Tiret L, Poirier O, Hallet V, McDonagh T A, Morrison C, McMurray J J, Dargie H J, Arveiler D, Ruidavets J B, Luc G, Evans A, Cambien F
INSERM U525, 17 rue du Fer à Moulin, 75005 Paris, France.
Hypertension. 1999 May;33(5):1169-74. doi: 10.1161/01.hyp.33.5.1169.
There is accumulating evidence that endothelin-1 plays an important role in vascular pathophysiology. Our objective was to examine whether molecular variations at the endothelin-1 locus were involved in susceptibility to myocardial infarction and variation in blood pressure. The entire coding sequence and 1.4 kb of the 5' flanking region were screened. Five polymorphisms were detected, which were genotyped in the ECTIM (Etude Cas-Témoin de l'Infarctus du Myocarde) Study, a multicenter study comparing 648 male patients who had survived a myocardial infarction and 760 population-based controls. The polymorphisms were not associated with myocardial infarction, nor did they contribute to blood pressure levels in the population at large. However, a G/T polymorphism predicting an Lys/Asn change (ET1/C198) strongly interacted (P<0.001) with body mass index in the determination of blood pressure levels. There was a steeper increase of blood pressure with body mass index in carriers of the T allele than in GG homozygotes. As a consequence, the T allele was associated with an increase of blood pressure in overweight subjects (body mass index >/=26 kg/m2), while no significant effect was observed in lean subjects (body mass index <26 kg/m2). To determine whether this finding could be replicated, the ET1/C198 was genotyped in the Glasgow Heart Scan Study, a population-based study including 619 men and 663 women. Subjects homozygous for the T allele had higher resting blood pressure levels than others (P<0.05). A similar interaction between the T allele and body mass index was observed on the maximum blood pressure achieved during a treadmill exercise test (P<0.001). In conclusion, results from 2 independent studies suggest that the ET1/C198 polymorphism is associated with blood pressure levels in overweight people.
越来越多的证据表明内皮素-1在血管病理生理学中起重要作用。我们的目的是研究内皮素-1基因座的分子变异是否与心肌梗死易感性及血压变化有关。对整个编码序列和5'侧翼区域的1.4 kb进行了筛查。检测到五个多态性位点,在ECTIM(心肌梗死病例对照研究)中对其进行了基因分型,这是一项多中心研究,比较了648例心肌梗死后存活的男性患者和760例基于人群的对照。这些多态性与心肌梗死无关,在总体人群中也对血压水平没有影响。然而,一个预测赖氨酸/天冬酰胺变化的G/T多态性(ET1/C198)在血压水平的测定中与体重指数有强烈的相互作用(P<0.001)。与GG纯合子相比,T等位基因携带者的血压随体重指数的升高更为陡峭。因此,T等位基因与超重受试者(体重指数≥26 kg/m2)的血压升高有关,而在瘦受试者(体重指数<26 kg/m2)中未观察到显著影响。为了确定这一发现是否可以重复,在格拉斯哥心脏扫描研究中对ET1/C198进行了基因分型,该研究是一项基于人群的研究,包括619名男性和663名女性。T等位基因纯合子受试者的静息血压水平高于其他受试者(P<0.05)。在跑步机运动试验中达到的最大血压上也观察到T等位基因与体重指数之间有类似的相互作用(P<0.001)。总之,两项独立研究的结果表明,ET1/C198多态性与超重人群的血压水平有关。