» Articles » PMID: 39332904

Genetics-driven Risk Predictions Leveraging the Mendelian Randomization Framework

Overview
Journal Genome Res
Specialty Genetics
Date 2024 Sep 27
PMID 39332904
Authors
Affiliations
Soon will be listed here.
Abstract

Accurate predictive models of future disease onset are crucial for effective preventive healthcare, yet longitudinal data sets linking early risk factors to subsequent health outcomes are limited. To overcome this challenge, we introduce a novel framework, redictive sk modeling using ndelian andomization (PRiMeR), which utilizes genetic effects as supervisory signals to learn disease risk predictors without relying on longitudinal data. To do so, PRiMeR leverages risk factors and genetic data from a healthy cohort, along with results from genome-wide association studies of diseases of interest. After training, the learned predictor can be used to assess risk for new patients solely based on risk factors. We validate PRiMeR through comprehensive simulations and in future type 2 diabetes predictions in UK Biobank participants without diabetes, using follow-up onset labels for validation. Moreover, we apply PRiMeR to predict future Alzheimer's disease onset from brain imaging biomarkers and future Parkinson's disease onset from accelerometer-derived traits. Overall, with PRiMeR we offer a new perspective in predictive modeling, showing it is possible to learn risk predictors leveraging genetics rather than longitudinal data.

References
1.
de Jong L, van der Hiele K, Veer I, Houwing J, Westendorp R, Bollen E . Strongly reduced volumes of putamen and thalamus in Alzheimer's disease: an MRI study. Brain. 2008; 131(Pt 12):3277-85. PMC: 2639208. DOI: 10.1093/brain/awn278. View

2.
Wichmann H, Horlein A, Ahrens W, Nauck M . [The biobank of the German National Cohort as a resource for epidemiologic research]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2016; 59(3):351-60. DOI: 10.1007/s00103-015-2305-4. View

3.
Pingault J, OReilly P, Schoeler T, Ploubidis G, Rijsdijk F, Dudbridge F . Using genetic data to strengthen causal inference in observational research. Nat Rev Genet. 2018; 19(9):566-580. DOI: 10.1038/s41576-018-0020-3. View

4.
Grabner G, Janke A, Budge M, Smith D, Pruessner J, Collins D . Symmetric atlasing and model based segmentation: an application to the hippocampus in older adults. Med Image Comput Comput Assist Interv. 2007; 9(Pt 2):58-66. DOI: 10.1007/11866763_8. View

5.
Cai M, Wang Z, Xiao J, Hu X, Chen G, Yang C . XMAP: Cross-population fine-mapping by leveraging genetic diversity and accounting for confounding bias. Nat Commun. 2023; 14(1):6870. PMC: 10613261. DOI: 10.1038/s41467-023-42614-7. View