Effect of gender on phenotypic expression of the S447X mutation in LPL -: The Copenhagen City Heart Study

被引:42
|
作者
Wittrup, HH
Nordestgaard, BG
Steffensen, R
Jensen, G
Tybjærg-Hansen, A
机构
[1] Univ Copenhagen Hosp, Rigshosp, Dept Clin Biochem KB3011, DK-2100 Copenhagen O, Denmark
[2] Herlev Univ Hosp, Dept Clin Biochem, Copenhagen, Denmark
[3] Univ Copenhagen Hosp, Rigshosp, Div Cardiol, Dept Med B, Copenhagen O, Denmark
[4] Univ Copenhagen, Bispebjerg Hosp, Copenhagen City Heart Study, Copenhagen O, Denmark
基金
英国医学研究理事会;
关键词
atherosclerosis; coronary disease; genes; lipids; lipoproteins;
D O I
10.1016/S0021-9150(02)00183-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The G188E, D9N, and N291S mutations in LPL increase TG, reduce HDL cholesterol, and increase risk of ischemic heart disease. The common S447X mutation may have opposite effects. We genotyped 8451 women and men from the Danish general population, and 854 women and men with ischemic heart disease. Participants carrying G188E, D9N, or N291S were excluded. Compared with non-carriers, female heterozygotes and homozygotes presented with a 0.11 and 0.18 mmol/l decrease in plasma TG (P = 0.001 and P = 0.37) and a 0.07 and 0.03 mmol/l increase in HDL cholesterol (P = 0.001 and P = 0.99). Male heterozygotes and homozygotes presented with a 0.20 and 0.41 mmol decrease in plasma TG (P < 0.001 and P = 0.06), which was twice that in women, and a 0.05 and 0. 17 mmol/l increase in plasma HDL cholesterol (P = 0.02 and P = 0.04), respectively. In meta-analyses by gender, the S447X mutation was associated with a significant 17% reduction in risk of ischemic heart disease in men (OR = 0.83; P = 0.01), whereas risk was unaffected in women (OR = 0.97; P = 0.98). The S447X mutation is associated with anti-atherogenic effects on TG and HDL cholesterol in both genders, and with a moderate protective effect on risk of ischemic heart disease in men. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
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页码:119 / 126
页数:8
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