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Alpha herpes virus type and viral load in intraocular fluids in patients with acute retinal necrosis.

Authors :
von Hofsten J
Bergström T
Zetterberg M
Source :
BMJ open ophthalmology [BMJ Open Ophthalmol] 2019 Apr 09; Vol. 4 (1), pp. e000247. Date of Electronic Publication: 2019 Apr 09 (Print Publication: 2019).
Publication Year :
2019

Abstract

Objectives: To identify all patients tested positive for herpes viruses in intraocular samples between 2007 and 2016 in South-Western Sweden and evaluate which of these met the criteria of acute retinal necrosis (ARN). To compare viral load in intraocular samples and virus type with clinical outcome.<br />Method and Analysis: Retrospective case series. Intraocular samples and serum were analysed with quantitative real-time PCR (qPCR) and presence of antibodies (IgG and IgM) were detected by ELISA in serum.<br />Results: Between 2007 and 2016, 13 patients met the clinical criteria of ARN and were PCR-positive in aqueous or vitreous for herpes simplex virus 1 (HSV1; n=4), herpes simplex virus 2 (HSV2; n=3) and varicella zoster virus (VZV; n=6). None of the patients tested positive for cytomegalovirus (n=13) or Epstein Barr virus (n=2) met the criteria of ARN. All ARN patients had specific serum IgG and three patients exhibited virus DNA in serum. There was no correlation between high viral load and worse visual outcome. However, higher viral loads were seen in samples taken earlier in the disease process. Median age was higher (p=0.049) in VZV-ARN than for HSV-ARN patients (60.5 and 45.4 years, respectively) with a tendency of worse best corrected visual acuity at presentation (1.62 and 0.79 log MAR, respectively; p=0.079).<br />Conclusion: ARN is a reactivation of alpha herpes virus and presence of herpes DNA in serum may occur. VZV-ARN are older than HSV-ARN patients. High viral load does not appear to be a predictor of worse visual outcome, but rather indicates earlier sampling.<br />Competing Interests: Competing interests: None declared.

Details

Language :
English
ISSN :
2397-3269
Volume :
4
Issue :
1
Database :
MEDLINE
Journal :
BMJ open ophthalmology
Publication Type :
Academic Journal
Accession number :
31179395
Full Text :
https://doi.org/10.1136/bmjophth-2018-000247