4.7 Article

Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations

期刊

GENOME MEDICINE
卷 14, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13073-022-01074-2

关键词

Polygenic risk score; Type 2 diabetes; Diverse populations; Clinical implementation

资金

  1. National Human Genome Research Institute (NHGRI) [U01HG006828, U01HG006830, U01HG006389, U01HG006382, U01HG006375, U01HG006379, U01HG006380, U01HG006388, U01HG006378, U01HG006385]
  2. NHGRI [U01HG008685, U01HG008680]
  3. University of Alabama at Birmingham [U01HG011167]
  4. REGARDS [R01HL136666]
  5. HyperGEN [R01HL055673]
  6. GenHAT [R01HL123782]
  7. WPC [R01HL092173, K24HL133373]
  8. National Heart, Lung, and Blood Institute (NHLBI)
  9. National Institute of Neurological Disorders and Stroke (NINDS) [U01NS041588]
  10. Doris Duke Charitable Foundation [2020096]
  11. NIH [R01HL092173, UL1TR001873, OT2OD026553, OT2HL161841, P30AR070253, P30AR069625, U01HG011723, U01DK105556, R01DK066358, R01DK078616, R01HL151855, R01AR063759, R21AR078339, R00AG054573, K25DK128563, K23DK114551]

向作者/读者索取更多资源

This study developed and validated a trans-ancestry PRS using multiple populations' T2D GWAS data, demonstrating its potential as a risk index in clinical settings among diverse patients.
Background Type 2 diabetes (T2D) is a worldwide scourge caused by both genetic and environmental risk factors that disproportionately afflicts communities of color. Leveraging existing large-scale genome-wide association studies (GWAS), polygenic risk scores (PRS) have shown promise to complement established clinical risk factors and intervention paradigms, and improve early diagnosis and prevention of T2D. However, to date, T2D PRS have been most widely developed and validated in individuals of European descent. Comprehensive assessment of T2D PRS in non-European populations is critical for equitable deployment of PRS to clinical practice that benefits global populations. Methods We integrated T2D GWAS in European, African, and East Asian populations to construct a trans-ancestry T2D PRS using a newly developed Bayesian polygenic modeling method, and assessed the prediction accuracy of the PRS in the multi-ethnic Electronic Medical Records and Genomics (eMERGE) study (11,945 cases; 57,694 controls), four Black cohorts (5137 cases; 9657 controls), and the Taiwan Biobank (4570 cases; 84,996 controls). We additionally evaluated a post hoc ancestry adjustment method that can express the polygenic risk on the same scale across ancestrally diverse individuals and facilitate the clinical implementation of the PRS in prospective cohorts. Results The trans-ancestry PRS was significantly associated with T2D status across the ancestral groups examined. The top 2% of the PRS distribution can identify individuals with an approximately 2.5-4.5-fold of increase in T2D risk, which corresponds to the increased risk of T2D for first-degree relatives. The post hoc ancestry adjustment method eliminated major distributional differences in the PRS across ancestries without compromising its predictive performance. Conclusions By integrating T2D GWAS from multiple populations, we developed and validated a trans-ancestry PRS, and demonstrated its potential as a meaningful index of risk among diverse patients in clinical settings. Our efforts represent the first step towards the implementation of the T2D PRS into routine healthcare.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据