The presence and impact of herpes virus DNA in recipient cornea and aqueous humor on graft survival following penetrating keratoplasty.
Autor: | Jeng YT; Department of Ophthalmology, Taipei City Hospital, Taipei, Taiwan., Tsai CY; Department of Ophthalmology, Taipei City Hospital, Taipei, Taiwan; Institute of Public Health, National Yang-Ming University, Taipei, Taiwan., Kuo LL; Department of Ophthalmology, Taipei City Hospital, Taipei, Taiwan; Department of Health Care Management, National Taipei University of Nursing and Health Sciences, Taipei, Taiwan., Woung LC; Department of Ophthalmology, Taipei City Hospital, Taipei, Taiwan; Department of Ophthalmology, National Taiwan University Hospital, Taipei, Taiwan., Lin SY; Department of Education and Research, Taipei City Hospital, Taipei, Taiwan., Tsai IL; Department of Ophthalmology, Taipei City Hospital, Taipei, Taiwan. Electronic address: ilunt@ms49.hinet.net. |
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Jazyk: | angličtina |
Zdroj: | Journal of the Formosan Medical Association = Taiwan yi zhi [J Formos Med Assoc] 2020 Nov; Vol. 119 (11), pp. 1650-1657. Date of Electronic Publication: 2020 Jan 13. |
DOI: | 10.1016/j.jfma.2019.12.009 |
Abstrakt: | Background/purpose: Reactivation of herpes viruses poses threat to corneal graft survival. This study evaluated the presence of herpes simplex virus type 1 (HSV-1), HSV type 2 (HSV-2), and cytomegalovirus (CMV) DNA in recipient corneas and the aqueous humor of patients undergoing penetrating keratoplasty (PKP), and the impact on graft survival. Methods: This retrospective study reviewed 90 eyes of 71 patients underwent PKP between 2008 and 2016. Cornea and aqueous humor samples were sent for polymerase chain reaction (PCR) testing for viral DNA. The main outcomes were PCR results and graft survival. Results: Recipient corneas tested positive for HSV-1 in 47 eyes (52.2%), for HSV-2 in 24 eyes (26.7%), and for CMV in seven eyes (7.8%). Aqueous humor tested positive for HSV-1 in 44 eyes (48.9%), for HSV-2 in 25 eyes (27.8%), and for CMV in eight eyes (8.9%). The presence of aqueous HSV-1 DNA was associated with higher risk of graft failure (p = 0.005), whereas corneal HSV-1 DNA was not. The presence of HSV-2 DNA had no significant impact on graft survival. Aqueous CMV DNA was associated with higher risk of graft failure in univariate model, but not in multivariate model. Conclusion: There were high positive rates of HSV-1, HSV-2, and CMV DNA in recipient corneas and aqueous humor at the time of PKP, even among patients not suspected of latent viral infection. The presence of aqueous HSV-1 DNA was associated with higher risk of graft failure. Competing Interests: Declaration of Competing Interest None. (Copyright © 2019 Formosan Medical Association. Published by Elsevier B.V. All rights reserved.) |
Databáze: | MEDLINE |
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