An integrated multi-tissue approach for endometriosis candidate biomarkers: a systematic review.

Biological compartments Candidate biomarkers Endometriosis Endometriosis phenotypes

Journal

Reproductive biology and endocrinology : RB&E
ISSN: 1477-7827
Titre abrégé: Reprod Biol Endocrinol
Pays: England
ID NLM: 101153627

Informations de publication

Date de publication:
10 Feb 2024
Historique:
received: 24 04 2023
accepted: 28 12 2023
medline: 11 2 2024
pubmed: 11 2 2024
entrez: 10 2 2024
Statut: epublish

Résumé

Biomarker identification could help in deciphering endometriosis pathophysiology in addition to their use in the development of non invasive diagnostic and prognostic approaches, that are essential to greatly improve patient care. Despite extensive efforts, no single potential biomarker or combination has been clinically validated for endometriosis.Many studies have investigated endometriosis-associated biological markers in specific tissues, but an integrative approach across tissues is lacking. The aim of this review is to propose a comprehensive overview of identified biomarkers based on tissue or biological compartment, while taking into account endometriosis phenotypes (superficial, ovarian or deep, or rASRM stages), menstrual cycle phases, treatments and symptoms.We searched PubMed and Embase databases for articles matching the following criteria: 'endometriosis' present in the title and the associated term 'biomarkers' found as Medical Subject Headings (MeSH) terms or in all fields. We restricted to publications in English and on human populations. Relevant articles published between 01 January 2005 (when endometriosis phenotypes start to be described in papers) and 01 September 2022 were critically analysed and discussed.Four hundred forty seven articles on endometriosis biomarkers that included a control group without endometriosis and provided specific information on endometriosis phenotypes are included in this review. Presence of information or adjustment controlling for menstrual cycle phase, symptoms and treatments is highlighted, and the results are further summarized by biological compartment. The 9 biological compartments studied for endometriosis biomarker research are in order of frequency: peripheral blood, eutopic endometrium, peritoneal fluid, ovaries, urine, menstrual blood, saliva, feces and cervical mucus. Adjustments of results on disease phenotypes, cycle phases, treatments and symptoms are present in 70%, 29%, 3% and 6% of selected articles, respectively. A total of 1107 biomarkers were identified in these biological compartments. Of these, 74 were found in several biological compartments by at least two independent research teams and only 4 (TNF-a, MMP-9, TIMP-1 and miR-451) are detected in at least 3 tissues with cohorts of 30 women or more.Integrative analysis is a crucial step to highlight potential pitfalls behind the lack of success in the search for clinically relevant endometriosis biomarkers, and to illuminate the physiopathology of this disease.

Identifiants

pubmed: 38341605
doi: 10.1186/s12958-023-01181-8
pii: 10.1186/s12958-023-01181-8
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

21

Subventions

Organisme : European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme
ID : grant agreement No 851360
Organisme : European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme
ID : grant agreement No 851360

Informations de copyright

© 2024. The Author(s).

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Auteurs

Axelle Brulport (A)

Institut Pasteur, Université Paris Cité, CNRS UMR 3525, INSERM UA12, Comparative Functional Genomics Group, Paris, 75015, France. axelle.brulport@inserm.fr.

Mathilde Bourdon (M)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.
Département de Gynécologie, Obstétrique et Médecine de la Reproduction, AP-HP, Centre Hospitalier Universitaire (CHU) Cochin, F-75014, Paris, France.

Daniel Vaiman (D)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.

Christian Drouet (C)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.
Université de Paris, Faculté de Santé, Faculté de Médecine Paris Centre, Paris, France, Service de Biologie de la Reproduction - CECOS, AP-HP, Centre Hospitalier Universitaire (CHU) Cochin, Paris, 75014, France.

Khaled Pocate-Cheriet (K)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.
Université de Paris, Faculté de Santé, Faculté de Médecine Paris Centre, Paris, France, Service de Biologie de la Reproduction - CECOS, AP-HP, Centre Hospitalier Universitaire (CHU) Cochin, Paris, 75014, France.

Kheira Bouzid (K)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.

Louis Marcellin (L)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.
Département de Gynécologie, Obstétrique et Médecine de la Reproduction, AP-HP, Centre Hospitalier Universitaire (CHU) Cochin, F-75014, Paris, France.

Pietro Santulli (P)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.
Département de Gynécologie, Obstétrique et Médecine de la Reproduction, AP-HP, Centre Hospitalier Universitaire (CHU) Cochin, F-75014, Paris, France.

Carole Abo (C)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.
Département de Gynécologie, Obstétrique et Médecine de la Reproduction, AP-HP, Centre Hospitalier Universitaire (CHU) Cochin, F-75014, Paris, France.

Maxime Jeljeli (M)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.
Service d'Immunologie Biologique, AP-HP, Centre Hospitalier Universitaire (CHU) Cochin, Paris, F-75014, France.

Sandrine Chouzenoux (S)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.

Charles Chapron (C)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.
Département de Gynécologie, Obstétrique et Médecine de la Reproduction, AP-HP, Centre Hospitalier Universitaire (CHU) Cochin, F-75014, Paris, France.

Frédéric Batteux (F)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.
Service d'Immunologie Biologique, AP-HP, Centre Hospitalier Universitaire (CHU) Cochin, Paris, F-75014, France.

Camille Berthelot (C)

Institut Pasteur, Université Paris Cité, CNRS UMR 3525, INSERM UA12, Comparative Functional Genomics Group, Paris, 75015, France.

Ludivine Doridot (L)

Université Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, Paris, France.

Classifications MeSH