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J-RAS研究中肾动脉支架置入术治疗高血压和慢性肾脏病长达12个月的临床结局——前瞻性、单臂、多中心临床研究

Clinical outcome of renal artery stenting for hypertension and chronic kidney disease up to 12 months in the J-RAS Study – prospective, single-arm, multicenter clinical study.

作者信息

Fujihara Masahiko, Yokoi Yoshiaki, Abe Takaaki, Soga Yoshimitsu, Yamashita Takehiro, Miyashita Yusuke, Nakamura Masato, Yokoi Hiroyoshi, Ito Sadayoshi

机构信息

Kishiwada Tokushukai Hospital Cardiovascular Center, Japan.

出版信息

Circ J. 2015;79(2):351-9. doi: 10.1253/circj.CJ-14-0908. Epub 2014 Dec 4.

DOI:10.1253/circj.CJ-14-0908
PMID:25476409
Abstract

BACKGROUND

Atherosclerotic renal artery stenosis (ARAS) causes renovascular hypertension (HTN) and impairs renal function, leading to chronic kidney disease (CKD). The J-RAS study was a prospective, multicenter study to assess the clinical outcome of renal artery stenting for up to 1 year in Japanese patients with ARAS.

METHODS AND RESULTS

One hundred and forty-nine patients were enrolled between November 2010 and January 2013. The patients were classified into an HTN (n=121) group and a CKD (n=108) group in the primary analysis. The primary efficacy endpoints were change in blood pressure for the HTN group and change in estimated glomerular filtration rate (eGFR) for the CKD group at 1 months. The primary safety endpoint was freedom from major cardiovascular or renal events at 12 months. In the HTN group, the mean systolic blood pressure (SBP) significantly decreased from 161.6 ± 21 mmHg at baseline to 137.0 ± 21 mmHg (P<0.0001). In the CKD group, there was no significant difference in eGFR from 40.7 ± 10 ml·min(-1)·1.73 m(-2)at baseline to 40.8 ± 13 ml·min(-1)·1.73 m(-2)(P=0.32). The primary safety endpoint was 89.4% at 12 months.

CONCLUSIONS

In the J-RAS trial, significant SBP reduction was seen in the HTN group, and stabilization of renal function in the CKD group. Renal artery stenting for ARAS is safe and effective in Japanese patients.

摘要

背景

动脉粥样硬化性肾动脉狭窄(ARAS)可导致肾血管性高血压(HTN)并损害肾功能,进而引发慢性肾脏病(CKD)。J-RAS研究是一项前瞻性、多中心研究,旨在评估日本ARAS患者接受肾动脉支架置入术长达1年的临床结局。

方法与结果

2010年11月至2013年1月期间共纳入149例患者。在初步分析中,患者被分为高血压组(n = 121)和慢性肾脏病组(n = 108)。主要疗效终点为高血压组1个月时血压的变化以及慢性肾脏病组1个月时估计肾小球滤过率(eGFR)的变化。主要安全终点为12个月时无重大心血管或肾脏事件。在高血压组中,平均收缩压(SBP)从基线时的161.6±21 mmHg显著降至137.0±21 mmHg(P<0.0001)。在慢性肾脏病组中,eGFR从基线时的40.7±10 ml·min⁻¹·1.73 m⁻² 至40.8±13 ml·min⁻¹·1.73 m⁻² 无显著差异(P = 0.32)。12个月时主要安全终点为89.4%。

结论

在J-RAS试验中,高血压组收缩压显著降低,慢性肾脏病组肾功能稳定。肾动脉支架置入术治疗ARAS在日本患者中安全有效。

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