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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
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.
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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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