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The effect of androgens on the risk of endometriosis sub-phenotypes and ovarian neoplasms : a Mendelian randomization study
ID Gjorgoska, Marija (Avtor), ID Lanišnik-Rižner, Tea (Avtor)

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Izvleček
Endometriosis is a complex gynecological pathology with a broad spectrum of symptoms, affecting around 10% of reproductive-aged women. Ovarian cancer (OC) is a heterogeneous disease for which we lack effective diagnostic and therapeutic strategies. The etiology and pathogenesis of both diseases remain ambiguous. Androgens in endometriosis could have a distinct role beyond serving as estrogen sources, whereas in the case of serous OC could be important in the formation of precursor lesions which ultimately lead to tumor formation. Here we performed two-sample Mendelian randomization (MR) analysis to examine the causal relationship between the androgen precursor - dehydroepiandrosterone sulphate (DHEAS), bioactive androgen - testosterone (T), androgen metabolite - androsterone sulphate, steroid hormone binding globulin (SHBG) and albumin and the risk of endometrioses of various sub-phenotypes and ovarian neoplasms across the benign-borderline-malignant spectrum. Stringent quality control procedures were followed to select eligible instrumental variables that were strongly associated with the selected exposures, sensitivity analyses were performed to assess the heterogeneities, horizontal pleiotropy, and stabilities of SNPs in endometriosis and ovarian neoplasms. We discovered an inverse association between genetically predicted levels of all androgens and risk of endometriosis, the same trend was most evident in the ovarian sub-phenotype. Total T levels were also inversely associated with peritoneal sub-phenotype of endometriosis. Likewise, T was causally associated with decreased risk of clear-cell OC, an endometriosis-associated OC subtype, and with malignant serous OC of both low- and high-grade, but with higher risk of their counterpart of low malignant potential. These findings support further investigation of androgen's action at a molecular level in ovary-associated endometriotic lesions, clear cell ovarian tumors and serous precursor lesions.

Jezik:Angleški jezik
Ključne besede:androgen hormones, endometriosis sub-phenotypes, ovarian neoplasms, two-sample Mendelian randomization
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:MF - Medicinska fakulteta
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2024
Št. strani:9 str.
Številčenje:Vol. 239, art. 106482
PID:20.500.12556/RUL-156244 Povezava se odpre v novem oknu
UDK:616-006:577
ISSN pri članku:1879-1220
DOI:10.1016/j.jsbmb.2024.106482 Povezava se odpre v novem oknu
COBISS.SI-ID:187494659 Povezava se odpre v novem oknu
Datum objave v RUL:15.05.2024
Število ogledov:411
Število prenosov:44
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Gradivo je del revije

Naslov:The journal of steroid biochemistry and molecular biology
Skrajšan naslov:J. steroid biochem. mol. biol.
Založnik:Elsevier
ISSN:1879-1220
COBISS.SI-ID:57401603 Povezava se odpre v novem oknu

Licence

Licenca:CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:androgeni hormoni, subfenotipi endometrioze, novotvorbe jajčnikov, Mendlova randomizacija dveh vzorcev

Projekti

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:J3-2535
Naslov:Vloga androgenov pri hormonsko odvisnih boleznih: pomen za diagnostiko in zdravljenje

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P3-0449
Naslov:Translacijska molekularna endokrinologija za zdravje žensk

Financer:EC - European Commission
Program financ.:H2020
Številka projekta:101008193
Naslov:Translational Research on Endometriosis
Akronim:TRENDO

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