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rs3764435 Associated With Parkinson's Disease in Mexican Mestizos: Case-Control Study Reveals Protective Effects Against Disease Development and Cognitive Impairment

Parkinson's disease (PD) is the second most common movement disorder. Genetic risk factors provide information about the pathophysiology of PD that could potentially be used as biomarkers. The ALDH1A1 gene encodes for the aldehyde dehydrogenase enzyme, which is involved in the disposal of toxic...

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Autores principales: Salas-Leal, Alma C., Sandoval-Carrillo, Ada, Romero-Gutiérrez, Elizabeth, Castellanos-Juárez, Francisco X., Méndez-Hernández, Edna M., La Llave-León, Osmel, Quiñones-Canales, Gerardo, Arias-Carrión, Oscar, Salas-Pacheco, José M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794556/
https://www.ncbi.nlm.nih.gov/pubmed/31649613
http://dx.doi.org/10.3389/fneur.2019.01066
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author Salas-Leal, Alma C.
Sandoval-Carrillo, Ada
Romero-Gutiérrez, Elizabeth
Castellanos-Juárez, Francisco X.
Méndez-Hernández, Edna M.
La Llave-León, Osmel
Quiñones-Canales, Gerardo
Arias-Carrión, Oscar
Salas-Pacheco, José M.
author_facet Salas-Leal, Alma C.
Sandoval-Carrillo, Ada
Romero-Gutiérrez, Elizabeth
Castellanos-Juárez, Francisco X.
Méndez-Hernández, Edna M.
La Llave-León, Osmel
Quiñones-Canales, Gerardo
Arias-Carrión, Oscar
Salas-Pacheco, José M.
author_sort Salas-Leal, Alma C.
collection PubMed
description Parkinson's disease (PD) is the second most common movement disorder. Genetic risk factors provide information about the pathophysiology of PD that could potentially be used as biomarkers. The ALDH1A1 gene encodes for the aldehyde dehydrogenase enzyme, which is involved in the disposal of toxic metabolites of dopamine. Due to the cytotoxic nature of aldehydes, their detoxification is essential for cellular homeostasis. It has been reported that ALDH1A1 expression levels and activity are decreased in PD patients. A deficit in ALDH1A1 activity in the substantia nigra, may lead to the accumulation of neurotoxic aldehydes and eventually the cell death seen in PD. One of the single nucleotide polymorphisms (SNP) that may modulate ALDH1A1 activity levels is rs3764435 (A/C). To investigate whether a statistical association exists between PD and the SNP rs3764435, we carried out a population-based Case-Control association study (120 PD patients and 178 non-PD subjects) in Mexican mestizos. DNA was extracted from blood samples and genotyped for rs3764435 using real-time PCR. A significant difference was found between PD cases and controls in both allelic and genotypic frequencies. The calculated OR showed that the C/C genotype is a protective factor under the codominant and recessive models of inheritance. However, after stratifying by sex, the protective role of this genotype is conserved only in men. Also, under the codominant and dominant models, rs3764435 appears to exert a protective effect against cognitive impairment in PD patients. Here for the first time, we show an association between PD and rs3764435 in a Mexican mestizo population, suggesting it confers neuroprotection for dementia in PD and is neuroprotective against developing PD in the males of this population. While analysis of the SNP looks favorable, replication of our study in cell lines or rs3764435 KO mice is required to validate these results.
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spelling pubmed-67945562019-10-24 rs3764435 Associated With Parkinson's Disease in Mexican Mestizos: Case-Control Study Reveals Protective Effects Against Disease Development and Cognitive Impairment Salas-Leal, Alma C. Sandoval-Carrillo, Ada Romero-Gutiérrez, Elizabeth Castellanos-Juárez, Francisco X. Méndez-Hernández, Edna M. La Llave-León, Osmel Quiñones-Canales, Gerardo Arias-Carrión, Oscar Salas-Pacheco, José M. Front Neurol Neurology Parkinson's disease (PD) is the second most common movement disorder. Genetic risk factors provide information about the pathophysiology of PD that could potentially be used as biomarkers. The ALDH1A1 gene encodes for the aldehyde dehydrogenase enzyme, which is involved in the disposal of toxic metabolites of dopamine. Due to the cytotoxic nature of aldehydes, their detoxification is essential for cellular homeostasis. It has been reported that ALDH1A1 expression levels and activity are decreased in PD patients. A deficit in ALDH1A1 activity in the substantia nigra, may lead to the accumulation of neurotoxic aldehydes and eventually the cell death seen in PD. One of the single nucleotide polymorphisms (SNP) that may modulate ALDH1A1 activity levels is rs3764435 (A/C). To investigate whether a statistical association exists between PD and the SNP rs3764435, we carried out a population-based Case-Control association study (120 PD patients and 178 non-PD subjects) in Mexican mestizos. DNA was extracted from blood samples and genotyped for rs3764435 using real-time PCR. A significant difference was found between PD cases and controls in both allelic and genotypic frequencies. The calculated OR showed that the C/C genotype is a protective factor under the codominant and recessive models of inheritance. However, after stratifying by sex, the protective role of this genotype is conserved only in men. Also, under the codominant and dominant models, rs3764435 appears to exert a protective effect against cognitive impairment in PD patients. Here for the first time, we show an association between PD and rs3764435 in a Mexican mestizo population, suggesting it confers neuroprotection for dementia in PD and is neuroprotective against developing PD in the males of this population. While analysis of the SNP looks favorable, replication of our study in cell lines or rs3764435 KO mice is required to validate these results. Frontiers Media S.A. 2019-10-09 /pmc/articles/PMC6794556/ /pubmed/31649613 http://dx.doi.org/10.3389/fneur.2019.01066 Text en Copyright © 2019 Salas-Leal, Sandoval-Carrillo, Romero-Gutiérrez, Castellanos-Juárez, Méndez-Hernández, La Llave-León, Quiñones-Canales, Arias-Carrión and Salas-Pacheco. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Salas-Leal, Alma C.
Sandoval-Carrillo, Ada
Romero-Gutiérrez, Elizabeth
Castellanos-Juárez, Francisco X.
Méndez-Hernández, Edna M.
La Llave-León, Osmel
Quiñones-Canales, Gerardo
Arias-Carrión, Oscar
Salas-Pacheco, José M.
rs3764435 Associated With Parkinson's Disease in Mexican Mestizos: Case-Control Study Reveals Protective Effects Against Disease Development and Cognitive Impairment
title rs3764435 Associated With Parkinson's Disease in Mexican Mestizos: Case-Control Study Reveals Protective Effects Against Disease Development and Cognitive Impairment
title_full rs3764435 Associated With Parkinson's Disease in Mexican Mestizos: Case-Control Study Reveals Protective Effects Against Disease Development and Cognitive Impairment
title_fullStr rs3764435 Associated With Parkinson's Disease in Mexican Mestizos: Case-Control Study Reveals Protective Effects Against Disease Development and Cognitive Impairment
title_full_unstemmed rs3764435 Associated With Parkinson's Disease in Mexican Mestizos: Case-Control Study Reveals Protective Effects Against Disease Development and Cognitive Impairment
title_short rs3764435 Associated With Parkinson's Disease in Mexican Mestizos: Case-Control Study Reveals Protective Effects Against Disease Development and Cognitive Impairment
title_sort rs3764435 associated with parkinson's disease in mexican mestizos: case-control study reveals protective effects against disease development and cognitive impairment
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794556/
https://www.ncbi.nlm.nih.gov/pubmed/31649613
http://dx.doi.org/10.3389/fneur.2019.01066
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