Melander O, Bengtsson K, Orho-Melander M, Lindblad U, Forsblom C, Råstam L, Groop L, Hulthén U L
Department of Endocrinology, Lund University, Malmö, Sweden.
J Hum Hypertens. 2000 Jan;14(1):43-6. doi: 10.1038/sj.jhh.1000942.
Previous studies have suggested that the Trp460 allele of the Gly460Trp polymorphism in the alpha-adducin gene is associated with salt sensitivity and primary hypertension. The present study was undertaken to evaluate if the Trp460 allele of this polymorphism is associated with primary hypertension in Scandinavians. To address this issue, 294 patients with primary hypertension and 265 normotensive control subjects from Sweden were examined and genotyped for the Gly460Trp polymorphism using polymerase chain reaction and restriction fragment length polymorphism methods. We then used a population of 80 patients with primary hypertension and 154 normotensive control subjects from Finland to replicate the findings. The frequency of the Trp460 allele was lower in hypertensive patients than in normotensive controls in the Swedish population (17.7% vs 23.0%; P = 0.03) and in the Finnish population (14.4% vs 19.5%; NS). Therefore we also performed a pooled analysis in which the frequency of the Trp460 allele was significantly lower in hypertensive patients than in normotensive controls (17.0% vs 21. 7%; P = 0.02). In subjects who did not receive antihypertensive medication (n = 447) there was no difference between carriers of the three different codon 460 genotypes (Trp-Trp; Trp-Gly and Gly-Gly) either for systolic (128 +/- 18; 127 +/- 15 and 129 +/- 17 mm Hg, NS) or for diastolic blood pressure (75.6 +/- 12.1; 74.7 +/- 9.3 and 75.0 +/- 10.4 mm Hg, NS). In conclusion, the lower frequency of the Trp460 allele in hypertensive patients than in normotensive controls strongly argues against a pathogenic role of this allele in primary hypertension. The results rather suggest that another variant in linkage disequilibrium with the Gly460Trp polymorphism increases susceptibility for hypertension. Journal of Human Hypertension (2000) 14, 43-46.
以往的研究表明,α-内收蛋白基因中Gly460Trp多态性的Trp460等位基因与盐敏感性及原发性高血压相关。本研究旨在评估该多态性的Trp460等位基因是否与斯堪的纳维亚人的原发性高血压相关。为解决这一问题,我们对来自瑞典的294例原发性高血压患者和265例血压正常的对照者进行了检查,并采用聚合酶链反应和限制性片段长度多态性方法对Gly460Trp多态性进行基因分型。然后,我们利用来自芬兰的80例原发性高血压患者和154例血压正常的对照者群体对研究结果进行重复验证。在瑞典人群中,高血压患者的Trp460等位基因频率低于血压正常的对照者(17.7%对23.0%;P = 0.03),在芬兰人群中也是如此(14.4%对19.5%;无显著性差异)。因此,我们还进行了一项汇总分析,结果显示高血压患者的Trp460等位基因频率显著低于血压正常的对照者(17.0%对21.7%;P = 0.02)。在未接受抗高血压药物治疗的受试者(n = 447)中,三种不同密码子460基因型(Trp-Trp;Trp-Gly和Gly-Gly)携带者的收缩压(128±18;127±15和129±17 mmHg,无显著性差异)或舒张压(75.6±12.1;74.7±9.3和75.0±10.4 mmHg,无显著性差异)均无差异。总之,高血压患者中Trp460等位基因频率低于血压正常的对照者,这有力地反驳了该等位基因在原发性高血压中起致病作用的观点。结果反而表明,与Gly460Trp多态性处于连锁不平衡状态的另一种变异增加了患高血压的易感性。《人类高血压杂志》(2000年)14卷,43 - 46页。