Fan Yue-Mei, Lehtimäki Terho, Rontu Riikka, Ilveskoski Erkki, Goebeler Sirkka, Kajander Olli, Mikkelsson Jussi, Perola Markus, Karhunen Pekka J
Laboratory of Atherosclerosis Genetics, Centre for Laboratory Medicine, Tampere University Hospital, Tampere, Finland.
Atherosclerosis. 2007 Jun;192(2):421-7. doi: 10.1016/j.atherosclerosis.2006.05.028. Epub 2006 Jun 21.
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).
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.
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 (> or =50%) than men with the CT or CC genotype (P=0.019).
The results suggest that HL C-480T polymorphism is a strong age-dependent risk factor of SCD in early middle-aged men.
我们研究了肝脂酶(HL)C-480T多态性与急性心肌梗死(AMI)风险以及院外心脏性猝死(SCD)之间的关联。
对700例中年(33 - 70岁,平均53岁)芬兰白人男性的院外猝死或非自然死亡病例进行了详细尸检(赫尔辛基猝死研究)。获得了682名男性的基因型数据。
在以年龄、体重指数、高血压、糖尿病、吸烟和饮酒作为协变量的逻辑回归分析中,与CC基因型携带者相比,TT基因型男性发生SCD和AMI的风险增加(OR = 3.0,P = 0.011;OR = 3.7,P = 0.003)。在SCD风险方面存在显著的年龄与基因型交互作用(P < 0.05)。与CC基因型携带者相比,TT基因型与SCD之间的关联在年龄<53岁的男性中尤为强烈(P = 0.001),但在老年男性中这种关联不显著。这主要是由于在没有血栓形成的情况下,TT基因型与严重冠状动脉疾病导致的AMI之间存在强烈关联。TT基因型携带者比CT或CC基因型男性更有可能出现严重冠状动脉狭窄(≥50%)(P = 0.019)。
结果表明,HL C-480T多态性是中年早期男性SCD的一个强烈的年龄依赖性风险因素。