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Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine

dc.contributor.authorHeddar, Abdelkader
dc.contributor.authorOgur, Cagri
dc.contributor.authorDa Costa, Sabrina
dc.contributor.authorBraham, Ines
dc.contributor.authorBillaud-Rist, Line
dc.contributor.authorFindikli, Necati
dc.contributor.authorBeneteau, Claire
dc.contributor.authorReynaud, Rachel
dc.contributor.authorMahmoud, Khaled
dc.contributor.authorLegrand, Stephanie
dc.contributor.authorMarchand, Maud
dc.contributor.authorCedrin-Durnerin, Isabelle
dc.contributor.authorCantalloube, Adele
dc.contributor.authorPeigne, Maeliss
dc.contributor.authorBretault, Marion
dc.contributor.authorDagher-Hayeck, Benedicte
dc.contributor.authorPerol, Sandrine
dc.contributor.authorDroumaguet, Celine
dc.contributor.authorCavkaytar, Sabri
dc.contributor.authorNicolas-Bonne, Carole
dc.contributor.authorElloumi, Hanen
dc.contributor.authorKhrouf, Mohamed
dc.contributor.authorRougier-LeMasle, Charlotte
dc.contributor.authorFradin, Melanie
dc.contributor.authorLe Boette, Elsa
dc.contributor.authorLuigi, Perrine
dc.contributor.authorGuerrot, Anne-Marie
dc.contributor.authorGinglinger, Emmanuelle
dc.contributor.authorZampa, Amandine
dc.contributor.authorFauconnier, Anais
dc.contributor.authorAuger, Nathalie
dc.contributor.authorParis, Francoise
dc.contributor.authorBrischoux-Boucher, Elise
dc.contributor.authorCabrol, Christelle
dc.contributor.authorBrun, Aurore
dc.contributor.authorGuyon, Laura
dc.contributor.authorBerard, Melanie
dc.contributor.authorRiviere, Axelle
dc.contributor.authorGruchy, Nicolas
dc.contributor.authorOdent, Sylvie
dc.contributor.authorGilbert-Dussardier, Brigitte
dc.contributor.authorIsidor, Bertrand
dc.contributor.authorPiard, Juliette
dc.contributor.authorLambert, Laetitia
dc.contributor.authorHamamah, Samir
dc.contributor.authorGuedj, Anne Marie
dc.contributor.authorde la Perriere, Aude Brac
dc.contributor.authorFernandez, Herve
dc.contributor.authorRaffin-Sanson, Marie-Laure
dc.contributor.authorPolak, Michel
dc.contributor.authorLetur, Helene
dc.contributor.authorEpelboin, Sylvie
dc.contributor.authorPlu-Bureau, Genevieve
dc.contributor.authorWolczynski, Slawomir
dc.contributor.authorHieronimus, Sylvie
dc.contributor.authorAittomaki, Kristiina
dc.contributor.authorCatteau-Jonard, Sophie
dc.contributor.authorMisrahi, Micheline
dc.date.accessioned2026-06-27T14:43:08Z
dc.date.issued2022
dc.description.abstractBackground Primary Ovarian Insufficiency (POI), a public health problem, affects 1-3.7% of women under 40 yield-ing infertility and a shorter lifespan. Most causes are unknown. Recently, genetic causes were identified, mostly in single families. We studied an unprecedented large cohort of POI to unravel its molecular pathophysiology.Methods 375 patients with 70 families were studied using targeted (88 genes) or whole exome sequencing with pathogenic/likely-pathogenic variant selection. Mitomycin-induced chromosome breakages were studied in patients' lymphocytes if necessary. Findings A high-yield of 29.3% supports a clinical genetic diagnosis of POI. In addition, we found strong evidence of pathogenicity for nine genes not previously related to a Mendelian phenotype or POI: ELAVL2, NLRP11, CENPE, SPATA33, CCDC150, CCDC185, including DNA repair genes: C17orf53(HROB), HELQ, SWI5 yielding high chromo-somal fragility. We confirmed the causal role of BRCA2, FANCM, BNC1, ERCC6, MSH4, BMPR1A, BMPR1B, BMPR2, ESR2, CAV1, SPIDR, RCBTB1 and ATG7 previously reported in isolated patients/families. In 8.5% of cases, POI is the only symptom of a multi-organ genetic disease. New pathways were identified: NF-kB, post-translational regulation, and mitophagy (mitochondrial autophagy), providing future therapeutic targets. Three new genes have been shown to affect the age of natural menopause supporting a genetic link.Interpretation We have developed high-performance genetic diagnostic of POI, dissecting the molecular pathogene-sis of POI and enabling personalized medicine to i) prevent/cure comorbidities for tumour/cancer susceptibility genes that could affect life-expectancy (37.4% of cases), or for genetically-revealed syndromic POI (8.5% of cases), ii) predict residual ovarian reserve (60.5% of cases). Genetic diagnosis could help to identify patients who may benefit from the promising in vitro activation-IVA technique in the near future, greatly improving its success in treating infertility.Funding Universite? Paris Saclay, Agence Nationale de Biome?decine.Copyright (c) 2022 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)en
dc.description.sponsorshipUniversite Paris Sud-Paris Saclay
dc.description.sponsorshipHopitaux Universitaires Paris Saclay
dc.description.sponsorshipInstitut National de la Sante et de la Recherche Medicale-INSERM
dc.description.sponsorshipAgence Nationale de Biomedecine
dc.description.urihttps://doi.org/10.1016/j.ebiom.2022.104246
dc.identifier.doi10.1016/j.ebiom.2022.104246
dc.identifier.issn2352-3964
dc.identifier.pubmed36099812
dc.identifier.urihttps://hdl.handle.net/20.500.14981/63896
dc.identifier.volume84
dc.identifier.wos000877614200002
dc.language.isoeng
dc.publisherELSEVIER
dc.relation.ispartofEBIOMEDICINE
dc.rightsopenAccess
dc.subjectPrimary ovarian insufficiency
dc.subjectPersonalized medicine
dc.subjectNF-KB
dc.subjectPost-translational regulation
dc.subjectMeiosis
dc.subjectDNA repair genes
dc.subjectMitophagy
dc.subjectPULMONARY ARTERIAL-HYPERTENSION
dc.subjectOF-FUNCTION MUTATIONS
dc.subjectVARIANTS
dc.subjectIDENTIFICATION
dc.subjectASSOCIATION
dc.subjectFERTILITY
dc.subjectCARRIERS
dc.subjectBMPR2
dc.subjectWOMEN
dc.subjectGeneral & Internal Medicine
dc.subjectResearch & Experimental Medicine
dc.titleGenetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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