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The effect of lipophilicity and dose on the frequency of statin-associated muscle symptoms: A systematic review and meta-analysis
journal contribution
posted on 2018-06-20, 00:00 authored by Jordon IrwinJordon Irwin, Saman KhalesiSaman Khalesi, Andrew FenningAndrew Fenning, Rebecca VellaRebecca VellaAddressing the factors which lead to the development of statin-associated muscle symptoms (SAMS) is vital for maintaining patient compliance with these pharmaceuticals, and thus improving patient outcomes. This study aimed to clarify the relationship between statin lipophilicity, or dose, and the frequency of adverse muscle symptoms using a systematic review of randomised controlled trials (RCTs). RCTs, including statin monotherapy and placebo groups, which reported data on muscle adverse events were identified through the PubMed and Scopus databases. Risk ratios (RRs) and 95% confidence intervals (CI) were pooled using a random-effects meta-analysis. A total of 135 RCTs were included in this review. Statin therapy was associated with a significant, but modest, increase in the risk of adverse muscle symptoms compared to placebo (RR = 1.050; 95% CI = 1.014–1.089; P = 0.007; I 2 = 3.291%). This significant association was primarily due to the inclusion of RCTs recruiting participants with a history of statin intolerance. Lipophilic statins had no appreciable impact on the development of SAMS compared to hydrophilic formulations. A univariate meta-regression of dose (sta ndardised to atorvastatin dose equivalents) and the risk of musculoskeletal complaints also showed no significant association. The results obtained from this meta-analysis indicate that there is a slight increase in the risk of SAMS, especially in individuals with a history of statin intolerance. There is limited evidence to suggest that the risk of SAMS would differ between the use of lipophilic and hydrophilic statins, or high- and low-dose therapy. © 2017 Elsevier Ltd
History
Volume
128Start Page
264End Page
273Number of Pages
10eISSN
1096-1186ISSN
1043-6618Publisher
Academic Press, UKPublisher DOI
Peer Reviewed
- Yes
Open Access
- No
Acceptance Date
2017-09-20Era Eligible
- Yes
Journal
Pharmacological ResearchUsage metrics
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