Thromb Haemost 2007; 97(01): 62-66
DOI: 10.1160/TH06-06-0314
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Polymorphism A36G of the tumor necrosis factor receptor 1 gene is associated with PAI-1 levels in obese women

Alenka Mavri
1   Inserm UMR 626 and Université de la Méditerranée, Marseille, France
2   University Medical Centre, Department of Vascular Disease, Ljubljana, Slovenia
,
Delphine Bastelica
1   Inserm UMR 626 and Université de la Méditerranée, Marseille, France
,
Marjorie Poggi
1   Inserm UMR 626 and Université de la Méditerranée, Marseille, France
,
Pierre Morange
1   Inserm UMR 626 and Université de la Méditerranée, Marseille, France
,
Franck Peiretti
1   Inserm UMR 626 and Université de la Méditerranée, Marseille, France
,
Monique Verdier
1   Inserm UMR 626 and Université de la Méditerranée, Marseille, France
,
Irène Juhan-Vague
1   Inserm UMR 626 and Université de la Méditerranée, Marseille, France
,
Marie-Christine Alessi
1   Inserm UMR 626 and Université de la Méditerranée, Marseille, France
› Author Affiliations
Financial support: This work was supported by grants from Institut National de la Santé et de la Recherche Médicale (Inserm), Centre d’Investigation Clinique de Marseille (CIC), and the Ministère de l’Education Nationale, de l’Enseignement Supérieur et de la Recherche (Contrat Quadriennal). A. Mavri was a recipient from the “Fondation pour la Recherche Médicale (accueil de chercheur étranger)”. D. Bastelica was a fellow from the “Association de Langue Française pour l’Etude du Diabète et des Maladies métaboliques / Astra Zeneca”. M. Poggi was a recipient of the “Groupe de Réflexion sur la Recherche Cardiovasculaire”.
Further Information

Publication History

Received 07 June 2006

Accepted after resubmission 14 November 2006

Publication Date:
28 November 2017 (online)

Summary

The tumor necrosis factor (TNF) pathway may be implicated in etiopathogenesis of PAI-1 overexpression during obesity. The aim of this study was to investigate the influence of polymorphismA36G of the TNF receptor 1 (TNFRSF1A +36A/G) on plasma concentrations of PAI-1 in 163 obese (31 with the metabolic syndrome, MetS) and 150 lean, healthy women. Genotypic and allele frequencies did not significantly differ between obese and lean subjects. TNFRSF1A genotypes were significantly associated with sTNFR1 plasma levels in obese women only (p<0.01); TNFRSF1A +36G/G obese carriers exhibited higher sTNFR1 and PAI-1 levels than A carriers (p<0.01 and p<0.05, respectively). In obese women, the presence of the MetS significantly potentiated the elevation of sTNFR1 and PAI-1 levels observed in the TNFRSF1A+36G/G carriers. Our results suggest that association between TNFRSF1A +36G/G genotype and the MetS renders obese women more prone to activation of the TNF pathway reflected by high circulating sTNFR1 and PAI-1 levels.

 
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