Identification of the Human Papillomavirus Genotypes, According to the Human Immunodeficiency Virus Status in a Cohort of Women from Maputo, Mozambique Show others and affiliations
2021 (English) In: Viruses, E-ISSN 1999-4915, Vol. 14, no 1, article id 24Article in journal (Refereed) Published
Abstract [en]
BACKGROUND: Human papillomavirus (HPV) infection is now a well-established cause of cervical cancer and other anogenital cancers. An association between human immunodeficiency virus (HIV) infection and higher HPV incidence and prevalence are commonly reported. This study was conducted to demonstrate HPV prevalence, genotypes and its characteristics, according to the HIV status in women from Maputo in Mozambique.
METHODS: A total of 233 participants with ages ranging from fourteen to forty-five were included. Cervical samples were collected, DNA extracted, and HPV genotyping was performed using the HPV Direct Flow CHIP Kit.
RESULTS: In total, 177 HIV-negative and 56 HIV-positive women were included in the analysis. The overall HPV prevalence was 63% and was significantly higher among HIV-positive women (79% versus 58% among HIV-negative women; p = 0.005). The prevalence of multiple HPV type infections was 32%. High-risk HPV types 52, 68, 35, 18 and 16 were the most frequent. A higher proportion of HIV-positive women had multiple HPV types compared with HIV-negative women.
CONCLUSIONS: This study demonstrated a high prevalence of HPV in the study cohort. HIV-positive women were identified as having the highest HPV prevalence and infection with multiple HPV types across all ages. High-risk genotypes were the most commonly found.
Place, publisher, year, edition, pages MDPI, 2021. Vol. 14, no 1, article id 24
Keywords [en]
human immunodeficiency virus, human papillomavirus, women
National Category
Cancer and Oncology Infectious Medicine
Identifiers URN: urn:nbn:se:oru:diva-96826 DOI: 10.3390/v14010024 ISI: 000748067800001 PubMedID: 35062228 Scopus ID: 2-s2.0-85121781549 OAI: oai:DiVA.org:oru-96826 DiVA, id: diva2:1633589
2022-01-312022-01-312024-01-17 Bibliographically approved