English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12500/13673 (91%)
Visitors : 2666032      Online Users : 612
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/16459


    Title: Genetic variants in severe hypertriglyceridemia among taiwanese participants - insights from genome-wide association and whole-exome sequencing analyses
    Authors: Fan, HY;Tsai, MC;Lai, CJ;Yeh, CL;Hsu, HY;Lai, PJ;Hsu, HC;Su, TC;Lin, HJ;Lin, YF;Lu, TP;Chien, KL
    Contributors: Center for Neuropsychiatric Research
    Abstract: BACKGROUND: There are limited data on the use of whole-exome sequencing (WES) to diagnose severe hypertriglyceridemia. Our aim was to identify candidate genes linked to triglyceride levels via a genome-wide association study (GWAS) and to recruit participants with severe hypertriglyceridemia for WES to assess allelic variants in the candidate genes. METHODS AND RESULTS: A GWAS was conducted involving 120,140 participants to identify lead loci associated with blood triglyceride levels. Following the identification of these lead loci, WES was performed on DNA samples from 29 participants with hypertriglyceridemia whose triglyceride levels exceeded 800 mg/dL to assess variations in the corresponding genes. In the GWAS of 120,140 participants, the apolipoprotein A5 (APOA5) locus on chromosome 11 showed the strongest association with blood triglyceride levels (lead single nucleotide polymorphism [SNP] rs2075291; P=3.07×10(-108)), along with 5 independent SNPs (most significant P=7.84×10(-167)). Other key loci included BUD13 homolog (BUD13; P=2.73×10(-62)), glucokinase regulator (GCKR; P=2.63×10(-24)), and lipoprotein lipase (LPL; P=1.50×10(-11)). WES in 29 hypertriglyceridemia patients identified additional genes, including ALDH1A2, APOC1, LPL, RGS7, and SIK3, showing significant allele frequency variations and potential roles in lipid metabolism. CONCLUSIONS: Our study confirms the role of known genetic loci in triglyceride metabolism and hypertriglyceridemia while uncovering novel loci, offering new perspectives on lipid regulation and potential avenues for therapeutic advancements.
    Date: 2025-02
    Relation: Circulation Journal. 2025 Feb 25;89(3):331-339.
    Link to: http://dx.doi.org/10.1253/circj.CJ-24-0491
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=&DestApp=IC2JCR
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85219376599
    Appears in Collections:[林彥鋒] 期刊論文

    Files in This Item:

    File SizeFormat
    PUB39662927.pdf1284KbAdobe PDF33View/Open


    All items in NHRI are protected by copyright, with all rights reserved.

    Related Items in TAIR

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