Ontology highlight
ABSTRACT: Objective
To assess the effect of statins compared with placebo on the risk of developing hypertransaminasemia.Patients and methods
We performed a systematic review of electronic databases and included articles published between January 1, 1965, and April 10, 2017. Randomized clinical trials (RCTs) comparing statins vs placebo were included. Odds ratios (ORs) were pooled in random-effect meta-analyses according to established methods recommended by the Cochrane Collaboration.Results
Seventy-three eligible RCTs, comprising 123,051 patients, were identified. Statins associated with a significantly risk of hypertransaminasemia (OR 1.45; 95% confidence interval [CI], 1.24-1.69; P<.001). Atorvastatin showed the highest odds (OR 2.66; 95% CI, 1.74-4.06; P<.001) followed by rosuvastatin (OR 1.35; 95% CI, 1.06-1.70; P=.01) and lovastatin (OR 1.53; 95% CI, 1.03-2.28; P=.04). Pravastatin, fluvastatin, and simvastatin yielded no statistically different odds compared with placebo.Conclusions
A dose-dependent risk of developing hypertransaminasemia occurs in patients taking atorvastatin, rosuvastatin, and lovastatin.
SUBMITTER: Villani R
PROVIDER: S-EPMC6544559 | biostudies-literature | 2019 Jun
REPOSITORIES: biostudies-literature
Villani Rosanna R Navarese Eliano Pio EP Cavallone Francesco F Kubica Jacek J Bellanti Francesco F Facciorusso Antonio A Vendemiale Gianluigi G Serviddio Gaetano G
Mayo Clinic proceedings. Innovations, quality & outcomes 20190505 2
<h4>Objective</h4>To assess the effect of statins compared with placebo on the risk of developing hypertransaminasemia.<h4>Patients and methods</h4>We performed a systematic review of electronic databases and included articles published between January 1, 1965, and April 10, 2017. Randomized clinical trials (RCTs) comparing statins vs placebo were included. Odds ratios (ORs) were pooled in random-effect meta-analyses according to established methods recommended by the Cochrane Collaboration.<h4> ...[more]