Association between obesity and remission in rheumatoid arthritis patients treated with disease-modifying anti-rheumatic drugs

The aim of this study was to investigate the association between body-mass index (BMI) and remission in RA patients receiving conventional synthetic (cs-) or the biological Disease-Modifying Antirheumatic Drug (DMARD), tocilizumab. Individual participant data (IPD) were pooled from five trials inves...

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Veröffentlicht in:Scientific reports 2020-10, Vol.10 (1), p.18634, Article 18634
Hauptverfasser: Abuhelwa, Ahmad Y., Hopkins, Ashley M., Sorich, Michael J., Proudman, Susanna, Foster, David J. R., Wiese, Michael D.
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container_title Scientific reports
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creator Abuhelwa, Ahmad Y.
Hopkins, Ashley M.
Sorich, Michael J.
Proudman, Susanna
Foster, David J. R.
Wiese, Michael D.
description The aim of this study was to investigate the association between body-mass index (BMI) and remission in RA patients receiving conventional synthetic (cs-) or the biological Disease-Modifying Antirheumatic Drug (DMARD), tocilizumab. Individual participant data (IPD) were pooled from five trials investigating tocilizumab and/or csDMARDs therapy (primarily methotrexate) for RA. Time to first remission was recorded according to the Simplified Disease Activity Index (SDAI) and Clinical Disease Activity Index (CDAI). BMI was classified according to WHO definitions. Associations between baseline BMI and remission were assessed by Cox-proportional hazard analysis. IPD were available from 5428 patients treated with tocilizumab ± csDMARDs (n = 4098) or csDMARDs alone (n = 1330). Of these, 1839 (33.9%) had normal BMI, 1780 (32.8%) overweight, 1652 (30.4%) obese and 157 (2.9%) were underweight. Obesity, compared to normal BMI, was associated with less frequent remission using SDAI (adjusted HR 0.80 [95% CI 0.70–0.92]) and CDAI (adjusted HR 0.77 [0.68–0.87]). As continuous variable, increased BMI was associated with less frequent SDAI (P = 0.001) and CDAI (P = 0.001) defined remission. No heterogeneity in identified associations was observed between studies (P = 0.08) or treatments (P = 0.22). Obesity was negatively associated with RA disease remission regardless of RA therapy, suggesting that baseline BMI should be considered as a stratification factor in future RA trials.
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R.</creatorcontrib><creatorcontrib>Wiese, Michael D.</creatorcontrib><title>Association between obesity and remission in rheumatoid arthritis patients treated with disease-modifying anti-rheumatic drugs</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>The aim of this study was to investigate the association between body-mass index (BMI) and remission in RA patients receiving conventional synthetic (cs-) or the biological Disease-Modifying Antirheumatic Drug (DMARD), tocilizumab. Individual participant data (IPD) were pooled from five trials investigating tocilizumab and/or csDMARDs therapy (primarily methotrexate) for RA. Time to first remission was recorded according to the Simplified Disease Activity Index (SDAI) and Clinical Disease Activity Index (CDAI). BMI was classified according to WHO definitions. Associations between baseline BMI and remission were assessed by Cox-proportional hazard analysis. 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R.</au><au>Wiese, Michael D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between obesity and remission in rheumatoid arthritis patients treated with disease-modifying anti-rheumatic drugs</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2020-10-29</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>18634</spage><pages>18634-</pages><artnum>18634</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>The aim of this study was to investigate the association between body-mass index (BMI) and remission in RA patients receiving conventional synthetic (cs-) or the biological Disease-Modifying Antirheumatic Drug (DMARD), tocilizumab. Individual participant data (IPD) were pooled from five trials investigating tocilizumab and/or csDMARDs therapy (primarily methotrexate) for RA. Time to first remission was recorded according to the Simplified Disease Activity Index (SDAI) and Clinical Disease Activity Index (CDAI). BMI was classified according to WHO definitions. Associations between baseline BMI and remission were assessed by Cox-proportional hazard analysis. IPD were available from 5428 patients treated with tocilizumab ± csDMARDs (n = 4098) or csDMARDs alone (n = 1330). Of these, 1839 (33.9%) had normal BMI, 1780 (32.8%) overweight, 1652 (30.4%) obese and 157 (2.9%) were underweight. Obesity, compared to normal BMI, was associated with less frequent remission using SDAI (adjusted HR 0.80 [95% CI 0.70–0.92]) and CDAI (adjusted HR 0.77 [0.68–0.87]). As continuous variable, increased BMI was associated with less frequent SDAI (P = 0.001) and CDAI (P = 0.001) defined remission. No heterogeneity in identified associations was observed between studies (P = 0.08) or treatments (P = 0.22). Obesity was negatively associated with RA disease remission regardless of RA therapy, suggesting that baseline BMI should be considered as a stratification factor in future RA trials.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33122725</pmid><doi>10.1038/s41598-020-75673-7</doi><orcidid>https://orcid.org/0000-0002-4182-065X</orcidid><oa>free_for_read</oa></addata></record>
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subjects 692/4023
692/4023/1670
692/4023/1670/498
692/53/2422
Adult
Antirheumatic Agents - therapeutic use
Arthritis, Rheumatoid - complications
Arthritis, Rheumatoid - drug therapy
Body Mass Index
Body weight
Clinical trials
Cohort Studies
Female
Heterogeneity
Humanities and Social Sciences
Humans
Male
Methotrexate
Middle Aged
multidisciplinary
Obesity
Obesity - complications
Overweight
Proportional Hazards Models
Remission
Remission (Medicine)
Remission Induction
Rheumatoid arthritis
Science
Science (multidisciplinary)
Underweight
title Association between obesity and remission in rheumatoid arthritis patients treated with disease-modifying anti-rheumatic drugs
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