Journal article
Effects of baricitinib on lipid, apolipoprotein, and lipoprotein particle profiles in a phase 2b study in patients with active rheumatoid arthritis
- Abstract:
-
Objective: To assess the effects of baricitinib on lipid profile in patients with moderate-to-severe rheumatoid arthritis.
Methods: Once-daily baricitinib (1, 2, 4, or 8-mg) or placebo was studied in 301 randomized patients. Changes in lipid profile, particle size, and number were assessed at weeks 12/24; associations with clinical efficacy were evaluated. Apolipoproteins were assessed at weeks 4/12 for the placebo, and 4- and 8-mg baricitinib groups.
Results: Baricitinib treatment resulted in dose-dependent increases by week 12 in serum lipids (low-density lipoprotein cholesterol [LDL-C]: 3.4 mg/dL increase from baseline to week 12 (1-mg) to 11.8 mg/dL (8-mg); high-density lipoprotein cholesterol [HDL-C]: 3.3 mg/dL (1-mg) to 8.1 mg/dL (8-mg); triglycerides: 6.4 mg/dL (1-mg) to 15.4 mg/dL (8-mg) baricitinib). Group-wise mean increases in LDL-C were coincident with mean increases in large LDL particles and mean reductions in small dense LDL particles. Increases from baseline to week 12 in apolipoprotein A-I, B, and total CIII were observed with 4-mg (9.5%, 6.8%, and 23.0%, respectively) and 8-mg (12.2%, 7.1%, and 19.7%, respectively) baricitinib with no increase in LDL-associated CIII (4-mg: -4.5%; 8-mg: -9.0). Baricitinib reduced HDL-associated serum amyloid A at 4-mg (-36.0%) and 8-mg (-32.0%); a significant reduction in lipoprotein (a) was observed only with 8-mg (-16.6%). Increased HDL cholesterol at week 12 correlated with improved Disease Activity Scores and Simplified Disease Activity Index; changes in total cholesterol, LDL cholesterol, and triglycerides did not reveal a similar relationship.
Conclusion: Baricitinib-associated increases in serum lipids were observed. HDL-C increases correlated with improved clinical outcomes. This article is protected by copyright. All rights reserved.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Access Document
- Files:
-
-
(Preview, Accepted manuscript, pdf, 555.3KB, Terms of use)
-
- Publisher copy:
- 10.1002/art.40036
Authors
- Publisher:
- Wiley
- Journal:
- Arthritis and Rheumatology More from this journal
- Volume:
- 69
- Issue:
- 5
- Pages:
- 943-952
- Publication date:
- 2017-04-26
- Acceptance date:
- 2016-12-22
- DOI:
- EISSN:
-
2326-5205
- ISSN:
-
2326-5191
- Keywords:
- Pubs id:
-
pubs:670811
- UUID:
-
uuid:9b4a686d-7b65-4a06-8d0c-240b0c107946
- Local pid:
-
pubs:670811
- Source identifiers:
-
670811
- Deposit date:
-
2017-01-13
- ARK identifier:
Terms of use
- Copyright holder:
- © 2016, American College of Rheumatology
- Copyright date:
- 2017
- Notes:
- This is the author accepted manuscript following peer review version of the article. The final version is available online from Wiley at: 10.1002/art.40036
If you are the owner of this record, you can report an update to it here: Report update to this record