Marzena Skrzypa
ID
Natalia Potocka
ID
Halina Bartosik-Psujek
ID
Izabela Zawlik
ID
 Email src
Laboratory of Molecular Biology, Centre for Innovative Research in Medical and Natural Sciences, Faculty of Medicine, University of Rzeszow, Rzeszow, Poland
Laboratory of Molecular Biology, Centre for Innovative Research in Medical and Natural Sciences, Faculty of Medicine, University of Rzeszow, Rzeszow, Poland
Department of Neurology, Clinical Voivodship Hospital No. 2 in Rzeszów, Rzeszów, Poland
Laboratory of Molecular Biology, Centre for Innovative Research in Medical and Natural Sciences, Faculty of Medicine, University of Rzeszow, Rzeszow, Poland
Received: 28 January 2019 / Accepted: 11 February 2019 / Published: 30 March 2019

Abstract

Introduction. Alzheimer’s disease (AD) is one of the most common neurodegenerative diseases, which is a serious health problem for societies that live longer. Spontaneous dominant mutations and polymorphisms of selected genes play an important role in development of AD.

Aim. Several polymorphisms in selected genes strongly associated with development of Alzheimer’s disease were highlighted in this review: APOE, CYP46, APP, PSEN1, PSEN2, UBQLN1, BACE1, PRND, APBB2, TOMM 40. These gene polymorphisms have a significant role in the development of Alzheimer’s disease and they have potential to be biomarkers. Researchers combine efforts to find significant polymorphisms that would ensure that a person is predisposed to the occurrence of disease symptoms. This topic is often taken up by scientists seeking to develop effective genetic tests for diagnosing AD.

Material and methods. Analysis of literature from web of knowledge: Web of Science (all database), NCBI and PubMed.

Results. We reviewed the selected important genes and polymorphisms which are most often associated with development of AD.

Conclusion. It should be noted that nowadays scientists strive not to focus on only one polymorphism in the gene but on several polymorphisms in different genes concomitantly and above all on interactions between them to the diagnosis of this disease. Only this approach to AD will contribute to the creation of appropriate identification methods. Moreover, we should use the new generation tools - the platform for collecting data and personalized medicine. 

 

Cite

Skrzypa M, Potocka N, Bartosik-Psujek H, Zawlik I. Genetic risk factors of Alzheimer’s disease. Eur J Clin Exp Med. 2019;17(1):57– 66. doi: 10.15584/ejcem.2019.1.10

This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited