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  • 标题:Adiposity significantly modifies genetic risk for dyslipidemia
  • 本地全文:下载
  • 作者:Christopher B. Cole ; Majid Nikpay ; Paulina Lau
  • 期刊名称:JLR Papers In Press
  • 印刷版ISSN:0022-2275
  • 电子版ISSN:1539-7262
  • 出版年度:2014
  • 卷号:55
  • 期号:11
  • 页码:2416-2422
  • DOI:10.1194/jlr.P052522
  • 语种:English
  • 出版社:American Society for Biochemistry and Molecular Biology
  • 摘要:Recent genome-wide association studies have identified multiple loci robustly associated with plasma lipids, which also contribute to extreme lipid phenotypes. However, these common genetic variants explain PInteraction = 2.87 × 10−4) and HDLc ( PInteraction = 1.05 × 10−3). These interactions were largely driven by SNPs tagging APOA5 , glucokinase receptor ( GCKR ), and LPL for TG, and cholesteryl ester transfer protein ( CETP ), GalNAc-transferase ( GALNT2 ), endothelial lipase ( LIPG ), and phospholipid transfer protein ( PLTP ) for HDLc. In contrast, the GRSLDL cholesterol × adiposity interaction was not significant. Sexual dimorphism was evident for the GRSHDL on HDLc in obese ( PInteraction = 0.016) but not lean subjects. SNP by BMI interactions may provide biological insight into specific genetic associations and missing heritability.
  • 关键词:obesity ; genetic risk score ; lipoproteins ; single nucleotide polymorphism ; statistical interaction
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