Quantitative Change of Hepatitis B Surface Antigen Leading to Final Hepatitis B Surface Antigen Loss in Patients with Chronic Hepatitis B Receiving Nucleos(t)ide Analogs in China.

IF 3 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Tianhui Zhou, Meng Shu, Fangyun Luo, Sijia Dong, Jiaming Teng, Yanan Du, Hong Qiu, Wei Cai
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引用次数: 0

Abstract

Introduction: Loss of hepatitis B surface antigen (HBsAg) is the pivotal component of functional cure in patients suffering from chronic hepatitis B (CHB). The predictive value of quantitative HBsAg (qHBsAg) in HBsAg loss among those undergoing nucleos(t)ide analog (NAs) therapy is an area of ongoing investigation.

Methods: A retrospective cohort study using electronic medical records was performed. CHB patients with NAs treatment between January 1, 2012, and December 31, 2020 were enrolled and followed up until discontinuation of NAs, as indicated by a gap more than 12 months in prescription refills, past medical record, or study end. Patients were grouped into NAs treatment-naïve cohort and treatment-experienced cohort. In both cohorts, Cox regression models assessed associations between 12-month reduction in qHBsAg, baseline qHBsAg, and HBsAg loss.

Results: Overall, 2,627 CHB patients with NAs treatment was identified, including 1,179 in treatment-naïve cohort and 1,448 in treatment-experienced cohort. In treatment-naïve cohort, 9 patients had HBsAg loss (0.51/100 person-years). In treatment-experienced cohort, 30 patients had HBsAg loss (1.03/100 person-years). HBsAg loss was significantly associated with a 0.5-1 log10 (treatment-naïve: adjusted hazard ratio [aHR] 8.06, 95% confidence interval [CI] 1.29-50.40; treatment-experienced: aHR 4.34, 95% CI 1.40-13.47) and >1 log10 qHBsAg decrease (treatment-naïve: aHR 9.19, 95% CI 1.47-57.65; treatment-experienced: aHR 8.02, 95% CI 1.76-36.57) compared with qHBsAg not reduced. HBsAg loss was significantly associated with lower baseline qHBsAg in treatment-experienced cohort, while such difference was not significant in treatment-naïve cohort.

Discussion: A rapid decline of qHBsAg in 12 months during NAs therapy, as opposed to merely maintaining a low level of qHBsAg, was associated with HBsAg loss.

中国接受核苷类似物治疗的慢性乙型肝炎患者乙型肝炎表面抗原的定量变化导致最终乙型肝炎表面抗原丢失
乙型肝炎表面抗原(HBsAg)的丧失是慢性乙型肝炎(CHB)患者功能性治愈的关键组成部分。在接受核苷类似物(NAs)治疗的患者中,定量HBsAg (qHBsAg)对HBsAg损失的预测价值是一个正在研究的领域。方法:采用电子病历进行回顾性队列研究。2012年1月1日至2020年12月31日期间接受NAs治疗的CHB患者入组并随访,直到停止NAs治疗,如处方补药、既往医疗记录或研究结束的间隔超过12个月。患者分为NAs treatment-naïve组和治疗经验组。在这两个队列中,Cox回归模型评估了12个月qHBsAg下降、基线qHBsAg和HBsAg损失之间的关系。结果:总体而言,确定了2627例接受NAs治疗的CHB患者,其中treatment-naïve队列1179例,治疗经历队列1448例。在treatment-naïve队列中,9例患者出现HBsAg损失(0.51/100人年)。在接受治疗的队列中,30例患者出现HBsAg损失(1.03/100人年)。HBsAg损失与0.5-1 log10显著相关(treatment-naïve:校正风险比[aHR] 8.06, 95%可信区间[CI] 1.29-50.40;治疗经历:aHR 4.34, 95% CI 1.40-13.47)和bbb1 log10 qHBsAg下降(treatment-naïve: aHR 9.19, 95% CI 1.47-57.65;治疗经历:aHR 8.02, 95% CI 1.76-36.57)与qHBsAg未降低相比。在治疗经历的队列中,HBsAg损失与较低的基线qHBsAg显著相关,而在treatment-naïve队列中,这种差异不显著。讨论:在NAs治疗期间,qHBsAg在12个月内迅速下降,而不是仅仅维持低水平的qHBsAg,与HBsAg损失有关。
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来源期刊
Clinical and Translational Gastroenterology
Clinical and Translational Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
7.00
自引率
0.00%
发文量
114
审稿时长
16 weeks
期刊介绍: Clinical and Translational Gastroenterology (CTG), published on behalf of the American College of Gastroenterology (ACG), is a peer-reviewed open access online journal dedicated to innovative clinical work in the field of gastroenterology and hepatology. CTG hopes to fulfill an unmet need for clinicians and scientists by welcoming novel cohort studies, early-phase clinical trials, qualitative and quantitative epidemiologic research, hypothesis-generating research, studies of novel mechanisms and methodologies including public health interventions, and integration of approaches across organs and disciplines. CTG also welcomes hypothesis-generating small studies, methods papers, and translational research with clear applications to human physiology or disease. Colon and small bowel Endoscopy and novel diagnostics Esophagus Functional GI disorders Immunology of the GI tract Microbiology of the GI tract Inflammatory bowel disease Pancreas and biliary tract Liver Pathology Pediatrics Preventative medicine Nutrition/obesity Stomach.
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