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Machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies
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 cogni...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539075/ https://www.ncbi.nlm.nih.gov/pubmed/37665736 http://dx.doi.org/10.1093/bioinformatics/btad534 |
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author | Park, Jun Young Lee, Jang Jae Lee, Younghwa Lee, Dongsoo Gim, Jungsoo Farrer, Lindsay Lee, Kun Ho Won, Sungho |
author_facet | Park, Jun Young Lee, Jang Jae Lee, Younghwa Lee, Dongsoo Gim, Jungsoo Farrer, Lindsay Lee, Kun Ho Won, Sungho |
author_sort | Park, Jun Young |
collection | PubMed |
description | 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< [Formula: see text]) 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. |
format | Online Article Text |
id | pubmed-10539075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105390752023-09-29 Machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies Park, Jun Young Lee, Jang Jae Lee, Younghwa Lee, Dongsoo Gim, Jungsoo Farrer, Lindsay Lee, Kun Ho Won, Sungho Bioinformatics Original Paper 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< [Formula: see text]) 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. Oxford University Press 2023-09-04 /pmc/articles/PMC10539075/ /pubmed/37665736 http://dx.doi.org/10.1093/bioinformatics/btad534 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Park, Jun Young Lee, Jang Jae Lee, Younghwa Lee, Dongsoo Gim, Jungsoo Farrer, Lindsay Lee, Kun Ho Won, Sungho Machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies |
title | Machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies |
title_full | Machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies |
title_fullStr | Machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies |
title_full_unstemmed | Machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies |
title_short | Machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies |
title_sort | machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539075/ https://www.ncbi.nlm.nih.gov/pubmed/37665736 http://dx.doi.org/10.1093/bioinformatics/btad534 |
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