血清碳酸酐酶IX在埃及肝硬化和/或肝细胞癌患者中的预后价值。

Heba M. Abd El Latif, I. El-Elaimy, O. Hendy, Naglaa Meghawry, A. Zied
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摘要

肝细胞癌(HCC)是最常见的原发性肝癌类型,大多数患者诊断为晚期或终末期,预后较差。此外,肝硬化是一种以纤维化和肝功能受损为特征的慢性肝病,是HCC发展的主要危险因素。因此,建立新的临床标志物对肝癌的早期诊断和分期至关重要。目的:我们的研究旨在评估碳酸酐酶IX (CA9)作为肝硬化埃及患者HCC诊断的早期血清生物标志物。材料与方法:本研究选择58例肝硬化患者和60例HCC患者以及58例健康对照。对所有纳入的患者进行常规肝脏检查、CBC、c反应蛋白、甲胎蛋白(AFP)和血清CA9。结果:与对照组相比,HCC和肝硬化患者血清CA9和AFP水平显著升高。CA9随着肝病的发展而增加,在HCC队列中,CA9与BCLC分期、儿童分型、腹水和脑病成正比,在肝硬化队列中,CA9与儿童分型和腹水成正比。我们的研究结果表明,CA9在区分HCC(临界值>85 pg/mL)或肝硬化患者(临界值>54.7 pg/mL)和对照组方面具有比AFP更高的准确性和特异性。另一方面,CA9区分肝硬化和HCC的敏感性和特异性均低于AFP,分别为51.67%和46.55%。结论:CA9可作为HCC早期诊断的生物标志物,CA9水平与HCC预后不良有密切关系,提示其在HCC发生和疾病进展中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic value of serum carbonic anhydrase IX in Egyptian patients with cirrhosis and/ or hepatocellular carcinoma.
Introduction : Hepatocellular carcinoma (HCC) is the commonest type of primary liver cancers, and most patients are diagnosed in advanced or terminal stages with poor prognosis. Furthermore, cirrhosis, a chronic liver disease characterized by fibrosis and impaired liver function, is a major risk factor for the development of HCC. Therefore, it is crucial to establish new clinical markers for early HCC diagnosis and staging. Aim: Our study aimed to evaluate carbonic anhydrase IX (CA9) as an early serum biomarker for HCC diagnosis within cirrhotic Egyptian patients. Material and methods: Fifty-eight cirrhotic patients and sixty HCC patients as well as fifty-eight healthy control subjects were selected for the current study. Routine liver tests, CBC, C-reactive protein, alpha-fetoprotein (AFP), and serum CA9 were done for all the patients included. Results: Serum CA9 and AFP levels increased significantly in HCC and cirrhotic patients compared to controls. CA9 increased with the development of hepatic disease through the direct proportion of CA9 with BCLC staging, child classification, ascites, and encephalopathy in the HCC cohort and the direct proportion with child classification and ascites in the cirrhotic cohort. Our findings showed that CA9 has higher accuracy than AFP to differentiate between HCC (at cutoff value>85 pg/mL) or cirrhotic patients (at cutoff value>54.7 pg/mL) and control with greater sensitivity and specificity than AFP. On the other hand, CA9 showed lower sensitivity and specificity than AFP in discrimination between cirrhosis and HCC only 51.67% and 46.55%, respectively. Conclusions: CA9 could be used as a biomarker for early HCC diagnosis and there is a strong relationship between CA9 level and HCC´s worse prognosis suggesting its potential role in HCC development and disease progression.
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