Women, men, and rheumatoid arthritis: analyses of disease activity, disease characteristics, and treatments in the QUEST-RA Study

Tuulikki Sokka(Central Finland Health Care District), Sergio Toloza(San Juan Bautista School of Medicine), Maurizio Cutolo(University of Genoa), Hannu Kautiainen(Vetcare (Finland)), Heidi Mäkinen(Central Finland Health Care District), Feride Göğüş(Gazi University), Vlado Skakić(University of Nis), Humeira Badsha(United States Bone and Joint Initiative), Tõnu Peets(East Tallinn Central Hospital), Asta Baranauskaitė(Kaunas University of Technology), Pál Géher(Hospital of the Brothers of St. John of God), Ilona Újfalussy(Health Center), Fotini N. Skopouli(National and Kapodistrian University of Athens), Maria Mavrommati(Athens Euroclinic), Rieke Alten(MSB Medical School Berlin), Christof Pohl(MSB Medical School Berlin), Jean Sibilia(Hôpital d'Hautepierre), Andrea Stancati(Marche Polytechnic University), Fausto Salaffi(Marche Polytechnic University), Wojciech Romanowski(Center for Rheumatology), Danuta Zarowny-Wierzbinska(Wojewódzki Szpital Zespolony), Dan Henrohn(Uppsala University Hospital), Barry Bresnihan(University College Dublin), Patricia Minnock(Our Lady's Hospital), Lene Surland Knudsen(Herlev Hospital), Johannes W. G. Jacobs(Utrecht University), Jaime Calvo‐Alén(Hospital Sierrallana), Juris Lazovskis, Geraldo da Rocha Castelar Pinheiro(Hospital Universitário Pedro Ernesto), Д. Е. Каратеев(Riga East University Hospital), Daina Andersone(Pauls Stradiņš Clinical University Hospital), Sylejman Rexhepi(University Clinical Center of Kosovo), Yusuf Yazıcı(New York University Langone Orthopedic Hospital), Theodore Pincus(New York University Langone Orthopedic Hospital), the QUEST-RA Group
Arthritis Research & Therapy
January 14, 2009
Cited by 473Open Access
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Abstract

INTRODUCTION: Gender as a predictor of outcomes of rheumatoid arthritis (RA) has evoked considerable interest over the decades. Historically, there is no consensus whether RA is worse in females or males. Recent reports suggest that females are less likely than males to achieve remission. Therefore, we aimed to study possible associations of gender and disease activity, disease characteristics, and treatments of RA in a large multinational cross-sectional cohort of patients with RA called Quantitative Standard Monitoring of Patients with RA (QUEST-RA). METHODS: The cohort includes clinical and questionnaire data from patients who were seen in usual care, including 6,004 patients at 70 sites in 25 countries as of April 2008. Gender differences were analyzed for American College of Rheumatology Core Data Set measures of disease activity, DAS28 (disease activity score using 28 joint counts), fatigue, the presence of rheumatoid factor, nodules and erosions, and the current use of prednisone, methotrexate, and biologic agents. RESULTS: Women had poorer scores than men in all Core Data Set measures. The mean values for females and males were swollen joint count-28 (SJC28) of 4.5 versus 3.8, tender joint count-28 of 6.9 versus 5.4, erythrocyte sedimentation rate of 30 versus 26, Health Assessment Questionnaire of 1.1 versus 0.8, visual analog scales for physician global estimate of 3.0 versus 2.5, pain of 4.3 versus 3.6, patient global status of 4.2 versus 3.7, DAS28 of 4.3 versus 3.8, and fatigue of 4.6 versus 3.7 (P < 0.001). However, effect sizes were small-medium and smallest (0.13) for SJC28. Among patients who had no or minimal disease activity (0 to 1) on SJC28, women had statistically significantly higher mean values compared with men in all other disease activity measures (P < 0.001) and met DAS28 remission less often than men. Rheumatoid factor was equally prevalent among genders. Men had nodules more often than women. Women had erosions more often than men, but the statistical significance was marginal. Similar proportions of females and males were taking different therapies. CONCLUSIONS: In this large multinational cohort, RA disease activity measures appear to be worse in women than in men. However, most of the gender differences in RA disease activity may originate from the measures of disease activity rather than from RA disease activity itself.


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