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首页> 外文期刊>AIDS Research and Human Retroviruses >Interleukin-6 is associated with noninvasive markers of liver fibrosis in HIV-infected patients with alcohol problems
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Interleukin-6 is associated with noninvasive markers of liver fibrosis in HIV-infected patients with alcohol problems

机译:白细胞介素6与HIV感染酒精中毒患者肝纤维化的非侵入性标志物相关

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Both HIV and hepatitis C virus (HCV) cause chronic inflammation and alterations in serum inflammatory cytokines. The impact of inflammatory cytokines on liver fibrosis is not well understood. We studied the association between interleukin (IL)-6, IL-10, and tumor necrosis factor (TNF)-α and liver fibrosis in HIV-infected patients with current or past alcohol problems (CAGE ≥2 or physician investigator diagnosis). Liver fibrosis was estimated with FIB-4 (FIB-4 <1.45 defined the absence of liver fibrosis and FIB-4 >3.25 defined advanced fibrosis). Logistic regression was used to assess the association between cytokines and fibrosis, adjusting for age, sex, CD4, HIV RNA, current antiretroviral therapy, body mass index, and HCV. Secondary analyses explored whether the association between HCV and liver fibrosis was mediated by these cytokines. Participants (n=308) were all HIV-infected; 73% were male with a mean age of 42 years; half had detectable HCV-RNA, 60.7% had an absence of liver fibrosis, and 10.1% had advanced fibrosis. In models that adjusted for each cytokine separately, higher levels of IL-6 were significantly associated with an absence of fibrosis [adjusted OR (95% CI): 0.43 (0.19, 0.98), p=0.05] and were borderline significant for advanced fibrosis [adjusted OR (95% CI): 8.16 (0.96, 69.54), p=0.055]. In the final model, only higher levels of IL-6 remained significantly associated with advanced liver fibrosis [adjusted OR (95% CI): 11.78 (1.17, 118.19), p=0.036]. Adjustment for inflammatory cytokines attenuated the adjusted OR for the association between HCV and fibrosis in the case of IL-6 [for the absence of fibrosis from 0.32 (0.17, 0.57) p<0.01 to 0.47 (0.23, 0.96) p=0.04; and for advanced fibrosis from 7.22 (2.01, 25.96) p<0.01 to 6.62 (1.20, 36.62) p=0.03], suggesting IL-6 may be a partial mediator of the association between HCV and liver fibrosis. IL-6 was strongly and significantly associated with liver fibrosis in a cohort of HIV-infected patients with alcohol problems. IL-6 may be a useful predictive marker for liver fibrosis for HIV-infected patients.
机译:HIV和丙型肝炎病毒(HCV)都会引起慢性炎症和血清炎性细胞因子的改变。炎症性细胞因子对肝纤维化的影响尚不清楚。我们研究了白细胞介素(IL)-6,IL-10和肿瘤坏死因子(TNF)-α与HIV感染的当前或既往酒精问题(CAGE≥2或医生调查)的患者之间的相关性。用FIB-4评估肝纤维化(FIB-4 <1.45定义为不存在肝纤维化,FIB-4> 3.25定义为晚期纤维化)。 Logistic回归用于评估细胞因子与纤维化之间的关联,调整年龄,性别,CD4,HIV RNA,当前的抗逆转录病毒疗法,体重指数和HCV。二级分析探讨了HCV和肝纤维化之间的联系是否由这些细胞因子介导。参与者(n = 308)全部感染了艾滋病毒; 73%是男性,平均年龄为42岁;一半具有可检测的HCV-RNA,60.7%没有肝纤维化,而10.1%有晚期纤维化。在分别针对每种细胞因子进行调整的模型中,较高的IL-6水平与无纤维化显着相关[调整后的OR(95%CI):0.43(0.19,0.98),p = 0.05],对于晚期纤维化具有临界意义[调整后的OR(95%CI):8.16(0.96,69.54),p = 0.055]。在最终模型中,只有更高水平的IL-6仍与晚期肝纤维化显着相关[校正OR(95%CI):11.78(1.17,118.19),p = 0.036]。在IL-6的情况下,对炎症细胞因子的调整减弱了HCV与纤维化之间相关性的调整后OR [对于没有纤维化的情况,从0.32(0.17,0.57)p <0.01降低到0.47(0.23,0.96)p = 0.04;对于晚期纤维化,从7.22(2.01,25.96)p <0.01到6.62(1.20,36.62)p = 0.03],提示IL-6可能是HCV与肝纤维化之间联系的部分介质。在一群患有酒精问题的HIV感染患者中,IL-6与肝纤维化密切相关。 IL-6可能是HIV感染患者肝纤维化的有用预测指标。

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