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Reducing cardiovascular risk with immunomodulators: a randomised active comparator trial among patients with rheumatoid arthritis

OBJECTIVE: Recent large-scale randomised trials demonstrate that immunomodulators reduce cardiovascular (CV) events among the general population. However, it is uncertain whether these effects apply to rheumatoid arthritis (RA) and if certain treatment strategies in RA reduce CV risk to a greater ex...

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Autores principales: Solomon, Daniel H, Giles, Jon T, Liao, Katherine P, Ridker, Paul M, Rist, Pamela M, Glynn, Robert J, Broderick, Rachel, Lu, Fengxin, Murray, Meredith T, Vanni, Kathleen, Santacroce, Leah M, Abohashem, Shady, Robson, Philip M, Fayad, Zahi, Mani, Venkatesh, Tawakol, Ahmed, Bathon, Joan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933165/
https://www.ncbi.nlm.nih.gov/pubmed/36450449
http://dx.doi.org/10.1136/ard-2022-223302
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author Solomon, Daniel H
Giles, Jon T
Liao, Katherine P
Ridker, Paul M
Rist, Pamela M
Glynn, Robert J
Broderick, Rachel
Lu, Fengxin
Murray, Meredith T
Vanni, Kathleen
Santacroce, Leah M
Abohashem, Shady
Robson, Philip M
Fayad, Zahi
Mani, Venkatesh
Tawakol, Ahmed
Bathon, Joan
author_facet Solomon, Daniel H
Giles, Jon T
Liao, Katherine P
Ridker, Paul M
Rist, Pamela M
Glynn, Robert J
Broderick, Rachel
Lu, Fengxin
Murray, Meredith T
Vanni, Kathleen
Santacroce, Leah M
Abohashem, Shady
Robson, Philip M
Fayad, Zahi
Mani, Venkatesh
Tawakol, Ahmed
Bathon, Joan
author_sort Solomon, Daniel H
collection PubMed
description OBJECTIVE: Recent large-scale randomised trials demonstrate that immunomodulators reduce cardiovascular (CV) events among the general population. However, it is uncertain whether these effects apply to rheumatoid arthritis (RA) and if certain treatment strategies in RA reduce CV risk to a greater extent. METHODS: Patients with active RA despite use of methotrexate were randomly assigned to addition of a tumour necrosis factor (TNF) inhibitor (TNFi) or addition of sulfasalazine and hydroxychloroquine (triple therapy) for 24 weeks. Baseline and follow-up (18)F-fluorodeoxyglucose-positron emission tomography/CT scans were assessed for change in arterial inflammation, an index of CV risk, measured as an arterial target-to-background ratio (TBR) in the carotid arteries and aorta. RESULTS: 115 patients completed the protocol. The two treatment groups were well balanced with a median age of 58 years, 71% women, 57% seropositive and a baseline disease activity score in 28 joints of 4.8 (IQR 4.0, 5.6). Baseline TBR was similar across the two groups. Significant TBR reductions were observed in both groups—ΔTNFi: −0.24 (SD=0.51), Δtriple therapy: −0.19 (SD=0.51)—without difference between groups (difference in Δs: −0.02, 95% CI −0.19 to 0.15, p=0.79). While disease activity was significantly reduced across both treatment groups, there was no association with change in TBR (β=0.04, 95% CI −0.03 to 0.10). CONCLUSION: We found that addition of either a TNFi or triple therapy resulted in clinically important improvements in vascular inflammation. However, the addition of a TNFi did not reduce arterial inflammation more than triple therapy. TRIAL REGISTRATION NUMBER: NCT02374021.
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spelling pubmed-99331652023-02-17 Reducing cardiovascular risk with immunomodulators: a randomised active comparator trial among patients with rheumatoid arthritis Solomon, Daniel H Giles, Jon T Liao, Katherine P Ridker, Paul M Rist, Pamela M Glynn, Robert J Broderick, Rachel Lu, Fengxin Murray, Meredith T Vanni, Kathleen Santacroce, Leah M Abohashem, Shady Robson, Philip M Fayad, Zahi Mani, Venkatesh Tawakol, Ahmed Bathon, Joan Ann Rheum Dis Rheumatoid Arthritis OBJECTIVE: Recent large-scale randomised trials demonstrate that immunomodulators reduce cardiovascular (CV) events among the general population. However, it is uncertain whether these effects apply to rheumatoid arthritis (RA) and if certain treatment strategies in RA reduce CV risk to a greater extent. METHODS: Patients with active RA despite use of methotrexate were randomly assigned to addition of a tumour necrosis factor (TNF) inhibitor (TNFi) or addition of sulfasalazine and hydroxychloroquine (triple therapy) for 24 weeks. Baseline and follow-up (18)F-fluorodeoxyglucose-positron emission tomography/CT scans were assessed for change in arterial inflammation, an index of CV risk, measured as an arterial target-to-background ratio (TBR) in the carotid arteries and aorta. RESULTS: 115 patients completed the protocol. The two treatment groups were well balanced with a median age of 58 years, 71% women, 57% seropositive and a baseline disease activity score in 28 joints of 4.8 (IQR 4.0, 5.6). Baseline TBR was similar across the two groups. Significant TBR reductions were observed in both groups—ΔTNFi: −0.24 (SD=0.51), Δtriple therapy: −0.19 (SD=0.51)—without difference between groups (difference in Δs: −0.02, 95% CI −0.19 to 0.15, p=0.79). While disease activity was significantly reduced across both treatment groups, there was no association with change in TBR (β=0.04, 95% CI −0.03 to 0.10). CONCLUSION: We found that addition of either a TNFi or triple therapy resulted in clinically important improvements in vascular inflammation. However, the addition of a TNFi did not reduce arterial inflammation more than triple therapy. TRIAL REGISTRATION NUMBER: NCT02374021. BMJ Publishing Group 2023-03 2022-11-30 /pmc/articles/PMC9933165/ /pubmed/36450449 http://dx.doi.org/10.1136/ard-2022-223302 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Rheumatoid Arthritis
Solomon, Daniel H
Giles, Jon T
Liao, Katherine P
Ridker, Paul M
Rist, Pamela M
Glynn, Robert J
Broderick, Rachel
Lu, Fengxin
Murray, Meredith T
Vanni, Kathleen
Santacroce, Leah M
Abohashem, Shady
Robson, Philip M
Fayad, Zahi
Mani, Venkatesh
Tawakol, Ahmed
Bathon, Joan
Reducing cardiovascular risk with immunomodulators: a randomised active comparator trial among patients with rheumatoid arthritis
title Reducing cardiovascular risk with immunomodulators: a randomised active comparator trial among patients with rheumatoid arthritis
title_full Reducing cardiovascular risk with immunomodulators: a randomised active comparator trial among patients with rheumatoid arthritis
title_fullStr Reducing cardiovascular risk with immunomodulators: a randomised active comparator trial among patients with rheumatoid arthritis
title_full_unstemmed Reducing cardiovascular risk with immunomodulators: a randomised active comparator trial among patients with rheumatoid arthritis
title_short Reducing cardiovascular risk with immunomodulators: a randomised active comparator trial among patients with rheumatoid arthritis
title_sort reducing cardiovascular risk with immunomodulators: a randomised active comparator trial among patients with rheumatoid arthritis
topic Rheumatoid Arthritis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933165/
https://www.ncbi.nlm.nih.gov/pubmed/36450449
http://dx.doi.org/10.1136/ard-2022-223302
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