4.7 Article

A genome-wide cross-trait analysis identifies shared loci and causal relationships of type 2 diabetes and glycaemic traits with polycystic ovary syndrome

Journal

DIABETOLOGIA
Volume 65, Issue 9, Pages 1483-1494

Publisher

SPRINGER
DOI: 10.1007/s00125-022-05746-x

Keywords

Genome-wide cross-trait analysis; Insulin resistance; Mendelian randomisation; Polycystic ovary syndrome; Type 2 diabetes

Funding

  1. Swedish Medical Research Council [2018-02435]
  2. Novo Nordisk Foundation [NNF19OC0056647]
  3. Diabetes Foundation [DIA2021633]
  4. Karolinska Institute
  5. Vinnova [2018-02435] Funding Source: Vinnova
  6. Swedish Research Council [2018-02435] Funding Source: Swedish Research Council
  7. Formas [2018-02435] Funding Source: Formas

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The genetic link between type 2 diabetes, glycaemic traits and PCOS was found, influenced by both biological pleiotropy and causal mediation, some of which is independent of BMI. The study highlights the importance of controlling fasting insulin levels to mitigate the risk of PCOS, as well as screening for and monitoring type 2 diabetes in all women with PCOS, irrespective of BMI.
Aims/hypothesis The link underlying abnormal glucose metabolism, type 2 diabetes and polycystic ovary syndrome (PCOS) that is independent of BMI remains unclear in observational studies. We aimed to clarify this association using a genome-wide cross-trait approach. Methods Summary statistics from the hitherto largest genome-wide association studies conducted for type 2 diabetes, type 2 diabetes mellitus adjusted for BMI (T2DM(adj)BMI), fasting glucose, fasting insulin, 2h glucose after an oral glucose challenge (all adjusted for BMI), HbA(1c) and PCOS, all in populations of European ancestry, were used. We quantified overall and local genetic correlations, identified pleiotropic loci and expression-trait associations, and made causal inferences across traits. Results A positive overall genetic correlation between type 2 diabetes and PCOS was observed, largely influenced by BMI (r(g)=0.31, p=1.63x10(-8)) but also independent of BMI (T2DM(adj)BMI-PCOS: r(g)=0.12, p=0.03). Sixteen pleiotropic loci affecting type 2 diabetes, glycaemic traits and PCOS were identified, suggesting mechanisms of association that are independent of BMI. Two shared expression-trait associations were found for type 2 diabetes/T2DM(adj)BMI and PCOS targeting tissues of the cardiovascular, exocrine/endocrine and digestive systems. A putative causal effect of fasting insulin adjusted for BMI and type 2 diabetes on PCOS was demonstrated. Conclusions/interpretation We found a genetic link underlying type 2 diabetes, glycaemic traits and PCOS, driven by both biological pleiotropy and causal mediation, some of which is independent of BMI. Our findings highlight the importance of controlling fasting insulin levels to mitigate the risk of PCOS, as well as screening for and long-term monitoring of type 2 diabetes in all women with PCOS, irrespective of BMI.

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