Association of Ocular Inflammation and Rubella Virus Persistence
IMPORTANCE: Metagenomic deep sequencing (MDS) demonstrates that persistent and active rubella virus (RV) infection is associated with Fuchs heterochromic iridocyclitis (FHI). OBJECTIVE: To assess the utility of MDS in identifying RV infection in patients with uveitis. DESIGN, SETTING, AND PARTICIPAN...
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Veröffentlicht in: | Archives of ophthalmology (1960) 2019-04, Vol.137 (4), p.435-438 |
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Sprache: | eng |
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Zusammenfassung: | IMPORTANCE: Metagenomic deep sequencing (MDS) demonstrates that persistent and active rubella virus (RV) infection is associated with Fuchs heterochromic iridocyclitis (FHI). OBJECTIVE: To assess the utility of MDS in identifying RV infection in patients with uveitis. DESIGN, SETTING, AND PARTICIPANTS: This case series assessed 6 patients diagnosed by MDS with RV-associated uveitis at a tertiary uveitis referral center in the United States. EXPOSURES: Prior RV infection. MAIN OUTCOMES AND MEASURES: Clinical examination findings, slitlamp photography, corneal confocal imaging, and infectious pathogen genome obtained from RNA sequencing. RESULTS: Six white men (age range, 36-61 years) were diagnosed with RV-associated uveitis by MDS. Three patients exhibited iris heterochromia associated with their uveitis in classic FHI fashion. The other 3 patients had less classic FHI features and exhibited anterior vitritis. Three patients had in vivo corneal confocal microscopy, with 2 demonstrating stellate keratic precipitates in addition to endothelial infiltration, spotlike holes, and enlarged intercellular boundaries. Of these 3 patients, 1 patient exhibited polymorphism and polymegathism of the endothelial cells. CONCLUSIONS AND RELEVANCE: These findings suggest that persistent RV infection is associated with recurrent or chronic anterior or anterior-intermediate uveitis as well as corneal endothelial cell damage. Ophthalmologists should consider RV infection as a potential cause of hypertensive anterior and intermediate uveitis. |
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ISSN: | 2168-6165 2168-6173 |
DOI: | 10.1001/jamaophthalmol.2018.6185 |