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丝裂原活化蛋白激酶激活蛋白1基因(MAPKAP1)rs10118570多态性与日本血吸虫病的抗感染及抗肝纤维化作用相关。

MAPKAP1 rs10118570 polymorphism is associated with anti-infection and anti-hepatic fibrogenesis in schistosomiasis japonica.

作者信息

Zhu Xiao, Zhang Jinfang, Fan Wenguo, Gong Yunguo, Yan Jianhua, Yuan Zhidong, Wu Lang, Cui Hongjing, Luo Haiqing, Kong Qingming, Tang Li, Leng Shuilong, Liao Yufeng, Fu Weiming, Xiao Qin, Li Dongpei

机构信息

Guangdong Province Key Laboratory of Medical Molecular Diagnosis, Department of Clinical Oncology, Guangdong Medical College, Zhanjiang/Dongguan, China; Peking University Shenzhen Hospital, Shenzhen Peking University - The Hong Kong University of Science and Technology Medical Center, Shenzhen, China.

Department of Orthopaedics & Traumatology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.

出版信息

PLoS One. 2014 Aug 25;9(8):e105995. doi: 10.1371/journal.pone.0105995. eCollection 2014.

Abstract

Chronic infection with Schistosoma japonicum is an important cause of hepatic fibrosis (HF). Human 9q33.3 is one of the most important loci for stress-related diseases. We examined the potential associations of 43 single-nucleotide polymorphisms (SNPs) with S. japonicum infection and HF in epidemic region in China. We identified a SNP (rs10118570 GG in mitogen-activated protein kinase associated protein 1, MAPKAP1) contributes to anti-infection (adjusted OR = 0.35) and anti-fibrogenesis (adjusted RR = 0.44) in the discovery study. Replicative and combined studies showed consistent protective quality for this genotype (replicative: adjusted OR = 0.37 for anti-infection, and adjusted RR = 0.40 for anti-fibrogenesis; Combined: adjusted OR = 0.45 for anti-infection, and adjusted RR = 0.42 for anti-fibrogenesis). Univariate and multivariate analysis in the discovery, replicative and combined studies, suggested that durations (years), splenomegaly, serum ALB and rs10118570 were independent predictors influencing the fibrogenesis. The analysis of gene-gene interaction showed rs10118570 functions independently. We conclude that MAPKAP1 may represent a novel anti-infection and anti-fibrogenesis genomic locus in chronic schistosomiasis japonica. And rs10118570 may be a potential biomarker and target for the treatment of this life-threatening ancient disease.

摘要

日本血吸虫慢性感染是肝纤维化(HF)的重要病因。人类9q33.3是与应激相关疾病最重要的基因座之一。我们在中国流行地区研究了43个单核苷酸多态性(SNP)与日本血吸虫感染及肝纤维化的潜在关联。我们在发现研究中鉴定出一个SNP(丝裂原活化蛋白激酶相关蛋白1,MAPKAP1中的rs10118570 GG)有助于抗感染(校正OR = 0.35)和抗纤维化(校正RR = 0.44)。重复和综合研究显示该基因型具有一致的保护作用(重复研究:抗感染校正OR = 0.37,抗纤维化校正RR = 0.40;综合研究:抗感染校正OR = 0.45,抗纤维化校正RR = 0.42)。在发现、重复和综合研究中的单变量和多变量分析表明,病程(年)、脾肿大、血清白蛋白和rs10118570是影响纤维化的独立预测因素。基因-基因相互作用分析显示rs10118570独立发挥作用。我们得出结论,MAPKAP1可能是日本血吸虫病慢性感染中一个新的抗感染和抗纤维化基因组位点。并且rs10118570可能是这种威胁生命的古老疾病治疗的潜在生物标志物和靶点。

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