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The Assessment of Infection Risk in Patients with Vitiligo Undergoing Dialysis for End-Stage Renal Disease: A Retrospective Cohort Study

*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Vitiligo is an autoimmune condition that causes patchy skin depigmentation. Although the mechanism by which vitiligo induces immunocompromise is unclear, other related autoimmune diseases are known to predispose those affected to infection. Individuals with vitiligo exhibit epidermal barrier disruption, which could potentially increase their susceptibility to systemic infections; patients with renal disease also show a predisposition to infection. Nevertheless, there is little research addressing the risk of infection in dialysis patients with vitiligo in comparison to those without it. A retrospective analysis was performed on patients with end-stage renal disease (ESRD) in the United States Renal Data System who started dialysis between 2004 and 2019 to determine if ESRD patients with vitiligo are at an increased risk of bacteremia, cellulitis, conjunctivitis, herpes zoster, or septicemia. Multivariable logistic regression modeling indicated that female sex, black compared to white race, Hispanic ethnicity, hepatitis C infection, and tobacco use were associated with an enhanced risk of vitiligo, whereas increasing age and catheter, versus arteriovenous fistula, and access type were associated with a decreased risk. After controlling for demographics and clinical covariates, vitiligo was found to be significantly associated with an increased risk of bacteremia, cellulitis, and herpes zoster but not with conjunctivitis and septicemia.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

94

Journal (Volume, Issue Number)

Pathogens (Volume 13, Issue 1)

Publication milestones

  • Published - 01/2024

Publication status

Published - 01/2024

Publication IDs

  • Scopus: 85183354620
  • ORCID: /0000-0003-3146-162X/work/157545363
  • ORCID: /0000-0003-4066-4541/work/157546156

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4
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0.57
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3
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0.43
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4
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1

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4
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Funding Details

This work was supported in part by the Translational Research Program of the Augusta University Department of Medicine. The data reported here were supplied by the USRDS. The interpretation and reporting of these data are the responsibility of the authors and in no way should be seen as official policy or as the interpretation of the USRDS or the United States Government. The contents of this article do not represent the views of the Department of Veterans Affairs or the United States Government. This research received no specific external funding. W.B.B. was supported by a VA Research Career Scientist Award (#IK6BX005691).
FundersFunding number
Augusta University Department of Medicine
-
VA Research
6BX005691