Shehata Mohamed, Hamza Mohamed
Department of Cardiology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Cardiovasc Ther. 2015 Apr;33(2):35-41. doi: 10.1111/1755-5922.12108.
The effectiveness of statin pretreatment in reducing the incidence of contrast-induced nephropathy (CIN) has been examined in some observational and randomized studies, yielding controversial results.
This study sought to evaluate the role of atorvastatin in prevention of CIN in diabetic patients with mild-to-moderate chronic kidney disease (CKD), undergoing elective percutaneous coronary intervention (PCI).
130 patients with mean glomerular filtration rate of 48.5 ± 16 mL/min/1.73 m were prospectively enrolled, then randomly (double blind) assigned in 1:1 ratio to receive atorvastatin (80 mg daily for 48 h) or placebo. Serum creatinine and glomerular filtration rate were measured preintervention, 72 h and 10 days thereafter. An increase in serum creatinine by >0.5 mg/dL (44.2 μmol/L) or >25% of baseline value was considered as CIN.
Mean age of the study cohort was 56 ± 5 years (males: 62%). Mean serum creatinine level in the placebo group increased significantly 3 days after coronary intervention and declined on the 10th day to a level that did not differ significantly from the baseline level, but still higher. However, in atorvastatin group, mean serum creatinine level showed a nonsignificant rise on the third day and then decreased to a level close to the baseline one, on the 10th day. Incidence of CIN was 7.7% in atorvastatin group and 20% in the placebo group (P < 0.05).
Atorvastatin dose of 80 mg per day for 48 h is associated with decreased incidence of CIN in diabetic patients with CKD undergoing PCI.
一些观察性研究和随机研究对他汀类药物预处理在降低造影剂肾病(CIN)发生率方面的有效性进行了检验,但结果存在争议。
本研究旨在评估阿托伐他汀在接受择期经皮冠状动脉介入治疗(PCI)的轻至中度慢性肾脏病(CKD)糖尿病患者中预防CIN的作用。
前瞻性纳入130例平均肾小球滤过率为48.5±16 mL/min/1.73 m²的患者,然后以1:1的比例随机(双盲)分配接受阿托伐他汀(每日80 mg,共48小时)或安慰剂。在干预前、干预后72小时和10天测量血清肌酐和肾小球滤过率。血清肌酐升高>0.5 mg/dL(44.2 μmol/L)或>基线值的25%被视为CIN。
研究队列的平均年龄为56±5岁(男性:62%)。安慰剂组的平均血清肌酐水平在冠状动脉介入治疗后3天显著升高,并在第10天下降至与基线水平无显著差异但仍较高的水平。然而,在阿托伐他汀组中,平均血清肌酐水平在第3天呈非显著升高,然后在第10天降至接近基线水平。阿托伐他汀组的CIN发生率为7.7%,安慰剂组为20%(P<0.05)。
对于接受PCI的CKD糖尿病患者,每日80 mg阿托伐他汀治疗48小时可降低CIN的发生率。