Zhu S S, Dong Y, Zhang H F, Wang L M, Xu Z Q, Zhang M, Gan Y, Chen D W, Wang F C, Yan J G, Zhao P
The Fifth Medical Center, Chinese PLA General Hospital, Pediatric Liver Disease Therapy and Research Center, Beijing 100039, China.
The Fifth Medical Center, Chinese PLA General Hospital, Clinical trial center, China.
Zhonghua Gan Zang Bing Za Zhi. 2019 Aug 20;27(8):604-609. doi: 10.3760/cma.j.issn.1007-3418.2019.08.004.
To investigate the curative effect of antiviral therapy and related factors influencing the curative affect in children with immune-tolerant phase chronic hepatitis B. From May 2014 to April 2015, 46 children with chronic hepatitis B, aged 1 to 16 years with immune-tolerant phase were enrolled as the treatment group. All cases in the treated group either received interferon alpha (3-5 MIU/m(2), once daily) in lamivudine combination (if HBV DNA decreased < 2 log(10)) or repeatedly received interferon-alpha alone (if HBV DNA decreased >2 log(10)) for 12 weeks. Interferon was discontinued at 72 weeks and followed-up period was continued with lamivudine for 24 weeks. At the same time, data of 23 cases of untreated children with immune-tolerant phase chronic hepatitis B were collected as the control group. The treatment group and the control group were divided into two age groups: 1-7 years old and 7-15 years old. Data measurements were compared using t-test, analysis of variance and single factor analysis methods, and the count data were analyzed by (2) test. Multiple logistic regression analysis was used to analyze the effects of different factors on response. (1) There were 22 cases aged 1-7 years in the treatment group (47.8%) and 12 cases aged 1-7 years in the control group (52.2%). The cases of mother-to-child transmission (MTCT) in treatment and control group were 34 (73.9%) and 17 (73.9%), while children with normal baseline ALT in the treatment and control group were 18 (39.1%) and 10 (43.5%). (2) At the end of follow-up, 15 cases in the treatment group (32.6%) had HBeAg serological conversion. Among them, nine (19.6%) cases had HBsAg clearance or HB-Ag seroconversion with anti-HBs, and one (2.2%) case had HBsAg clearance, but both HBeAg and anti-HBe were positive. In the control group, one case had HBV DNA lower than the lower limit of detection level, and one case had HBeAg seroconversion without HBsAg clearance. (3) At the end of follow-up, the seroconversion rates of HBeAg in patients aged 1 to 7 years and patients aged 7 to 15 years were 45.5% and 20.8%, respectively ( = 0.078) and the clearance rates of HBsAg were 36.4% and 8.3% ( = 0.023). The serum conversion rates of normal and abnormal baseline alanine aminotransferase levels were 5.6% and 50.0% ( = 0.005), and the clearance rates of HBsAg were 5.6% and 32.1% ( = 0.077), respectively. There was no statistically significant difference in gender, mother-to-child transmission, HBV DNA genotyping and baseline HBsAg level in antiviral efficacy among children ( > 0.05). (4) HBsAg and HBeAg clearance occurred in 100% of patients at the end of follow-up who had HBsAg < 3 000 IU/ml at 24 weeks of treatment. (5) Multivariate logistic regression analysis showed that serum HBeAg conversion rate had relation with non-MTCT transmission and abnormal baseline alanine aminotransferase. Furthermore, HBsAg clearance rate was associated with the age of children. Sequential combination of interferon and lamivudine with a prolonged course can improve the HBV DNA negative conversion rate, HBeAg seroconversion rate, HBsAg loss rate and mild ALT abnormalities at baseline in children under the age of 7 years with immune-tolerant phase chronic hepatitis B.
探讨抗病毒治疗对免疫耐受期慢性乙型肝炎患儿的疗效及影响疗效的相关因素。选取2014年5月至2015年4月收治的46例1~16岁免疫耐受期慢性乙型肝炎患儿作为治疗组。治疗组所有病例,若HBV DNA下降<2 log(10),则接受α干扰素(3 - 5 MIU/m²,每日1次)联合拉米夫定治疗;若HBV DNA下降>2 log(10),则重复单独使用α干扰素治疗,疗程均为12周。72周时停用干扰素,继续使用拉米夫定随访24周。同时,收集23例未经治疗的免疫耐受期慢性乙型肝炎患儿资料作为对照组。治疗组和对照组再分为两个年龄组:1~7岁和7~15岁。采用t检验、方差分析和单因素分析方法比较数据测量值,计数资料采用(2)检验分析。采用多因素logistic回归分析不同因素对疗效的影响。(1)治疗组1~7岁患儿22例(47.8%),对照组1~7岁患儿12例(52.2%)。治疗组和对照组母婴传播(MTCT)病例分别为34例(73.9%)和17例(73.9%),治疗组和对照组基线ALT正常的患儿分别为18例(39.1%)和10例(43.5%)。(2)随访结束时,治疗组15例(32.6%)发生HBeAg血清学转换。其中,9例(19.6%)出现HBsAg清除或HB-Ag血清学转换伴抗-HBs产生,1例(2.2%)出现HBsAg清除,但HBeAg和抗-HBe均为阳性。对照组1例HBV DNA低于检测下限,1例发生HBeAg血清学转换但未出现HBsAg清除。(3)随访结束时,1~7岁患儿和7~15岁患儿的HBeAg血清学转换率分别为45.5%和20.8%(=0.078),HBsAg清除率分别为36.4%和8.3%(=0.023)。基线丙氨酸氨基转移酶水平正常和异常患儿的血清学转换率分别为5.6%和50.0%(=0.005),HBsAg清除率分别为5.6%和32.1%(=0.077)。儿童抗病毒疗效在性别、母婴传播、HBV DNA基因分型及基线HBsAg水平方面差异无统计学意义(>0.05)。(4)治疗24周时HBsAg<3 000 IU/ml的患儿随访结束时100%发生HBsAg和HBeAg清除。(5)多因素logistic回归分析显示,血清HBeAg转换率与非母婴传播及基线丙氨酸氨基转移酶异常有关。此外,HBsAg清除率与患儿年龄有关。干扰素与拉米夫定序贯联合并延长疗程可提高免疫耐受期慢性乙型肝炎7岁以下患儿的HBV DNA阴转率、HBeAg血清学转换率、HBsAg消失率及基线轻度ALT异常情况。