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Genetics of Alzheimer’s disease

Alzheimer’s disease (AD) is the leading cause of neurodegeneration in the elderly and is clinically characterized by slowly progressing cognitive decline, which most commonly affects episodic memory function. This eventually leads to difficulties in activities of daily living. Biomarker studies show...

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Autores principales: König, Theresa, Stögmann, Elisabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397623/
https://www.ncbi.nlm.nih.gov/pubmed/33616797
http://dx.doi.org/10.1007/s10354-021-00819-9
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author König, Theresa
Stögmann, Elisabeth
author_facet König, Theresa
Stögmann, Elisabeth
author_sort König, Theresa
collection PubMed
description Alzheimer’s disease (AD) is the leading cause of neurodegeneration in the elderly and is clinically characterized by slowly progressing cognitive decline, which most commonly affects episodic memory function. This eventually leads to difficulties in activities of daily living. Biomarker studies show that the underlying pathology of AD begins 20 years before clinical symptoms. This results in the need to define specific targets and preclinical stages in order to address the problems of this disease at an earlier point in time. Genetic studies are indispensable for gaining insight into the etiology of neurodegenerative diseases and can play a major role in the early definition of the individual disease risk. This review provides an overview of the currently known genetic features of AD.
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spelling pubmed-83976232021-09-14 Genetics of Alzheimer’s disease König, Theresa Stögmann, Elisabeth Wien Med Wochenschr Main Topic Alzheimer’s disease (AD) is the leading cause of neurodegeneration in the elderly and is clinically characterized by slowly progressing cognitive decline, which most commonly affects episodic memory function. This eventually leads to difficulties in activities of daily living. Biomarker studies show that the underlying pathology of AD begins 20 years before clinical symptoms. This results in the need to define specific targets and preclinical stages in order to address the problems of this disease at an earlier point in time. Genetic studies are indispensable for gaining insight into the etiology of neurodegenerative diseases and can play a major role in the early definition of the individual disease risk. This review provides an overview of the currently known genetic features of AD. Springer Vienna 2021-02-22 2021 /pmc/articles/PMC8397623/ /pubmed/33616797 http://dx.doi.org/10.1007/s10354-021-00819-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Main Topic
König, Theresa
Stögmann, Elisabeth
Genetics of Alzheimer’s disease
title Genetics of Alzheimer’s disease
title_full Genetics of Alzheimer’s disease
title_fullStr Genetics of Alzheimer’s disease
title_full_unstemmed Genetics of Alzheimer’s disease
title_short Genetics of Alzheimer’s disease
title_sort genetics of alzheimer’s disease
topic Main Topic
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397623/
https://www.ncbi.nlm.nih.gov/pubmed/33616797
http://dx.doi.org/10.1007/s10354-021-00819-9
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