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Gender and ethnicity differences in patients with diffuse systemic sclerosis--analysis from three large randomized clinical trials.

Authors :
Nashid M
Khanna PP
Furst DE
Clements PJ
Maranian P
Seibold J
Postlethwaite AE
Louie JS
Mayes MD
Agrawal H
Khanna D
Source :
Rheumatology (Oxford, England) [Rheumatology (Oxford)] 2011 Feb; Vol. 50 (2), pp. 335-42. Date of Electronic Publication: 2010 Oct 01.
Publication Year :
2011

Abstract

Objective: Although the incidence of dcSSc is higher in African-American and Hispanic populations compared with European Caucasian patients, it is not clear whether there are differences in subsequent disease course. Also, the potential impact of gender on the disease course of dcSSc is not well defined. Our objective was to assess the course of modified Rodnan skin score (MRSS), HAQ-disability index (HAQ-DI) and forced vital capacity per cent (FVC%) predicted between men vs women and three ethnic groups with dcSSc participating in three randomized clinical trials (RCTs).<br />Method: Data from RCTs (n = 495) were pooled and analysed. Baseline characteristics were compared in men vs women and among ethnic groups. A linear mixed effects model was used to assess the predictors of MRSS, HAQ-DI and FVC%. The primary independent variables were time-in-study and its interaction with gender and ethnicity. The models were adjusted for other covariates that were significant at baseline between gender and ethnicity analyses.<br />Results: Men had lower HAQI-DI scores compared with women (P < 0.05). Among the three ethnic groups, Caucasians were older, African-Americans had lower FVC% predicted and Hispanics had greater tender joint counts (P < 0.05). The course of MRSS, HAQ-DI and FVC% predicted during the study period was not significantly different between gender and three ethnicities. Time-in-study was an independent predictor of improvement in MRSS and HAQ-DI.<br />Conclusion: Our analysis explores the influence of gender and ethnicity on disease course in RCTs. These findings are relevant to issues of future trial design.

Details

Language :
English
ISSN :
1462-0332
Volume :
50
Issue :
2
Database :
MEDLINE
Journal :
Rheumatology (Oxford, England)
Publication Type :
Academic Journal
Accession number :
20889574
Full Text :
https://doi.org/10.1093/rheumatology/keq294