Open Access Research

Identification of haplotype tag single nucleotide polymorphisms within the receptor for advanced glycation end products gene and their clinical relevance in patients with major trauma

Ling Zeng1, An-qiang Zhang1, Wei Gu1, Jian Zhou2, Lian-yang Zhang2, Ding-yuan Du3, Mao Zhang4, Hai-yan Wang1, Jun Yan1, Ce Yang1 and Jian-xin Jiang1*

  • * Corresponding author: Jian-xin Jiang hellojjx@126.com

  • † Equal contributors

Author Affiliations

1 State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Changjiang Road 10, Yuzhong District, Chongqing, 400042, China

2 Department of Traumatic Surgery, Daping Hospital, Third Military Medical University, Changjiang Road 10, Yuzhong District, Chongqing, 400042, China

3 Chongqing Emergency Medical Center, Jiankang Road, Yuzhong District, Chongqing, 400042, China

4 Department of Emergency Medical Center, the Second Affiliated Hospital, Zhejiang University, Jiefang Road 88, Zhejiang, 310009, China

For all author emails, please log on.

Critical Care 2012, 16:R131 doi:10.1186/cc11436

Published: 24 July 2012

Abstract

Introduction

The receptor for advanced glycation end products (RAGE) has been considered as one of the major pattern recognition receptors and plays an important role in the development of sepsis and multiple organ dysfunction in critical illnesses. Although genetic variants of the RAGE gene have been shown to be well associated with susceptibility to some inflammatory diseases, little is known about their clinical relevance in the development of sepsis in critical ill patients.

Methods

Four genetic variants were selected from the entire RAGE gene and genotyped using pyrosequencing and polymerase chain reaction-length polymorphism methods. Association studies were performed in two independent Chinese Han populations.

Results

Among the four genetic variants, only the rs1800625 polymorphism was significantly associated with sepsis morbidity rate and multiple organ dysfunction (MOD) scores in patients with major trauma both in Chongqing (n = 496) and Zhejiang (n = 232) districts, respectively. Results from ex vivo responsiveness of peripheral blood leukocytes indicated that the rs1800625 polymorphism was well associated with decreased production of TNFα. In addition, the rs1800625 polymorphism could significantly inhibit the promoter activities of the RAGE gene.

Conclusions

The rs1800625 polymorphism is a functional variant, which might be used as a relevant risk estimate for the development of sepsis and multiple organ dysfunction syndrome in patients with major trauma.