Lipid Profiles in Patients With Ulcerative Colitis Receiving Tofacitinib-Implications for Cardiovascular Risk and Patient Management
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Titre | Lipid Profiles in Patients With Ulcerative Colitis Receiving Tofacitinib-Implications for Cardiovascular Risk and Patient Management |
Type de publication | Journal Article |
Year of Publication | 2021 |
Auteurs | Sands BE, Colombel J-F, Ha C, Farnier M, Armuzzi A, Quirk D, Friedman GS, Kwok K, Salese L, Su C, Taub PR |
Journal | INFLAMMATORY BOWEL DISEASES |
Volume | 27 |
Pagination | 797-808 |
Date Published | JUN |
Type of Article | Article |
ISSN | 1078-0998 |
Mots-clés | Clinical 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. |
DOI | 10.1093/ibd/izaa227 |