Apolipoprotein A5-1131T>C polymorphism, but not APOE genotypes, increases susceptibility for dyslipidemia in children and adolescents

Apolipoprotein A5 (APOA5) and apolipoprotein E (APOE) play important roles in the metabolism of cholesterol and triglycerides. The aim of this study was to determine the allelic and genotypic distributions of the APOA5 - 1131T > C (rs 662799) and the APOE Hha I polymorphisms and to identify the a...

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Veröffentlicht in:Molecular biology reports 2011-10, Vol.38 (7), p.4381-4388
Hauptverfasser: Brito, D. D. V., Fernandes, A. P., Gomes, K. B., Coelho, F. F., Cruz, N. G., Sabino, A. P., Cardoso, J. E., Figueiredo-Filho, P. P., Diamante, R., Norton, C. R., Sousa, M. O.
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container_end_page 4388
container_issue 7
container_start_page 4381
container_title Molecular biology reports
container_volume 38
creator Brito, D. D. V.
Fernandes, A. P.
Gomes, K. B.
Coelho, F. F.
Cruz, N. G.
Sabino, A. P.
Cardoso, J. E.
Figueiredo-Filho, P. P.
Diamante, R.
Norton, C. R.
Sousa, M. O.
description Apolipoprotein A5 (APOA5) and apolipoprotein E (APOE) play important roles in the metabolism of cholesterol and triglycerides. The aim of this study was to determine the allelic and genotypic distributions of the APOA5 - 1131T > C (rs 662799) and the APOE Hha I polymorphisms and to identify the association of both individual and combined APOA5 – APOE genetic variants and the risk for dyslipidemia in children and adolescents. We genotyped 53 dyslipidemic and 77 normolipidemic individuals. The total cholesterol, triglycerides and HDL cholesterol were determined enzymatically. For APOA5 polymorphism, the presence of the allele C confers an individual risk for dyslipidemia (OR = 2.38, 95% CI = 1.15–4.89; P  = 0.018). No significant differences were observed for lipid parameters among the APOA5 groups, except for a higher value of HDLc ( P  = 0.024) in C-carriers. The allelic and genotypic frequencies of APOE polymorphism were similar between groups and did not increase the susceptibility for dyslipidemia. None of the combined APOA5 – APOE polymorphisms increased risk for dyslipidemia. We demonstrated an association between APOA5 - 1131T > C polymorphism and dyslipidemia in children and adolescents. This finding may be useful to guide new studies with genetic markers down a path toward a better characterization of the genetic risk factors for dyslipidemia and atherosclerotic diseases.
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D. V. ; Fernandes, A. P. ; Gomes, K. B. ; Coelho, F. F. ; Cruz, N. G. ; Sabino, A. P. ; Cardoso, J. E. ; Figueiredo-Filho, P. P. ; Diamante, R. ; Norton, C. R. ; Sousa, M. O.</creator><creatorcontrib>Brito, D. D. V. ; Fernandes, A. P. ; Gomes, K. B. ; Coelho, F. F. ; Cruz, N. G. ; Sabino, A. P. ; Cardoso, J. E. ; Figueiredo-Filho, P. P. ; Diamante, R. ; Norton, C. R. ; Sousa, M. O.</creatorcontrib><description>Apolipoprotein A5 (APOA5) and apolipoprotein E (APOE) play important roles in the metabolism of cholesterol and triglycerides. The aim of this study was to determine the allelic and genotypic distributions of the APOA5 - 1131T &gt; C (rs 662799) and the APOE Hha I polymorphisms and to identify the association of both individual and combined APOA5 – APOE genetic variants and the risk for dyslipidemia in children and adolescents. We genotyped 53 dyslipidemic and 77 normolipidemic individuals. The total cholesterol, triglycerides and HDL cholesterol were determined enzymatically. For APOA5 polymorphism, the presence of the allele C confers an individual risk for dyslipidemia (OR = 2.38, 95% CI = 1.15–4.89; P  = 0.018). No significant differences were observed for lipid parameters among the APOA5 groups, except for a higher value of HDLc ( P  = 0.024) in C-carriers. The allelic and genotypic frequencies of APOE polymorphism were similar between groups and did not increase the susceptibility for dyslipidemia. None of the combined APOA5 – APOE polymorphisms increased risk for dyslipidemia. We demonstrated an association between APOA5 - 1131T &gt; C polymorphism and dyslipidemia in children and adolescents. 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D. V.</au><au>Fernandes, A. P.</au><au>Gomes, K. B.</au><au>Coelho, F. F.</au><au>Cruz, N. G.</au><au>Sabino, A. P.</au><au>Cardoso, J. E.</au><au>Figueiredo-Filho, P. P.</au><au>Diamante, R.</au><au>Norton, C. R.</au><au>Sousa, M. O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Apolipoprotein A5-1131T&gt;C polymorphism, but not APOE genotypes, increases susceptibility for dyslipidemia in children and adolescents</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><addtitle>Mol Biol Rep</addtitle><date>2011-10-01</date><risdate>2011</risdate><volume>38</volume><issue>7</issue><spage>4381</spage><epage>4388</epage><pages>4381-4388</pages><issn>0301-4851</issn><eissn>1573-4978</eissn><abstract>Apolipoprotein A5 (APOA5) and apolipoprotein E (APOE) play important roles in the metabolism of cholesterol and triglycerides. The aim of this study was to determine the allelic and genotypic distributions of the APOA5 - 1131T &gt; C (rs 662799) and the APOE Hha I polymorphisms and to identify the association of both individual and combined APOA5 – APOE genetic variants and the risk for dyslipidemia in children and adolescents. We genotyped 53 dyslipidemic and 77 normolipidemic individuals. The total cholesterol, triglycerides and HDL cholesterol were determined enzymatically. For APOA5 polymorphism, the presence of the allele C confers an individual risk for dyslipidemia (OR = 2.38, 95% CI = 1.15–4.89; P  = 0.018). No significant differences were observed for lipid parameters among the APOA5 groups, except for a higher value of HDLc ( P  = 0.024) in C-carriers. The allelic and genotypic frequencies of APOE polymorphism were similar between groups and did not increase the susceptibility for dyslipidemia. None of the combined APOA5 – APOE polymorphisms increased risk for dyslipidemia. We demonstrated an association between APOA5 - 1131T &gt; C polymorphism and dyslipidemia in children and adolescents. This finding may be useful to guide new studies with genetic markers down a path toward a better characterization of the genetic risk factors for dyslipidemia and atherosclerotic diseases.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>21132386</pmid><doi>10.1007/s11033-010-0565-5</doi><tpages>8</tpages></addata></record>
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subjects Adolescent
Animal Anatomy
Animal Biochemistry
Apolipoprotein A-V
Apolipoproteins
Apolipoproteins A - genetics
Apolipoproteins E - genetics
Biomedical and Life Sciences
Child
Children & youth
Demography
Dyslipidemias - blood
Dyslipidemias - genetics
Female
Gene Frequency - genetics
Genetic Association Studies
Genetic Predisposition to Disease
Genotype & phenotype
Histology
Humans
Life Sciences
Lipids
Lipids - blood
Male
Molecular biology
Morphology
Polymorphism
Polymorphism, Single Nucleotide - genetics
Teenagers
Young Adult
title Apolipoprotein A5-1131T>C polymorphism, but not APOE genotypes, increases susceptibility for dyslipidemia in children and adolescents
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