American Diabetes Association
Browse

Type 1 diabetes genetic risk score differentiates subgroups of Ketosis-Prone Diabetes

Download (285.59 kB)
figure
posted on 2023-07-28, 20:05 authored by Deborah Osafehinti, Surya N Mulukutla, Christiane S Hampe, Ruchi Gaba, Nalini Ram, Michael N Weedon, Richard A Oram, Ashok Balasubramanyam
<p><strong>Objective: </strong>To determine if genetic risk for type 1 diabetes (T1D) differentiates the four “Ab” subgroups of Ketosis-Prone Diabetes (KPD), where “A+” and “A-” define presence or absence of islet autoantibodies and “b+” and “b-” define presence or absence of beta cell function.</p> <p><strong>Research Design and Methods:</strong> We compared T1D genetic risk scores (GRS) of KPD patients across subgroups, race/ethnicity, beta cell function and glycemia. </p> <p><strong>Results:</strong> Among 426 KPD patients (54% Hispanic, 31% African American, 11% White), rank-order of GRS was A+b- > A+b+ = A-b- > A-b+. GRS of A+b- KPD was lower than that of a T1D cohort and GRS of A-b+ KPD was higher than that of a T2D cohort. GRS was lowest among African American patients with a similar distribution across KPD subgroups.</p> <p><strong>Conclusions:</strong> T1D genetic risk delineates etiological differences between KPD subgroups. A+b- KPD patients have the highest and A-b+ KPD patients the lowest GRS. </p>

Funding

This work was supported by funds from NIH R01-DK056689 and the Rutherford Chair, Baylor-St. Luke’s Medical Center / Baylor College of Medicine (to AB), and a Diabetes UK Harry Keen Fellowship (16/0005529) (to RAO).

History

Usage metrics

    Diabetes Care

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC