{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,24]],"date-time":"2026-10-24T02:12:55Z","timestamp":1792807975729,"version":"4.5.0"},"reference-count":48,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2022,11,28]],"date-time":"2022-11-28T00:00:00Z","timestamp":1669593600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100003132","name":"Agentschap voor Innovatie door Wetenschap en Technologie","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100003132","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100003130","name":"Fonds Wetenschappelijk Onderzoek","doi-asserted-by":"publisher","award":["1S85521N"],"award-info":[{"award-number":["1S85521N"]}],"id":[{"id":"10.13039\/501100003130","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["acrjournals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Arthritis Care &amp;amp; Research"],"published-print":{"date-parts":[[2023,4]]},"abstract":"<jats:sec><jats:title>Objective<\/jats:title><jats:p>This study investigated how psychosocial aspects of disease affect the probability of achieving sustained remission in early rheumatoid arthritis (RA) and explored the directionality of this relationship.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Data were analyzed from the randomized controlled Care in Early RA trial. Sustained remission was defined as a continued Disease Activity Score in 28 joints using the C\u2010reactive protein level (DAS28\u2010CRP) of &lt;2.6 from weeks 16 to 104. Patients completed the Short Form 36 (SF\u201036) health survey, Revised Illness Perception Questionnaire (IPQ\u2010R), and the Utrecht Coping List. These psychosocial variables were studied at baseline and at week 16 as predictors of sustained remission with logistic regression. Next, subgroups of patients in remission at week 16 were identified by Latent Profile Analysis based on these psychosocial indicators. Time to first loss of remission was then compared between groups by Cox proportional hazards regression. Finally, directionality of associations between psychosocial indicators and DAS28\u2010CRP was explored with cross\u2010lagged panel models (CLPMs).<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Sustained DAS28\u2010CRP remission was associated with higher SF\u201036 scores and less passive coping at baseline and with higher SF\u201036 scores and more positive IPQ\u2010R outcomes at week 16. Among patients in DAS28\u2010CRP remission at week 16 (n\u00a0=\u00a0287), 2 subgroups were identified: a low psychosocial burden group (n\u00a0=\u00a0231 of 287) and a high psychosocial burden group (n\u00a0=\u00a056 of 287). The low psychosocial burden group retained remission longer (hazard ratio 0.51 [0.35\u20130.73]). In the CLPM, temporal relationships between psychosocial well\u2010being and DAS28\u2010CRP were complex, bidirectional, and disease\u2010phase dependent.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Suboptimal psychosocial well\u2010being and negative illness perceptions predicted lower probability of sustained remission in an early RA cohort. Illness perceptions appeared to become more clinically relevant with time. Finally, 1 in 5 patients showed worse psychosocial outcomes despite early remission, and these patients tended to lose remission earlier.<\/jats:p><\/jats:sec>","DOI":"10.1002\/acr.24847","type":"journal-article","created":{"date-parts":[[2021,12,21]],"date-time":"2021-12-21T01:10:26Z","timestamp":1640049026000},"page":"758-767","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":21,"title":["Psychosocial Burden Predicts Sustained Remission in Early Rheumatoid Arthritis: Unraveling the Complex Interplay of <scp>Well\u2010Being<\/scp> and Disease Activity"],"prefix":"10.1002","volume":"75","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6073-7635","authenticated-orcid":false,"given":"Micha\u00ebl","family":"Doumen","sequence":"first","affiliation":[{"name":"Skeletal Biology and Engineering Research Center, Katholieke Universiteit Leuven, Leuven, Belgium, and University Hospitals Leuven  Leuven 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