Department of Nephrology, Hippokration Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Protypo Hemodialysis Unit, Thessaloniki, Greece.
Blood Purif. 2021;50(1):73-83. doi: 10.1159/000507913. Epub 2020 Oct 5.
Intradialytic hypertension occurs in 5-15% of hemodialysis patients and is associated with increased cardiovascular risk, but the responsible mechanisms remain unknown. This study examined the effects of nebivolol and irbesartan on ambulatory central blood pressure (BP), arterial stiffness, and wave-reflection parameters in patients with intradialytic hypertension.
This is a prespecified analysis of a single-blind, randomized, cross-over study in 38 hemodialysis patients with intradialytic hypertension. Patients were randomized to nebivolol 5 mg followed byirbesartan 150 mg, or vice versa. In a non-randomized manner, the first half of the patients (n = 19) received a single drug dose 1 h prior to dialysis session and the remaining received the drugs for a whole week before the evaluation. Ambulatory central BP, arterial stiffness, and wave-reflection parameters were estimated with Mobil-O-Graph NG device, during a midweek dialysis day.
Intake of a single dose of nebivolol or irbesartan resulted in lower postdialysis central systolic BP (c-SBP) (baseline: 140.9 ± 15.4; nebivolol: 130.3 ± 19.5, p = 0.009; irbesartan: 127.3 ± 24.4 mm Hg, p = 0.007). Single-dose nebivolol also produced marginally lower 24-h c-SBP (p = 0.064) and lower 24-h central diastolic BP (c-DBP) (p = 0.029). Weekly administration of both drugs reduced postdialysis c-SBP (baseline: 144.1 ± 15.3; nebivolol: 131.8 ± 14.1, p = 0.014; irbesartan: 126.4 ± 17.8, p = 0.001) and 24-h c-SBP and c-DBP (baseline: 135.5 ± 10.3/91.9 ± 9.2; nebivolol: 126.4 ± 8.4/86.6 ± 7.2, p < 0.001/p = 0.002; irbesartan: 128.7 ± 11.6/87.0 ± 9.4, p = 0.061/p = 0.051 mm Hg). Single-dose intake of both drugs did not affect heart rate-adjusted augmentation index [AIx(75)], but decreased postdialysis pulse wave velocity (PWV). Importantly, weekly administration of both drugs reduced 24-h PWV (baseline: 10.0 ± 2.5; nebivolol: 9.7 ± 2.5, p = 0.012; irbesartan: 9.7 ± 2.7, p = 0.041). In between drug-group comparisons, no significant differences were noted.
This is the first randomized evaluation on the effects of pharmacological interventions on central BP and PWV in patients with intradialytic hypertension. Weekly administration of both nebivolol and irbesartan reduced 24-h central BP and PWV, but not AIx(75).
透析期间高血压发生在 5-15%的血液透析患者中,与心血管风险增加有关,但负责的机制仍不清楚。本研究旨在观察比索洛尔和厄贝沙坦对透析期间高血压患者的动态中心血压(BP)、动脉僵硬度和波反射参数的影响。
这是一项对 38 例透析期间高血压患者进行的单盲、随机、交叉研究的预设分析。患者随机分为比索洛尔 5mg 后给予厄贝沙坦 150mg,或反之。以非随机方式,前半部分患者(n=19)在透析前 1 小时给予单药剂量,其余患者在评估前一周内给予药物。在一周透析日期间,使用 Mobil-O-Graph NG 设备估计动态中心 BP、动脉僵硬度和波反射参数。
单次服用比索洛尔或厄贝沙坦可降低透析后中心收缩压(c-SBP)(基线:140.9±15.4;比索洛尔:130.3±19.5,p=0.009;厄贝沙坦:127.3±24.4mmHg,p=0.007)。单次剂量的比索洛尔也使 24 小时 c-SBP 略有降低(p=0.064)和 24 小时中心舒张压(c-DBP)降低(p=0.029)。两种药物的每周给药均可降低透析后 c-SBP(基线:144.1±15.3;比索洛尔:131.8±14.1,p=0.014;厄贝沙坦:126.4±17.8,p=0.001)和 24 小时 c-SBP 和 c-DBP(基线:135.5±10.3/91.9±9.2;比索洛尔:126.4±8.4/86.6±7.2,p<0.001/p=0.002;厄贝沙坦:128.7±11.6/87.0±9.4,p=0.061/p=0.051mmHg)。两种药物的单次摄入均不影响心率校正后的增强指数[AIx(75)],但可降低透析后脉搏波速度(PWV)。重要的是,两种药物的每周给药均可降低 24 小时 PWV(基线:10.0±2.5;比索洛尔:9.7±2.5,p=0.012;厄贝沙坦:9.7±2.7,p=0.041)。在药物组之间的比较中,未观察到显著差异。
这是第一项关于药物干预对透析期间高血压患者中心 BP 和 PWV 影响的随机评估。比索洛尔和厄贝沙坦的每周给药均可降低 24 小时中心 BP 和 PWV,但不能降低 AIx(75)。