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Biochemical and Biophysical Research Communications
Volume 346, Issue 4, 11 August 2006, Pages 1303-1306
 
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doi:10.1016/j.bbrc.2006.06.048    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2006 Elsevier Inc. All rights reserved.

Paraoxonase-1 expression is up-regulated in Down syndrome fetal liver

Nathalie Janela, Corresponding Author Contact Information, E-mail The Corresponding Author, Olivier Christopheb, Emilie Aït Yahya-Graisona, c, Julien Hameleta, Evelyne Palya, Marguerite Prieurd, Anne-Lise Delezoïdee and Jean Maurice Delabara

aEA 3508, Université Paris 7—Denis Diderot, Paris, France bINSERM U770, hôpital du Kremlin-Bicêtre, Le Kremlin-Bicêtre, France cNeurobiologie et diversité cellulaire, UMR 7637, ESPCI, Paris, France dService de cytogénétique, hôpital Necker, Paris, France eService de biologie du Développement, hôpital Robert Debré, Paris, France

Received 23 May 2006. 
Available online 16 June 2006.

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Abstract

Patients with Down syndrome appear to be protected from the development of atherosclerosis. On the contrary, hyperhomocysteinemia is associated with an increased risk for atherosclerosis. As hyperhomocysteinemia due to cystathionine β synthase deficiency is associated with a decreased expression of paraoxonase-1, a major anti-atherosclerotic component secreted by the liver, we aimed to analyze the expression of paraoxonase-1 and cystathionine β synthase in Down syndrome fetal liver by quantitative real-time reverse transcriptase-polymerase chain reaction. Paraoxonase-1 was up-regulated in Down syndrome fetal liver, while cystathionine β synthase gene expression in Down syndrome fetuses was similar to the gene level in control fetuses. Moreover, there was no evidence for an association between paraoxonase-1 genotypes influencing paraoxonase-1 gene expression and Down syndrome. Since most serum paraoxonase-1 is synthesized in the liver, an increase of hepatic paraoxonase-1 expression might be one of the factors which could explain the low incidence of atherosclerotic vascular disease in Down syndrome.

Keywords: Down syndrome; Paraoxonase-1; Liver; Fetus; Gene expression; Polymorphisms

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