Immunosuppressive treatment and the risk of diabetes in rheumatoid arthritis.

<h4>Objective</h4>Inflammation and anti-inflammatory treatments might influence the risk of diabetes. The objective of this study was to assess factors associated with incident diabetes in rheumatoid arthritis (RA).<h4>Methods</h4>The study population consisted of RA patients...

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Main Authors: Siri Lillegraven, Jeffrey D Greenberg, George W Reed, Katherine Saunders, Jeffrey R Curtis, Leslie Harrold, Marc C Hochberg, Dimitrios A Pappas, Joel M Kremer, Daniel H Solomon
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0210459
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author Siri Lillegraven
Jeffrey D Greenberg
George W Reed
Katherine Saunders
Jeffrey R Curtis
Leslie Harrold
Marc C Hochberg
Dimitrios A Pappas
Joel M Kremer
Daniel H Solomon
author_facet Siri Lillegraven
Jeffrey D Greenberg
George W Reed
Katherine Saunders
Jeffrey R Curtis
Leslie Harrold
Marc C Hochberg
Dimitrios A Pappas
Joel M Kremer
Daniel H Solomon
author_sort Siri Lillegraven
collection DOAJ
description <h4>Objective</h4>Inflammation and anti-inflammatory treatments might influence the risk of diabetes. The objective of this study was to assess factors associated with incident diabetes in rheumatoid arthritis (RA).<h4>Methods</h4>The study population consisted of RA patients from a multi-center cohort study, Corrona. To assess risk associated with disease modifying antirheumatic drug (DMARD) exposure, we assessed five mutually exclusive DMARD groups. Additionally, we assessed the risk associated with body mass index (BMI, <25, 25-30, >30 kg/m2) and glucocorticoid usage. Incident cases of diabetes were confirmed through adjudication, and Cox regression models were fit to estimate the risk of incident diabetes.<h4>Results</h4>We identified 21,775 DMARD treatment regimens, the mean (SD) age at the index visit was 58 (13) years, disease duration 10 (10) years, and 30% used oral glucocorticoids at the time. Eighty-four incident cases of diabetes were confirmed within the treatment exposure periods. The hazard ratio (HR, 95% confidence interval) for diabetes was significantly reduced in patients receiving TNF inhibitors, HR 0.35 (0.13, 0.91), compared to patients treated with non-biologic DMARDs other than hydroxychloroquine and methotrexate. Hydroxychloroquine, methotrexate and use of other biologic DMARDs had a numerically reduced risk compared to the same group. Patients prescribed ≥7.5 mg of glucocorticoids had a HR of 2.33 (1.68, 3.22) of incident diabetes compared with patients not prescribed oral glucocorticoids. RA patients with a BMI >30 had a HR of 6.27 (2.97, 13.25) compared to patients with BMI ≤25.<h4>Conclusion</h4>DMARDs, glucocorticoids and obesity influenced the risk of incident diabetes in a large cohort of RA patients. Monitoring for the occurrence of diabetes should be part of routine RA management with a focus on specific subgroups.
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spelling doaj.art-e35121fcf08d4ca8be74b90dbf5359942022-12-21T18:24:50ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01141e021045910.1371/journal.pone.0210459Immunosuppressive treatment and the risk of diabetes in rheumatoid arthritis.Siri LillegravenJeffrey D GreenbergGeorge W ReedKatherine SaundersJeffrey R CurtisLeslie HarroldMarc C HochbergDimitrios A PappasJoel M KremerDaniel H Solomon<h4>Objective</h4>Inflammation and anti-inflammatory treatments might influence the risk of diabetes. The objective of this study was to assess factors associated with incident diabetes in rheumatoid arthritis (RA).<h4>Methods</h4>The study population consisted of RA patients from a multi-center cohort study, Corrona. To assess risk associated with disease modifying antirheumatic drug (DMARD) exposure, we assessed five mutually exclusive DMARD groups. Additionally, we assessed the risk associated with body mass index (BMI, <25, 25-30, >30 kg/m2) and glucocorticoid usage. Incident cases of diabetes were confirmed through adjudication, and Cox regression models were fit to estimate the risk of incident diabetes.<h4>Results</h4>We identified 21,775 DMARD treatment regimens, the mean (SD) age at the index visit was 58 (13) years, disease duration 10 (10) years, and 30% used oral glucocorticoids at the time. Eighty-four incident cases of diabetes were confirmed within the treatment exposure periods. The hazard ratio (HR, 95% confidence interval) for diabetes was significantly reduced in patients receiving TNF inhibitors, HR 0.35 (0.13, 0.91), compared to patients treated with non-biologic DMARDs other than hydroxychloroquine and methotrexate. Hydroxychloroquine, methotrexate and use of other biologic DMARDs had a numerically reduced risk compared to the same group. Patients prescribed ≥7.5 mg of glucocorticoids had a HR of 2.33 (1.68, 3.22) of incident diabetes compared with patients not prescribed oral glucocorticoids. RA patients with a BMI >30 had a HR of 6.27 (2.97, 13.25) compared to patients with BMI ≤25.<h4>Conclusion</h4>DMARDs, glucocorticoids and obesity influenced the risk of incident diabetes in a large cohort of RA patients. Monitoring for the occurrence of diabetes should be part of routine RA management with a focus on specific subgroups.https://doi.org/10.1371/journal.pone.0210459
spellingShingle Siri Lillegraven
Jeffrey D Greenberg
George W Reed
Katherine Saunders
Jeffrey R Curtis
Leslie Harrold
Marc C Hochberg
Dimitrios A Pappas
Joel M Kremer
Daniel H Solomon
Immunosuppressive treatment and the risk of diabetes in rheumatoid arthritis.
PLoS ONE
title Immunosuppressive treatment and the risk of diabetes in rheumatoid arthritis.
title_full Immunosuppressive treatment and the risk of diabetes in rheumatoid arthritis.
title_fullStr Immunosuppressive treatment and the risk of diabetes in rheumatoid arthritis.
title_full_unstemmed Immunosuppressive treatment and the risk of diabetes in rheumatoid arthritis.
title_short Immunosuppressive treatment and the risk of diabetes in rheumatoid arthritis.
title_sort immunosuppressive treatment and the risk of diabetes in rheumatoid arthritis
url https://doi.org/10.1371/journal.pone.0210459
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