Integration of polygenic and gut metagenomic risk prediction for common diseases
Liu Yang; Ritchie Scott C.; Teo Shu Mei; Ruuskanen Matti O.; Kambur Oleg; Zhu Qiyun; Sanders Jon; Vázquez-Baeza Yoshiki; Verspoor Karin; Jousilahti Pekka; Lahti Leo; Niiranen Teemu; Salomaa Veikko; Havulinna Aki S.; Knight Rob; Méric Guillaume; Inouye Michael
Integration of polygenic and gut metagenomic risk prediction for common diseases
Liu Yang
Ritchie Scott C.
Teo Shu Mei
Ruuskanen Matti O.
Kambur Oleg
Zhu Qiyun
Sanders Jon
Vázquez-Baeza Yoshiki
Verspoor Karin
Jousilahti Pekka
Lahti Leo
Niiranen Teemu
Salomaa Veikko
Havulinna Aki S.
Knight Rob
Méric Guillaume
Inouye Michael
Nature
Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2025082785030
https://urn.fi/URN:NBN:fi-fe2025082785030
Tiivistelmä
Multiomics has shown promise in noninvasive risk profiling and early detection of various common diseases. In the present study, in a prospective population-based cohort with ~18 years of e-health record follow-up, we investigated the incremental and combined value of genomic and gut metagenomic risk assessment compared with conventional risk factors for predicting incident coronary artery disease (CAD), type 2 diabetes (T2D), Alzheimer disease and prostate cancer. We found that polygenic risk scores (PRSs) improved prediction over conventional risk factors for all diseases. Gut microbiome scores improved predictive capacity over baseline age for CAD, T2D and prostate cancer. Integrated risk models of PRSs, gut microbiome scores and conventional risk factors achieved the highest predictive performance for all diseases studied compared with models based on conventional risk factors alone. The present study demonstrates that integrated PRSs and gut metagenomic risk models improve the predictive value over conventional risk factors for common chronic diseases.
Kokoelmat
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