Association of genetic variants with myocardial infarction in Japanese individuals with different lipid profiles

被引:8
作者
Yoshida, Tetsuro [2 ]
Kato, Kimihiko [3 ]
Yokoi, Kiyoshi [3 ]
Oguri, Mitsutoshi [4 ]
Watanabe, Sachiro [5 ]
Metoki, Norifumi [6 ]
Yoshida, Hidemi [7 ]
Satoh, Kei [7 ]
Aoyagi, Yukitoshi [8 ]
Nozawa, Yoshinori [9 ,10 ]
Yamada, Yoshiji [1 ]
机构
[1] Mie Univ, Life Sci Res Ctr, Dept Human Funct Genom, Tsu, Mie 5148507, Japan
[2] Inabe Gen Hosp, Dept Cardiovasc Med, Inabe, Japan
[3] Gifu Prefectural Tajimi Hosp, Dept Cardiovasc Med, Tajimi, Japan
[4] Japanese Red Cross Nagoya First Hosp, Dept Cardiol, Nagoya, Aichi, Japan
[5] Gifu Prefectural Gen Med Ctr, Dept Cardiol, Gifu, Japan
[6] Hirosaki Stroke Ctr, Dept Internal Med, Hirosaki, Aomori, Japan
[7] Hirosaki Univ, Grad Sch Med, Dept Vasc Biol, Inst Brain Sci, Hirosaki, Aomori, Japan
[8] Tokyo Metropolitan Inst Gerontol, Dept Genom Longev & Hlth, Tokyo, Japan
[9] Gifu Int Inst Biotechnol, Kakamigahara, Japan
[10] Tokai Gakuin Univ, Kakamigahara, Japan
关键词
genetics; polymorphism; myocardial infarction; lipid profiles; triglycerides; high density lipoprotein cholesterol; low density lipoprotein cholesterol; POLYMORPHISMS; RISK; IDENTIFICATION; FAMILY; NEUROPILIN-2; RECEPTOR;
D O I
10.3892/ijmm_00000383
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Dyslipidemia is an important risk factor for mvocardial infarction (MI) We previously Showed that gene polymorphisms associated with MI differed among individuals with different lipid profiles. We further examined whether variants that confer susceptibility to MI might differ genetic among individuals with low or high serum concenterations of triglycerides, high density lipoprotein (HDL)-cholesterol, or density lipoprotein (LDL)-cholesterol. The, study population comprised 5270 Japanese individuals, including 1188 subjects with M I and 4082 controls The 150 polymorphisms examined in the present study were selected by genome-wide association studies of MI and ischemic Stroke with the Use of file Affymetrix GeneChip Human Mapping, 500K Array Set. The Initial Chi-square test revealed that the A-G polymorphism (rs12632110) of SEMA3F was significantly ((false discovery rate <005) associated with MI among with high serum HDL-cholesterol or among those with low serum LDL-cholesterol Subsequent multivariable logistic regression analysis with adjustment For covariates revealed that rs12632110 was significantly (P<0.01) associated with MI in individuals with high serum HDL-cholesterol of with low serum LDL-cholesterol The genetic variants that confer susceptibility to MI differ among individuals with different lipid profiles. and the genetic component for the development of MI is more apparent in individuals at low-development (high HDL and low LDL-cholesterol levels) compared to those at high-risk. Stratification of subjects according to lipid profiles may thus be important for personalized prevention of IMI based on genetic information
引用
收藏
页码:607 / 616
页数:10
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