Age-dependent association between hepatic lipase gene C-480T polymorphism and the risk of pre-hospital sudden cardiac death:: The Helsinki Sudden Death Study

被引:7
作者
Fan, Yue-Mei
Lehtimaki, Terho
Rontu, Riikka
Ilveskoski, Erkki
Goebeler, Sirkka
Kajander, Olli
Mikkelsson, Jussi
Perola, Markus
Karhunen, Pekka J.
机构
[1] Tampere Univ Hosp, Ctr Lab Med, Lab Atherosclerosis Genet, FI-33521 Tampere, Finland
[2] Tampere Univ, FinnMedi 2, Sch Med, Dept Clin Chem, FI-33521 Tampere, Finland
[3] Tampere Univ Hosp, Ctr Lab Med, Tampere, Finland
[4] Tampere Univ, Sch Med, Dept Forens Med, FIN-33101 Tampere, Finland
[5] Natl Publ Hlth Inst, Dept Human Mol Genet, Helsinki, Finland
基金
芬兰科学院;
关键词
acute myocardial infarction; hepatic lipase; polymorphism; sudden cardiac death;
D O I
10.1016/j.atherosclerosis.2006.05.028
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: We investigated the association between hepatic lipase (HL) C-480T polymorphism and the risk of acute myocardial infarction (AMI) as well as pre-hospital sudden cardiac death (SCD). Methods: Seven hundred sudden or unnatural pre-hospital deaths of middle-aged (33-70 years, mean 53 years) Caucasian Finnish men were subjected to detailed autopsy (Helsinki Sudden Death Study). Genotype data were obtained for 682 men. Results: In logistic regression analysis with age, body mass index, hypertension, diabetes, smoking and alcohol consumption as covariates, men with the TT genotype had an increased risk for SCD and AMI compared to CC carriers (OR = 3.0, P = 0.011; and OR = 3.7, P = 0.003). There was a significant age-by-genotype interaction (P < 0.05) on the risk of SCD. Compared to CC genotype carriers, the association between the TT genotype and SCD was particularly strong (P = 0.001) among men <53 years of age, but this association was non-significant among older men. This was mainly due to a strong association between the TT genotype and AMI due to severe coronary disease in the absence of thrombosis. Carriers of the TT genotype were more likely to have severe coronary stenoses (>= 50%) than men with the CT or CC genotype (P = 0.019). Conclusions: The results suggest that HL C-480T polymorphism, is a strong age-dependent risk factor of SCD in early middle-aged men. (C) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:421 / 427
页数:7
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