蒙古乙型肝炎表面抗原患者中三角肝炎 (D) 的流行率、特征和病毒学相关性。

IF 1.9 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Sarantuya Gidaagaya, Akinori Rokuhara, Masaya Sugiyama, Sumiya Dorj, Batnasan Barsuren, Bira Namdag, Batmunkh Munkhbat, Shinichi Oka, Masashi Mizokami
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引用次数: 0

摘要

蒙古的乙型肝炎病毒(HDV)感染的临床和生化特征在很大程度上仍不为人所知。我们的目的是利用几种标记物调查蒙古 HDV 患者的临床特征。根据 HDV RNA 阳性程度将 143 名乙肝表面抗原(HBsAg)阳性患者分为 122 名 HDV 阳性患者和 21 名 HDV 阴性患者。对乙肝 e 抗原(HBeAg)阳性和 HDV 阴性患者进行了分组分析。对肝功能、定量 HBsAg(qHBsAg)、抗 HDV 免疫球蛋白(Ig)M、Mac-2 结合蛋白糖基化异构体(M2BPGi)、乙型肝炎病毒(HBV)DNA 水平和 HDV RNA 水平进行了检测。在显示抗 HDV IgG 的患者中,85.3%(122/143)的患者 HDV RNA 呈阳性。HDV 阳性患者的肝病活动度高于 HDV 阴性患者。HDV 阳性组中,qHBsAg 和 M2BPGi 水平较高的患者比例更高(p < 0.001)。HDV 阳性组的抗 HDV IgM 阳性率明显更高(p < 0.001)。在HBeAg阳性-HDV阳性患者中,HDV RNA水平与qHBsAg水平呈反相关(r = -0.49,p = 0.034),而在HBeAg阴性患者中,HDV RNA水平与qHBsAg水平呈正相关(r = 0.35,p < 0.001)。乙型肝炎病毒(HBV)DNA 和 HDV RNA 水平不存在任何相关性。M2BPGi 水平与 HDV RNA 水平同样没有相关性。使用高灵敏度的 HDV RNA 检测法,蒙古的 HBV 患者 HDV RNA 阳性率很高。HDV RNA 阳性患者的抗 HDV IgM 阳性率也很高。HDV RNA 阳性组的肝病严重程度和 M2BPGi 水平都很高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence, characteristics, and virologic correlations of hepatitis delta (D) among patients with hepatitis B surface antigen in Mongolia.

Clinical and biochemical features of hepatitis delta virus (HDV) infections in Mongolia remain largely unknown. We aimed to investigate the clinical characteristics of HDV patients in Mongolia using several markers. The 143 hepatitis B surface antigen (HBsAg)-positive patients were divided into 122 HDV-positive and 21 HDV-negative patients by HDV RNA positivity. Subgroup analysis was performed between hepatitis B e antigen (HBeAg)-positive and -negative HDV-positive patients. Liver function, quantitative HBsAg (qHBsAg), anti-HDV Immunoglobulin (Ig) M, Mac-2 binding protein glycosylation isomer (M2BPGi), hepatitis B virus (HBV) DNA level, and HDV RNA level were tested. HDV RNA was positive in 85.3% (122/143) of patients showing anti-HDV IgG. Liver disease activity was higher in HDV-positive patients than in HDV-negative patients. The HDV-positive group included a higher proportion of patients with high qHBsAg and M2BPGi levels (p < 0.001). The positivity rate for anti-HDV IgM was significantly higher in the HDV-positive group (p < 0.001). HDV RNA levels showed an inverse correlation with qHBsAg levels in HBeAg-positive-HDV-positive patients (r = -0.49, p = 0.034), and a positive correlation with qHBsAg levels in HBeAg-negative patients (r = 0.35, p < 0.001). Hepatitis B virus (HBV) DNA and HDV RNA levels did not show any correlation. M2BPGi levels likewise did not correlate with HDV RNA levels. A high positivity rate for HDV RNA was observed for HBV patients in Mongolia using the highly sensitive HDV RNA assay. The positivity rate for anti-HDV IgM was high in HDV RNA-positive patients. Severity of liver disease and M2BPGi levels were both high in the HDV RNA-positive group.

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