Evaluation of Host Gene Methylation as a Triage Test for HPV-Positive Women-A Cohort Study.


Journal

Journal of lower genital tract disease
ISSN: 1526-0976
Titre abrégé: J Low Genit Tract Dis
Pays: United States
ID NLM: 9704963

Informations de publication

Date de publication:
26 Jul 2024
Historique:
medline: 26 7 2024
pubmed: 26 7 2024
entrez: 26 7 2024
Statut: aheadofprint

Résumé

This study was designed to evaluate the performance of a host gene methylation marker panel (ASTN1, DLX1, ITGA4, RXFP3, SOX17, and ZNF671) in the triage of human papillomavirus (HPV)-positive women, its possible impact in a cervical cancer screening program, and the possible influence of the variation of the rate of HPV16/18 in its performance. Cohort study in which consecutive women referred for colposcopy in an organized cervical cancer screening program had repeated HPV testing, colposcopy, and biopsies. The women that remained HPV positive at the time of colposcopy were tested with the panel of DNA methylation markers. The performance of the test was evaluated and compared to standard practice. The study test had a sensitivity and specificity for cervical intraepithelial neoplasia (CIN) 2+ of 60.8% (49.1-71.6%) and 88.4% (83.2-92.5%), respectively. For CIN3+, it was of 78.0% (64.0-88.5%) and 86.0% (80.8-90.2%), respectively.The rate and level of methylation positively correlated with the severity of disease. The use of methylation reduces the referral for colposcopy to 25.5%, while detecting 78.0% of the CIN3+ cases. Referral of all HPV16/18-positive cases and triage of the other high-risk HPV-positive cases with methylation, detects 90.0% of the cases of CIN3+, while reducing the number of referrals to 43.2%.The variation in the rate of HPV16/18 does not relevantly affect the performance of the methylation panel. The studied methylation panel has a high sensitivity and specificity for CIN3+ and reduces the rate of referrals for colposcopy, without relevant variation according to the rate of HPV16/18.

Identifiants

pubmed: 39058311
doi: 10.1097/LGT.0000000000000830
pii: 00128360-990000000-00129
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the ASCCP.

Déclaration de conflit d'intérêts

Conflicts of interest: PVB received speaker fees from Seegene.

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Auteurs

Mariana Costa (M)

Unilabs Portugal, Laboratório de Biologia Molecular, Porto, Portugal.

Juliane Hippe (J)

Oncgnostics GmbH, Jena, Germany.

Carlos Sousa (C)

Unilabs Portugal, Laboratório de Biologia Molecular, Porto, Portugal.

Martina Schmitz (M)

Oncgnostics GmbH, Jena, Germany.

Ana-Rita Silva (AR)

Unilabs Portugal, Laboratório de Biologia Molecular, Porto, Portugal.

Alfred Hansel (A)

Oncgnostics GmbH, Jena, Germany.

Mario Preti (M)

Department of Surgical Sciences University of Torino, Italy.

Classifications MeSH