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dc.contributor.authorD’Urso, Shannon
dc.contributor.authorArumugam, Pooja
dc.contributor.authorWeider, Therese
dc.contributor.authorHwang, Liang-Dar
dc.contributor.authorBond, Tom A.
dc.contributor.authorKemp, John P.
dc.contributor.authorWarrington, Nicole Maree
dc.contributor.authorEvans, David M.
dc.contributor.authorO’Mara, Tracy A.
dc.contributor.authorMoen, Gunn-Helen Øiseth
dc.date.accessioned2023-02-08T10:29:18Z
dc.date.available2023-02-08T10:29:18Z
dc.date.created2022-11-21T12:06:33Z
dc.date.issued2022
dc.identifier.citationBMC Medicine. 2022, 20:419 1-17.en_US
dc.identifier.issn1741-7015
dc.identifier.urihttps://hdl.handle.net/11250/3049209
dc.description.abstractBackground Observational epidemiological studies suggest a link between several factors related to ovulation and reproductive function and endometrial cancer (EC) risk; however, it is not clear whether these relationships are causal, and whether the risk factors act independently of each other. The aim of this study was to investigate putative causal relationships between the number of live births, age at last live birth, and years ovulating and EC risk. Methods We conducted a series of observational analyses to investigate various risk factors and EC risk in the UK Biobank (UKBB). Additionally, multivariate analysis was performed to elucidate the relationship between the number of live births, age at last live birth, and years ovulating and other related factors such as age at natural menopause, age at menarche, and body mass index (BMI). Secondly, we used Mendelian randomization (MR) to assess if these observed relationships were causal. Genome-wide significant single nucleotide polymorphisms (SNPs) were extracted from previous studies of woman’s number of live births, age at menopause and menarche, and BMI. We conducted a genome-wide association analysis using the UKBB to identify SNPs associated with years ovulating, years using the contraceptive pill, and age at last live birth. Results We found evidence for a causal effect of the number of live births (inverse variance weighted (IVW) odds ratio (OR): 0.537, p = 0.006), the number of years ovulating (IVW OR: 1.051, p = 0.014), in addition to the known risk factors BMI, age at menarche, and age at menopause on EC risk in the univariate MR analyses. Due to the close relationships between these factors, we followed up with multivariable MR (MVMR) analysis. Results from the MVMR analysis showed that number of live births had a causal effect on EC risk (OR: 0.783, p = 0.036) independent of BMI, age at menarche and age at menopause. Conclusions MVMR analysis showed that the number of live births causally reduced the risk of EC.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleMendelian randomization analysis of factors related to ovulation and reproductive function and endometrial cancer risken_US
dc.title.alternativeMendelian randomization analysis of factors related to ovulation and reproductive function and endometrial cancer risken_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-17en_US
dc.source.volume20:419en_US
dc.source.journalBMC Medicineen_US
dc.identifier.doi10.1186/s12916-022-02585-w
dc.identifier.cristin2077199
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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