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The Genetics of Alzheimer’s Disease in the Chinese Population

Alzheimer’s disease (AD) is a neurodegenerative disease characterized by progressive cognitive dysfunction and behavioral impairment. In China, the number of AD patients is growing rapidly, which poses a considerable burden on society and families. In recent years, through the advancement of genome-...

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Autores principales: Gan, Chen-Ling, Zhang, Tao, Lee, Tae Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178026/
https://www.ncbi.nlm.nih.gov/pubmed/32235595
http://dx.doi.org/10.3390/ijms21072381
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author Gan, Chen-Ling
Zhang, Tao
Lee, Tae Ho
author_facet Gan, Chen-Ling
Zhang, Tao
Lee, Tae Ho
author_sort Gan, Chen-Ling
collection PubMed
description Alzheimer’s disease (AD) is a neurodegenerative disease characterized by progressive cognitive dysfunction and behavioral impairment. In China, the number of AD patients is growing rapidly, which poses a considerable burden on society and families. In recent years, through the advancement of genome-wide association studies, second-generation gene sequencing technology, and their application in AD genetic research, more genetic loci associated with the risk for AD have been discovered, including KCNJ15, TREM2, and GCH1, which provides new ideas for the etiology and treatment of AD. This review summarizes three early-onset AD causative genes (APP, PSEN1, and PSEN2) and some late-onset AD susceptibility genes and their mutation sites newly discovered in China, and briefly introduces the potential mechanisms of these genetic susceptibilities in the pathogenesis of AD, which would help in understanding the genetic mechanisms underlying this devastating disease.
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spelling pubmed-71780262020-04-28 The Genetics of Alzheimer’s Disease in the Chinese Population Gan, Chen-Ling Zhang, Tao Lee, Tae Ho Int J Mol Sci Review Alzheimer’s disease (AD) is a neurodegenerative disease characterized by progressive cognitive dysfunction and behavioral impairment. In China, the number of AD patients is growing rapidly, which poses a considerable burden on society and families. In recent years, through the advancement of genome-wide association studies, second-generation gene sequencing technology, and their application in AD genetic research, more genetic loci associated with the risk for AD have been discovered, including KCNJ15, TREM2, and GCH1, which provides new ideas for the etiology and treatment of AD. This review summarizes three early-onset AD causative genes (APP, PSEN1, and PSEN2) and some late-onset AD susceptibility genes and their mutation sites newly discovered in China, and briefly introduces the potential mechanisms of these genetic susceptibilities in the pathogenesis of AD, which would help in understanding the genetic mechanisms underlying this devastating disease. MDPI 2020-03-30 /pmc/articles/PMC7178026/ /pubmed/32235595 http://dx.doi.org/10.3390/ijms21072381 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Gan, Chen-Ling
Zhang, Tao
Lee, Tae Ho
The Genetics of Alzheimer’s Disease in the Chinese Population
title The Genetics of Alzheimer’s Disease in the Chinese Population
title_full The Genetics of Alzheimer’s Disease in the Chinese Population
title_fullStr The Genetics of Alzheimer’s Disease in the Chinese Population
title_full_unstemmed The Genetics of Alzheimer’s Disease in the Chinese Population
title_short The Genetics of Alzheimer’s Disease in the Chinese Population
title_sort genetics of alzheimer’s disease in the chinese population
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178026/
https://www.ncbi.nlm.nih.gov/pubmed/32235595
http://dx.doi.org/10.3390/ijms21072381
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