The Association of Methotrexate, Sulfasalazine, and Hydroxychloroquine Use With Fracture in Postmenopausal Women With Rheumatoid Arthritis: Findings From the Women's Health Initiative

ABSTRACT This study was conducted to evaluate the extent to which disease‐modifying antirheumatic medications (DMARDs) used as part of a triple therapy for the treatment of rheumatoid arthritis (RA) including methotrexate, sulfasalazine, and hydroxychloroquine are associated with fractures in postme...

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Main Authors: Laura Carbone, Sowmya Vasan, Rachel Elam, Sandeepkumar Gupta, Omar Tolaymat, Carolyn Crandall, Jean Wactawski‐Wende, Karen C Johnson
Format: Article
Language:English
Published: Wiley 2020-10-01
Series:JBMR Plus
Subjects:
Online Access:https://doi.org/10.1002/jbm4.10393
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spelling doaj-9e6c1a3c33104eae90fe10909f3d3b992021-05-02T18:23:58ZengWileyJBMR Plus2473-40392020-10-01410n/an/a10.1002/jbm4.10393The Association of Methotrexate, Sulfasalazine, and Hydroxychloroquine Use With Fracture in Postmenopausal Women With Rheumatoid Arthritis: Findings From the Women's Health InitiativeLaura Carbone0Sowmya Vasan1Rachel Elam2Sandeepkumar Gupta3Omar Tolaymat4Carolyn Crandall5Jean Wactawski‐Wende6Karen C Johnson7Department of Medicine, Division of Rheumatology, J. Harold Harrison MD, Distinguished University Chair in Rheumatology Medical College of Georgia at Augusta University Augusta GA USAFred Hutchinson Cancer Research Center Seattle WA USADepartment of Rheumatology Charlie Norwood Veterans Affairs Medical Center Augusta GA USADepartment of Medicine, Division of Rheumatology Medical College of Georgia at Augusta University Augusta GA USADepartment of Medicine, Division of Rheumatology Medical College of Georgia at Augusta University Augusta GA USADepartment of Medicine, Division of General Internal Medicine and Health Services Research David Geffen School of Medicine at University of California, Los Angeles Los Angeles CA USADepartment of Epidemiology and Environmental Health, School of Public Health and Health Professions University at Buffalo Buffalo NY USADepartment of Preventive Medicine University of Tennessee Health Science Center Memphis TN USAABSTRACT This study was conducted to evaluate the extent to which disease‐modifying antirheumatic medications (DMARDs) used as part of a triple therapy for the treatment of rheumatoid arthritis (RA) including methotrexate, sulfasalazine, and hydroxychloroquine are associated with fractures in postmenopausal women with RA. Incident fractures following use of methotrexate, sulfasalazine, and/or hydroxychloroquine in postmenopausal women with RA in the Women's Health Initiative were estimated by Cox proportional hazards using hazard ratios (HRs) and 95% CIs after consideration of potential confounders. There were 1201 women with RA enrolled in the Women's Health Initiative included in these analyses, of which 74% were white, 17% were black, and 9% were of other or unknown race/ethnicity. Of the women with RA, 421 (35%) had not used methotrexate, sulfasalazine, or hydroxychloroquine, whereas 519 (43%) women had used methotrexate, 83 (7%) sulfasalazine, and 363 (30%) hydroxychloroquine alone or in combination at some time during study follow‐up. Over a median length of 6.46 years of follow‐up, in multivariable adjusted models, no statistically significant association was found between methotrexate (HR, 1.1; 95% CI, 0.8–1.6), sulfasalazine (HR, 0.6; 95% CI, 0.2–1.5), or hydroxychloroquine (HR, 1.0; 95% CI, 0.7–1.5) use and incident fractures or between combination therapy with methotrexate and sulfasalazine or methotrexate and hydroxychloroquine use (HR, 0.9; 95% CI, 0.5–1.6) and incident fractures. In conclusion, postmenopausal women with RA receiving any component of triple therapy should not be expected to have any substantial reduction in fracture risk from use of these DMARDs. © 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.https://doi.org/10.1002/jbm4.10393COX PROPORTIONAL HAZARDS MODELINGDISEASE MODIFYING ANTIRHEUMATIC DRUGSFRACTURE RISK ASSESSMENTOSTEOPOROSISRHEUMATOID ARTHRITIS
collection DOAJ
language English
format Article
sources DOAJ
author Laura Carbone
Sowmya Vasan
Rachel Elam
Sandeepkumar Gupta
Omar Tolaymat
Carolyn Crandall
Jean Wactawski‐Wende
Karen C Johnson
spellingShingle Laura Carbone
Sowmya Vasan
Rachel Elam
Sandeepkumar Gupta
Omar Tolaymat
Carolyn Crandall
Jean Wactawski‐Wende
Karen C Johnson
The Association of Methotrexate, Sulfasalazine, and Hydroxychloroquine Use With Fracture in Postmenopausal Women With Rheumatoid Arthritis: Findings From the Women's Health Initiative
JBMR Plus
COX PROPORTIONAL HAZARDS MODELING
DISEASE MODIFYING ANTIRHEUMATIC DRUGS
FRACTURE RISK ASSESSMENT
OSTEOPOROSIS
RHEUMATOID ARTHRITIS
author_facet Laura Carbone
Sowmya Vasan
Rachel Elam
Sandeepkumar Gupta
Omar Tolaymat
Carolyn Crandall
Jean Wactawski‐Wende
Karen C Johnson
author_sort Laura Carbone
title The Association of Methotrexate, Sulfasalazine, and Hydroxychloroquine Use With Fracture in Postmenopausal Women With Rheumatoid Arthritis: Findings From the Women's Health Initiative
title_short The Association of Methotrexate, Sulfasalazine, and Hydroxychloroquine Use With Fracture in Postmenopausal Women With Rheumatoid Arthritis: Findings From the Women's Health Initiative
title_full The Association of Methotrexate, Sulfasalazine, and Hydroxychloroquine Use With Fracture in Postmenopausal Women With Rheumatoid Arthritis: Findings From the Women's Health Initiative
title_fullStr The Association of Methotrexate, Sulfasalazine, and Hydroxychloroquine Use With Fracture in Postmenopausal Women With Rheumatoid Arthritis: Findings From the Women's Health Initiative
title_full_unstemmed The Association of Methotrexate, Sulfasalazine, and Hydroxychloroquine Use With Fracture in Postmenopausal Women With Rheumatoid Arthritis: Findings From the Women's Health Initiative
title_sort association of methotrexate, sulfasalazine, and hydroxychloroquine use with fracture in postmenopausal women with rheumatoid arthritis: findings from the women's health initiative
publisher Wiley
series JBMR Plus
issn 2473-4039
publishDate 2020-10-01
description ABSTRACT This study was conducted to evaluate the extent to which disease‐modifying antirheumatic medications (DMARDs) used as part of a triple therapy for the treatment of rheumatoid arthritis (RA) including methotrexate, sulfasalazine, and hydroxychloroquine are associated with fractures in postmenopausal women with RA. Incident fractures following use of methotrexate, sulfasalazine, and/or hydroxychloroquine in postmenopausal women with RA in the Women's Health Initiative were estimated by Cox proportional hazards using hazard ratios (HRs) and 95% CIs after consideration of potential confounders. There were 1201 women with RA enrolled in the Women's Health Initiative included in these analyses, of which 74% were white, 17% were black, and 9% were of other or unknown race/ethnicity. Of the women with RA, 421 (35%) had not used methotrexate, sulfasalazine, or hydroxychloroquine, whereas 519 (43%) women had used methotrexate, 83 (7%) sulfasalazine, and 363 (30%) hydroxychloroquine alone or in combination at some time during study follow‐up. Over a median length of 6.46 years of follow‐up, in multivariable adjusted models, no statistically significant association was found between methotrexate (HR, 1.1; 95% CI, 0.8–1.6), sulfasalazine (HR, 0.6; 95% CI, 0.2–1.5), or hydroxychloroquine (HR, 1.0; 95% CI, 0.7–1.5) use and incident fractures or between combination therapy with methotrexate and sulfasalazine or methotrexate and hydroxychloroquine use (HR, 0.9; 95% CI, 0.5–1.6) and incident fractures. In conclusion, postmenopausal women with RA receiving any component of triple therapy should not be expected to have any substantial reduction in fracture risk from use of these DMARDs. © 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
topic COX PROPORTIONAL HAZARDS MODELING
DISEASE MODIFYING ANTIRHEUMATIC DRUGS
FRACTURE RISK ASSESSMENT
OSTEOPOROSIS
RHEUMATOID ARTHRITIS
url https://doi.org/10.1002/jbm4.10393
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