Determinants of social participation in patients living with systemic lupus erythematosus: the Psy-LUP multicentre study

Objective Systemic lupus erythematosus (SLE) can negatively impact patients’ social participation. The aim of this study was to identify the determinants of social participation in patients with SLE.Methods A cross-sectional evaluation was carried out in 100 adult outpatients with SLE enrolled in th...

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Main Authors: Eric Hachulla, Nathalie Costedoat-Chalumeau, Nicolas Schleinitz, Antoine Huart, Viviane Queyrel, Nathalie Tieulie, Laurent Chiche, Aurelie Hummel, Noémie Jourde-Chiche, Eric Daugas, Jean-Robert Harle, Gilles Kaplanski, Karin Mazodier, Julien Mancini, Laure Swiader, Cécile Manet, Marie-Anastasie Aim, Julien Faraut, Francoise Sarrot- Reynauld, Philippe Manet, Lionel Dany
Format: Article
Language:English
Published: BMJ Publishing Group 2025-06-01
Series:RMD Open
Online Access:https://rmdopen.bmj.com/content/11/2/e005661.full
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Summary:Objective Systemic lupus erythematosus (SLE) can negatively impact patients’ social participation. The aim of this study was to identify the determinants of social participation in patients with SLE.Methods A cross-sectional evaluation was carried out in 100 adult outpatients with SLE enrolled in the multicentre psychosocial lupus (Psy-LUP) study. Participants completed the following standardised questionnaires: Participation Scale (social participation); Zimbardo Time Perspective Inventory; Sarason’s Social Support Questionnaire; Couples Satisfaction Index; Brief Illness Perceptions; Short Form-36 and Lupus-QoL. Stepwise multivariate regression analysis identified determinants of social participation.Results 92 women and eight men were included. Mean age was 44 years, mean SLE duration was 14 years, 52% of patients had a history of lupus nephritis and 38% were currently receiving immunosuppressants and/or biologics. 73% were in a couple and 64% were employed. Social participation was reduced in 29% of patients (compared with 46% in rheumatoid arthritis or multiple sclerosis), who reported different illness perceptions than those with preserved social participation. In multivariate linear regression, female sex (p=0.006), smoking (p=0.04), osteoporotic fractures (p=0.03), anti-cardiolipin antibodies (p=0.01) and ‘Past Negative’ time perspective (p=0.002) were associated with reduced social participation, while haematological involvement (p=0.005) and ‘Present Hedonistic’ time perspective (p=0.02) were protective. Reduced social participation was also associated with illness representations and with lower health-related quality of life (HR-QoL) scores.Conclusions Social participation is frequently altered in patients with SLE and correlates with illness representations, time perspective and HR-QoL. Psychological support and therapeutic education may help improve patients’ time perspective.Trial registration number NCT03913754.
ISSN:2056-5933