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Impact of Genetic Variants of Apolipoprotein E on Lipid Profile in Patients with Parkinson's Disease
The pathogenesis of Parkinson's disease (PD) seems to involve genetic susceptibility to neurodegeneration. APOE gene has been considered a risk factor for PD. This study aimed to evaluate the association of APOE polymorphism with PD and its influence on lipid profile. We studied 232 PD patients...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794554/ https://www.ncbi.nlm.nih.gov/pubmed/24175296 http://dx.doi.org/10.1155/2013/641515 |
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author | Gregório, Michele L. Pinhel, Marcela A. S. Sado, Caroline L. Longo, Gabriela S. Oliveira, Fábio N. Amorim, Gisele S. Nakazone, Marcelo A. Florim, Greiciane M. Mazeti, Camila M. Martins, Denise P. Tognola, Waldir A. Brandão, Antonio C. Júnior, Sidney Pinheiro de Godoy, Moacir F. Souza, Dorotéia R. S. |
author_facet | Gregório, Michele L. Pinhel, Marcela A. S. Sado, Caroline L. Longo, Gabriela S. Oliveira, Fábio N. Amorim, Gisele S. Nakazone, Marcelo A. Florim, Greiciane M. Mazeti, Camila M. Martins, Denise P. Tognola, Waldir A. Brandão, Antonio C. Júnior, Sidney Pinheiro de Godoy, Moacir F. Souza, Dorotéia R. S. |
author_sort | Gregório, Michele L. |
collection | PubMed |
description | The pathogenesis of Parkinson's disease (PD) seems to involve genetic susceptibility to neurodegeneration. APOE gene has been considered a risk factor for PD. This study aimed to evaluate the association of APOE polymorphism with PD and its influence on lipid profile. We studied 232 PD patients (PD) and 169 individuals without the disease. The studied polymorphism was analyzed by PCR/RFLP. The Fisher's exact test, chi-square, ANOVA, and t-test (P < 0.05) were applied. The APOE3/3 genotype was prevalent in PD patients and Controls (P = 0.713) followed by APOE3/4 (P = 0.772). Both groups showed recommended values for lipid profile, with increase in the values of total cholesterol and LDLc, as well as decreased values of triglycerides in PD patients compared with Controls (P < 0.05 for all of them). Increased levels of HDLc, in PD patients, were associated with the APOE3/3 versus APOE-/4 genotypes (P = 0.012). The APOE polymorphism does not distinguish PD patients from Controls, as opposed to the lipid profile alone or in association with APOE. Furthermore, a relationship between increase of HDLc levels and APOE3 in homozygous was found in PD patients only. |
format | Online Article Text |
id | pubmed-3794554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-37945542013-10-30 Impact of Genetic Variants of Apolipoprotein E on Lipid Profile in Patients with Parkinson's Disease Gregório, Michele L. Pinhel, Marcela A. S. Sado, Caroline L. Longo, Gabriela S. Oliveira, Fábio N. Amorim, Gisele S. Nakazone, Marcelo A. Florim, Greiciane M. Mazeti, Camila M. Martins, Denise P. Tognola, Waldir A. Brandão, Antonio C. Júnior, Sidney Pinheiro de Godoy, Moacir F. Souza, Dorotéia R. S. Biomed Res Int Clinical Study The pathogenesis of Parkinson's disease (PD) seems to involve genetic susceptibility to neurodegeneration. APOE gene has been considered a risk factor for PD. This study aimed to evaluate the association of APOE polymorphism with PD and its influence on lipid profile. We studied 232 PD patients (PD) and 169 individuals without the disease. The studied polymorphism was analyzed by PCR/RFLP. The Fisher's exact test, chi-square, ANOVA, and t-test (P < 0.05) were applied. The APOE3/3 genotype was prevalent in PD patients and Controls (P = 0.713) followed by APOE3/4 (P = 0.772). Both groups showed recommended values for lipid profile, with increase in the values of total cholesterol and LDLc, as well as decreased values of triglycerides in PD patients compared with Controls (P < 0.05 for all of them). Increased levels of HDLc, in PD patients, were associated with the APOE3/3 versus APOE-/4 genotypes (P = 0.012). The APOE polymorphism does not distinguish PD patients from Controls, as opposed to the lipid profile alone or in association with APOE. Furthermore, a relationship between increase of HDLc levels and APOE3 in homozygous was found in PD patients only. Hindawi Publishing Corporation 2013 2013-09-24 /pmc/articles/PMC3794554/ /pubmed/24175296 http://dx.doi.org/10.1155/2013/641515 Text en Copyright © 2013 Michele L. Gregório et al. https://creativecommons.org/licenses/by/3.0/ 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. |
spellingShingle | Clinical Study Gregório, Michele L. Pinhel, Marcela A. S. Sado, Caroline L. Longo, Gabriela S. Oliveira, Fábio N. Amorim, Gisele S. Nakazone, Marcelo A. Florim, Greiciane M. Mazeti, Camila M. Martins, Denise P. Tognola, Waldir A. Brandão, Antonio C. Júnior, Sidney Pinheiro de Godoy, Moacir F. Souza, Dorotéia R. S. Impact of Genetic Variants of Apolipoprotein E on Lipid Profile in Patients with Parkinson's Disease |
title | Impact of Genetic Variants of Apolipoprotein E on Lipid Profile in Patients with Parkinson's Disease |
title_full | Impact of Genetic Variants of Apolipoprotein E on Lipid Profile in Patients with Parkinson's Disease |
title_fullStr | Impact of Genetic Variants of Apolipoprotein E on Lipid Profile in Patients with Parkinson's Disease |
title_full_unstemmed | Impact of Genetic Variants of Apolipoprotein E on Lipid Profile in Patients with Parkinson's Disease |
title_short | Impact of Genetic Variants of Apolipoprotein E on Lipid Profile in Patients with Parkinson's Disease |
title_sort | impact of genetic variants of apolipoprotein e on lipid profile in patients with parkinson's disease |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794554/ https://www.ncbi.nlm.nih.gov/pubmed/24175296 http://dx.doi.org/10.1155/2013/641515 |
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