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Cutaneous viral infections associated with ultraviolet radiation exposure

The complex interplay between ultraviolet radiation (UVR) and cutaneous viral infections in the context of cancer etiology is challenging to unravel, given the limited information on the independent association between UVR and cutaneous viral infections. Using multiple biomarkers of infection with 2...

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Detalles Bibliográficos
Autores principales: Zhao, Yayi, Amorrortu, Rossybelle P., Fenske, Neil A., Cherpelis, Basil, Messina, Jane L., Sondak, Vernon K., Giuliano, Anna R., Schell, Michael J., Waterboer, Tim, Pawlita, Michael, McKay‐Chopin, Sandrine, Gheit, Tarik, Tommasino, Massimo, Rollison, Dana E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754468/
https://www.ncbi.nlm.nih.gov/pubmed/32818302
http://dx.doi.org/10.1002/ijc.33263
Descripción
Sumario:The complex interplay between ultraviolet radiation (UVR) and cutaneous viral infections in the context of cancer etiology is challenging to unravel, given the limited information on the independent association between UVR and cutaneous viral infections. Using multiple biomarkers of infection with 24 types of cutaneous human papillomavirus (HPV) and 4 types of polyomaviruses (HPyV), we investigated cross‐sectional associations with recent UVR exposure, using skin pigmentation measured by spectrophotometer. Age‐ and sex‐adjusted associations between UVR and viral seropositivity, viral DNA present in eyebrow hairs (EBH) and skin swabs (SSW) were estimated using logistic regression. Beta‐HPV seropositivity was associated with viral DNA positivity in EBH (OR = 1.40, 95% CI = 1.05‐1.88) and SSW (OR = 1.86, 95% CI = 1.25‐2.74). Similar associations were observed for Merkel cell polyomavirus. Participants in the highest tertile of UVR exposure were more likely to be seropositive for beta‐HPV (OR = 1.81, 95% CI = 1.16‐2.38), and have beta‐HPV DNA in EBH (OR = 1.57, 95% CI = 1.06‐2.33) and SSW (OR = 2.22, 95% CI = 1.25‐3.96), compared to participants with the lowest tertile of UVR exposure. UVR exposure was positively associated with three different markers of beta‐HPV infection. Therefore, future studies of HPV associated KC development should address more directly the role of HPV and UVR exposure as potential co‐carcinogens.