Mayo Clinic Proceedings: Innovations, Quality & Outcomes (Jun 2019)

Risk of Statin-Induced Hypertransaminasemia

  • Rosanna Villani, MD, PhD,
  • Eliano Pio Navarese, MD, PhD,
  • Francesco Cavallone, MD,
  • Jacek Kubica, MD, PhD,
  • Francesco Bellanti, MD, PhD,
  • Antonio Facciorusso, MD,
  • Gianluigi Vendemiale, MD,
  • Gaetano Serviddio, MD

Journal volume & issue
Vol. 3, no. 2
pp. 131 – 140

Abstract

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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.