Impact of cervicovaginal microbiome on the risk of cervical abnormalities development

Author:

Rosário Andreia12ORCID,Sousa Ana13ORCID,Varandas Tatiana2ORCID,Marinho‐Dias Joana2ORCID,Medeiros Rui124ORCID,Martins Gabriela2ORCID,Monteiro Paula5ORCID,Sousa Hugo12678ORCID

Affiliation:

1. Molecular Oncology & Viral Pathology Group, Research Center (CI‐IPOP)/RISE@CI‐IPOP (Health Research Network) Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (Porto.CCC) Porto Portugal

2. Clinical Pathology Service, Department of Pathology and Laboratory Medicine Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (Porto.CCC) Porto Portugal

3. Department of Health Sciences Escola Superior de Saúde do Instituto Politécnico de Bragança Bragança Portugal

4. Research Department Portuguese League Against Cancer (LPCC‐NRNorte) Porto Portugal

5. Department of Pathology and Laboratory Medicine, Anatomic Pathology Service Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (Porto.CCC) Porto Portugal

6. Early Phase Clinical Trial Unit, Clinical Research Unit Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center Raquel Seruca (Porto.CCC) Porto Portugal

7. Instituto Superior de Saúde ‐ ISAVE Amares Portugal

8. Department of Biological Sciences, FFUP – Faculty of Pharmacy University of Porto Porto Portugal

Abstract

AbstractThe vaginal microbiome has emerged as potentially influencing the natural history of Human Papillomavirus (HPV) infections and their clinical impact. We aimed to characterize the vaginal microbiome in samples from 807 high‐risk HPVs (Hr‐HPV) positive women with a mean age of 41.45 ± 10.79 years who participated in the Regional Cervical Cancer Screening Program from the Northern Region of Portugal. Microbiome analysis was performed with commercial kits for the detection of 21 microorganisms. The most frequent microorganisms were Ureaplasma parvum (52.5%), Gardnerella vaginalis (GV) (34.5%), Atopobium vaginae (AV) (32.6%), Lacto (30.7%), and Mycoplasma hominis (MH) (23.5%). The distribution according to age reveals that MH, Mega1, GV, BVab2, AV, and Mob were more prevalent in women older than 41 years of age (p < 0.050), while Lacto is significantly decreased in this group (23.5% vs. 39.4%, p < 0.001; RR = 0.47). The risk analysis showed that Hr‐HPV‐16/‐18 and Hr‐HPV‐9val genotypes are associated with an increased risk of developing cervical abnormalities, while Lacto (p < 0.001; odd ratio [OR] = 0.33), GV (p = 0.0111; OR = 0.41), AV (p = 0.033; OR = 0.53) and Mob (p = 0.022; OR = 0.29) are associated with protection. Similar results were found for the risk of development atypical squamous cells cannot exclude HSIL/high‐grade squamous intraepithelial lesion. Overall, the multivariate analysis confirmed that lactobacillus and bacteria associated with bacterial vaginosis (GV, AV, and Mob) are associated with protection against the development of cervical abnormalities. This study provides important data to be included in the future management of risk stratification for Hr‐HPV‐positive women.

Publisher

Wiley

Subject

Infectious Diseases,Virology

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