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Socioeconomic Aspects of Systemic Lupus Erythematosus

*Corresponding author for this work
  • Universidad de Antioquia
    ,
  • ,
  • Universidad Científica del Sur
    ,
  • Hospital Guillermo Almenara Irigoyen
    ,
  • The University of Alabama at Birmingham
Research Output:
Chapter in Book/Report/Conference proceeding
Chapter
Peer-review

Publication Information

Output type

Research Output:
Chapter in Book/Report/Conference proceeding
Chapter
Peer-review

Host publication Subtitle

Basic, Applied and Clinical Aspects

Original language

English

Pages from-to (Number of pages)

Pages 39-42 (4 pages)

Publication milestones

  • Published - 2016

Publication status

Published - 2016

Publisher

Elsevier Inc.
9780128019177

ISBN (Electronic)

9780128020098

Publication IDs

  • Scopus: 84966948840

Host publication title

Systemic Lupus Erythematosus

Abstract

Lower socioeconomic status (SES) can affect systemic lupus erythematosus (SLE) outcomes by several possible mechanisms, such as inadequate access to quality care services, communication barriers, and malnutrition. SES should be systematically measured at the individual level (education, income, and occupation), as well as at the household and neighborhood levels. Lower SES has been associated with higher disease activity, mainly over the disease course, higher damage accrual, mortality, and disability. Furthermore, outcome differences between Caucasians and non-Caucasians are partially explained by socioeconomic factors. The association between non-Caucasian ethnicities and lower SES makes genetic and environmental risks difficult to disentangle.

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