Infection as a potential cofactor in the genetic-epigenetic pathophysiology of endometriosis: a systematic review
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Reviews
VOLUME: 11 ISSUE: 3
P: 209 - 216
September 2019

Infection as a potential cofactor in the genetic-epigenetic pathophysiology of endometriosis: a systematic review

Facts Views Vis ObGyn 2019;11(3):209-216
1. Latifa Hospital, Dubai, United Arab Emirates
2. KU, Leuven, Belgium
3. Gruppo Italo-Belga, Villa Del Rosario, Rome, Italy
4. University of Oxford-Hon Consultant, Oxford,UK
5. Università Cattolica, Roma Italy
6. Department of Operative Gynecology, V. I. Kulakov Research Centre for Obstetrics, Gynecology, and Perinatology, Russian Federation
7. Department of Reproductive Medicine and Surgery, Moscow State University of Medicine and Dentistry, Moscow, Russia
8. Department of Obstetrics and Gynaecology, University of Strasbourg, France
9. School of Medicine, University of Tennessee Health Science Centre, Memphis Tennessee, USA
10. Virginia Commonwealth University, Richmond, Virginia, USA
11. Department of Obstetrics and Gynecology, University of British Columbia and Women’s Hospital, Vancouver, BC, Canada
No information available.
No information available
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Abstract

Background

The genetic-epigenetic theory postulates that endometriosis is triggered by a cumulative set of genetic-epigenetic (GE) incidents. Pelvic and upper genital tract infection might induce GE incidents and thusplay a role in the pathogenesis of endometriosis. Thus, this article aims to review the association of endometriosis with upper genital tract and pelvic infections.

Methods

Pubmed, Scopus and Google Scholar were searched for ‘endometriosis AND (infection OR PID OR bacteria OR viruses OR microbiome OR microbiota)’, for ‘reproductive microbiome’ and for ‘reproductive microbiome AND endometriosis’, respectively. All 384 articles, the first 120 ‘best match’ articles in PubMed for ‘reproductive microbiome’ and the first 160 hits in Google Scholar for ‘reproductive microbiome AND endomytriosis’ were hand searched for data describing an association between endometriosis and bacterial, viral or other infections. All 31 articles found were included in this manuscript.

Results

Women with endometriosis have a significantly increased risk of lower genital tract infection, chronic endometritis, severe PID and surgical site infections after hysterectomy. They have more colony forming units of Gardnerella, Streptococcus, Enterococci and Escherichia coli in the endometrium. In the cervix Atopobium is absent, but Gardnerella, Streptococcus, Escherichia, Shigella, and Ureoplasma are increased. They have higher concentrations of Escherichia Coli and higher concentrations of bacterial endotoxins in menstrual blood. A Shigella/Escherichia dominant stool microbiome is more frequent. The peritoneal fluid of women with endometriosis contains higher concentrations of bacterial endotoxins and an increased incidence of mollicutes and of HPV viruses. Endometriosis lesions have a specific bacterial colonisation with more frequently mollicutes (54%) and both high and medium-risk HPV infections (11%). They contain DNA with 96% homology with Shigella. In mice transplanted endometrium changes the gut microbiome while the gut microbiome influences the growth of these endometriosis lesions.

Conclusions

Endometriosis is associated with more upper genital tract and peritoneal infections. These infections might be co-factors causing GE incidents and influencing endometriosis growth.

Keywords:
Endometriosis, pathophysiology, infection, prevention of endometriosis, adolescent endometriosis