Your browser doesn't support javascript.
loading
FAM19A4/miR124-2 Methylation Testing and Human Papillomavirus (HPV) 16/18 Genotyping in HPV-Positive Women Under the Age of 30 Years.
Vink, Frederique J; Meijer, Chris J L M; Hesselink, Albertus T; Floore, Arno N; Lissenberg-Witte, Birgit I; Bonde, Jesper H; Pedersen, Helle; Cuschieri, Kate; Bhatia, Ramya; Poljak, Mario; Ostrbenk Valencak, Anja; Hillemanns, Peter; Quint, Wim G V; Del Pino, Marta; Kenter, Gemma G; Steenbergen, Renske D M; Heideman, Daniëlle A M; Bleeker, Maaike C G.
Afiliação
  • Vink FJ; Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands.
  • Meijer CJLM; Imaging and Biomarkers, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Hesselink AT; Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands.
  • Floore AN; Imaging and Biomarkers, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Lissenberg-Witte BI; Self-screen B.V., Amsterdam, The Netherlands.
  • Bonde JH; Self-screen B.V., Amsterdam, The Netherlands.
  • Pedersen H; Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Epidemiology and Data Science, Amsterdam, the Netherlands.
  • Cuschieri K; Molecular Pathology Laboratory, Department of Pathology, Copenhagen University Hospital, Hvidovre Hospital, Hvidovre, Denmark.
  • Bhatia R; Molecular Pathology Laboratory, Department of Pathology, Copenhagen University Hospital, Hvidovre Hospital, Hvidovre, Denmark.
  • Poljak M; Scottish HPV Reference Laboratory, Royal Infirmary of Edinburgh, NHS Lothian, Edinburgh, Scotland.
  • Ostrbenk Valencak A; Centre for Reproductive Health, University of Edinburgh, Edinburgh, Scotland.
  • Hillemanns P; Scottish HPV Reference Laboratory, Royal Infirmary of Edinburgh, NHS Lothian, Edinburgh, Scotland.
  • Quint WGV; Centre for Reproductive Health, University of Edinburgh, Edinburgh, Scotland.
  • Del Pino M; Institute of Microbiology and Immunology, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • Kenter GG; Institute of Microbiology and Immunology, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • Steenbergen RDM; Department of Obstetrics and Gynaecology, Hannover Medical School, Hannover, Germany.
  • Heideman DAM; DDL Diagnostic Laboratory, Rijswijk, The Netherlands.
  • Bleeker MCG; Institut Clinic of Gynecology, Obstetrics and Neonatology, Gynecology Oncology Unit, Hospital Clínic-Institut d'Investigacions Biomèdiques August Pi i Sunyer, Faculty of Medicine, University of Barcelona, Barcelona, Spain.
Clin Infect Dis ; 76(3): e827-e834, 2023 02 08.
Article em En | MEDLINE | ID: mdl-35686306
ABSTRACT

BACKGROUND:

High-grade squamous intraepithelial lesions (HSIL) or cervical intraepithelial neoplasia (CIN) grade 2/3 lesions in human papillomavirus (HPV)-positive women <30 years of age have high spontaneous regression rates. To reduce overtreatment, biomarkers are needed to delineate advanced CIN lesions that require treatment. We analyzed the FAM19A4/miR124-2 methylation test and HPV16/18 genotyping in HPV-positive women aged <30 years, aiming to identify CIN2/3 lesions in need of treatment.

METHODS:

A European multicenter retrospective study was designed evaluating the FAM19A4/miR124-2 methylation test and HPV16/18 genotyping in cervical scrapes of 1061 HPV-positive women aged 15-29 years (690 ≤CIN1, 166 CIN2, and 205 CIN3+). A subset of 62 CIN2 and 103 CIN3 were immunohistochemically characterized by HPV E4 expression, a marker for a productive HPV infection, and p16ink4a and Ki-67, markers indicative for a transforming infection. CIN2/3 lesions with low HPV E4 expression and high p16ink4a/Ki-67 expression were considered as nonproductive, transforming CIN, compatible with advanced CIN2/3 lesions in need of treatment.

RESULTS:

FAM19A4/miR124-2 methylation positivity increased significantly with CIN grade and age groups (<25, 25-29, and ≥30 years), while HPV16/18 positivity was comparable across age groups. FAM19A4/miR124-2 methylation positivity was HPV type independent. Methylation-positive CIN2/3 lesions had higher p16ink4a/Ki-67-immunoscores (P = .003) and expressed less HPV E4 (P = .033) compared with methylation-negative CIN2/3 lesions. These differences in HPV E4 and p16ink4a/Ki-67 expression were not found between HPV16/18-positive and non-16/18 HPV-positive lesions.

CONCLUSIONS:

Compared with HPV16/18 genotyping, the FAM19A4/miR124-2 methylation test detects nonproductive, transforming CIN2/3 lesions with high specificity in women aged <30 years, providing clinicians supportive information about the need for treatment of CIN2/3 in young HPV-positive women.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Displasia do Colo do Útero / Neoplasias do Colo do Útero / Infecções por Papillomavirus / MicroRNAs Tipo de estudo: Observational_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Displasia do Colo do Útero / Neoplasias do Colo do Útero / Infecções por Papillomavirus / MicroRNAs Tipo de estudo: Observational_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article