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Large-scale analysis to identify risk factors for ovarian cancer
by
Iqbal Madakkatel
, Mäenpää, Johanna
, Oehler, Martin K
, Hyppönen, Elina
, Anwar Mulugeta
, Lumsden, Amanda L
in
Biobanks
/ Biomarkers
/ Decision trees
/ Disease prevention
/ Ethnicity
/ Interactive computer systems
/ Machine learning
/ Medical prognosis
/ Ovarian cancer
/ Questionnaires
/ Regression analysis
/ Risk factors
/ Womens health
2025
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Large-scale analysis to identify risk factors for ovarian cancer
by
Iqbal Madakkatel
, Mäenpää, Johanna
, Oehler, Martin K
, Hyppönen, Elina
, Anwar Mulugeta
, Lumsden, Amanda L
in
Biobanks
/ Biomarkers
/ Decision trees
/ Disease prevention
/ Ethnicity
/ Interactive computer systems
/ Machine learning
/ Medical prognosis
/ Ovarian cancer
/ Questionnaires
/ Regression analysis
/ Risk factors
/ Womens health
2025
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Do you wish to request the book?
Large-scale analysis to identify risk factors for ovarian cancer
by
Iqbal Madakkatel
, Mäenpää, Johanna
, Oehler, Martin K
, Hyppönen, Elina
, Anwar Mulugeta
, Lumsden, Amanda L
in
Biobanks
/ Biomarkers
/ Decision trees
/ Disease prevention
/ Ethnicity
/ Interactive computer systems
/ Machine learning
/ Medical prognosis
/ Ovarian cancer
/ Questionnaires
/ Regression analysis
/ Risk factors
/ Womens health
2025
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Large-scale analysis to identify risk factors for ovarian cancer
Journal Article
Large-scale analysis to identify risk factors for ovarian cancer
2025
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Overview
ObjectiveOvarian cancer is characterized by late-stage diagnoses and poor prognosis. We aimed to identify factors that can inform prevention and early detection of ovarian cancer.MethodsWe used a data-driven machine learning approach to identify predictors of epithelial ovarian cancer from 2920 input features measured 12.6 years (IQR 11.9 to 13.3 years) before diagnoses. Analyses included 221 732 female participants in the UK Biobank without a history of cancer. During the follow-up 1441 women developed ovarian cancer. For factors that contributed to model prediction, we used multivariate logistic regression to evaluate the association with ovarian cancer, with evidence for causality tested by Mendelian randomization (MR) analyses in the Ovarian Cancer Genetics Consortium (25 509 cases).ResultsGreater parity and ever-use of oral contraception were associated with lower ovarian cancer risk (ever vs never OR 0.74, 95% CI 0.66 to 0.84). After adjustment for established risk factors, greater height, weight, and greater red blood cell distribution width were associated with increased ovarian cancer risk, while higher aspartate aminotransferase levels and mean corpuscular volume were associated with lower risk. MR analyses confirmed observational associations with anthropometric/adiposity traits (eg, body fat percentage per standard deviation (SD); OR inverse-variance weighted (ORIVW) 1.28, 95% CI 1.13 to 1.46) and aspartate aminotransferase (ORIVW 0.87, 95% CI 0.78 to 0.98). MR also provided genetic evidence for a protective association of higher total serum protein on ovarian cancer, higher lymphocyte count on serous and endometrioid ovarian cancer, and greater forced expiratory volume in 1 s on serous ovarian cancer among other findings.ConclusionsThis study shows that certain risk factors for ovarian cancer are modifiable, suggesting that weight reduction and interventions to reduce the number of ovulations may provide potential for future prevention. We also identified blood biomarkers associated with ovarian cancer years before diagnoses, warranting further investigation.
Publisher
Elsevier Limited
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