Department of Clinical Sciences, Lund University and Center for Emergency Medicine, Malmö University Hospital, Malmö, Sweden.
J Hypertens. 2011 Feb;29(2):388-95. doi: 10.1097/HJH.0b013e3283410390.
The capability of the protein NEDD4L to reduce renal tubular expression of epithelial Na+ channel (ENaC) is influenced by a functional rs4149601 G→A NEDD4L polymorphism. As diuretics and β-blockers inhibit renal sodium reabsorption and renin release, respectively, we hypothesized that the β-blocker or diuretic-induced blood pressure reduction and prevention of cardiovascular disease would be greater in patients with the highest ENaC expression (rs4149601 G-allele), whereas there would be no such genetically mediated differences in treatment efficacy among patients treated with the vasodilator diltiazem.
We related rs4149601 status to 6-month blood pressure reduction and risk of cardiovascular events in 5152 hypertensive patients (DBP ≥ 100 mmHg) from the Nordic Diltiazem Study (NORDIL) randomized to either β-blocker and/or diuretic-based treatment or diltiazem-based treatment.
In patients on β-blocker or diuretic monotherapy, carriers of the G-allele had greater SBP reduction (19.5 ± 16.8 vs. 15.0 ± 19.3 mmHg, P < 0.001) and DBP reduction (15.4 ± 8.3vs. 14.1 ± 8.4 mmHg, P = 0.02) and during 4.5 years of follow-up among patients randomized to β-blockers and/or diuretics, carriers of the G-allele had greater protection from cardiovascular events [relative risk (RR) = 0.52, 95% confidence interval (CI) = 0.36-0.74, P < 0.001] as compared to AA homozygotes. Within the diltiazem group, there was no difference in blood pressure reduction or risk of cardiovascular events according to genotype.
The functional NEDD4L rs4149601 polymorphism influences the efficacy of β-blocker and/or diuretic-based antihypertensive treatment both in terms of blood pressure reduction and cardiovascular disease protection, whereas diltiazem-based antihypertensive treatment efficacy is not influenced by this NEDD4L polymorphism.
蛋白 NEDD4L 降低上皮钠通道 (ENaC) 肾小管表达的能力受到功能性 rs4149601 G→A NEDD4L 多态性的影响。由于利尿剂和β-受体阻滞剂分别抑制肾钠重吸收和肾素释放,因此我们假设β-受体阻滞剂或利尿剂引起的血压降低和心血管疾病预防作用在 ENaC 表达最高(rs4149601 G 等位基因)的患者中更大,而在接受血管扩张剂地尔硫卓治疗的患者中,治疗效果则没有这种遗传介导的差异。
我们将 rs4149601 状态与北欧地尔硫卓研究(NORDIL)中 5152 名高血压患者(DBP≥100mmHg)的 6 个月血压降低和心血管事件风险相关联,这些患者被随机分配至β-受体阻滞剂和/或利尿剂为基础的治疗或地尔硫卓为基础的治疗。
在接受β-受体阻滞剂或利尿剂单药治疗的患者中,G 等位基因携带者的 SBP 降低幅度更大(19.5±16.8 与 15.0±19.3mmHg,P<0.001),DBP 降低幅度更大(15.4±8.3 与 14.1±8.4mmHg,P=0.02),在接受β-受体阻滞剂和/或利尿剂治疗的患者中,随访 4.5 年期间,G 等位基因携带者发生心血管事件的保护作用更大[相对风险(RR)=0.52,95%置信区间(CI)=0.36-0.74,P<0.001],与 AA 纯合子相比。在地尔硫卓组中,根据基因型,血压降低或心血管事件风险没有差异。
功能性 NEDD4L rs4149601 多态性影响基于β-受体阻滞剂和/或利尿剂的抗高血压治疗的疗效,无论是在血压降低还是心血管疾病保护方面,而地尔硫卓为基础的降压治疗效果不受该 NEDD4L 多态性的影响。