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高血浆 CXCL10 水平与 HCV 基因型 1 以及 HIV/HCV 合并感染患者的更高胰岛素抵抗、纤维化和 HIV 病毒载量相关。

High plasma CXCL10 levels are associated with HCV-genotype 1, and higher insulin resistance, fibrosis, and HIV viral load in HIV/HCV coinfected patients.

机构信息

Infectious Diseases-HIV Unit, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

出版信息

Cytokine. 2012 Jan;57(1):25-9. doi: 10.1016/j.cyto.2011.10.020. Epub 2011 Dec 3.

Abstract

BACKGROUND

CXCL10 may contribute to the host immune response against the hepatitis C virus (HCV), liver disease progression, and response to HCV antiviral therapy. The aim of our study was to analyze the relationship among virological, immunological, and clinical characteristics with plasma CXCL10 levels in human immunodeficiency virus (HIV)/HCV-coinfected patients.

METHODS

We carried out a cross-sectional study on 144 patients. CXCL10 and insulin were measured using an immunoassay kit. The degree of insulin resistance was estimated for each patient using the homeostatic model assessment (HOMA) method. Insulin resistance was defined as a HOMA index higher than or equal to 3.8. Aspartate aminotransferase (AST) to platelet ratio (APRI), FIB-4, Forns index, HGM1, and HGM2 were calculated.

RESULTS

The variables associated with log(10) CXCL10 levels by univariate analysis were age (b=0.013; p=0.023), prior AIDS-defining condition (b=0.127; p=0.045), detectable plasma HIV viral load (b=0.092; p=0.006), log(10) HOMA (b=0.216; p=0.002), HCV-genotype 1 (b=0.114; p=0.071), and liver fibrosis assessed by all non-invasive indexes (log(10) APRI (b=0.296; p=0.001), log(10) FIB-4 (b=0.436; p<0.001), log(10) Forns index (b=0.591; p<0.001), log(10) HGM1 (b=0.351; p=0.021), and log(10) HGM2 (b=0.215; p=0.018)). However, in multivariate analysis, CXCL10 levels were only associated with HOMA, detectable plasma HIV viral load, HCV-genotype 1 and FIB-4 (R-square=0.235; p<0.001).

CONCLUSION

Plasma CXCL10 levels were influenced by several characteristics of patients related to HIV and HCV infections, insulin resistance, and liver fibrosis, indicating that CXCL10 may play an important role in the pathogenesis of both HCV and HIV infections.

摘要

背景

趋化因子(CXCL)10 可能有助于宿主对丙型肝炎病毒 (HCV)的免疫反应、肝病进展和对 HCV 抗病毒治疗的反应。我们的研究目的是分析病毒学、免疫学和临床特征与人类免疫缺陷病毒 (HIV)/HCV 合并感染患者血浆 CXCL10 水平之间的关系。

方法

我们对 144 例患者进行了横断面研究。使用免疫测定试剂盒测量 CXCL10 和胰岛素。使用稳态模型评估 (HOMA) 方法估算每位患者的胰岛素抵抗程度。胰岛素抵抗定义为 HOMA 指数高于或等于 3.8。计算天冬氨酸氨基转移酶 (AST)与血小板比值 (APRI)、FIB-4、Forns 指数、HGM1 和 HGM2。

结果

单因素分析中与 log(10)CXCL10 水平相关的变量为年龄(b=0.013;p=0.023)、既往 AIDS 定义性疾病(b=0.127;p=0.045)、可检测的血浆 HIV 病毒载量(b=0.092;p=0.006)、log(10)HOMA(b=0.216;p=0.002)、HCV 基因型 1(b=0.114;p=0.071)和所有非侵入性指标评估的肝纤维化(log(10)APRI(b=0.296;p=0.001)、log(10)FIB-4(b=0.436;p<0.001)、log(10)Forns 指数(b=0.591;p<0.001)、log(10)HGM1(b=0.351;p=0.021)和 log(10)HGM2(b=0.215;p=0.018))。然而,在多变量分析中,CXCL10 水平仅与 HOMA、可检测的血浆 HIV 病毒载量、HCV 基因型 1 和 FIB-4 相关(R 平方=0.235;p<0.001)。

结论

血浆 CXCL10 水平受与 HIV 和 HCV 感染、胰岛素抵抗和肝纤维化相关的患者的多个特征影响,表明 CXCL10 可能在 HCV 和 HIV 感染的发病机制中发挥重要作用。

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