Male origin microchimerism and ovarian cancer.


Journal

International journal of epidemiology
ISSN: 1464-3685
Titre abrégé: Int J Epidemiol
Pays: England
ID NLM: 7802871

Informations de publication

Date de publication:
03 03 2021
Historique:
accepted: 21 01 2020
pubmed: 18 2 2020
medline: 3 6 2021
entrez: 18 2 2020
Statut: ppublish

Résumé

Reduced risk of ovarian cancer is commonly ascribed to reduced exposure to endogenous hormones during pregnancy, using oral contraceptives or not using hormone replacement therapy. However, exposure to hormones alone account for less than half of all cases. Many women carry small amounts of male cells-known as male origin microchimerism-in their circulation and remarkable impacts of these cells on women's health are being published. Here, we pursue the possibility that male origin microchimerism has a role in reducing ovarian cancer risk. We conducted a prospective case-cohort study using blood samples and questionnaire data from 700 women participating in the Danish Diet, Cancer, and Health cohort. Blood samples were analysed for Y chromosome presence as a marker of male microchimerism. We evaluated the association between male microchimerism and ovarian cancer, using weighted Cox regression models reporting hazard ratios (HRs) and corresponding 95% confidence intervals (CIs). Male microchimerism was detected in 46% of cases and 65.9% of controls. Women testing positive for male microchimerism had a reduced hazard rate of ovarian cancer compared with women testing negative (HR = 0.44, 95% CI: 0.29-0.68). We found no evidence of interaction with measures of hormonal exposures (P = 0.50). For the first time we report that women who test positive for male microchimerism in their circulation have reduced rates of ovarian cancer compared with women who test negative. Although the underlying mechanisms are presently unknown, we believe male microchimerism is potent in preventing ovarian cancer.

Sections du résumé

BACKGROUND
Reduced risk of ovarian cancer is commonly ascribed to reduced exposure to endogenous hormones during pregnancy, using oral contraceptives or not using hormone replacement therapy. However, exposure to hormones alone account for less than half of all cases. Many women carry small amounts of male cells-known as male origin microchimerism-in their circulation and remarkable impacts of these cells on women's health are being published. Here, we pursue the possibility that male origin microchimerism has a role in reducing ovarian cancer risk.
METHODS
We conducted a prospective case-cohort study using blood samples and questionnaire data from 700 women participating in the Danish Diet, Cancer, and Health cohort. Blood samples were analysed for Y chromosome presence as a marker of male microchimerism. We evaluated the association between male microchimerism and ovarian cancer, using weighted Cox regression models reporting hazard ratios (HRs) and corresponding 95% confidence intervals (CIs).
RESULTS
Male microchimerism was detected in 46% of cases and 65.9% of controls. Women testing positive for male microchimerism had a reduced hazard rate of ovarian cancer compared with women testing negative (HR = 0.44, 95% CI: 0.29-0.68). We found no evidence of interaction with measures of hormonal exposures (P = 0.50).
CONCLUSIONS
For the first time we report that women who test positive for male microchimerism in their circulation have reduced rates of ovarian cancer compared with women who test negative. Although the underlying mechanisms are presently unknown, we believe male microchimerism is potent in preventing ovarian cancer.

Identifiants

pubmed: 32065627
pii: 5739464
doi: 10.1093/ije/dyaa019
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

87-94

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2020; all rights reserved. Published by Oxford University Press on behalf of the International Epidemiological Association.

Auteurs

Sara Hallum (S)

Section of Epidemiology, Department of Public Health, University of Copenhagen, Copenhagen, Denmark.

Marianne Antonius Jakobsen (MA)

Department of Clinical Immunology, Odense University Hospital, Odense, Denmark.

Thomas Alexander Gerds (TA)

Section of Biostatistics, Department of Public Health, University of Copenhagen, Copenhagen, Denmark.

Anja Pinborg (A)

Fertility Clinic, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Anne Tjønneland (A)

Section of Epidemiology, Department of Public Health, University of Copenhagen, Copenhagen, Denmark.
Danish Cancer Society Research Center, Institute of Cancer Epidemiology, Copenhagen, Denmark.

Mads Kamper-Jørgensen (M)

Section of Epidemiology, Department of Public Health, University of Copenhagen, Copenhagen, Denmark.

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