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中国人群中胃饥饿素基因多态性及血清胃饥饿素水平与乙型肝炎病毒相关肝病风险的关联

Association of Ghrelin Gene Polymorphisms and Serum Ghrelin Levels with the Risk of Hepatitis B Virus-Related Liver Diseases in a Chinese Population.

作者信息

Zhang Xiaolian, Zhai Limin, Rong Chengzhi, Qin Xue, Li Shan

机构信息

Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.

出版信息

PLoS One. 2015 Nov 23;10(11):e0143069. doi: 10.1371/journal.pone.0143069. eCollection 2015.

Abstract

BACKGROUND

The functions of ghrelin (GHRL) include anti-inflammatory effects, reduction of the fibrogenic response, protection of liver tissue, and regulation of cell proliferation. Genetic variations in the GHRL gene may play an important role in the development of chronic hepatitis B (CHB), liver cirrhosis (LC) and hepatocellular carcinoma (HCC). Therefore, we investigated whether GHRL gene polymorphisms and its serum levels are associated with hepatitis B virus (HBV)-related diseases risk in a Chinese population.

METHODS

176 patients with CHB, 106 patients with HBV-related LC, 151 patients with HBV-related HCC, and 167 healthy controls were recruited in the study. Genotyping of GHRL rs26311, rs27647, rs696217, and rs34911341 polymorphisms were determined with the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and DNA sequencing. The serum GHRL concentrations were determined using enzyme-linked immunosorbent assay (ELISA).

RESULTS

Binary logistic regression analyses adjusting for gender and age revealed that a significant increased risk of LC was found in the GHRL rs26311 GC genotype and combined GC+CC genotypes when compared with the GG genotype (GC vs. GG: OR = 1.671, 95% CI = 1.013-2.757, P = 0.044; GC+CC vs. GG: OR = 1.674, 95% CI = 1.040-2.696, P = 0.034). In subgroup analysis by gender, binary logistic regression analyses adjusting for age showed that the GHRL rs26311 C allele and combined GC+CC genotypes were associated with a significantly increased risk to LC in males (C vs. G OR = 1.416, 95% CI = 1.017-1.972, P = 0.040; GC+CC vs. GG: OR = 1.729, 95% CI = 1.019-2.933, P = 0.042). In addition, we found significant decreased serum GHRL levels in LC patients compared with the healthy controls. However, there was no significant association of the GHRL rs26311 polymorphism with serum GHRL levels in LC patients.

CONCLUSIONS

These observations suggest that the GHRL rs26311 polymorphism is associated with an increased risk to HBV-related LC, especially in men. We also found an inverse association of serum GHRL levels with LC.

摘要

背景

胃饥饿素(GHRL)的功能包括抗炎作用、降低纤维化反应、保护肝组织以及调节细胞增殖。GHRL基因的遗传变异可能在慢性乙型肝炎(CHB)、肝硬化(LC)和肝细胞癌(HCC)的发生发展中起重要作用。因此,我们调查了GHRL基因多态性及其血清水平是否与中国人群中乙型肝炎病毒(HBV)相关疾病的风险有关。

方法

本研究招募了176例CHB患者、106例HBV相关LC患者、151例HBV相关HCC患者和167例健康对照。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和DNA测序法对GHRL rs26311、rs27647、rs696217和rs34911341多态性进行基因分型。采用酶联免疫吸附测定(ELISA)法测定血清GHRL浓度。

结果

经性别和年龄校正的二元logistic回归分析显示,与GG基因型相比,GHRL rs26311 GC基因型和GC+CC基因型联合存在时,LC风险显著增加(GC与GG比较:OR = 1.671,95%CI = 1.013 - 2.757,P = 0.044;GC+CC与GG比较:OR = 1.674,95%CI = 1.040 - 2.696,P = 0.034)。在按性别进行的亚组分析中,经年龄校正的二元logistic回归分析显示,GHRL rs26311 C等位基因和GC+CC基因型联合存在时,男性患LC的风险显著增加(C与G比较:OR = 1.416,95%CI = 1.017 - 1.972,P = 0.040;GC+CC与GG比较:OR = 1.729,95%CI = 1.019 - 2.933,P = 0.042)。此外,我们发现LC患者的血清GHRL水平与健康对照相比显著降低。然而,LC患者中GHRL rs26311多态性与血清GHRL水平之间无显著关联。

结论

这些观察结果表明,GHRL rs26311多态性与HBV相关LC风险增加有关,尤其是在男性中。我们还发现血清GHRL水平与LC呈负相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72de/4658098/aebe11eb8bd0/pone.0143069.g001.jpg

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