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Association between Alzheimer’s Disease and Apolipoprotein E Polymorphisms

BACKGROUND: Alzheimer’s disease as a neurodegenerative disorder is the commonest type of dementia. A growing number of genes have been reported as the risk factors, which increase the susceptibility to Alzheimer’s disease. Apolipoprotein E (APOE), which its ε4 allele has been reported as a risk fact...

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Autores principales: Gozalpour, E, Kamali, K, Mohammd, K, Khorshid, HR Khorram, Ohadi, M, Karimloo, M, Mirabzadeh, A, Fotouhi, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481764/
https://www.ncbi.nlm.nih.gov/pubmed/23112999
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author Gozalpour, E
Kamali, K
Mohammd, K
Khorshid, HR Khorram
Ohadi, M
Karimloo, M
Mirabzadeh, A
Fotouhi, A
author_facet Gozalpour, E
Kamali, K
Mohammd, K
Khorshid, HR Khorram
Ohadi, M
Karimloo, M
Mirabzadeh, A
Fotouhi, A
author_sort Gozalpour, E
collection PubMed
description BACKGROUND: Alzheimer’s disease as a neurodegenerative disorder is the commonest type of dementia. A growing number of genes have been reported as the risk factors, which increase the susceptibility to Alzheimer’s disease. Apolipoprotein E (APOE), which its ε4 allele has been reported as a risk factor in late onset Alzheimer’s disease (AD), is the main cholesterol carrier in the brain. The main goal of this study was to assess the role of APOE genotypes and alleles in AD in Iranian population. METHODS: This study was performed in Tehran, Iran from 2007 to 2008. Totally, 154 AD cases and 162 control subjects from Iranian population were genotyped for APOE using PCR method. Genotype and alleles frequencies for APOE were calculated and compared between AD case and control subjects by χ2 or Fisher’s exact test. Type one error assumed less than 0.05. RESULTS: The frequency of ε2ε3 genotype was significantly higher in control subjects than AD patients was (13.5% versus 5.2%, P< 0.05) and ε3ε4 genotype frequency was significantly higher in AD cases compared with control subjects. APOE -ε2 allele frequency in cases was lower than that of control subjects but this difference was not significant (4.2% versus 7.7%). CONCLUSION: It seems that individuals carrying ε4 allele, develop AD 6.5 times more than non-carriers do (OR= 6.566, 95% CI= 2.89–14.92). It has been reported that ε4 allele acts in dose- age-dependent manner but we have shown that the risk of developing AD in male APOE -ε4 allele carriers is higher than that of female ε4 carriers.
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spelling pubmed-34817642012-10-30 Association between Alzheimer’s Disease and Apolipoprotein E Polymorphisms Gozalpour, E Kamali, K Mohammd, K Khorshid, HR Khorram Ohadi, M Karimloo, M Mirabzadeh, A Fotouhi, A Iran J Public Health Original Article BACKGROUND: Alzheimer’s disease as a neurodegenerative disorder is the commonest type of dementia. A growing number of genes have been reported as the risk factors, which increase the susceptibility to Alzheimer’s disease. Apolipoprotein E (APOE), which its ε4 allele has been reported as a risk factor in late onset Alzheimer’s disease (AD), is the main cholesterol carrier in the brain. The main goal of this study was to assess the role of APOE genotypes and alleles in AD in Iranian population. METHODS: This study was performed in Tehran, Iran from 2007 to 2008. Totally, 154 AD cases and 162 control subjects from Iranian population were genotyped for APOE using PCR method. Genotype and alleles frequencies for APOE were calculated and compared between AD case and control subjects by χ2 or Fisher’s exact test. Type one error assumed less than 0.05. RESULTS: The frequency of ε2ε3 genotype was significantly higher in control subjects than AD patients was (13.5% versus 5.2%, P< 0.05) and ε3ε4 genotype frequency was significantly higher in AD cases compared with control subjects. APOE -ε2 allele frequency in cases was lower than that of control subjects but this difference was not significant (4.2% versus 7.7%). CONCLUSION: It seems that individuals carrying ε4 allele, develop AD 6.5 times more than non-carriers do (OR= 6.566, 95% CI= 2.89–14.92). It has been reported that ε4 allele acts in dose- age-dependent manner but we have shown that the risk of developing AD in male APOE -ε4 allele carriers is higher than that of female ε4 carriers. Tehran University of Medical Sciences 2010-06-30 /pmc/articles/PMC3481764/ /pubmed/23112999 Text en Copyright © Iranian Public Health Association & Tehran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0), which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Gozalpour, E
Kamali, K
Mohammd, K
Khorshid, HR Khorram
Ohadi, M
Karimloo, M
Mirabzadeh, A
Fotouhi, A
Association between Alzheimer’s Disease and Apolipoprotein E Polymorphisms
title Association between Alzheimer’s Disease and Apolipoprotein E Polymorphisms
title_full Association between Alzheimer’s Disease and Apolipoprotein E Polymorphisms
title_fullStr Association between Alzheimer’s Disease and Apolipoprotein E Polymorphisms
title_full_unstemmed Association between Alzheimer’s Disease and Apolipoprotein E Polymorphisms
title_short Association between Alzheimer’s Disease and Apolipoprotein E Polymorphisms
title_sort association between alzheimer’s disease and apolipoprotein e polymorphisms
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481764/
https://www.ncbi.nlm.nih.gov/pubmed/23112999
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