Davis B R, Arnett D K, Boerwinkle E, Ford C E, Leiendecker-Foster C, Miller M B, Black H, Eckfeldt J H
School of Public Health, University of Texas-Houston, Houston, TX 77030, USA.
Pharmacogenomics J. 2007 Apr;7(2):112-22. doi: 10.1038/sj.tpj.6500395. Epub 2006 May 16.
In a double-blind, outcome trial conducted in hypertensive patients randomized to chlorthalidone (C), amlodipine (A), lisinopril (L), or doxazosin (D), the alpha-adducin Gly460Trp polymorphism was typed (n=36 913). Mean follow-up was 4.9 years. Relative risks (RRs) of chlorthalidone versus other treatments were compared between genotypes (Gly/Gly+Gly/Trp versus Trp/Trp). Primary outcome was coronary heart disease (CHD). Coronary heart disease incidence did not differ among treatments or genotypes nor was there any interaction between treatment and genotype (P=0.660). Subgroup analyses indicated that Trp allele carriers had greater CHD risk with C versus A+L in women (RR=1.31) but not men (RR=0.91) with no RR gender differences for non-carriers (gender-gene-treatment interaction, P=0.002). The alpha-adducin gene is not an important modifier of antihypertensive treatment on cardiovascular risk, but women Trp allele carriers may have increased CHD risk if treated with C versus A or L. This must be confirmed to have implications for hypertension treatment.
在一项针对高血压患者的双盲结局试验中,将患者随机分为服用氯噻酮(C)、氨氯地平(A)、赖诺普利(L)或多沙唑嗪(D)组,并对α-内收蛋白Gly460Trp多态性进行分型(n = 36913)。平均随访时间为4.9年。比较了氯噻酮与其他治疗方法在不同基因型(Gly/Gly + Gly/Trp与Trp/Trp)之间的相对风险(RRs)。主要结局是冠心病(CHD)。冠心病发病率在各治疗组或基因型之间无差异,治疗与基因型之间也无任何相互作用(P = 0.660)。亚组分析表明,在女性中,Trp等位基因携带者服用C时患冠心病的风险高于服用A + L时(RR = 1.31),而男性中则不然(RR = 0.91),非携带者的RR无性别差异(性别-基因-治疗相互作用,P = 0.002)。α-内收蛋白基因不是抗高血压治疗对心血管风险的重要修饰因子,但女性Trp等位基因携带者若服用C而非A或L,可能会增加患冠心病的风险。这一点必须得到证实,才能对高血压治疗产生影响。