Department of Nephrology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Department of Scientific Research, Xiangya Hospital, Central South University, Changsha, Hunan, China.
PLoS One. 2020 May 29;15(5):e0233233. doi: 10.1371/journal.pone.0233233. eCollection 2020.
Previous studies have shown that visit-to-visit blood pressure variability (BPV) is associated with chronic kidney disease (CKD). However, the results have not been consistent among studies. This systematic review and meta-analysis was conducted to comprehensively assess the association between visit-to-visit BPV and the risk of CKD.
Medline, Embase, and the Cochrane Library were searched from the date of inception through 1 August 2019 using the terms "blood pressure variability," "chronic kidney disease," "nephropathy," and other comparable terms. The primary outcome was the development of CKD. Two reviewers extracted the data independently. Meta-analysis was performed using a random effects model.
Fourteen studies were included in the systematic review and meta-analysis. The risk of CKD was significantly greater in patients with high baseline systolic blood pressure variability (SBPV) than in patients with low baseline SBPV: the standard deviation (SD) showed relative risk (RR) of 1.69 and 95% CI of 1.38-2.08, the coefficient of variation (CV) showed RR of 1.23 and 95% CI of 1.12-1.36, and variance independent of mean (VIM) showed RR of 1.40 and 95% CI of 1.15-1.71. RRs for each unit increase in visit-to-visit SBPV and risk of CKD were 1.05 (95% CI: 1.03-1.07) for SD, 1.06 (95% CI: 1.03-1.09) for CV, and 1.1 (95% CI: 0.96-1.25) for VIM. Diastolic BPV was similarly predictive of CKD based on SD and CV.
Increased visit-to-visit BPV might be an independent risk factor for CKD. However, significant heterogeneity was present; thus, future prospective studies are needed to confirm our findings. Our results indicate that treatment of hypertension should control blood pressure levels and prevent abnormal fluctuations in blood pressure to reduce the risk of CKD.
先前的研究表明,血压变异性(BPV)与慢性肾脏病(CKD)有关。然而,研究结果并不一致。本系统评价和荟萃分析旨在全面评估 BPV 与 CKD 风险之间的关系。
使用“血压变异性”、“慢性肾脏病”、“肾病”等术语,从建库日期到 2019 年 8 月 1 日,在 Medline、Embase 和 Cochrane 图书馆进行检索。主要结局是 CKD 的发生。两名审查员独立提取数据。使用随机效应模型进行荟萃分析。
系统评价和荟萃分析共纳入 14 项研究。与基线 SBPV 较低的患者相比,基线 SBPV 较高的患者发生 CKD 的风险显著增加:标准差(SD)的相对危险度(RR)为 1.69,95%置信区间(CI)为 1.38-2.08,变异系数(CV)RR 为 1.23,95%CI 为 1.12-1.36,均值独立方差(VIM)RR 为 1.40,95%CI 为 1.15-1.71。每单位 SBPV 波动增加与 CKD 风险的 RR 分别为 SD 为 1.05(95%CI:1.03-1.07),CV 为 1.06(95%CI:1.03-1.09),VIM 为 1.1(95%CI:0.96-1.25)。基于 SD 和 CV,DBPV 也同样可以预测 CKD。
增加的 BPV 可能是 CKD 的独立危险因素。然而,存在显著的异质性;因此,需要进一步开展前瞻性研究来证实我们的研究结果。我们的结果表明,高血压的治疗应控制血压水平并预防血压异常波动,以降低 CKD 的风险。