Genetic Biomarkers for Endometriosis
Seven genomic regions associated with endometriosis risk explain minimal phenotypic variance and lack individual predictive power, necessitating larger sample sizes or combined data for improved risk prediction.
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The paper studied whether known common genetic variants associated with endometriosis risk from GWAS can predict individual endometriosis development. Using effect sizes from seven genome-wide significant loci and simulations incorporating an estimated heritability from all common SNPs (h² = 0.26), it found that combining the seven markers explained only 1.85% of phenotypic variance on the liability scale and provided no meaningful individual predictive power; even with ~30,000 cases, the simulated variance explained by a genetic risk predictor was only ~0.08. A major caveat stated is that current effect sizes are small and predictive accuracy remains limited under present sample sizes. This paper is centrally about endometriosis — evaluating genetic biomarkers and polygenic prediction accuracy for endometriosis risk.
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References (35)
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Cited by (5)
- Unified Predictive Model for Endometriosis: Merging Clinical, Self-reporting and Genetic Information 2022
- Revisiting the Risk Factors for Endometriosis: A Machine Learning Approach 2022
- Challenges in uncovering non-invasive biomarkers of endometriosis 2020
- Should Genetics Now Be Considered the Pre-eminent Etiologic Factor in Endometriosis? 2019
- Genetics of endometriosis: State of the art on genetic risk factors for endometriosis 2018
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- last seen: 2026-06-10T17:14:06.276822+00:00