| Literature DB >> 30334266 |
Takuya Imatoh1,2, Loic Yengo3, Ghislain Rocheleau3, Seiichiro Kamimura4, Shiro Maeda5,6, Motonobu Miyazaki7, Philippe Froguel3,8.
Abstract
It has been reported that polymorphisms within the gene-encoding enzymes related to alcohol metabolism are associated with levels of serum HDL-cholesterol (HDL-C) in East Asian populations. We evaluated the effects of genetic variants within the aldehyde dehydrogenase-2 (ALDH2) gene and the alcohol dehydrogenase-1B (ADH1B) gene on changes in the lipid profile in an 11-year longitudinal study. We genotyped rs1229984 within ADH1B and rs671 within ALDH2. We combined the genetic data with longitudinal clinical and biochemical data from 2002 to 2013 and designed a retrospective longitudinal study of 1436 Japanese males. There were significant negative relationships between rs671 within ALDH2 and HDL-C levels according to multiple linear regression analysis. Next, we assessed the association between the development of hypo-HDL cholesterolemia and rs1229984 within ADH1B or rs671 within ALDH2. In logistic regression analysis, rs671 A allele homozygote carriers have 2.65 times higher risk of developing hypo-HDL cholesterolemia than G allele homozygote carriers. Even after adjusting for possible confounding factors, a significant association was observed. However, no association between rs1229984 within ADH1B and the development of hypo-HDL cholesterolemia was observed. Rs671 within ALDH2 but not rs1229984 within ADH1B was associated with lower HDL-C levels in Japanese males.Entities:
Keywords: Alcohol dehydrogenase-1B; Aldehyde dehydrogenase-2; Epidemiological study; High-density lipoprotein; Single nucleotide polymorphisms
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Year: 2018 PMID: 30334266 DOI: 10.1002/lipd.12087
Source DB: PubMed Journal: Lipids ISSN: 0024-4201 Impact factor: 1.880