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MicroRNome analysis generates a blood-based signature for endometriosis
Endometriosis, characterized by endometrial-like tissue outside the uterus, is thought to affect 2–10% of women of reproductive age: representing about 190 million women worldwide. Numerous studies have evaluated the diagnostic value of blood biomarkers but with disappointing results. Thus, the gold...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8902281/ https://www.ncbi.nlm.nih.gov/pubmed/35260677 http://dx.doi.org/10.1038/s41598-022-07771-7 |
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author | Bendifallah, Sofiane Dabi, Yohann Suisse, Stéphane Jornea, Ludmila Bouteiller, Delphine Touboul, Cyril Puchar, Anne Daraï, Emile |
author_facet | Bendifallah, Sofiane Dabi, Yohann Suisse, Stéphane Jornea, Ludmila Bouteiller, Delphine Touboul, Cyril Puchar, Anne Daraï, Emile |
author_sort | Bendifallah, Sofiane |
collection | PubMed |
description | Endometriosis, characterized by endometrial-like tissue outside the uterus, is thought to affect 2–10% of women of reproductive age: representing about 190 million women worldwide. Numerous studies have evaluated the diagnostic value of blood biomarkers but with disappointing results. Thus, the gold standard for diagnosing endometriosis remains laparoscopy. We performed a prospective trial, the ENDO-miRNA study, using both Artificial Intelligence (AI) and Machine Learning (ML), to analyze the current human miRNome to differentiate between patients with and without endometriosis, and to develop a blood-based microRNA (miRNA) diagnostic signature for endometriosis. Here, we present the first blood-based diagnostic signature obtained from a combination of two robust and disruptive technologies merging the intrinsic quality of miRNAs to condense the endometriosis phenotype (and its heterogeneity) with the modeling power of AI. The most accurate signature provides a sensitivity, specificity, and Area Under the Curve (AUC) of 96.8%, 100%, and 98.4%, respectively, and is sufficiently robust and reproducible to replace the gold standard of diagnostic surgery. Such a diagnostic approach for this debilitating disorder could impact recommendations from national and international learned societies. |
format | Online Article Text |
id | pubmed-8902281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89022812022-03-08 MicroRNome analysis generates a blood-based signature for endometriosis Bendifallah, Sofiane Dabi, Yohann Suisse, Stéphane Jornea, Ludmila Bouteiller, Delphine Touboul, Cyril Puchar, Anne Daraï, Emile Sci Rep Article Endometriosis, characterized by endometrial-like tissue outside the uterus, is thought to affect 2–10% of women of reproductive age: representing about 190 million women worldwide. Numerous studies have evaluated the diagnostic value of blood biomarkers but with disappointing results. Thus, the gold standard for diagnosing endometriosis remains laparoscopy. We performed a prospective trial, the ENDO-miRNA study, using both Artificial Intelligence (AI) and Machine Learning (ML), to analyze the current human miRNome to differentiate between patients with and without endometriosis, and to develop a blood-based microRNA (miRNA) diagnostic signature for endometriosis. Here, we present the first blood-based diagnostic signature obtained from a combination of two robust and disruptive technologies merging the intrinsic quality of miRNAs to condense the endometriosis phenotype (and its heterogeneity) with the modeling power of AI. The most accurate signature provides a sensitivity, specificity, and Area Under the Curve (AUC) of 96.8%, 100%, and 98.4%, respectively, and is sufficiently robust and reproducible to replace the gold standard of diagnostic surgery. Such a diagnostic approach for this debilitating disorder could impact recommendations from national and international learned societies. Nature Publishing Group UK 2022-03-08 /pmc/articles/PMC8902281/ /pubmed/35260677 http://dx.doi.org/10.1038/s41598-022-07771-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Bendifallah, Sofiane Dabi, Yohann Suisse, Stéphane Jornea, Ludmila Bouteiller, Delphine Touboul, Cyril Puchar, Anne Daraï, Emile MicroRNome analysis generates a blood-based signature for endometriosis |
title | MicroRNome analysis generates a blood-based signature for endometriosis |
title_full | MicroRNome analysis generates a blood-based signature for endometriosis |
title_fullStr | MicroRNome analysis generates a blood-based signature for endometriosis |
title_full_unstemmed | MicroRNome analysis generates a blood-based signature for endometriosis |
title_short | MicroRNome analysis generates a blood-based signature for endometriosis |
title_sort | micrornome analysis generates a blood-based signature for endometriosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8902281/ https://www.ncbi.nlm.nih.gov/pubmed/35260677 http://dx.doi.org/10.1038/s41598-022-07771-7 |
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