From the Department of Geriatric Medicine (M.H.M., T.B.W.), Oslo University Hospital Ullevaal, Oslo, Norway.
Institute of Clinical Medicine (M.H.M., S.E.K., T.B.W.), University of Oslo, Norway.
Hypertension. 2020 Jun;75(6):1584-1592. doi: 10.1161/HYPERTENSIONAHA.119.14443. Epub 2020 Apr 27.
Blood pressure-lowering drugs have different blood pressure-lowering profiles. We studied if differences in blood pressure mean and variability can explain the differences in risks of cardiovascular events and death among 15 245 high-risk hypertensive patients randomized to valsartan or amlodipine and followed for 4.2 years in the VALUE trial (Valsartan Antihypertensive Long-Term Use Evaluation). We selected patients with ≥3 visits and performed Cox regression analyses, defining mean blood pressure as a time-dependent covariate and visit-to-visit and within-visit blood pressure variability as the SD. Of 14 996 eligible patients, participants in the valsartan group had higher systolic mean blood pressure by 2.2 mm Hg, higher visit-to-visit systolic variability by 1.4 mm Hg, and higher within-visit systolic variability by 0.2 mm Hg ( values <0.0001). The higher risks of myocardial infarction and stroke in the valsartan group was attenuated after adjustment for mean and variability of systolic blood pressure, from HR 1.19 (95% CI, 1.02-1.39) to 1.11 (0.96-1.30) and from HR 1.13 (0.96-1.33) to 1.00 (0.85-1.18), respectively. The lower risk of congestive heart failure in the valsartan group was accentuated after adjustment, from HR 0.86 (0.74-1.00) to 0.76 (0.65-0.89). A smaller effect was seen on risk of death, from 1.01 (0.92-1.12) to 0.94 (0.85-1.04). In conclusion, the higher risks of myocardial infarction and stroke in patients randomized to valsartan versus amlodipine were related to the drugs' different blood pressure modulating profiles. The risk of congestive heart failure with valsartan was lower, independent of the less favorable blood pressure modulating profile.
降压药物具有不同的降压特征。我们研究了在 VAL-UE 试验(缬沙坦抗高血压长期疗效评估)中,15245 例高危高血压患者随机分为缬沙坦或氨氯地平组,随访 4.2 年后,血压均值和变异性的差异是否可以解释心血管事件和死亡风险的差异。我们选择了有≥3 次就诊的患者,并进行了 Cox 回归分析,将血压均值定义为时间依赖性协变量,将就诊间和就诊内血压变异性定义为 SD。在 14996 例合格患者中,缬沙坦组的收缩压均值高 2.2mmHg,就诊间收缩压变异性高 1.4mmHg,就诊内收缩压变异性高 0.2mmHg(P<0.0001)。缬沙坦组的心肌梗死和卒中风险较高,经调整收缩压均值和变异性后,风险从 HR 1.19(95%CI,1.02-1.39)降至 1.11(0.96-1.30),从 HR 1.13(0.96-1.33)降至 1.00(0.85-1.18)。缬沙坦组心力衰竭风险较低,经调整后,风险从 HR 0.86(0.74-1.00)降至 0.76(0.65-0.89)。死亡风险的影响较小,从 HR 1.01(0.92-1.12)降至 0.94(0.85-1.04)。总之,与氨氯地平相比,缬沙坦组患者的心肌梗死和卒中风险较高与药物的不同血压调节特征有关。缬沙坦心力衰竭风险较低,与血压调节特征不理想无关。