TY - JOUR
T1 - Lipid Profiles in Patients with Ulcerative Colitis Receiving Tofacitinib - Implications for Cardiovascular Risk and Patient Management
AU - Sands, Bruce E.
AU - Colombel, Jean Frédéric
AU - Ha, Christina
AU - Farnier, Michel
AU - Armuzzi, Alessandro
AU - Quirk, Daniel
AU - Friedman, Gary S.
AU - Kwok, Kenneth
AU - Salese, Leonardo
AU - Su, Chinyu
AU - Taub, Pam R.
N1 - Publisher Copyright:
© 2020 Crohn's & Colitis Foundation. Published by Oxford University Press on behalf of Crohn's & Colitis Foundation.
PY - 2021/6/1
Y1 - 2021/6/1
N2 - 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 tofacitinib 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. ClinicalTrials.gov
AB - 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 tofacitinib 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. ClinicalTrials.gov
KW - clinical trials
KW - lipids
KW - tofacitinib
UR - http://www.scopus.com/inward/record.url?scp=85104830381&partnerID=8YFLogxK
U2 - 10.1093/ibd/izaa227
DO - 10.1093/ibd/izaa227
M3 - Article
C2 - 32870265
AN - SCOPUS:85104830381
SN - 1078-0998
VL - 27
SP - 797
EP - 808
JO - Inflammatory Bowel Diseases
JF - Inflammatory Bowel Diseases
IS - 6
ER -