Zacharakis George, Koskinas John, Kotsiou Stamatia, Tzara Fevronia, Vafeiadis Nikolaos, Papoutselis Menelaos, Maltezos Eustratios, Sivridis Eleftherios, Papoutselis Kostantinos
Unit of Preventive Medicine, Social Security Institute, Alexandroupolis, Greece.
J Hepatol. 2008 Dec;49(6):884-91. doi: 10.1016/j.jhep.2008.06.009. Epub 2008 Jul 2.
BACKGROUND/AIMS: To evaluate the fluctuating course of serum HBV-DNA levels during the natural history of chronic HBV infection in the general population of North-Eastern Greece, in association with liver disease progression.
Two hundred and sixty-three adults with chronic HBV, median 34 years of age, were randomly selected and prospectively followed-up for a maximum period of 12 years. Viral markers, liver biochemistry and physical examination were performed every 6 months, and liver biopsy/abdominal ultrasound every 2-4 years.
At entry, 195/263 (76%) were HBeAg (-)/anti-HBe (+) inactive carriers: (a) almost all 195 individuals with undetectable or HBV-DNA levels <2000IU/ml had no liver disease at entry and at follow-up period by imaging or liver histology evaluation (b) only 4/195 (2%) showed HBV reactivation with HBV-DNA >2000IU/ml. At entry, 48/263 (18%) patients were chronic HBeAg(-); (a) 1/3 patients had intermittently HBV-DNA <2000IU/ml for at least one occasion and were misclassified as inactive carriers (b) 22/48 (46%) had moderate/severe histology at entry and 5/48 (10%) showed liver disease progression during follow-up. Logistic regression analysis was used to derive OR (95%CI) for factors associated with liver disease progression.
Close monitoring of serum HBV-DNA levels is useful in the management of chronic HBeAg(-) patients, as associated with liver disease progression.
背景/目的:评估希腊东北部普通人群慢性乙型肝炎病毒(HBV)感染自然史期间血清HBV-DNA水平的波动过程及其与肝病进展的关系。
随机选取263例慢性HBV感染的成年人,年龄中位数为34岁,进行前瞻性随访,最长随访12年。每6个月检测病毒标志物、肝生化指标并进行体格检查,每2至4年进行肝活检/腹部超声检查。
入组时,195/263(76%)为HBeAg(-)/抗-HBe(+)非活动性携带者:(a)几乎所有195例HBV-DNA检测不到或水平<2000IU/ml的个体在入组时及随访期间经影像学或肝组织学评估均无肝病;(b)仅4/195(2%)出现HBV再激活,HBV-DNA>2000IU/ml。入组时,48/263(18%)患者为慢性HBeAg(-);(a)1/3患者至少有一次HBV-DNA间歇性<2000IU/ml,被误分类为非活动性携带者;(b)22/48(46%)入组时组织学表现为中度/重度,5/48(10%)在随访期间出现肝病进展。采用逻辑回归分析得出与肝病进展相关因素的比值比(OR)(95%可信区间)。
密切监测血清HBV-DNA水平对慢性HBeAg(-)患者的管理有用,因为其与肝病进展相关。