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1000 Titel
  • Polygenic risk score phenome-wide association study reveals an association between endometriosis and testosterone
1000 Autor/in
  1. MCGRATH, Isabelle |
  2. International Endometriosis Genetics Consortium |
  3. Montgomery, Grant |
  4. Mortlock, Sally-Anne |
1000 Erscheinungsjahr 2023
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2023-12-05
1000 Erschienen in
1000 Quellenangabe
  • 21(1):482
1000 Copyrightjahr
  • 2023
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s12916-023-03184-z |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696845/ |
1000 Ergänzendes Material
  • https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-023-03184-z#Sec12 |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • BACKGROUND: Endometriosis affects 1 in 9 women, yet it is poorly understood with long diagnostic delays, invasive diagnoses, and poor treatment outcomes. Characterised by the presence of endometrial-like tissue outside of the uterus, its main symptoms are pain and infertility. Endometriosis often co-occurs with other conditions, which may provide insights into the origins of endometriosis. METHODS: Here a polygenic risk score phenome-wide association study of endometriosis was conducted in the UK Biobank to investigate the pleiotropic effects of a genetic liability to endometriosis. The relationship between the polygenic risk score for endometriosis and health conditions, blood and urine biomarkers and reproductive factors were investigated separately in females, males and females without an endometriosis diagnosis. The relationship between endometriosis and the blood and urine biomarkers was further investigated using genetic correlation and Mendelian randomisation approaches to identify causal relationships. RESULTS: Multiple health conditions, blood and urine biomarkers and reproductive factors were associated with genetic liability to endometriosis in each group, indicating many endometriosis comorbidities are not dependent on the physical manifestation of endometriosis. Differences in the associated traits between males and females highlighted the importance of sex-specific pathways in the overlap of endometriosis with many other traits. Notably, an association of genetic liability to endometriosis with lower testosterone levels was identified. Follow-up analysis utilising Mendelian randomisation approaches suggested lower testosterone may be causal for both endometriosis and clear cell ovarian cancer. CONCLUSIONS: This study highlights the diversity of the pleiotropic effects of genetic risk to endometriosis irrespective of a diagnosis of endometriosis. A key finding was the identification of a causal effect of the genetic liability to lower testosterone on endometriosis using Mendelian randomisation.
1000 Sacherschließung
lokal Genetic
lokal Endometriosis
lokal Ovarian cancer
lokal Testosterone
lokal PheWAS
lokal Mendelian randomisation
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0003-4244-8842|https://frl.publisso.de/adhoc/uri/IEludGVybmF0aW9uYWwgRW5kb21ldHJpb3NpcyBHZW5ldGljcyBDb25zb3J0aXVt|https://orcid.org/0000-0002-4140-8139|https://orcid.org/0000-0003-2327-9465
1000 Label
1000 Förderer
  1. National Health and Medical Research Council |
  2. Department of Health and Aged Care, Australian Government |
1000 Fördernummer
  1. GNT1177194
  2. MRF1199785
1000 Förderprogramm
  1. -
  2. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer National Health and Medical Research Council |
    1000 Förderprogramm -
    1000 Fördernummer GNT1177194
  2. 1000 joinedFunding-child
    1000 Förderer Department of Health and Aged Care, Australian Government |
    1000 Förderprogramm -
    1000 Fördernummer MRF1199785
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6472620.rdf
1000 Erstellt am 2023-12-11T15:19:11.033+0100
1000 Erstellt von 339
1000 beschreibt frl:6472620
1000 Bearbeitet von 317
1000 Zuletzt bearbeitet 2023-12-12T12:12:42.080+0100
1000 Objekt bearb. Tue Dec 12 12:12:30 CET 2023
1000 Vgl. frl:6472620
1000 Oai Id
  1. oai:frl.publisso.de:frl:6472620 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
1000 Gegenstand von

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