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Comparison of machine learning tools for the prediction of AMD based on genetic, age, and diabetes-related variables in the Chinese population

INTRODUCTION: Age-related macular degeneration (AMD) is the main cause of visual impairment and the most important cause of blindness in older people. However, there is currently no effective treatment for this disease, so it is necessary to establish a risk model to predict AMD development. METHODS...

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Autores principales: Hao, Shaofeng, Bai, Junye, Liu, Huimin, Wang, Lijun, Liu, Tao, Lin, Chaobin, Luo, Xiangguang, Gao, Junhui, Zhao, Jiangman, Li, Huilin, Tang, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770346/
https://www.ncbi.nlm.nih.gov/pubmed/33426217
http://dx.doi.org/10.1016/j.reth.2020.09.001
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author Hao, Shaofeng
Bai, Junye
Liu, Huimin
Wang, Lijun
Liu, Tao
Lin, Chaobin
Luo, Xiangguang
Gao, Junhui
Zhao, Jiangman
Li, Huilin
Tang, Hui
author_facet Hao, Shaofeng
Bai, Junye
Liu, Huimin
Wang, Lijun
Liu, Tao
Lin, Chaobin
Luo, Xiangguang
Gao, Junhui
Zhao, Jiangman
Li, Huilin
Tang, Hui
author_sort Hao, Shaofeng
collection PubMed
description INTRODUCTION: Age-related macular degeneration (AMD) is the main cause of visual impairment and the most important cause of blindness in older people. However, there is currently no effective treatment for this disease, so it is necessary to establish a risk model to predict AMD development. METHODS: This study included a total of 202 subjects, comprising 82 AMD patients and 120 control subjects. Sixty-six single-nucleotide polymorphisms (SNPs) were identified using the MassArray assay. Considering 14 independent clinical variables as well as SNPs, four predictive models were established in the training set and evaluated by the confusion matrix, area under the receiver operating characteristic (ROC) curve (AUROC). The difference distributions of the 14 independent clinical features between the AMD and control groups were tested using the chi-squared test. Age and diabetes were adjusted using logistic regression analysis and the “genomic-control” method was used for multiple testing correction. RESULTS: Three SNPs (rs10490924, OR = 1.686, genomic-control corrected p-value (GC) = 0.030; rs2338104, OR = 1.794, GC = 0.025 and rs1864163, OR = 2.125, GC = 0.038) were significant risk factors for AMD development. In the training set, four models obtained AUROC values above 0.72. CONCLUSIONS: We believe machine learning tools will be useful for the early prediction of AMD and for the development of relevant intervention strategies.
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spelling pubmed-77703462021-01-08 Comparison of machine learning tools for the prediction of AMD based on genetic, age, and diabetes-related variables in the Chinese population Hao, Shaofeng Bai, Junye Liu, Huimin Wang, Lijun Liu, Tao Lin, Chaobin Luo, Xiangguang Gao, Junhui Zhao, Jiangman Li, Huilin Tang, Hui Regen Ther Original Article INTRODUCTION: Age-related macular degeneration (AMD) is the main cause of visual impairment and the most important cause of blindness in older people. However, there is currently no effective treatment for this disease, so it is necessary to establish a risk model to predict AMD development. METHODS: This study included a total of 202 subjects, comprising 82 AMD patients and 120 control subjects. Sixty-six single-nucleotide polymorphisms (SNPs) were identified using the MassArray assay. Considering 14 independent clinical variables as well as SNPs, four predictive models were established in the training set and evaluated by the confusion matrix, area under the receiver operating characteristic (ROC) curve (AUROC). The difference distributions of the 14 independent clinical features between the AMD and control groups were tested using the chi-squared test. Age and diabetes were adjusted using logistic regression analysis and the “genomic-control” method was used for multiple testing correction. RESULTS: Three SNPs (rs10490924, OR = 1.686, genomic-control corrected p-value (GC) = 0.030; rs2338104, OR = 1.794, GC = 0.025 and rs1864163, OR = 2.125, GC = 0.038) were significant risk factors for AMD development. In the training set, four models obtained AUROC values above 0.72. CONCLUSIONS: We believe machine learning tools will be useful for the early prediction of AMD and for the development of relevant intervention strategies. Japanese Society for Regenerative Medicine 2020-09-29 /pmc/articles/PMC7770346/ /pubmed/33426217 http://dx.doi.org/10.1016/j.reth.2020.09.001 Text en © 2020 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Hao, Shaofeng
Bai, Junye
Liu, Huimin
Wang, Lijun
Liu, Tao
Lin, Chaobin
Luo, Xiangguang
Gao, Junhui
Zhao, Jiangman
Li, Huilin
Tang, Hui
Comparison of machine learning tools for the prediction of AMD based on genetic, age, and diabetes-related variables in the Chinese population
title Comparison of machine learning tools for the prediction of AMD based on genetic, age, and diabetes-related variables in the Chinese population
title_full Comparison of machine learning tools for the prediction of AMD based on genetic, age, and diabetes-related variables in the Chinese population
title_fullStr Comparison of machine learning tools for the prediction of AMD based on genetic, age, and diabetes-related variables in the Chinese population
title_full_unstemmed Comparison of machine learning tools for the prediction of AMD based on genetic, age, and diabetes-related variables in the Chinese population
title_short Comparison of machine learning tools for the prediction of AMD based on genetic, age, and diabetes-related variables in the Chinese population
title_sort comparison of machine learning tools for the prediction of amd based on genetic, age, and diabetes-related variables in the chinese population
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770346/
https://www.ncbi.nlm.nih.gov/pubmed/33426217
http://dx.doi.org/10.1016/j.reth.2020.09.001
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