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首页> 外文期刊>Biological trace element research >Prognostic Value of Serum Iron, Ferritin, and Transferrin in Chronic Alcoholic Liver Disease
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Prognostic Value of Serum Iron, Ferritin, and Transferrin in Chronic Alcoholic Liver Disease

机译:血清铁,铁素和转铁蛋白在慢性酒精性肝病中的预后价值

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摘要

Ethanol increases iron absorption. Therefore, increased amount of iron reaches the liver, and exerts pro-oxidant effects and stimulates ferritin synthesis and hepatic stellate cell activation, promoting fibrosis and inflammation. These mechanisms would theoretically support a role of ferritin as a marker of the transition to liver cirrhosis, and, consequently, as a prognostic factor, but there is controversy regarding its behavior in alcoholics. We analyzed among 238 severe alcoholics the prognostic value of iron, ferritin, transferrin, transferrin saturation index (TSI) and total iron binding capacity (TIBC), and the relationships of these variables with liver function, proinflammatory markers (C-reactive protein (CRP), interleukin (IL)-6, IL-8, and tumor necrosis factor alpha), and the presence of cirrhosis. Patients showed higher serum ferritin (Z = 2.50, p = 0.031) but lower transferrin (t(264) = 4.81, p < 0.001), TIBC (t(262) = 4.44, p < 0.001), and iron (Z = 3.19, p = 0.001) values compared with 32 age- and sex-matched controls. Ferritin was related to inflammatory cytokines such as IL-8 (rho = 0.18, p = 0.012) and to IL-6 (rho = 0.16, p = 0.016), but not to liver function. On the contrary, cirrhotics showed lower transferrin (t(234) = 4.77, p < 0.001) and TIBC (t(232) = 4.67, p < 0.001), but higher TSI (Z = 3.35, p < 0.001) than non-cirrhotics. Transferrin, TSI, and TIBC were related to liver function impairment (marked differences among the Child's groups regarding transferrin (KW (2) = 22.83, p < 0.001), TSI (KW (2) = 15.81, p < 0.001), and TIBC (KW (2) = 21.38, p < 0.001) but only weakly to inflammation (inverse relationships between IL-6 and total iron (rho = - 0.16, p = 0.017), TIBC (rho = - 0.20, p = 0.002), and transferrin (rho = - 0.20, p = 0.003). In accordance, albumin, IL-6, alcohol quitting, and TSI, in this order, were independently related to mortality, but not ferritin or iron.
机译:乙醇增加了铁吸收。因此,含铁量增加达到肝脏,并施加促氧化剂效果并刺激铁蛋白合成和肝星状细胞活化,促进纤维化和炎症。理论上,这些机制可以支持铁蛋白作为转型给肝硬化的标志物的作用,因此作为预后因素,但对酗酒者的行为存在争议。我们分析了238个严重的酗酒者铁,铁蛋白,转移素,转移素饱和度指数(TSI)和总铁结合能力(TIBC)的预后值以及这些变量与肝功能,促炎标记物(C-反应蛋白(CRP)的关系的关系),白细胞介素(IL)-6,IL-8和肿瘤坏死因子α),以及肝硬化的存在。患者显示出更高的血清铁蛋白(Z = 2.50,P = 0.031),但下降素(T(264)= 4.81,P <0.001),TIBC(T(262)= 4.44,P <0.001)和铁(Z = 3.19 ,p = 0.001)值与32年龄和性别匹配的对照相比。铁蛋白与炎性细胞因子有关,例如IL-8(rhO = 0.18,p = 0.012)和IL-6(rho = 0.16,p = 0.016),但不是肝功能。相反,循环表现出较低的转铁蛋白(T(234)= 4.77,p <0.001)和TIBC(t(232)= 4.67,p <0.001),但较高的TSI(Z = 3.35,P <0.001)而不是非 - 循环。转铁素,TSI和TIBC与肝功能障碍有关(儿童群体的有关转移素的显着差异(KW(2)= 22.83,P <0.001),TSI(KW(2)= 15.81,P <0.001)和TIBC (kw(2)= 21.38,p <0.001),但仅弱到炎症(IL-6和总铁之间的反向关系(rho = - 0.16,p = 0.017),TIBC(rho = - 0.20,p = 0.002),和转铁蛋白(Rho = - 0.20,p = 0.003)。根据白蛋白,IL-6,酒精戒烟和TSI,与死亡率独立相关,但不是铁蛋白或铁。

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