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短期中等剂量或高剂量瑞舒伐他汀预防对比剂肾病的疗效:15项随机对照试验的荟萃分析

Efficacy of short-term moderate or high-dose rosuvastatin in preventing contrast-induced nephropathy: A meta-analysis of 15 randomized controlled trials.

作者信息

Liang Min, Yang Shicheng, Fu Naikuan

机构信息

Graduate School of Tianjin Medical University Department of Cardiology, Tianjin Chest Hospital, Tianjin, China.

出版信息

Medicine (Baltimore). 2017 Jul;96(27):e7384. doi: 10.1097/MD.0000000000007384.

Abstract

BACKGROUND

The prophylactic efficacy of statin pretreatment for the prevention of contrast-induced nephropathy (CIN) in patients undergoing coronary angiography (CAG) or percutaneous coronary intervention (PCI) remains controversial. The aim of the study was to perform a meta-analysis of randomized controlled trials (RCTs) to assess the effectiveness of short-term moderate or high-dose rosuvastatin pretreatment in preventing CIN.

METHODS

We included RCTs comparing short-term moderate or high-dose rosuvastatin treatment versus low-dose rosuvastatin treatment or placebo for preventing CIN. The primary endpoint was the incidence of CIN within 2 to 5 days after contrast administration, and related-parameters including serum creatinine (SCr), cystatin C (CysC), hypersensitive C-reactive protein (hs-CRP), urine microalbumin (mALB) were also extracted.

RESULTS

Fifteen RCTs with a total of 2673 patients were identified and analyzed. Patients who received moderate or high-dose rosuvastatin pretreatment had a 55% lower risk of CIN compared with low-dose rosuvastatin pretreatment or placebo group based on a fixed effect model (RR = 0.45, 95% CI 0.35-0.58, P < .0001). The benefit of moderate or high-dose rosuvastatin was consistent in both comparisons with low-dose rosuvastatin (RR = 0.40, 95% CI 0.27-0.59, P < .0001) or placebo (RR = 0.45, 95% CI 0.35-0.58, P < .0001). And moderate (20 mg) or high dose (≥40 mg) rosuvastatin significantly reduced the incidence of CIN compared with the control (RR = 0.39, 95% CI 0.29-0.54, P < .0001, RR = 0.56, 95% CI 0.37-0.85, P = .006, respectively). Subgroup analysis showed that moderate or high-dose rosuvastatin pretreatment could decrease the incidence of CIN in patients with chronic kidney disease (CKD) (RR = 0.53, 95% CI 0.30-0.93, P = .03) or diabetes mellitus (DM) (RR = 0.51, 95% CI 0.31-0.86, P = .01) or acute coronary syndrome (ACS) patients undergoing PCI (RR = 0.52, 95% CI 0.35-0.76, P = .0009) or in studies which received mean contrast volume ≥110 mL (RR = 0.43, 95% CI 0.32-0.58, P < .0001). The SCr, CysC, hs-CRP, and mALB after the operation in the moderate or high-dose rosuvastatin group were lower than those of low-dose rosuvastatin group.

CONCLUSION

This meta-analysis demonstrated that moderate or high-dose rosuvastatin treatment could reduce the incidence of CIN in patients undergoing CAG or PCI. Moreover, moderate or high-dose rosuvastatin would be beneficial in high-risk patients with CKD or DM or undergoing PCI.

摘要

背景

他汀类药物预处理对接受冠状动脉造影(CAG)或经皮冠状动脉介入治疗(PCI)患者预防造影剂肾病(CIN)的疗效仍存在争议。本研究的目的是对随机对照试验(RCT)进行荟萃分析,以评估短期中等剂量或高剂量瑞舒伐他汀预处理预防CIN的有效性。

方法

我们纳入了比较短期中等剂量或高剂量瑞舒伐他汀治疗与低剂量瑞舒伐他汀治疗或安慰剂预防CIN的RCT。主要终点是造影剂给药后2至5天内CIN的发生率,还提取了包括血清肌酐(SCr)、胱抑素C(CysC)、超敏C反应蛋白(hs-CRP)、尿微量白蛋白(mALB)等相关参数。

结果

共纳入并分析了15项RCT,总计2673例患者。基于固定效应模型,接受中等剂量或高剂量瑞舒伐他汀预处理的患者发生CIN的风险比低剂量瑞舒伐他汀预处理或安慰剂组低55%(RR = 0.45,95%CI 0.35 - 0.58,P <.0001)。中等剂量或高剂量瑞舒伐他汀在与低剂量瑞舒伐他汀(RR = 0.40,95%CI 0.27 - 0.59,P <.0001)或安慰剂(RR = 0.45,95%CI 0.35 - 0.58,P <.0001)的比较中获益一致。与对照组相比,中等剂量(20mg)或高剂量(≥40mg)瑞舒伐他汀显著降低了CIN的发生率(RR分别为0.39,95%CI 0.29 - 0.54,P <.0001;RR = 0.56,95%CI 0.37 - 0.85,P =.006)。亚组分析表明,中等剂量或高剂量瑞舒伐他汀预处理可降低慢性肾脏病(CKD)患者(RR = 0.53,95%CI 0.30 - 0.93,P =.03)、糖尿病(DM)患者(RR = 0.51,95%CI 0.31 - 0.86,P =.01)、接受PCI的急性冠状动脉综合征(ACS)患者(RR = 0.52,95%CI 0.35 - 0.76,P =.0009)或平均造影剂用量≥110mL的研究中的CIN发生率(RR = 0.43,95%CI 0.32 - 0.58,P <.0001)。中等剂量或高剂量瑞舒伐他汀组术后SCr、CysC、hs-CRP和mALB低于低剂量瑞舒伐他汀组。

结论

本荟萃分析表明,中等剂量或高剂量瑞舒伐他汀治疗可降低接受CAG或PCI患者的CIN发生率。此外,中等剂量或高剂量瑞舒伐他汀对CKD或DM高危患者或接受PCI的患者有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb8/5502163/8388bea6ae14/medi-96-e7384-g001.jpg

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