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Impact of Genetic Variants of Apolipoprotein E on Lipid Profile in Patients with Parkinson's Disease

Identifieur interne : 000117 ( Main/Merge ); précédent : 000116; suivant : 000118

Impact of Genetic Variants of Apolipoprotein E on Lipid Profile in Patients with Parkinson's Disease

Auteurs : Michele Greg [Brésil] ; Marcela Pinhel [Brésil] ; Caroline Sado [Brésil] ; Gabriela Longo [Brésil] ; Fábio Oliveira [Brésil] ; Gisele Amorim [Brésil] ; Marcelo Nakazone [Brésil] ; Greiciane Florim [Brésil] ; Camila Mazeti [Brésil] ; Denise Martins [Brésil] ; Waldir Tognola [Brésil] ; Antonio Brandão [Brésil] ; Sidney Júnior [Brésil] ; Moacir De [Brésil] ; Dorotéia Souza [Brésil]

Source :

RBID : PMC:3794554

Abstract

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.


Url:
DOI: 10.1155/2013/641515
PubMed: 24175296
PubMed Central: 3794554

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PMC:3794554

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<name sortKey="De Godoy, Moacir F" sort="De Godoy, Moacir F" uniqKey="De Godoy M" first="Moacir" last="De">Moacir De</name>
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<name sortKey="Souza, Doroteia R S" sort="Souza, Doroteia R S" uniqKey="Souza D" first="Dorotéia" last="Souza">Dorotéia Souza</name>
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<name sortKey="Pinhel, Marcela A S" sort="Pinhel, Marcela A S" uniqKey="Pinhel M" first="Marcela" last="Pinhel">Marcela Pinhel</name>
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<name sortKey="Sado, Caroline L" sort="Sado, Caroline L" uniqKey="Sado C" first="Caroline" last="Sado">Caroline Sado</name>
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<nlm:aff id="I3">Federal University of São Paulo (UNIFESP), 04021001 São Paulo, SP, Brazil</nlm:aff>
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<name sortKey="Oliveira, Fabio N" sort="Oliveira, Fabio N" uniqKey="Oliveira F" first="Fábio" last="Oliveira">Fábio Oliveira</name>
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<nlm:aff id="I4">Hospital de Base, 15090000 Sao Jose do Rio Preto, SP, Brazil</nlm:aff>
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<name sortKey="Nakazone, Marcelo A" sort="Nakazone, Marcelo A" uniqKey="Nakazone M" first="Marcelo" last="Nakazone">Marcelo Nakazone</name>
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<name sortKey="Florim, Greiciane M" sort="Florim, Greiciane M" uniqKey="Florim G" first="Greiciane" last="Florim">Greiciane Florim</name>
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<name sortKey="Martins, Denise P" sort="Martins, Denise P" uniqKey="Martins D" first="Denise" last="Martins">Denise Martins</name>
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<country xml:lang="fr">Brésil</country>
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<name sortKey="Tognola, Waldir A" sort="Tognola, Waldir A" uniqKey="Tognola W" first="Waldir" last="Tognola">Waldir Tognola</name>
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<nlm:aff id="I6">Department of Neuroscience/Molecular Biology, Sao Jose do Rio Preto Medical School (FAMERP), 15090000 Sao Jose do Rio Preto, SP, Brazil</nlm:aff>
<country xml:lang="fr">Brésil</country>
<wicri:regionArea>Department of Neuroscience/Molecular Biology, Sao Jose do Rio Preto Medical School (FAMERP), 15090000 Sao Jose do Rio Preto, SP</wicri:regionArea>
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<region type="state">État de São Paulo</region>
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<name sortKey="Brandao, Antonio C" sort="Brandao, Antonio C" uniqKey="Brandao A" first="Antonio" last="Brandão">Antonio Brandão</name>
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<nlm:aff id="I6">Department of Neuroscience/Molecular Biology, Sao Jose do Rio Preto Medical School (FAMERP), 15090000 Sao Jose do Rio Preto, SP, Brazil</nlm:aff>
<country xml:lang="fr">Brésil</country>
<wicri:regionArea>Department of Neuroscience/Molecular Biology, Sao Jose do Rio Preto Medical School (FAMERP), 15090000 Sao Jose do Rio Preto, SP</wicri:regionArea>
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<region type="state">État de São Paulo</region>
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<name sortKey="Junior, Sidney Pinheiro" sort="Junior, Sidney Pinheiro" uniqKey="Junior S" first="Sidney" last="Júnior">Sidney Júnior</name>
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<nlm:aff id="I7">Department of Molecular Biology, Sao Jose do Rio Preto Medical School—FAMERP, 15090000 Sao Jose do Rio Preto, SP, Brazil</nlm:aff>
<country xml:lang="fr">Brésil</country>
<wicri:regionArea>Department of Molecular Biology, Sao Jose do Rio Preto Medical School—FAMERP, 15090000 Sao Jose do Rio Preto, SP</wicri:regionArea>
<placeName>
<region type="state">État de São Paulo</region>
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<author>
<name sortKey="De Godoy, Moacir F" sort="De Godoy, Moacir F" uniqKey="De Godoy M" first="Moacir" last="De">Moacir De</name>
<affiliation wicri:level="2">
<nlm:aff id="I4">Hospital de Base, 15090000 Sao Jose do Rio Preto, SP, Brazil</nlm:aff>
<country xml:lang="fr">Brésil</country>
<wicri:regionArea>Hospital de Base, 15090000 Sao Jose do Rio Preto, SP</wicri:regionArea>
<placeName>
<region type="state">État de São Paulo</region>
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<author>
<name sortKey="Souza, Doroteia R S" sort="Souza, Doroteia R S" uniqKey="Souza D" first="Dorotéia" last="Souza">Dorotéia Souza</name>
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<nlm:aff id="I3">Federal University of São Paulo (UNIFESP), 04021001 São Paulo, SP, Brazil</nlm:aff>
<country xml:lang="fr">Brésil</country>
<wicri:regionArea>Federal University of São Paulo (UNIFESP), 04021001 São Paulo, SP</wicri:regionArea>
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<region type="state">État de São Paulo</region>
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<series>
<title level="j">BioMed Research International</title>
<idno type="ISSN">2314-6133</idno>
<idno type="e-ISSN">2314-6141</idno>
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<div type="abstract" xml:lang="en">
<p>The pathogenesis of Parkinson's disease (PD) seems to involve genetic susceptibility to neurodegeneration.
<italic>APOE</italic>
gene has been considered a risk factor for PD. This study aimed to evaluate the association of
<italic>APOE</italic>
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
<italic>t</italic>
-test (
<italic>P</italic>
< 0.05) were applied. The
<italic>APOE3/3</italic>
genotype was prevalent in PD patients and Controls (
<italic>P</italic>
= 0.713) followed by
<italic>APOE3/4</italic>
(
<italic>P</italic>
= 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 (
<italic>P</italic>
< 0.05 for all of them). Increased levels of HDLc, in PD patients, were associated with the
<italic>APOE3/3</italic>
versus
<italic>APOE-/4</italic>
genotypes (
<italic>P</italic>
= 0.012). The
<italic>APOE </italic>
polymorphism does not distinguish PD patients from Controls, as opposed to the lipid profile alone or in association with
<italic>APOE</italic>
. Furthermore, a relationship between increase of HDLc levels and
<italic>APOE3</italic>
in homozygous was found in PD patients only.</p>
</div>
</front>
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