AI Article Synopsis

  • - The study investigated the link between a type 1 diabetes (T1D) polygenic score and the risk of developing type 2 diabetes (T2D) using large datasets from the CHARGE consortium and MGB Biobank.
  • - Researchers found no significant association between the T1D polygenic score and T2D prevalence in both biobanks, although a specific human leukocyte antigen score showed a slight association with T2D in one cohort.
  • - While the T1D score had a weak association with insulin use among T2D cases in one dataset, the overall results suggest that a common variant score for T1D does not reliably predict T2D risk, highlighting the need for further studies

Article Abstract

Context: Both type 1 diabetes (T1D) and type 2 diabetes (T2D) have significant genetic contributions to risk and understanding their overlap can offer clinical insight.

Objective: We examined whether a T1D polygenic score (PS) was associated with a diagnosis of T2D in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.

Methods: We constructed a T1D PS using 79 known single nucleotide polymorphisms associated with T1D risk. We analyzed 13 792 T2D cases and 14 169 controls from CHARGE cohorts to determine the association between the T1D PS and T2D prevalence. We validated findings in an independent sample of 2256 T2D cases and 27 052 controls from the Mass General Brigham Biobank (MGB Biobank). As secondary analyses in 5228 T2D cases from CHARGE, we used multivariable regression models to assess the association of the T1D PS with clinical outcomes associated with T1D.

Results: The T1D PS was not associated with T2D both in CHARGE ( = .15) and in the MGB Biobank ( = .87). The partitioned human leukocyte antigens only PS was associated with T2D in CHARGE (OR 1.02 per 1 SD increase in PS, 95% CI 1.01-1.03, = .006) but not in the MGB Biobank. The T1D PS was weakly associated with insulin use (OR 1.007, 95% CI 1.001-1.012, = .03) in CHARGE T2D cases but not with other outcomes.

Conclusion: In large biobank samples, a common variant PS for T1D was not consistently associated with prevalent T2D. However, possible heterogeneity in T2D cannot be ruled out and future studies are needed do subphenotyping.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10576255PMC
http://dx.doi.org/10.1210/jendso/bvad123DOI Listing

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