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替米沙坦-瑞舒伐他汀单片复方制剂对高血压合并血脂异常患者降压作用的初步研究。

Central blood pressure lowering effect of telmisartan-rosuvastatin single-pill combination in hypertensive patients combined with dyslipidemia: A pilot study.

机构信息

Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.

Division of Cardiology, Department of Internal Medicine, School of Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University, Seoul, Republic of Korea.

出版信息

J Clin Hypertens (Greenwich). 2021 Sep;23(9):1664-1674. doi: 10.1111/jch.14345. Epub 2021 Aug 12.

Abstract

This multicenter, phase 4, Prospective Randomized Open, Blinded End-point (PROBE) study aimed to evaluate safety and efficacy of telmisartan/rosuvastatin single-pill combination (SPC) therapy on lowering central blood pressure (BP) compared with telmisartan monotherapy in hypertensive patients with dyslipidemia in Korea. Study was terminated earlier than planned due to COVID-19 pandemic, thus should be considered as a pilot study. Among 125 patients who met the inclusion criteria of hypertension and dyslipidemia (defined as 10-year Atherosclerotic Cardiovascular Disease risk score over 5%), 80 patients went through 4-week single-group run-in period with telmisartan 40-80 mg, then randomized to telmisartan 80 mg + rosuvastatin (10 or 20 mg) SPC group or telmisartan 80 mg monotherapy group. The central/brachial BP, brachial-ankle pulse wave velocity (baPWV), and augmentation index (AIx) were assessed at baseline and 16 weeks later. Mean brachial SBP changed from 135.80 ± 14.22 mmHg to 130.69 ± 13.23 mmHg in telmisartan/rosuvastatin group and from 134.37 ± 12.50 mmHg to 133.75 ± 12.30 mmHg in telmisartan monotherapy group without significant difference (between-group difference p = .149). Mean central SBP were reduced significantly in the telmisartan/rosuvastatin group with change from 126.72 ± 14.44 mmHg to 121.56 ± 14.56 mmHg while telmisartan monotherapy group showed no significant change (between-group difference p = .028). BaPWV changed from 1672.57 ± 371.72 m/s to 1591.75 ± 272.16 m/s in telmisartan/rosuvastatin group and from 1542.85 ± 263.70 m/s to 1586.12 ± 297.45 m/s in telmisartan group with no significance (between-group difference p = .078). Change of AIx had no significant difference (between-group difference p = .314). Both groups showed excellent compliance rate of 96.9 ± 4.5% with no significant difference in adverse rate. Telmisartan/rosuvastatin SPC therapy was more effective in lowering central BP compared with the telmisartan monotherapy. The results of this study showed benefit of additive statin therapy in hypertensive patients combined with dyslipidemia.

摘要

这项多中心、4 期、前瞻性随机开放、盲终点(PROBE)研究旨在评估替米沙坦/瑞舒伐他汀单片复方(SPC)治疗与替米沙坦单药治疗相比,在降低高血压伴血脂异常患者中心血压(BP)方面的安全性和疗效。由于 COVID-19 大流行,该研究提前终止,因此应视为一项试点研究。在符合高血压和血脂异常纳入标准(定义为 10 年动脉粥样硬化性心血管疾病风险评分超过 5%)的 125 名患者中,80 名患者接受了 4 周的替米沙坦 40-80mg 单组导入期治疗,然后随机分为替米沙坦 80mg+瑞舒伐他汀(10 或 20mg)SPC 组或替米沙坦 80mg 单药组。在基线和 16 周后评估中心/肱动脉血压、肱踝脉搏波速度(baPWV)和增强指数(AIx)。替米沙坦/瑞舒伐他汀组的平均肱动脉收缩压从 135.80±14.22mmHg 降至 130.69±13.23mmHg,替米沙坦单药组从 134.37±12.50mmHg 降至 133.75±12.30mmHg,两组间差异无统计学意义(组间差异 p=0.149)。替米沙坦/瑞舒伐他汀组的平均中心收缩压显著降低,从 126.72±14.44mmHg 降至 121.56±14.56mmHg,而替米沙坦单药组无显著变化(组间差异 p=0.028)。替米沙坦/瑞舒伐他汀组的 baPWV 从 1672.57±371.72m/s 降至 1591.75±272.16m/s,替米沙坦组从 1542.85±263.70m/s 降至 1586.12±297.45m/s,两组间差异无统计学意义(组间差异 p=0.078)。AIx 的变化无统计学意义(组间差异 p=0.314)。两组的依从率均为 96.9±4.5%,不良反应发生率无显著差异。与替米沙坦单药治疗相比,替米沙坦/瑞舒伐他汀 SPC 治疗更能有效降低中心血压。这项研究的结果显示,在高血压合并血脂异常患者中,他汀类药物联合治疗具有额外的益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a42d/8678791/0d5ab46f7ec9/JCH-23-1664-g001.jpg

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