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Fetal/maternal-determined birth weight and adulthood type 2 diabetes and its subtypes: a Mendelian randomization study.
Wang, Wenxiu; Xiao, Wendi; Song, Zimin; Zhuang, Zhenhuang; Huang, Ninghao; Zhao, Yimin; Huang, Tao.
Affiliation
  • Wang W; Department of Epidemiology & Biostatistics, School of Public Health, Peking University, Beijing, China.
  • Xiao W; Department of Epidemiology & Biostatistics, School of Public Health, Peking University, Beijing, China.
  • Song Z; Department of Epidemiology & Biostatistics, School of Public Health, Peking University, Beijing, China.
  • Zhuang Z; Department of Epidemiology & Biostatistics, School of Public Health, Peking University, Beijing, China.
  • Huang N; Department of Epidemiology & Biostatistics, School of Public Health, Peking University, Beijing, China.
  • Zhao Y; Department of Sports Medicine, Peking University Third Hospital, Peking University, Beijing, China.
  • Huang T; Department of Epidemiology & Biostatistics, School of Public Health, Peking University, Beijing, China.
Article in En | MEDLINE | ID: mdl-38961757
ABSTRACT

BACKGROUND:

Lower birth weight (BW) might increase the risk of adulthood type 2 diabetes, but its associations with the highly heterogeneous type 2 diabetes subtypes remain to be studied. In addition, whether the associations between lower BW and adulthood type 2 diabetes risks depend on fetal or maternal effect is largely unknown.

METHODS:

In this study, we performed a two-sample Mendelian Randomization analysis to study the associations between overall, fetal-determined, and maternal-determined BW and the risks of type 2 diabetes and its subtypes, namely mild age-related diabetes (MARD), mild obesity-related diabetes (MOD), severe insulin-deficient diabetes (SIDD), and severe insulin-resistant diabetes (SIRD).

RESULTS:

Lower BW was genetically associated with increased risks of type 2 diabetes (odds ratio (OR) 1.86; 95% confidence interval (CI) 1.53, 2.26), MARD (OR 2.15; 95%CI 1.43, 3.23), MOD (OR 1.75; 95%CI 1.10, 2.77), SIDD (OR 1.86; 95%CI 1.11, 3.10), and SIRD (OR 1.66; 95%CI 1.06, 2.60). When examining the fetal-determined genetic effects independently, lower BW remained associated with type 2 diabetes and its subtypes, except for MOD. Using maternal-determined BW-lowering genotypes to proxy for an adverse intrauterine environment provided no evidence that it raised offspring risks of type 2 diabetes.

CONCLUSIONS:

Fetal-determined but not maternal-determined lower BW were associated with increased risks of adulthood type 2 diabetes and its subtypes. Our results underscored the importance of early targeted management among people with a low BW in the prevention of type 2 diabetes.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Clin Endocrinol Metab Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Clin Endocrinol Metab Year: 2024 Document type: Article Affiliation country: China