Genetic prediction of age at menarche, age at natural menopause and type 2 diabetes: A Mendelian randomization study

Nutr Metab Cardiovasc Dis. 2023 Apr;33(4):873-882. doi: 10.1016/j.numecd.2023.01.011. Epub 2023 Jan 29.

Abstract

Background and aims: The relationship between reproductive factors and type 2 diabetes (T2D) is controversial; therefore, we explored the causal relationship of age at menarche (AAM), age at natural menopause (ANM), with the risk of T2D and glycemic traits using two-sample Mendelian randomization.

Methods and results: We used publicly available data at the summary level of genome-wide association studies, where AAM (N = 329,345), ANM (N = 69,360), T2D (N = 464,389). The inverse variance weighting (IVW) method was employed as the primary method. To demonstrate the robustness of the results, we also conducted various sensitivity analysis methods including the MR-Egger regression, the weighted median (WM) and the MR Pleiotropy RESidual Sum and Outlier (MR-PRESSO) test. After excluding IVs associated with confounders, we found a causal association between later AAM and reduced risk of T2D (OR 0.81 [95% CI 0.75, 0.87]; P = 2.20 × 10-8), lower levels of FI (β -0.04 [95% CI -0.06, -0.01]; P = 2.19 × 10-3), FPG (β -0.03 [95% CI -0.05, -0.007]; P = 9.67 × 10-5) and HOMA-IR (β -0.04 [95% CI -0.06, -0.01]; P = 4,95 × 10-3). As for ANM, we only found a causal effect with HOMA-IR (β -0.01 [95% CI -0.02, -0.005]; P = 1.77 × 10-3), but not with T2D.

Conclusions: Our MR study showed a causal relationship between later AAM and lower risk of developing T2D, lower FI, FPG and HOMA-IR levels. This may provide new insights into the prevention of T2D in women.

Keywords: Age at menarche; Age at natural menopause; Mendelian randomization; Type 2 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Diabetes Mellitus, Type 2* / diagnosis
  • Diabetes Mellitus, Type 2* / epidemiology
  • Diabetes Mellitus, Type 2* / genetics
  • Female
  • Genome-Wide Association Study / methods
  • Humans
  • Menarche / genetics
  • Mendelian Randomization Analysis
  • Menopause / genetics
  • Polymorphism, Single Nucleotide