Frailty assessment in patients with Behçet's syndrome: A cross-sectional monocentric study

Evidence evaluating the association between pre-frailty and frailty, and risk of adverse health outcomes in patients with Behçet's syndrome (BS) is limited in the literature. The aim of this study was to characterize the prevalence of frailty and associated factors in a single-centre cohort of...

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Veröffentlicht in:Reumatología clinica (Barcelona) 2024-10, Vol.20 (8), p.409-415
Hauptverfasser: Apaydin, Hakan, Güven, Serdar Can, Koçak Ulucaköy, Rezan, Babaoğlu, Hakan, Kayacan Erdoğan, Esra, Orhan, Kevser, Armağan, Berkan
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container_title Reumatología clinica (Barcelona)
container_volume 20
creator Apaydin, Hakan
Güven, Serdar Can
Koçak Ulucaköy, Rezan
Babaoğlu, Hakan
Kayacan Erdoğan, Esra
Orhan, Kevser
Armağan, Berkan
description Evidence evaluating the association between pre-frailty and frailty, and risk of adverse health outcomes in patients with Behçet's syndrome (BS) is limited in the literature. The aim of this study was to characterize the prevalence of frailty and associated factors in a single-centre cohort of patients with BS. Based on the International Study Group's criteria, this was a monocentric cross-sectional study of BS patients. The Fried frailty criteria were used to define frailty. The Turkish version of the Behçet's Disease Current Activity Form was used to measure the disease activity of BS. Damage index was assessed with the Behçet's Syndrome Overall Damage Index. Forty-four patients were enrolled. According to Fried frailty criteria, patients were classified as 13.6% frail, 59% pre-frail, and 27.2% robust, respectively. Compared to pre-frail and robust patients, frail patients had higher levels of inflammatory markers at the time of diagnosis. CRP levels at time of diagnosis and at the last visit were higher in the frail group than in the pre-frail and robust groups (p=0.039 and p=0.023, respectively). When active drugs for BS were evaluated, systemic glucocorticoid (50%, p=0.030) and cyclophosphamide (33.3%, p=0.006) treatments were higher in the frail group. Frailty and pre-frailty are commonly detected even in younger patients with BS. Inflammation can be described as potential determinants of frailty status. La evidencia que evalúa la asociación entre prefragilidad y fragilidad, y el riesgo de resultados adversos para la salud en los pacientes con síndrome de Behçet (SB) es limitada en la literatura. El objetivo de este estudio fue caracterizar la prevalencia de fragilidad y los factores asociados en una cohorte de pacientes con SB. Basado en los criterios del Grupo Internacional de Estudio, este fue un estudio monocéntrico transversal de pacientes con SB. Se utilizaron los criterios de fragilidad de Fried para definir la fragilidad. Se utilizó la versión turca del Behçet's Disease Current Activity Form para medir la actividad de la enfermedad. El índice de daño se evaluó con el Índice de Daño Global del Síndrome de Behçet. Se incluyeron 44 pacientes. Según los criterios de fragilidad de Fried, los pacientes fueron clasificados como 13,6% frágiles, 59% prefrágiles y 27,2% robustos, respectivamente. En comparación con los pacientes prefrágiles y robustos, los pacientes frágiles tenían niveles más altos de marcadores inflamatorios en el momento del diagnós
doi_str_mv 10.1016/j.reumae.2024.09.005
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The aim of this study was to characterize the prevalence of frailty and associated factors in a single-centre cohort of patients with BS. Based on the International Study Group's criteria, this was a monocentric cross-sectional study of BS patients. The Fried frailty criteria were used to define frailty. The Turkish version of the Behçet's Disease Current Activity Form was used to measure the disease activity of BS. Damage index was assessed with the Behçet's Syndrome Overall Damage Index. Forty-four patients were enrolled. According to Fried frailty criteria, patients were classified as 13.6% frail, 59% pre-frail, and 27.2% robust, respectively. Compared to pre-frail and robust patients, frail patients had higher levels of inflammatory markers at the time of diagnosis. CRP levels at time of diagnosis and at the last visit were higher in the frail group than in the pre-frail and robust groups (p=0.039 and p=0.023, respectively). When active drugs for BS were evaluated, systemic glucocorticoid (50%, p=0.030) and cyclophosphamide (33.3%, p=0.006) treatments were higher in the frail group. Frailty and pre-frailty are commonly detected even in younger patients with BS. Inflammation can be described as potential determinants of frailty status. La evidencia que evalúa la asociación entre prefragilidad y fragilidad, y el riesgo de resultados adversos para la salud en los pacientes con síndrome de Behçet (SB) es limitada en la literatura. El objetivo de este estudio fue caracterizar la prevalencia de fragilidad y los factores asociados en una cohorte de pacientes con SB. Basado en los criterios del Grupo Internacional de Estudio, este fue un estudio monocéntrico transversal de pacientes con SB. Se utilizaron los criterios de fragilidad de Fried para definir la fragilidad. Se utilizó la versión turca del Behçet's Disease Current Activity Form para medir la actividad de la enfermedad. El índice de daño se evaluó con el Índice de Daño Global del Síndrome de Behçet. Se incluyeron 44 pacientes. Según los criterios de fragilidad de Fried, los pacientes fueron clasificados como 13,6% frágiles, 59% prefrágiles y 27,2% robustos, respectivamente. En comparación con los pacientes prefrágiles y robustos, los pacientes frágiles tenían niveles más altos de marcadores inflamatorios en el momento del diagnóstico. Los niveles de PCR en el momento del diagnóstico y en la última visita fueron más altos en el grupo frágil que en los grupos prefrágil y robusto (p=0,039 y p=0,023, respectivamente). Cuando se evaluaron los fármacos activos para el SB, los tratamientos sistémicos con glucocorticoides (50%, p=0,030) y ciclofosfamida (33,3%, p=0,006) fueron mayores en el grupo frágil. La fragilidad y la prefragilidad se detectan comúnmente incluso en pacientes jóvenes con SB. La inflamación puede ser descrita como un potencial determinante del estado de fragilidad.</description><identifier>ISSN: 2173-5743</identifier><identifier>EISSN: 2173-5743</identifier><identifier>DOI: 10.1016/j.reumae.2024.09.005</identifier><identifier>PMID: 39396353</identifier><language>eng</language><publisher>Spain: Elsevier España, S.L.U</publisher><subject>Adult ; Behcet Syndrome - complications ; Behcet Syndrome - diagnosis ; Behçet's syndrome ; Cross-Sectional Studies ; Female ; Fragilidad ; Frailty ; Frailty - complications ; Frailty - etiology ; Glucocorticoides ; Glucocorticoids ; Humans ; Immunosuppresion ; Inflamación ; Inflammaging ; Inmunosupresión ; Male ; Middle Aged ; Prevalence ; Síndrome de Behçet ; Turkey - epidemiology</subject><ispartof>Reumatología clinica (Barcelona), 2024-10, Vol.20 (8), p.409-415</ispartof><rights>2024 Sociedad Española de Reumatología (SER), Colegio Mexicano de Reumatología (CMR) and Elsevier España, S.L.U.</rights><rights>Copyright © 2024 Sociedad Española de Reumatología (SER), Colegio Mexicano de Reumatología (CMR) and Elsevier España, S.L.U. 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The aim of this study was to characterize the prevalence of frailty and associated factors in a single-centre cohort of patients with BS. Based on the International Study Group's criteria, this was a monocentric cross-sectional study of BS patients. The Fried frailty criteria were used to define frailty. The Turkish version of the Behçet's Disease Current Activity Form was used to measure the disease activity of BS. Damage index was assessed with the Behçet's Syndrome Overall Damage Index. Forty-four patients were enrolled. According to Fried frailty criteria, patients were classified as 13.6% frail, 59% pre-frail, and 27.2% robust, respectively. Compared to pre-frail and robust patients, frail patients had higher levels of inflammatory markers at the time of diagnosis. CRP levels at time of diagnosis and at the last visit were higher in the frail group than in the pre-frail and robust groups (p=0.039 and p=0.023, respectively). When active drugs for BS were evaluated, systemic glucocorticoid (50%, p=0.030) and cyclophosphamide (33.3%, p=0.006) treatments were higher in the frail group. Frailty and pre-frailty are commonly detected even in younger patients with BS. Inflammation can be described as potential determinants of frailty status. La evidencia que evalúa la asociación entre prefragilidad y fragilidad, y el riesgo de resultados adversos para la salud en los pacientes con síndrome de Behçet (SB) es limitada en la literatura. El objetivo de este estudio fue caracterizar la prevalencia de fragilidad y los factores asociados en una cohorte de pacientes con SB. Basado en los criterios del Grupo Internacional de Estudio, este fue un estudio monocéntrico transversal de pacientes con SB. Se utilizaron los criterios de fragilidad de Fried para definir la fragilidad. Se utilizó la versión turca del Behçet's Disease Current Activity Form para medir la actividad de la enfermedad. El índice de daño se evaluó con el Índice de Daño Global del Síndrome de Behçet. Se incluyeron 44 pacientes. Según los criterios de fragilidad de Fried, los pacientes fueron clasificados como 13,6% frágiles, 59% prefrágiles y 27,2% robustos, respectivamente. En comparación con los pacientes prefrágiles y robustos, los pacientes frágiles tenían niveles más altos de marcadores inflamatorios en el momento del diagnóstico. Los niveles de PCR en el momento del diagnóstico y en la última visita fueron más altos en el grupo frágil que en los grupos prefrágil y robusto (p=0,039 y p=0,023, respectivamente). Cuando se evaluaron los fármacos activos para el SB, los tratamientos sistémicos con glucocorticoides (50%, p=0,030) y ciclofosfamida (33,3%, p=0,006) fueron mayores en el grupo frágil. La fragilidad y la prefragilidad se detectan comúnmente incluso en pacientes jóvenes con SB. La inflamación puede ser descrita como un potencial determinante del estado de fragilidad.</description><subject>Adult</subject><subject>Behcet Syndrome - complications</subject><subject>Behcet Syndrome - diagnosis</subject><subject>Behçet's syndrome</subject><subject>Cross-Sectional Studies</subject><subject>Female</subject><subject>Fragilidad</subject><subject>Frailty</subject><subject>Frailty - complications</subject><subject>Frailty - etiology</subject><subject>Glucocorticoides</subject><subject>Glucocorticoids</subject><subject>Humans</subject><subject>Immunosuppresion</subject><subject>Inflamación</subject><subject>Inflammaging</subject><subject>Inmunosupresión</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Prevalence</subject><subject>Síndrome de Behçet</subject><subject>Turkey - epidemiology</subject><issn>2173-5743</issn><issn>2173-5743</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtOwzAQhi0EAlR6A4S8g02CHSdOwgIJEC-pEpvuWFiOPVFd5VE8Cagn4iBcDJcCYsVsPIvvnxl_hBxzFnPG5fky9jC2GuKEJWnMypixbIccJjwXUZanYvdPf0CmiEsWqkiyUub75ECUopQiE4fk-c5r1wxrqhEBsYVuoK6jKz240CJ9c8OCXsPi4x2GU6S47qzvW7igV9T4HjFCMIPrO93Qtu96E0LeGYrDaNdHZK_WDcL0-52Q-d3t_OYhmj3dP95czSLDMymiWnJpueVQ8FTyPGOs4nmZJqCNqXLD01oIUdSZzSpr8oAmojK2yuuiLoqUiQk5245d-f5lBBxU69BA0-gO-hGV4FwKkfJCBjTdol-3e6jVyrtW-7XiTG3EqqXailUbsYqVKogNsZPvDWPVgv0N_WgMwOUWgPDNVwdeoQn-DFjngx9le_f_hk8M9Iym</recordid><startdate>202410</startdate><enddate>202410</enddate><creator>Apaydin, Hakan</creator><creator>Güven, Serdar Can</creator><creator>Koçak Ulucaköy, Rezan</creator><creator>Babaoğlu, Hakan</creator><creator>Kayacan Erdoğan, Esra</creator><creator>Orhan, Kevser</creator><creator>Armağan, Berkan</creator><general>Elsevier España, S.L.U</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202410</creationdate><title>Frailty assessment in patients with Behçet's syndrome: A cross-sectional monocentric study</title><author>Apaydin, Hakan ; Güven, Serdar Can ; Koçak Ulucaköy, Rezan ; Babaoğlu, Hakan ; Kayacan Erdoğan, Esra ; Orhan, Kevser ; Armağan, Berkan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1563-f616d1d1e814617500b17942eaccb7c14f3338f5d5bdc76d123bcdb7f8f88403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Behcet Syndrome - complications</topic><topic>Behcet Syndrome - diagnosis</topic><topic>Behçet's syndrome</topic><topic>Cross-Sectional Studies</topic><topic>Female</topic><topic>Fragilidad</topic><topic>Frailty</topic><topic>Frailty - complications</topic><topic>Frailty - etiology</topic><topic>Glucocorticoides</topic><topic>Glucocorticoids</topic><topic>Humans</topic><topic>Immunosuppresion</topic><topic>Inflamación</topic><topic>Inflammaging</topic><topic>Inmunosupresión</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prevalence</topic><topic>Síndrome de Behçet</topic><topic>Turkey - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Apaydin, Hakan</creatorcontrib><creatorcontrib>Güven, Serdar Can</creatorcontrib><creatorcontrib>Koçak Ulucaköy, Rezan</creatorcontrib><creatorcontrib>Babaoğlu, Hakan</creatorcontrib><creatorcontrib>Kayacan Erdoğan, Esra</creatorcontrib><creatorcontrib>Orhan, Kevser</creatorcontrib><creatorcontrib>Armağan, Berkan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Reumatología clinica (Barcelona)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Apaydin, Hakan</au><au>Güven, Serdar Can</au><au>Koçak Ulucaköy, Rezan</au><au>Babaoğlu, Hakan</au><au>Kayacan Erdoğan, Esra</au><au>Orhan, Kevser</au><au>Armağan, Berkan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Frailty assessment in patients with Behçet's syndrome: A cross-sectional monocentric study</atitle><jtitle>Reumatología clinica (Barcelona)</jtitle><addtitle>Reumatol Clin (Engl Ed)</addtitle><date>2024-10</date><risdate>2024</risdate><volume>20</volume><issue>8</issue><spage>409</spage><epage>415</epage><pages>409-415</pages><issn>2173-5743</issn><eissn>2173-5743</eissn><abstract>Evidence evaluating the association between pre-frailty and frailty, and risk of adverse health outcomes in patients with Behçet's syndrome (BS) is limited in the literature. The aim of this study was to characterize the prevalence of frailty and associated factors in a single-centre cohort of patients with BS. Based on the International Study Group's criteria, this was a monocentric cross-sectional study of BS patients. The Fried frailty criteria were used to define frailty. The Turkish version of the Behçet's Disease Current Activity Form was used to measure the disease activity of BS. Damage index was assessed with the Behçet's Syndrome Overall Damage Index. Forty-four patients were enrolled. According to Fried frailty criteria, patients were classified as 13.6% frail, 59% pre-frail, and 27.2% robust, respectively. Compared to pre-frail and robust patients, frail patients had higher levels of inflammatory markers at the time of diagnosis. CRP levels at time of diagnosis and at the last visit were higher in the frail group than in the pre-frail and robust groups (p=0.039 and p=0.023, respectively). When active drugs for BS were evaluated, systemic glucocorticoid (50%, p=0.030) and cyclophosphamide (33.3%, p=0.006) treatments were higher in the frail group. Frailty and pre-frailty are commonly detected even in younger patients with BS. Inflammation can be described as potential determinants of frailty status. La evidencia que evalúa la asociación entre prefragilidad y fragilidad, y el riesgo de resultados adversos para la salud en los pacientes con síndrome de Behçet (SB) es limitada en la literatura. El objetivo de este estudio fue caracterizar la prevalencia de fragilidad y los factores asociados en una cohorte de pacientes con SB. Basado en los criterios del Grupo Internacional de Estudio, este fue un estudio monocéntrico transversal de pacientes con SB. Se utilizaron los criterios de fragilidad de Fried para definir la fragilidad. Se utilizó la versión turca del Behçet's Disease Current Activity Form para medir la actividad de la enfermedad. El índice de daño se evaluó con el Índice de Daño Global del Síndrome de Behçet. Se incluyeron 44 pacientes. Según los criterios de fragilidad de Fried, los pacientes fueron clasificados como 13,6% frágiles, 59% prefrágiles y 27,2% robustos, respectivamente. En comparación con los pacientes prefrágiles y robustos, los pacientes frágiles tenían niveles más altos de marcadores inflamatorios en el momento del diagnóstico. Los niveles de PCR en el momento del diagnóstico y en la última visita fueron más altos en el grupo frágil que en los grupos prefrágil y robusto (p=0,039 y p=0,023, respectivamente). Cuando se evaluaron los fármacos activos para el SB, los tratamientos sistémicos con glucocorticoides (50%, p=0,030) y ciclofosfamida (33,3%, p=0,006) fueron mayores en el grupo frágil. La fragilidad y la prefragilidad se detectan comúnmente incluso en pacientes jóvenes con SB. La inflamación puede ser descrita como un potencial determinante del estado de fragilidad.</abstract><cop>Spain</cop><pub>Elsevier España, S.L.U</pub><pmid>39396353</pmid><doi>10.1016/j.reumae.2024.09.005</doi><tpages>7</tpages></addata></record>
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subjects Adult
Behcet Syndrome - complications
Behcet Syndrome - diagnosis
Behçet's syndrome
Cross-Sectional Studies
Female
Fragilidad
Frailty
Frailty - complications
Frailty - etiology
Glucocorticoides
Glucocorticoids
Humans
Immunosuppresion
Inflamación
Inflammaging
Inmunosupresión
Male
Middle Aged
Prevalence
Síndrome de Behçet
Turkey - epidemiology
title Frailty assessment in patients with Behçet's syndrome: A cross-sectional monocentric study
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