Causal relationship between body mass index and insulin resistance: Linear and nonlinear Mendelian randomization study in a Japanese population
Author(s) -
Ishida Noriyuki,
Harada Sei,
Toki Ryota,
Hirata Aya,
Matsumoto Minako,
Miyagawa Naoko,
Iida Miho,
Edagawa Shun,
Miyake Atsuko,
Kuwabara Kazuyo,
Shibuki Takuma,
Kato Suzuka,
Arakawa Kazuharu,
Kinoshita Kengo,
SakuraiYageta Mika,
Tamiya Gen,
Nagashima Kengo,
Muraoka Hirokazu,
Sato Yasunori,
Takebayashi Toru
Publication year - 2025
Publication title -
journal of diabetes investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.089
H-Index - 50
eISSN - 2040-1124
pISSN - 2040-1116
DOI - 10.1111/jdi.14377
Subject(s) - mendelian randomization , insulin resistance , medicine , body mass index , obesity , type 2 diabetes , diabetes mellitus , population , homeostatic model assessment , endocrinology , type 2 diabetes mellitus , insulin , genotype , biology , genetics , environmental health , genetic variants , gene
ABSTRACT Aims/Introduction Obesity is a known risk factor for several chronic diseases, including type 2 diabetes mellitus, which results from increased insulin resistance and impaired insulin secretion. However, the association between obesity and insulin resistance in Asian populations has not yet been fully elucidated. Therefore, we aimed to investigate the causal relationship between body mass index (BMI) and glycemic traits using Mendelian randomization (MR). Materials and Methods We performed individual‐level MR analyses using genetic risk scores based on BMI‐related variants in 3,745 individuals without diabetes mellitus from a Japanese cohort. We examined heterogeneity through subgroup analyses based on potential modifiers and determined the shape of the causal relationship using nonlinear MR analyses to further assess the impact of BMI on the homeostasis model assessment of insulin resistance (HOMA‐IR). Results MR analyses revealed a significant positive association between BMI and HOMA‐IR (β = 0.077; 95% confidence interval, 0.014–0.141; P = 0.016; outcome variable was log‐transformed and standardized). Additional analyses revealed heterogeneity among subgroups differentiated by age, sex, lifestyle habits, and cardiometabolic traits. Nonlinear MR analyses suggested a potential J‐shaped causal relationship between BMI and HOMA‐IR. Conclusions Our findings demonstrated that obesity and low BMI may contribute to increased insulin resistance. Furthermore, the impact of BMI on insulin resistance could vary owing to effect modification. Managing BMI is crucial in individuals at high risk of increased insulin resistance and may have important implications for preventing type 2 diabetes, especially given the low insulin secretory capacity observed in East Asian populations.
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