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Risk Prediction Using Genome-Wide Association Studies on Type 2 Diabetes
The success of genome-wide association studies (GWASs) has enabled us to improve risk assessment and provide novel genetic variants for diagnosis, prevention, and treatment. However, most variants discovered by GWASs have been reported to have very small effect sizes on complex human diseases, which...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korea Genome Organization
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287117/ https://www.ncbi.nlm.nih.gov/pubmed/28154504 http://dx.doi.org/10.5808/GI.2016.14.4.138 |
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author | Choi, Sungkyoung Bae, Sunghwan Park, Taesung |
author_facet | Choi, Sungkyoung Bae, Sunghwan Park, Taesung |
author_sort | Choi, Sungkyoung |
collection | PubMed |
description | The success of genome-wide association studies (GWASs) has enabled us to improve risk assessment and provide novel genetic variants for diagnosis, prevention, and treatment. However, most variants discovered by GWASs have been reported to have very small effect sizes on complex human diseases, which has been a big hurdle in building risk prediction models. Recently, many statistical approaches based on penalized regression have been developed to solve the “large p and small n” problem. In this report, we evaluated the performance of several statistical methods for predicting a binary trait: stepwise logistic regression (SLR), least absolute shrinkage and selection operator (LASSO), and Elastic-Net (EN). We first built a prediction model by combining variable selection and prediction methods for type 2 diabetes using Affymetrix Genome-Wide Human SNP Array 5.0 from the Korean Association Resource project. We assessed the risk prediction performance using area under the receiver operating characteristic curve (AUC) for the internal and external validation datasets. In the internal validation, SLR-LASSO and SLR-EN tended to yield more accurate predictions than other combinations. During the external validation, the SLR-SLR and SLR-EN combinations achieved the highest AUC of 0.726. We propose these combinations as a potentially powerful risk prediction model for type 2 diabetes. |
format | Online Article Text |
id | pubmed-5287117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korea Genome Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-52871172017-02-02 Risk Prediction Using Genome-Wide Association Studies on Type 2 Diabetes Choi, Sungkyoung Bae, Sunghwan Park, Taesung Genomics Inform Original Article The success of genome-wide association studies (GWASs) has enabled us to improve risk assessment and provide novel genetic variants for diagnosis, prevention, and treatment. However, most variants discovered by GWASs have been reported to have very small effect sizes on complex human diseases, which has been a big hurdle in building risk prediction models. Recently, many statistical approaches based on penalized regression have been developed to solve the “large p and small n” problem. In this report, we evaluated the performance of several statistical methods for predicting a binary trait: stepwise logistic regression (SLR), least absolute shrinkage and selection operator (LASSO), and Elastic-Net (EN). We first built a prediction model by combining variable selection and prediction methods for type 2 diabetes using Affymetrix Genome-Wide Human SNP Array 5.0 from the Korean Association Resource project. We assessed the risk prediction performance using area under the receiver operating characteristic curve (AUC) for the internal and external validation datasets. In the internal validation, SLR-LASSO and SLR-EN tended to yield more accurate predictions than other combinations. During the external validation, the SLR-SLR and SLR-EN combinations achieved the highest AUC of 0.726. We propose these combinations as a potentially powerful risk prediction model for type 2 diabetes. Korea Genome Organization 2016-12 2016-12-30 /pmc/articles/PMC5287117/ /pubmed/28154504 http://dx.doi.org/10.5808/GI.2016.14.4.138 Text en Copyright © 2016 by the Korea Genome Organization http://creativecommons.org/licenses/by-nc/4.0/ It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/). |
spellingShingle | Original Article Choi, Sungkyoung Bae, Sunghwan Park, Taesung Risk Prediction Using Genome-Wide Association Studies on Type 2 Diabetes |
title | Risk Prediction Using Genome-Wide Association Studies on Type 2 Diabetes |
title_full | Risk Prediction Using Genome-Wide Association Studies on Type 2 Diabetes |
title_fullStr | Risk Prediction Using Genome-Wide Association Studies on Type 2 Diabetes |
title_full_unstemmed | Risk Prediction Using Genome-Wide Association Studies on Type 2 Diabetes |
title_short | Risk Prediction Using Genome-Wide Association Studies on Type 2 Diabetes |
title_sort | risk prediction using genome-wide association studies on type 2 diabetes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287117/ https://www.ncbi.nlm.nih.gov/pubmed/28154504 http://dx.doi.org/10.5808/GI.2016.14.4.138 |
work_keys_str_mv | AT choisungkyoung riskpredictionusinggenomewideassociationstudiesontype2diabetes AT baesunghwan riskpredictionusinggenomewideassociationstudiesontype2diabetes AT parktaesung riskpredictionusinggenomewideassociationstudiesontype2diabetes |