Persico Marcello, Bruno Savino, Costantino Andrea, Mazza Marta, Almasio Piero Luigi
Internal Medicine and Hepatology Division, Second University of Naples, Via Del Parco Carelli 36, 80123 Naples, Italy.
Int J Hepatol. 2011;2011:314301. doi: 10.4061/2011/314301. Epub 2011 Nov 15.
virus features, coinfections and host characteristics. In particular, a peculiar genetic background of the host by conditioning the occurrence of intracellular metabolic derangements (i.e., insulin resistance) might contribute to accelerate the rate of progression to cirrhosis and eventually the occurrence of hepatocellular carcinoma (HCC) and death. Likely, direct interplays between virus genotype and host genetic background might be hypothesized at this level. Morbidity and mortality in cirrhosis is primarily associated with complications of liver cirrhosis (ascites, hepatic encephalopathy, jaundice, and gastroesophageal bleeding) and HCC occurrence. Therefore the main goal of therapy is to clear viral infection and decrease liver necro-inflammation that directly relates to development of cirrhosis and HCC. Among patients treated with Interferon-based therapy, those with sustained viral response showed a significant reduction of progression to cirrhosis and development of HCC. However, a residual risk of hepatocellular carcinoma still remains indicating the need for careful follow-up using ultrasonography every six months in cirrhotic patients, even in those showing persistently normal ALT and undetectable HCV RNA levels after antiviral therapy.
病毒特征、合并感染和宿主特征。特别是,宿主独特的遗传背景通过调节细胞内代谢紊乱(即胰岛素抵抗)的发生,可能会加速肝硬化的进展速度,并最终导致肝细胞癌(HCC)的发生和死亡。在此层面上,可能存在病毒基因型与宿主遗传背景之间的直接相互作用。肝硬化的发病率和死亡率主要与肝硬化并发症(腹水、肝性脑病、黄疸和胃食管出血)以及HCC的发生有关。因此,治疗的主要目标是清除病毒感染并减轻肝脏坏死性炎症,而这直接关系到肝硬化和HCC的发展。在接受基于干扰素治疗的患者中,实现持续病毒学应答的患者向肝硬化进展和发生HCC的情况显著减少。然而,肝细胞癌的残余风险仍然存在,这表明即使在抗病毒治疗后谷丙转氨酶(ALT)持续正常且丙型肝炎病毒(HCV)RNA水平检测不到的肝硬化患者中,仍需要每六个月使用超声进行仔细随访。