Literature DB >> 24140479

Impact of endothelial nitric oxide synthase gene polymorphism on severity of enterovirus 71-infection in Chinese children.

Ji-an Li1, Zong-bo Chen, Tie-gang Lv, Zhen-liang Han, Pei-pei Liu.   

Abstract

OBJECTIVES: Genetic polymorphism G894T on the endothelial nitric oxide synthase (eNOS) gene has been reported as a susceptibility factor in a number of diseases, but evidence of its effect on enterovirus 71 (EV71) infection is lacking. This study investigated the possible association between this polymorphism (rs1799983) and disease severity in Chinese children with EV71 infection. DESIGN AND METHODS: 185 children with EV71 infection (83 with severe and 102 with mild disease) and 234 control healthy children underwent testing with polymerase chain reaction-restriction fragment length polymorphism (PCR-RLFP) to detect G894T polymorphism. In addition, plasma levels of nitric oxide (NO), interleukin 1 beta (IL-1β), interleukin 6 (IL-6), and tumor necrosis factor-alpha (TNF-α) and serum eNOS activity were measured according to genotype.
RESULTS: The presence of GT+TT genotypes and T allele were associated with severe cases compared to genotype GG (OR 2.5, 95% CI 1.2-5.3, P=0.017) and G (OR 2.4, 95% CI 1.2-4.8, P=0.011). Furthermore, in EV71 encephalitis, GT+TT genotype and T allele were also more frequent than GG and G (P<0.05). The NO level and eNOS activity in T carriers (GT+TT) (84.3±2.5μmol/L and 14.4±1.8U/mL) were significantly less compared to in G carriers (GG) (92.0±1.5μmol/L and 19.1±1.7U/mL, P<0.001). But T carriers had higher plasma levels of IL-1β, IL-6, and TNF-α than people without a T allele (P<0.001), and a significant negative correlation was observed between NO and cytokine levels.
CONCLUSION: The results indicate that carrying the T allele of the eNOS G894T gene polymorphism was associated with EV71 infection, and could be a susceptibility factor in the development of EV71 infection in Chinese children.
© 2013.

Entities:  

Keywords:  Cytokines; Endothelial nitric oxide synthase; Enterovirus 71; Gene polymorphism

Mesh:

Substances:

Year:  2013        PMID: 24140479     DOI: 10.1016/j.clinbiochem.2013.10.009

Source DB:  PubMed          Journal:  Clin Biochem        ISSN: 0009-9120            Impact factor:   3.281


  4 in total

1.  Association of Chemotactic Chemokine Ligand 5 Polymorphisms with the Risk of Developing Severe Enterovirus 71 Infection.

Authors:  Mao-Zhong Li; Li-Li Pang; Ai-Ying Bai; Shi-Cheng Yu; Xun Gong; Na Liu; Kun Cai; Guang-Cheng Xie; Wen-Juan Gao; Yu Jin; Zhao-Jun Duan
Journal:  Am J Trop Med Hyg       Date:  2015-08-24       Impact factor: 2.345

2.  Elevated expression of circulating miR876-5p is a specific response to severe EV71 infections.

Authors:  Robert Y L Wang; Kuo-Feng Weng; Yhu-Chering Huang; Chih-Jung Chen
Journal:  Sci Rep       Date:  2016-04-07       Impact factor: 4.379

3.  A functional polymorphism in IFNAR1 gene is associated with susceptibility and severity of HFMD with EV71 infection.

Authors:  Rongrong Zou; Guoliang Zhang; Shaoyuan Li; Wenfei Wang; Jing Yuan; Jianming Li; Yanrong Wang; Yimin Lin; Yong Deng; Boping Zhou; George Fu Gao; Yingxia Liu
Journal:  Sci Rep       Date:  2015-12-18       Impact factor: 4.379

Review 4.  Immunocompetent and Immunodeficient Mouse Models for Enterovirus 71 Pathogenesis and Therapy.

Authors:  Chiaho Shih; Chun-Che Liao; Ya-Shu Chang; Szu-Yao Wu; Chih-Shin Chang; An-Ting Liou
Journal:  Viruses       Date:  2018-11-28       Impact factor: 5.048

  4 in total

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