Efficacy of short-term moderate or high-dose statin therapy for the prevention of contrast-induced nephropathy in high-risk patients with chronic kidney disease: systematic review and meta-analysis
Author(s) -
Yanlin Zhou,
Liqun Chen,
Xiaogang Du
Publication year - 2021
Publication title -
clinics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.618
H-Index - 61
eISSN - 1980-5322
pISSN - 1807-5932
DOI - 10.6061/clinics/2021/e1876
Subject(s) - medicine , rosuvastatin , placebo , kidney disease , statin , atorvastatin , meta analysis , cochrane library , rosuvastatin calcium , subgroup analysis , relative risk , randomized controlled trial , contrast induced nephropathy , gastroenterology , confidence interval , pathology , alternative medicine , percutaneous coronary intervention , myocardial infarction
Although previous studies have indicated that statin therapy can effectively prevent the development of CIN, this observation remains controversial, especially in high-risk patients. A meta-analysis was performed to evaluate the efficacy of statin pretreatment for preventing the development of CIN in patients with chronic kidney disease (CKD) and to determine its effectiveness in various subgroups. We searched the online databases PubMed, EMBASE, and the Cochrane Library. RCTs that involved the comparison of the short-term moderate or high-dose statin pretreatment with placebo for CIN prevention in CKD patients undergoing angiography were included. The primary outcome was CIN prevalence. Seven RCTs comprising 4256 participants were investigated in this analysis. The risk of developing CIN in patients pretreated with statins was significantly lower than that in patients pretreated with placebo (RR=0.57, 95%CI=0.43-0.76, p =0.000). The SCr values of the statin group, when analyzed 48h after angiography were lower than those of the placebo group ((SMD=-0.15, 95% CI=-0.27 to -0.04, p =0.011). In the subgroup analysis, statin pretreatment could decrease the risk of CIN in CKD patients with DM (RR=0.54, 95% CI=0.39-0.76, p =0.000), but not in CKD patients without DM (RR=0.84, 95% CI=0.44-1.60, p =0.606). The efficacy of atorvastatin for preventing CIN was consistent with that observed with the use of rosuvastatin. The risk ratios (RR) were 0.51 (95% CI=0.32-0.81, p =0.004) and 0.60 (95% CI=0.41-0.88, p =0.009), respectively. Our study demonstrated that statin pretreatment could prevent the development of CIN in CKD patients. However, subgroup analysis demonstrated that statin pretreatment, despite being effective in preventing CIN in patients with CKD and DM, was not helpful for CKD patients without DM. Rosuvastatin and atorvastatin exhibited similar preventive effects with respect to CIN.
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