Correlation of serum ferritin with severity of liver disease

Garyll Ryan Tariang Blah, RS Tonk
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Abstract

Background and Aim: Serum ferritin is a marker of hepatic inflammation and has been studied to predict mortality in decompensated cirrhotics. No study has been done to evaluate ferritin as an independent marker of liver disease severity. We investigated whether serum ferritin levels can be correlated with Child–Pugh and Model for End-stage Liver Disease (MELD) scores. Materials and Methods: Seventy-five patients fulfilling the criteria were included and a cross-sectional observational study was done. Results: Seventy-five patients (68 males and 7 females) were evaluated. Serum ferritin levels were found to be significantly elevated in patients having higher Child–Pugh and MELD scores and showed a significant correlation with Child–Pugh score (P = 0.001) and MELD score (P = 0.027). On univariate analysis, serum ferritin, bilirubin, international normalized ratio, ascites, and sodium were found to be significantly associated with severity of liver disease. On multivariate analysis, however, serum ferritin was not found to have a significant association with severity of liver disease. AUROC was also determined which showed that serum ferritin had relatively poor discriminative ability. Conclusion: Elevation of serum ferritin is prevalent in chronic liver disease (CLD). In patients of CLD, severity is associated with a higher serum ferritin level. In future, a study may be designed, to obtain a prognostic model in incorporating serum ferritin into MELD similar to MELD-Na scoring system.
血清铁蛋白与肝病严重程度的相关性
背景与目的:血清铁蛋白是肝脏炎症的标志物,已被研究用于预测失代偿肝硬化的死亡率。目前还没有研究评估铁蛋白作为肝病严重程度的独立标志物。我们研究了血清铁蛋白水平是否与Child-Pugh和终末期肝病模型(MELD)评分相关。材料和方法:纳入75例符合标准的患者,并进行横断面观察研究。结果:共纳入75例患者,其中男68例,女7例。Child-Pugh和MELD评分较高的患者血清铁蛋白水平显著升高,且与Child-Pugh评分(P = 0.001)和MELD评分(P = 0.027)显著相关。单因素分析发现,血清铁蛋白、胆红素、国际标准化比值、腹水和钠与肝病严重程度显著相关。然而,在多变量分析中,血清铁蛋白并没有发现与肝病严重程度有显著关联。AUROC测定表明,血清铁蛋白的鉴别能力相对较差。结论:血清铁蛋白升高在慢性肝病(CLD)中普遍存在。在CLD患者中,严重程度与较高的血清铁蛋白水平相关。未来,可能会设计一项研究,以获得将血清铁蛋白纳入MELD的预后模型,类似于MELD- na评分系统。
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12
审稿时长
26 weeks
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