Department of Cardiology, Anzhen Hospital.
Department of Cardiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.
J Hypertens. 2024 Jul 1;42(7):1203-1211. doi: 10.1097/HJH.0000000000003715. Epub 2024 Mar 8.
Blood pressure variability (BPV) is a risk factor for poor kidney function independent of blood pressure (BP) in chronic kidney disease (CKD). Little is known about the association between kidney function decline and BPV in hypertensive patients without CKD.
A post-hoc analysis of the Systolic Blood Pressure Intervention Trial (SPRINT) was performed. BPV was measured as standard deviation (SD) and average real variability (ARV). Cox proportional hazard models were employed to explore the relationship between BPV and incident CKD and albuminuria.
A total of 5700 patients were included, with a mean age of 66.4 years old. During a median of 3.29 years follow-up, 150 (2.6%) patients developed CKD and 222 (7.2%) patients developed albuminuria. Patients were divided into four groups according to the quartiles of BPV. Compared with SBPV Q1, the incidence of CKD was higher in SBPV Q2-Q4; hazard ratios and 95% confidence interval were 1.81 (1.07-3.04), 1.85 (1.10-3.12) and 1.90 (1.13-3.19), respectively. The association between incident CKD and albuminuria with DBPV was less significant than SBPV. Similar results were found when measuring BPV as ARV and SD. No interaction was detected in BP-lowering strategy and SBPV on incident CKD and albuminuria ( P > 0.05).
This study found that BPV was a risk factor for incident CKD and albuminuria in patients without CKD, especially SBPV. Although intensive BP control increased the risk of CKD, the association between SBPV and kidney function decline did not differ between the two treatment groups.
URL: https://clinicaltrials.gov/ , Unique identifier: NCT01206062.
血压变异性(BPV)是慢性肾脏病(CKD)患者血压(BP)以外肾功能不良的危险因素。在没有 CKD 的高血压患者中,肾功能下降与 BPV 之间的关系知之甚少。
对收缩压干预试验(SPRINT)进行了事后分析。BPV 以标准差(SD)和平均真实变异性(ARV)来衡量。使用 Cox 比例风险模型探讨了 BPV 与新发 CKD 和白蛋白尿之间的关系。
共纳入 5700 例患者,平均年龄 66.4 岁。在中位数为 3.29 年的随访期间,150 例(2.6%)患者发生 CKD,222 例(7.2%)患者发生白蛋白尿。根据 BPV 的四分位数将患者分为四组。与 SBPV Q1 相比,SBPV Q2-Q4 的 CKD 发生率更高;风险比和 95%置信区间分别为 1.81(1.07-3.04)、1.85(1.10-3.12)和 1.90(1.13-3.19)。DBPV 与新发 CKD 和白蛋白尿之间的关联不如 SBPV 明显。以 ARV 和 SD 衡量 BPV 时,也得到了类似的结果。在降压策略和 SBPV 对新发 CKD 和白蛋白尿的影响中,未检测到交互作用(P>0.05)。
本研究发现,BPV 是无 CKD 患者新发 CKD 和白蛋白尿的危险因素,尤其是 SBPV。尽管强化 BP 控制增加了 CKD 的风险,但两组治疗中 SBPV 与肾功能下降之间的关联并无差异。
网址:https://clinicaltrials.gov/ ,独特标识符:NCT01206062。