Lipid Profiles in Patients With Ulcerative Colitis Receiving Tofacitinib-Implications for Cardiovascular Risk and Patient Management

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TitreLipid Profiles in Patients With Ulcerative Colitis Receiving Tofacitinib-Implications for Cardiovascular Risk and Patient Management
Type de publicationJournal Article
Year of Publication2021
AuteursSands BE, Colombel J-F, Ha C, Farnier M, Armuzzi A, Quirk D, Friedman GS, Kwok K, Salese L, Su C, Taub PR
JournalINFLAMMATORY BOWEL DISEASES
Volume27
Pagination797-808
Date PublishedJUN
Type of ArticleArticle
ISSN1078-0998
Mots-clésClinical trials, lipids, tofacitinib
Résumé

Background: Patients with ulcerative colitis (UC) are at elevated risk of cardiovascular disease vs the general population, despite a lower prevalence of traditional risk factors, including hyperlipidemia. Mechanistic studies in patients with rheumatoid arthritis and psoriasis suggest that tofacitinib restores serum lipids to preinflammation levels by reversing inflammation-induced cholesterol metabolism changes. We reviewed data on lipid levels and cardiovascular events, alongside recommendations for managing lipid levels during tofacitinib treatment in patients with UC, based on up-to-date expert guidelines. Methods: Data were identified from a phase 3/open-label, long-term extension (OLE) tofacitinib UC clinical program (cutoff May 27, 2019). Literature was identified from PubMed (search terms ``lipid,'' ``cholesterol,'' ``lipoprotein,'' ``cardiovascular,'' ``inflammation,'' ``atherosclerosis,'' ``tofacitinib,'' ``rheumatoid arthritis,'' ``psoriasis,'' ``inflammatory bowel disease,'' ``ulcerative colitis,'' ``hyperlipidemia,'' and ``guidelines'') and author knowledge. Data were available from 4 phase 3 clinical trials of 1124 patients with moderately to severely active UC who received >= 1 dose of to facitinib 5 or 10 mg twice daily in induction (two identical trials), maintenance, and OLE studies (treatment duration <= 6.8 years; 2576.4 patient-years of drug exposure). Results: In the OLE study, tofacitinib treatment was not associated with major changes from baseline in total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triglycerides, total cholesterol/high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol/high-density lipoprotein cholesterol, with lipid levels and ratios generally remaining stable over time. The major adverse cardiovascular events incidence rate was 0.26/100 patient-years (95% confidence interval, 0.11-0.54). Conclusions: Lipid levels and ratios remained generally unchanged from baseline in the OLE study after tofacitinib treatment, and major adverse cardiovascular events were infrequent. Long-term studies are ongoing.

DOI10.1093/ibd/izaa227