Yuen Man-Fung, Sablon Erwin, Wong Danny Ka-Ho, Yuan He-Jun, Wong Benjamin Chun-Yu, Chan Annie On-On, Lai Ching-Lung
Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong.
Clin Infect Dis. 2003 Aug 15;37(4):593-7. doi: 10.1086/376988. Epub 2003 Jul 29.
Hepatitis B virus (HBV) genotypes and precore and core promoter mutations were determined in 318 patients with HBV. Patients infected with HBV genotype B had a higher median alanine aminotransferase level and bilirubin level and a lower median albumin level during exacerbations of disease, compared with patients infected with HBV genotype C (all P<.001). By logistic regression analysis, HBV genotype B infection (P=.014) and low albumin levels (P=.006) were independently associated with a higher risk of hepatic decompensation during severe exacerbations of disease. Patients infected with genotype B had a significantly higher mortality due to hepatic decompensation than did patients with genotype C (70% vs. 27.8%; P=.05).
在318例乙肝病毒(HBV)感染者中测定了HBV基因型以及前核心和核心启动子突变情况。与感染HBV C基因型的患者相比,感染HBV B基因型的患者在疾病加重期的丙氨酸转氨酶水平中位数和胆红素水平更高,而白蛋白水平中位数更低(所有P<0.001)。通过逻辑回归分析,HBV B基因型感染(P=0.014)和低白蛋白水平(P=0.006)与疾病严重加重期肝失代偿风险较高独立相关。感染B基因型的患者因肝失代偿导致的死亡率显著高于C基因型患者(70%对27.8%;P=0.05)。