Clinical aspects
Determinants of health-related quality of life in a multinational systemic sclerosis inception cohort
K. Morrisroe1, M. Hudson2, M. Baron3, J. De vries-Bouwstra4, P.E. Carreira5, D.M. Wuttge6, M. Wang7, T.M. Frech8, W. Stevens9, S.M. Proudman10, M. Nikpour11
- Department of Medicine, The University of Melbourne at St Vincent’s Hospital; and Department of Rheumatology, St Vincent’s Hospital, Melbourne, Australia.
- Jewish General Hospital, Montreal; and Lady Davis Research Institute, Montreal, Canada.
- Jewish General Hospital, Montreal; and Lady Davis Research Institute, Montreal, Canada.
- Department of Rheumatology, Leiden University Medical Center (LUMC), the Netherlands.
- Rheumatology Department, Hospital Universitario 12 de Octubre, Madrid, Spain.
- Lund University, Skane University Hospital, Department of Clinical Sciences, Rheumatology, Lund, Sweden.
- Jewish General Hospital, Montreal; and Lady Davis Research Institute, Montreal, Canada.
- Division of Rheumatology, Department of Internal Medicine, University of Utah and Salt Lake Regional Veterans Affair Medical Center, USA.
- Department of Rheumatology, St Vincent’s Hospital, Melbourne, Australia.
- Rheumatology Unit, Royal Adelaide Hospital, North Terrace, Australia; and Discipline of Medicine, University of Adelaide, Australia.
- Department of Medicine, The University of Melbourne at St Vincent’s Hospital; and Department of Rheumatology, St Vincent’s Hospital, Melbourne, Australia. m.nikpour@unimelb.edu.au
for the International Systemic Sclerosis Inception Cohort (INSYNC) collaboration
CER10745
2018 Vol.36, N°4 ,Suppl.113
PI 0053, PF 0060
Clinical aspects
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PMID: 30183603 [PubMed]
Received: 09/08/2017
Accepted : 26/02/2018
In Press: 31/08/2018
Published: 29/09/2018
Abstract
OBJECTIVES:
To evaluate health-related quality of life (HRQoL) and its determinants in a systemic sclerosis (SSc) multinational inception cohort. We performed a meta-analysis of data from individual countries, and compared the meta-analysis to individual country results by pooling data from each of the countries.
METHODS:
SSc patients within 2 years of disease onset were recruited from 5 countries participating in the International Systemic Sclerosis Inception Cohort (INSYNC). Data from each country’s database were exported for analysis using a harmonised platform. HRQoL was assessed using the Medical Outcomes Short Form-36 (SF-36). Multivariate linear regression assessed associations between HRQoL and predictors in cohorts separately and meta-analyzed to generate pooled estimates. The analyses were repeated using individual patient data.
RESULTS:
Of the 637 SSc patients recruited, the majority was female (80.2%-83.3%), aged between 52.4-56.7 years with limited cutaneous disease subtype (48.6%-66.7%). HRQoL scores were lower for SSc patients than the general population (SF-36 physical component summary (PCS) score (36.4-39.6), mental component summary (MCS) score (41.0-46.4)). Determinants of SF-36 PCS by meta-analysis included increasing age (β=-0.1, 95%CI -0.2, -0.01), diffuse cutaneous disease subtype (β=-8.4, 95%CI -10.6, -6.3), and pulmonary arterial hypertension (β=-10.9, 95%CI -16.6, -5.3). Increasing age (β=0.09, 95%CI 0.0, 0.18) was the only variable associated with SF-36 MCS. Analyses using individual patient data revealed similar results to those of the meta-analysis of cohort data.
CONCLUSIONS:
Our study provides estimates of HRQoL in a large inception SSc cohort and provides evidence that individual patient data analysis is valid in the INSYNC dataset.