GENETIC VARIANTS RELATED TO LIPID METABOLISM AS A RISK FACTOR TO LATE-ONSET ALZHEIMER’S DISEASE
Author(s) -
Marcela Augusta Souza Pinhel,
Alessandro Crestani,
G.F. Sousa-Amorim,
Michele Lima Gregório,
João Castilho Cação,
Waldir Antônio Tognola,
Dorotéia Rossi Silva Souza
Publication year - 2017
Publication title -
journal of aging research and lifestyle
Language(s) - English
Resource type - Journals
ISSN - 2534-773X
DOI - 10.14283/jarcp.2017.3
Subject(s) - abca1 , genotype , apolipoprotein e , allele , genetics , restriction fragment length polymorphism , alzheimer's disease , dementia , polymorphism (computer science) , biology , allele frequency , disease , medicine , single nucleotide polymorphism , apolipoprotein b , endocrinology , cholesterol , gene , transporter
Background: Genetic polymorphisms in genes regulating cholesterol metabolism have been suggested to risk factor of developing Alzheimer’s disease (AD). Objective: to analyze the frequency of polymorphisms apolipoprotein E (APOE-HhaI) and adenosine triphosphate binding cassette transporter 1 (ABCA1-StyI) in patients with late-onset AD. Design: case-control study. Participants: We studied 166 subjects (≥65 years old): Study Group (SG)- 88 patients and Control Group (CG)- 88 without dementia. Setting: The polymorphisms were determined using the polymorphism chain reaction and restriction fragment length polymorphism (PCR-RFLP) methods. It was applied Fisher's exact/chi-square tests (P<0.05). Results: Genotypes with APOE*4 prevailed in SG. The genotypic combination between APOE-HhaI and ABCA1-StyI polymorphisms showed a prevalence of heterozygous genotypes of risk for AD. Conclusion: Although genetic variants for ABCA1-StyI alone does not differentiate patients and controls, the G allele in synergy with APOE*4 allele is highlighted in patients suggesting the influence of ABCA1 in the disease.
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