Is There an Anti-inflammatory Effect of Statins in Rheumatoid Arthritis? Analysis of a Large Routinely Collected Claims Database
Overview
Affiliations
What Is Already Known About This Subject: * The increasing evidence of the anti-inflammatory action of statins has stimulated interest in whether these might be beneficial in disease management of rheumatoid arthritis (RA), a chronic diseases characterized by high levels of inflammation. * The TARA trial (McCarey 2004) suggested a significant reduction in disease activity outcomes in RA patients randomized to atorvastatin compared with those assigned to the placebo harm. * However, as the signal reported by the trial was small, more evidence is needed.
What This Paper Adds: * We investigated the possible anti-inflammatory effect of statins in a cohort of RA patients using a large health insurance claims database. * To our knowledge, this is the largest study ever conducted on the anti-inflammatory effects of statins. * Our data do not show any beneficial effect of statins in reducing disease inflammation in RA patients.
Aim: To investigate the possible anti-inflammatory effect of statins in a cohort of rheumatoid arthritis (RA) patients.
Methods: We conducted a cohort study consisting of all patients with at least one claim for RA using LifeLink, a health insurance claims database. Initiation and cessation of oral steroid (OS) therapy were treated as surrogate for inflammatory flare-up and controlled inflammation, respectively. We split the RA patients into two sub-cohorts based on whether they were using OS within a specified time window of the RA index date (first recorded claim for RA in the database). Cox proportional hazard models were used to evaluate the association between time-varying exposure to any statins and (i) initiation of OS therapy in the non-users of OS at RA index date and (ii) cessation of OS therapy in the users of OS at RA index date controlling for potential confounders.
Results: We found 31 451 non-users of OS at RA index date and 6026 users of OS within the time window at RA index date. The results on both sub-cohorts were both consistent with no association of statin exposure with the risk of initiation/cessation of OS: the hazard ratio (HR) of initiating OS therapy was 0.96 (95% confidence interval 0.9, 1.01) in the sub-cohort of non-users and the HR of cessation of OS therapy was 0.95 (0.87, 1.05) in the sub-cohort of users of OS therapy at RA diagnosis.
Conclusions: These data do not show any beneficial effect of statins in reducing disease inflammation in RA patients.
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PMID: 37713899 PMC: 10508553. DOI: 10.1097/MD.0000000000035088.
Precision medicine: the precision gap in rheumatic disease.
Lin C, Cooles F, Isaacs J Nat Rev Rheumatol. 2022; 18(12):725-733.
PMID: 36216923 DOI: 10.1038/s41584-022-00845-w.
Free Fatty Acids in Bone Pathophysiology of Rheumatic Diseases.
Frommer K, Hasseli R, Schaffler A, Lange U, Rehart S, Steinmeyer J Front Immunol. 2019; 10:2757.
PMID: 31849953 PMC: 6901602. DOI: 10.3389/fimmu.2019.02757.
Mowla K, Rajai E, Ghorbani A, Dargahi-Malamir M, Bahadoram M, Mohammadi S J Clin Diagn Res. 2016; 10(5):OC32-6.
PMID: 27437268 PMC: 4948444. DOI: 10.7860/JCDR/2016/16538.7814.
Villafradez-Diaz M, Santiago-Casas Y, Nieves-Plaza M, Morales M, Rodriguez V, Rios G P R Health Sci J. 2014; 33(1):3-8.
PMID: 24665602 PMC: 4198336.