal-weight and obese subjects by metabolic health status. GCKR, ABCB11, CDKAL1, LPL, CDKN2B, NT5C2, APOA5, CETP and APOC1 were associated with metabolically unhealthy status among normal-weight individuals, while LPL, APOA5 and CETP were associated with metabolically unhealthy status among obese individuals. The genes shared across both comparisons, LPL, APOA5 and CETP, relate to lipid metabolism, while genes specific to the normal-weight comparison, GCKR, CDKAL1 and CDKN2B, relate to insulin or glucose metabolism. The authors present this as a map of the genetic architecture distinguishing metabolically healthy from unhealthy phenotypes within weight categories in a Korean population, with CETP identified as a shared lipid-metabolism contributor rather than the central focus of the study.
Original abstract
Understanding the mechanisms underlying the metabolically unhealthy normal weight (MUHNW) and metabolically healthy obese (MHO) phenotypes is important for developing strategies to prevent cardiometabolic diseases. Here, we conducted genome-wide association studies (GWASs) to identify the MUHNW and MHO genetic indices. The study dataset comprised genome-wide single-nucleotide polymorphism genotypes and epidemiological data from 49,915 subjects categorised into four phenotypes-metabolically healthy normal weight (MHNW), MUHNW, MHO, and metabolically unhealthy obese (MUHO). We conducted two GWASs using logistic regression analyses and adjustments for confounding variables (model 1: MHNW versus MUHNW and model 2: MHO versus MUHO). GCKR, ABCB11, CDKAL1, LPL, CDKN2B, NT5C2, APOA5, CETP, and APOC1 were associated with metabolically unhealthy phenotypes among normal weight individuals (model 1). LPL, APOA5, and CETP were associated with metabolically unhealthy phenotypes among obese individuals (model 2). The genes common to both models are related to lipid metabolism (LPL, APOA5, and CETP), and those associated with model 1 are related to insulin or glucose metabolism (GCKR, CDKAL1, and CDKN2B). This study reveals the genetic architecture of the MUHNW and MHO phenotypes in a Korean population-based cohort. These findings could help identify individuals at a high metabolic risk in normal weight and obese populations and provide potential novel targets for the management of metabolically unhealthy phenotypes.
ancestrygeneticsmetabolic syndrome
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.