Functional significance of CD14 promoter polymorphisms and their clinical relevance in a Chinese Han population

被引:29
作者
Gu, Wei [1 ]
Dong, Hong [1 ]
Jiang, Dong-Po [1 ]
Zhou, Jian [1 ]
Du, Ding-Yuan [2 ]
Gao, Jin-Mou [2 ]
Yao, Yuan-Zhang [1 ]
Zhang, Lian-Yang [1 ]
Wen, Ai-Qing [1 ]
Liu, Qing [1 ]
Wang, Zheng-Guo [1 ]
Jiang, Jian-Xin [1 ]
机构
[1] Third Mil Med Univ, Daping Hosp, Inst Surg Res, State Key Lab Trauma, Chongqing, Peoples R China
[2] Chongqing Emergency Med Ctr, Chongqing, Peoples R China
关键词
CD14; gene polymorphisms; functional study; trauma; multiple organ dysfunction; sepsis;
D O I
10.1097/CCM.0b013e318180b1ed
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective. Several polymorphisms in the CD14 promoter have been reported to be associated with various inflammatory diseases. However, conflicting results have been shown in association studies in different populations. This study aimed to investigate the possible functional significance of both the G-1145A and T-159C polymorphisms in the CD14 promoter and their association with organ dysfunction and sepsis in adult trauma patients. Design: Genetic, functional, and association studies. Setting: National Key Laboratory of Trauma and Departments of Traumatic Surgery in two teaching hospitals. Subjects. Three hundred twenty-five healthy volunteers and 105 patients with major trauma. Interventions: None. Measurements and Main Results: Among the five single nucleotide polymorphisms identified within CD14 promoter in a Chinese Han population, two single nucleotide polymorphisms (G-1145A and T-159C) were selected according to bioinformatics analysis. Promoter activity Of polymorphisms was determined using the reporter gene assay. Plasma sCD14 and tumor necrosis factor-alpha levels were measured by enzyme-linked immunosorbent assay. Both single nucleotide polymorphisms significantly reduced transcriptional activity of the promoter, and were significantly associated with a decrease of inducible sCD14 and tumor necrosis factor-alpha production in an allele-dose effect. Moreover, trauma patients carrying the - 1145 A or - 159 C allele appeared to have a decreased risk of multiple organ dysfunction and sepsis. In addition, both polymorphisms had a marked synergistic effect. Conclusions: The CD14/-1145 and -159 polymorphisms are functional variants, which may function in a synergistic fashion, and could be used as biological risk predictors of multiorgan dysfunction and sepsis in trauma patients.
引用
收藏
页码:2274 / 2280
页数:7
相关论文
共 65 条
[1]  
[Anonymous], ABBR INJ SCAL 1998 R
[2]   Genetic polymorphisms and sepsis [J].
Arcaroli, J ;
Fessler, MB ;
Abraham, E .
SHOCK, 2005, 24 (04) :300-312
[3]   Tandemly repeated DNA: Why should anyone care? [J].
Armour, John A. L. .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2006, 598 (1-2) :6-14
[4]   A polymorphism* in the 5′ flanking region of the CD14 gene is associated with circulating soluble CD14 levels and with total serum immunoglobulin E [J].
Baldini, M ;
Lohman, IC ;
Halonen, M ;
Erickson, RP ;
Holt, PG ;
Martinez, FD .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 20 (05) :976-983
[5]   Increased serum concentration of soluble CD14 is a prognostic marker in gram-positive sepsis [J].
Burgmann, H ;
Winkler, S ;
Locker, GJ ;
Presterl, E ;
Laczika, K ;
Staudinger, T ;
Knapp, S ;
Thalhammer, F ;
Wenisch, C ;
ZedwitzLiebenstein, K ;
Frass, M ;
Graninger, W .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1996, 80 (03) :307-310
[6]   Early elevation of soluble CD14 may help identify trauma patients at high risk for infection [J].
Carrillo, EH ;
Gordon, L ;
Goode, E ;
Davis, E ;
Polk, HC .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 2001, 50 (05) :810-815
[7]   CD14 promoter polymorphism in Chinese alcoholic patients with cirrhosis of liver and acute pancreatitis [J].
Chao, You-Chen ;
Chu, Heng-Cheng ;
Chang, Wei-Kuo ;
Huang, Hsin-Hung ;
Hsieh, Tsai-Yuan .
WORLD JOURNAL OF GASTROENTEROLOGY, 2005, 11 (38) :6043-6048
[8]   CD14-dependent alterations in c-Jun expression in the liver after burn injury [J].
Cho, K ;
Adamson, LK ;
Jeong, J ;
Crivello, SD ;
Vanhook, TG ;
Palmieri, T ;
Greenhalgh, DG .
JOURNAL OF SURGICAL RESEARCH, 2004, 122 (01) :36-42
[9]   Peptidoglycan recognition in innate immunity [J].
Dziarski, R ;
Gupta, D .
JOURNAL OF ENDOTOXIN RESEARCH, 2005, 11 (05) :304-310
[10]   Differences in the expression of LPS-receptors are not responsible for the sex-specific immune response after trauma and hemorrhagic shock [J].
Elsenmenger, SJ ;
Wichmann, MW ;
Angele, P ;
Faist, E ;
Hatz, R ;
Chaudry, IH ;
Jauch, KW ;
Angele, MK .
CELLULAR IMMUNOLOGY, 2004, 230 (01) :17-22