慢性丙型肝炎患儿血清α -胰蛋白酶抑制剂重链4 (ITIH4)与肝纤维化和病毒血症的关系

Hepatitis research and treatment Pub Date : 2014-01-01 Epub Date: 2014-09-14 DOI:10.1155/2014/307942
Mostafa M Sira, Behairy E Behairy, Azza M Abd-Elaziz, Sameh A Abd Elnaby, Ehab E Eltahan
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引用次数: 21

摘要

肝纤维化和病毒血症是慢性丙型肝炎病毒(HCV)感染治疗政策及其结果的决定因素。目的探讨慢性丙型肝炎患儿血清α -胰蛋白酶抑制剂重链4 (ITIH4)水平及其与肝纤维化和病毒血症的关系。采用ELISA法检测33例未接受治疗的慢性HCV患儿的ih4水平,并根据不同的临床、实验室和组织病理学参数进行比较。采用Ishak评分评估肝脏组织病理学变化,并与天门冬氨酸转氨酶与血小板比值(APRI)和FIB-4指数作为简单的无创纤维化指标进行比较。在30名年龄和性别匹配的健康对照中测量了ih4。患者的ITIH4水平明显高于对照组(54.2±30.78 pg/mL vs 37.21±5.39 pg/mL);P = 0.021)。ITIH4与纤维化分期直接相关(P = 0.015, 0.961, 0.389, P = 0.071),而ITIH4与HCV病毒血症负相关(P = 0.071),与APRI、FIB-4无显著相关性。总之,ITIH4与较高阶段的纤维化显著相关,表明其可能与肝纤维化发生有关。高ITIH4与低病毒血症的趋势表明其具有潜在的抗病毒特性,值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Serum Inter-Alpha-Trypsin Inhibitor Heavy Chain 4 (ITIH4) in Children with Chronic Hepatitis C: Relation to Liver Fibrosis and Viremia.

Serum Inter-Alpha-Trypsin Inhibitor Heavy Chain 4 (ITIH4) in Children with Chronic Hepatitis C: Relation to Liver Fibrosis and Viremia.

Serum Inter-Alpha-Trypsin Inhibitor Heavy Chain 4 (ITIH4) in Children with Chronic Hepatitis C: Relation to Liver Fibrosis and Viremia.

Liver fibrosis and viremia are determinant factors for the treatment policy and its outcome in chronic hepatitis C virus (HCV) infection. We aimed to investigate serum level of inter-alpha-trypsin inhibitor heavy chain 4 (ITIH4) and its relation to liver fibrosis and viremia in children with chronic HCV. ITIH4 was measured by ELISA in 33 treatment-naive children with proved chronic HCV and compared according to different clinical, laboratory and histopathological parameters. Liver histopathological changes were assessed using Ishak score and compared with aspartate transaminase-to-platelet ratio (APRI) and FIB-4 indices as simple noninvasive markers of fibrosis. ITIH4 was measured in a group of 30 age- and sex-matched healthy controls. ITIH4 was significantly higher in patients than in controls (54.2 ± 30.78 pg/mL versus 37.21 ± 5.39 pg/mL; P = 0.021). ITIH4, but not APRI or FIB-4, had a significant direct correlation with fibrosis stage (P = 0.015, 0.961, and 0.389, resp.), whereas, the negative correlation of ITIH4 with HCV viremia was of marginal significance (P = 0.071). In conclusion, ITIH4 significantly correlated with higher stages of fibrosis indicating a possible relation to liver fibrogenesis. The trend of higher ITIH4 with lower viremia points out a potential antiviral properties and further studies in this regard are worthwhile.

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