國家衛生研究院 NHRI:Item 3990099045/14353
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 12145/12927 (94%)
造访人次 : 908741      在线人数 : 1042
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻
    主页登入上传说明关于NHRI管理 到手机版


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.nhri.org.tw/handle/3990099045/14353


    题名: Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations
    作者: Ge, T;Irvin, MR;Patki, A;Srinivasasainagendra, V;Lin, YF;Tiwari, HK;Armstrong, ND;Benoit, B;Chen, CY;Choi, KW;Cimino, JJ;Davis, BH;Dikilitas, O;Etheridge, B;Feng, YA;Gainer, V;Huang, H;Jarvik, GP;Kachulis, C;Kenny, EE;Khan, A;Kiryluk, K;Kottyan, L;Kullo, IJ;Lange, C;Lennon, N;Leong, A;Malolepsza, E;Miles, AD;Murphy, S;Namjou, B;Narayan, R;O'Connor, MJ;Pacheco, JA;Perez, E;Rasmussen-Torvik, LJ;Rosenthal, EA;Schaid, D;Stamou, M;Udler, MS;Wei, WQ;Weiss, ST;Ng, MCY;Smoller, JW;Lebo, MS;Meigs, JB;Limdi, NA;Karlson, EW
    贡献者: Center for Neuropsychiatric Research
    摘要: 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.
    日期: 2022-06-29
    關聯: Genome Medicine. 2022 Jun 29;14:Article number 70.
    Link to: http://dx.doi.org/10.1186/s13073-022-01074-2
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1756-994X&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000819007300001
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85133024033
    显示于类别:[林彥鋒] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    PUB35765100.pdf1389KbAdobe PDF169检视/开启


    在NHRI中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈