Virology Department, Tropical Medicine Foundation Dr. Heitor Vieira Dourado, Manaus, Amazonas, Brazil.
Virology Department, Tropical Medicine Foundation Dr. Heitor Vieira Dourado, Manaus, Amazonas, Brazil; Multidisciplinar Center, Federal University of Amazonas, Manaus, Amazonas, Brazil.
J Hepatol. 2014 Dec;61(6):1205-11. doi: 10.1016/j.jhep.2014.05.041. Epub 2014 Jun 4.
BACKGROUND & AIMS: Chronic HDV/HBV co-infection is perhaps the most intriguing amongst all viral hepatitis. Only few studies focus deeply on this topic, particularly with patients infected with HDV-3. This study aimed to identify predictors of advanced disease, examining a cross-sectional data of 64 patients.
Histological grading was used to characterize the disease stages and viral loads were tested as predictors of necroinflammatory activity and fibrosis.
We identified three HDV/HBV co-infection patterns: patients with predominant HDV replication (56.3%), patients with similar viral loads of both viruses (40.6%), and patients with predominant HBV replication (3.1%). Mean HDV-RNA showed a positive trend regarding inflammatory activity and grade of fibrosis. HDV viral load correlated positively with serum levels of liver enzymes and inversely with platelets count. HBV viral load showed no correlation with any of the above parameters. Advanced fibrosis was associated with age, splenomegaly, and HDV viral load of more than 2 log10. Multiple logistic regression confirmed the independent effect of HDV viral predominance. Advanced necroinflammatory activity was independently associated with HDV viral load and splenomegaly.
HDV may possibly play an important and direct role in the establishment of necroinflammatory activity and fibrosis. Data show an indigenous HDV genotype, HDV-3, similar to those described in the Amazon region.
慢性 HDV/HBV 合并感染可能是所有病毒性肝炎中最引人关注的一种。只有少数研究深入探讨了这一主题,特别是针对感染 HDV-3 的患者。本研究旨在确定进展性疾病的预测因素,通过对 64 名患者的横断面数据进行分析。
采用组织学分级来描述疾病分期,并检测病毒载量作为坏死性炎症活动和纤维化的预测因子。
我们发现了三种 HDV/HBV 合并感染模式:以 HDV 复制为主的患者(56.3%)、两种病毒载量相似的患者(40.6%)和以 HBV 复制为主的患者(3.1%)。平均 HDV-RNA 显示出与炎症活动和纤维化程度呈正相关的趋势。HDV 病毒载量与血清肝酶水平呈正相关,与血小板计数呈负相关。HBV 病毒载量与上述任何参数均无相关性。晚期纤维化与年龄、脾肿大和 HDV 病毒载量超过 2log10 有关。多因素逻辑回归证实了 HDV 病毒优势的独立作用。晚期坏死性炎症活动与 HDV 病毒载量和脾肿大独立相关。
HDV 可能在坏死性炎症活动和纤维化的建立中发挥重要而直接的作用。数据显示,HDV-3 是一种本土基因型,与亚马逊地区描述的基因型相似。