Stigma, discrimination-related events, and determinants among adult people living with systemic lupus erythematosus (SLE): Systematic review and indicator-level meta-analysis.

LupusAug 8, 2026 (epub)
Clinical ResearchRheumatologyPsychiatryOpen access

Hebatullah M Abdulazeem, Syrine Bellakhal, Rym Abida et al.

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In 30 seconds

This systematic review and meta-analysis examined stigma and discrimination among 2254 adults with systemic lupus erythematosus (SLE). The study found a moderate overall burden of stigma at 34.71, with 46% of participants experiencing at least one form of stigma or discrimination, primarily social isolation and unfair treatment. The findings highlight the psychological impact of stigma on this population.

Key findings

  • Moderate overall burden of stigma reported at 34.71 (95% CI 26.15, 43.27).
  • 46% of individuals experienced at least one form of stigma or discrimination.
  • Common forms of stigma included social isolation and unfair treatment.
  • Higher stigma burden correlated with mental health issues.

Why it matters

Understanding the prevalence and impact of stigma in SLE patients is crucial for healthcare providers. It emphasizes the need for comprehensive assessments that include psychological and social factors, which can significantly affect patient outcomes and quality of life.

Source

Published in Lupus. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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