Minnich A, DeLangavant G, Lavigne J, Roederer G, Lussier-Cacan S, Davignon J
Clinical Research Institute of Montreal, Canada.
Arterioscler Thromb Vasc Biol. 1995 Oct;15(10):1740-5. doi: 10.1161/01.atv.15.10.1740.
The present study sought to resolve the contradictory evidence as to whether the G-->A substitution at position -75 of the apoA-I gene promoter raises HDL cholesterol (HDL-C) levels by examining the effect of this polymorphism in French Canadians, a relatively genetically homogeneous population. Among 308 women, carriers of the A allele displayed 12% and 10% higher mean plasma HDL-C and apoA-I concentrations, respectively, than did noncarriers. Among 345 men, no effect of the A allele was noted. The frequency distribution of HDL-C levels in women carrying the A but not the G allele appeared bimodal, with one peak corresponding to the mean of the noncarriers and a second to higher HDL-C. Thus it appears that only a subset of A alleles confers high HDL-C levels. This hypothesis was supported by data from four kindreds within which some but not all A alleles segregated with hyperalphalipoproteinemia. The data suggest that the A substitution in the apoA-I gene promoter does not directly confer high HDL-C levels but may be in linkage disequilibrium with other sequence polymorphism(s) at this locus in a subset of alleles that raise HDL-C levels.
本研究旨在通过检测法国裔加拿大人(一个遗传上相对同质的群体)中载脂蛋白A-I(apoA-I)基因启动子-75位G→A替换对高密度脂蛋白胆固醇(HDL-C)水平的影响,来解决关于该替换是否会提高HDL-C水平的相互矛盾的证据。在308名女性中,A等位基因携带者的平均血浆HDL-C和apoA-I浓度分别比非携带者高12%和10%。在345名男性中,未观察到A等位基因的影响。携带A而非G等位基因的女性中HDL-C水平的频率分布呈双峰,一个峰值对应非携带者的平均值,另一个对应较高的HDL-C。因此,似乎只有一部分A等位基因会导致HDL-C水平升高。这一假设得到了来自四个家族的数据支持,在这些家族中,部分而非所有A等位基因与高α脂蛋白血症相关。数据表明,apoA-I基因启动子中的A替换并不直接导致HDL-C水平升高,而是可能与该位点上一组能提高HDL-C水平的其他序列多态性处于连锁不平衡状态。