Machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies

Author:

Park Jun Young123ORCID,Lee Jang Jae3,Lee Younghwa1,Lee Dongsoo1,Gim Jungsoo34,Farrer Lindsay56ORCID,Lee Kun Ho347,Won Sungho18910

Affiliation:

1. Department of Public Health Sciences, Graduate School of Public Health, Seoul National University , Seoul 08826, Korea

2. Neurozen Inc. , Seoul 06168, Korea

3. Gwangju Alzheimer’s & Related Dementia Cohort Research Center, Chosun University , Gwangju 61452, Korea

4. Department of Biomedical Science, Chosun University , Gwangju 61452, Korea

5. Departments of Medicine (Biomedical Genetics), Neurology, and Ophthalmology, Boston University Chobanian & Avedisian School of Medicine , Boston, MA 02118, United States

6. Departments of Epidemiology and Biostatistics, Boston University School of Public Health , Boston, MA 02118, United States

7. Korea Brain Research Institute , Daegu 41068, Korea

8. Interdisciplinary Program in Bioinformatics, Seoul National University , Seoul 08826, Korea

9. Institute of Health and Environment, Seoul National University , Seoul 08826, Korea

10. RexSoft Inc , Seoul 08826, Korea

Abstract

Abstract Motivation Allowance for increasingly large samples is a key to identify the association of genetic variants with Alzheimer’s disease (AD) in genome-wide association studies (GWAS). Accordingly, we aimed to develop a method that incorporates patients with mild cognitive impairment and unknown cognitive status in GWAS using a machine learning-based AD prediction model. Results Simulation analyses showed that weighting imputed phenotypes method increased the statistical power compared to ordinary logistic regression using only AD cases and controls. Applied to real-world data, the penalized logistic method had the highest AUC (0.96) for AD prediction and weighting imputed phenotypes method performed well in terms of power. We identified an association (P<5.0×10-8) of AD with several variants in the APOE region and rs143625563 in LMX1A. Our method, which allows the inclusion of individuals with mild cognitive impairment, improves the statistical power of GWAS for AD. We discovered a novel association with LMX1A. Availability and implementation Simulation codes can be accessed at https://github.com/Junkkkk/wGEE_GWAS.

Funder

Healthcare AI Convergence Research & Development Program through the National IT Industry Promotion Agency of Korea (NIPA) funded by the Ministry of Science and ICT

KBRI basic research program through Korea Brain Research Institute funded by Ministry of Science and ICT

National Research Foundation (NRF) grant funded by the Korean Government

Basic Science Research Program through the National Research Foundation (NRF) funded by the Ministry of Education

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

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