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Progressive multifocal leukoencephalopathy in patients with systemic lupus erythematosus: a systematic literature review.

Publication ,  Journal Article
Henegar, CE; Eudy, AM; Kharat, V; Hill, DD; Bennett, D; Haight, B
Published in: Lupus
May 2016

OBJECTIVE: To determine risk factors for progressive multifocal leukoencephalopathy (PML) in systemic lupus erythematosus (SLE) patients, and understand how underlying disease or treatment for SLE may be associated with PML in this population. METHODS: Studies published in English between January 1, 1984 and October 31, 2014 that reported PML in adult SLE patients were included. Immunosuppression was defined as exposure to ≥1 immunosuppressant drug of interest at PML diagnosis: belimumab, rituximab, mycophenolate mofetil, azathioprine, cyclophosphamide, methotrexate and high-dose corticosteroids (>15 mg/day). Minimal immunosuppression was defined as low-dose corticosteroids (≤15 mg/day) and/or anti-malarials. RESULTS: Thirty-five publications met our inclusion criteria: four observational studies, two large case series, and 29 case reports that described 35 cases. Reported PML incidence rates among SLE patients based on observational studies ranged from 1.0 to 2.4 cases/100,000 person-years. Of the 35 case reports, three cases were exposed to no immunosuppressant drugs at PML diagnosis, five cases had minimal immunosuppression, 23 cases had immunosuppression, and four cases were indeterminate. CONCLUSIONS: The evidence from this literature review suggests that, while PML is a very rare disease in SLE patients, there does appear to be an increased risk of PML associated with SLE compared to the general population, potentially due to immunosuppression, other contributing factors in their underlying disease, treatments prescribed to manage disease, or some combination of these factors. Additional large observational studies, designed to assess exposure to drugs of interest and complicated treatment histories, are needed to provide further evidence about potential mechanisms contributing to the onset of PML in SLE patients.

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Published In

Lupus

DOI

EISSN

1477-0962

Publication Date

May 2016

Volume

25

Issue

6

Start / End Page

617 / 626

Location

England

Related Subject Headings

  • Risk Factors
  • Lupus Erythematosus, Systemic
  • Leukoencephalopathy, Progressive Multifocal
  • Incidence
  • Immunosuppressive Agents
  • Humans
  • Arthritis & Rheumatology
  • Adult
  • 3202 Clinical sciences
  • 1103 Clinical Sciences
 

Citation

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ICMJE
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Henegar, C. E., Eudy, A. M., Kharat, V., Hill, D. D., Bennett, D., & Haight, B. (2016). Progressive multifocal leukoencephalopathy in patients with systemic lupus erythematosus: a systematic literature review. Lupus, 25(6), 617–626. https://doi.org/10.1177/0961203315622819
Henegar, C. E., A. M. Eudy, V. Kharat, D. D. Hill, D. Bennett, and B. Haight. “Progressive multifocal leukoencephalopathy in patients with systemic lupus erythematosus: a systematic literature review.Lupus 25, no. 6 (May 2016): 617–26. https://doi.org/10.1177/0961203315622819.
Henegar CE, Eudy AM, Kharat V, Hill DD, Bennett D, Haight B. Progressive multifocal leukoencephalopathy in patients with systemic lupus erythematosus: a systematic literature review. Lupus. 2016 May;25(6):617–26.
Henegar, C. E., et al. “Progressive multifocal leukoencephalopathy in patients with systemic lupus erythematosus: a systematic literature review.Lupus, vol. 25, no. 6, May 2016, pp. 617–26. Pubmed, doi:10.1177/0961203315622819.
Henegar CE, Eudy AM, Kharat V, Hill DD, Bennett D, Haight B. Progressive multifocal leukoencephalopathy in patients with systemic lupus erythematosus: a systematic literature review. Lupus. 2016 May;25(6):617–626.
Journal cover image

Published In

Lupus

DOI

EISSN

1477-0962

Publication Date

May 2016

Volume

25

Issue

6

Start / End Page

617 / 626

Location

England

Related Subject Headings

  • Risk Factors
  • Lupus Erythematosus, Systemic
  • Leukoencephalopathy, Progressive Multifocal
  • Incidence
  • Immunosuppressive Agents
  • Humans
  • Arthritis & Rheumatology
  • Adult
  • 3202 Clinical sciences
  • 1103 Clinical Sciences