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2
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Genet Med. 2019 May;21(5):1155-1163. doi: 10.1038/s41436-018-0309-9. Epub 2018 Sep 26.
3
Age and Sex but Not ATP7B Genotype Effectively Influence the Clinical Phenotype of Wilson Disease.年龄和性别而非 ATP7B 基因型有效影响威尔逊病的临床表型。
Hepatology. 2019 Apr;69(4):1464-1476. doi: 10.1002/hep.30280. Epub 2019 Mar 1.
4
Global prevalence, treatment, and prevention of hepatitis B virus infection in 2016: a modelling study.2016 年全球乙型肝炎病毒感染的流行率、治疗和预防:一项建模研究。
Lancet Gastroenterol Hepatol. 2018 Jun;3(6):383-403. doi: 10.1016/S2468-1253(18)30056-6. Epub 2018 Mar 27.
5
Impact of previous hepatitis B infection on the clinical outcomes from chronic hepatitis C? A population-level analysis.既往乙型肝炎感染对慢性丙型肝炎临床结局的影响?一项基于人群的分析。
J Viral Hepat. 2018 Aug;25(8):930-938. doi: 10.1111/jvh.12897. Epub 2018 Apr 15.
6
The prevalence of hepatitis B infection in central China: An adult population-based serological survey of a large sample size.中国中部地区乙型肝炎感染的流行情况:一项基于大样本的成人血清学调查。
J Med Virol. 2017 Mar;89(3):450-457. doi: 10.1002/jmv.24649. Epub 2016 Aug 9.
7
An epidemiological serosurvey of hepatitis B virus shows evidence of declining prevalence due to hepatitis B vaccination in central China.一项关于乙型肝炎病毒的流行病学血清学调查显示,由于在中国中部地区进行了乙肝疫苗接种,其流行率有下降的迹象。
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8
Prospective evaluation of the diagnostic accuracy of hepatic copper content, as determined using the entire core of a liver biopsy sample.对使用肝活检样本整个核心部分测定的肝铜含量诊断准确性的前瞻性评估。
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9
A genetic study of Wilson's disease in the United Kingdom.英国的威尔逊病遗传研究。
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10
HBV and HCV infections in Wilson's disease patients: copper overload could be protective?威尔逊病患者中的乙肝病毒和丙肝病毒感染:铜过载可能具有保护作用?
Clin Biochem. 2012 Sep;45(13-14):1095-6. doi: 10.1016/j.clinbiochem.2012.04.026. Epub 2012 May 5.

Wilson 病患者乙型肝炎病毒感染:一项大型回顾性研究。

Hepatitis B virus infection in patients with Wilson disease: A large retrospective study.

机构信息

Department of Infectious Diseases, Institute of Hepatology, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan Province, China.

出版信息

World J Gastroenterol. 2023 Aug 28;29(32):4900-4911. doi: 10.3748/wjg.v29.i32.4900.

DOI:10.3748/wjg.v29.i32.4900
PMID:37701133
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10494763/
Abstract

BACKGROUND

Wilson disease (WD) is the most common genetic metabolic liver disease. Some studies have shown that comorbidities may have important effects on WD. Data on hepatitis B virus (HBV) infection in patients with WD are limited.

AIM

To investigate the prevalence and clinical impact of HBV infection in patients with WD.

METHODS

The clinical data of patients with WD were analyzed retrospectively, and the data of patients with concurrent WD and HBV infection were compared with those of patients with isolated WD.

RESULTS

Among a total of 915 WD patients recruited, the total prevalence of current and previous HBV infection was 2.1% [95% confidence interval (CI): 1.2%-3.0%] and 9.2% (95%CI: 7.3%-11.1%), respectively. The main finding of this study was the identification of 19 patients with concurrent WD and chronic hepatitis B (CHB) infection. The diagnosis of WD was missed in all but two patients with CHB infection. The mean delay in the diagnosis of WD in patients with concurrent WD and CHB infection was 32.5 mo, which was significantly longer than that in patients with isolated WD (10.5 mo). The rates of severe liver disease and mortality in patients with concurrent WD and CHB infection were significantly higher than those in patients with isolated WD (63.1% 19.3%, = 0.000 and 36.8% 4.1%, < 0.001, respectively). Binary logistic regression analysis revealed a significantly higher risk of severe liver disease at the diagnosis of WD in patients with current HBV infection [odds ratio (OR) = 7.748; 95%CI: 2.890-20.774; = 0.000)] or previous HBV infection (OR = 5.525; 95%CI: 3.159-8.739; = 0.000) than in patients with isolated WD.

CONCLUSION

The total prevalence of current HBV infection in patients with WD was 2.1%. The diagnosis of WD in CHB patients is usually missed. HBV infection is an independent risk factor for severe liver disease in WD patients. The diagnosis of WD should be ruled out in some patients with CHB infection.

摘要

背景

威尔逊病(WD)是最常见的遗传性代谢性肝病。一些研究表明,合并症可能对 WD 有重要影响。关于 WD 患者乙型肝炎病毒(HBV)感染的数据有限。

目的

探讨 WD 患者 HBV 感染的流行情况及其对 WD 的临床影响。

方法

回顾性分析 WD 患者的临床资料,并比较合并 WD 和 HBV 感染患者与单纯 WD 患者的资料。

结果

共纳入 915 例 WD 患者,HBV 现症和既往感染的总患病率分别为 2.1%(95%可信区间:1.2%-3.0%)和 9.2%(95%可信区间:7.3%-11.1%)。本研究的主要发现是鉴定出 19 例合并 WD 和慢性乙型肝炎(CHB)感染的患者。在所有合并 CHB 感染的患者中,除 2 例外,均漏诊了 WD 的诊断。合并 WD 和 CHB 感染的患者诊断为 WD 的平均延迟时间为 32.5 个月,明显长于单纯 WD 患者(10.5 个月)。合并 WD 和 CHB 感染患者严重肝病和死亡率显著高于单纯 WD 患者(63.1%比 19.3%,=0.000 和 36.8%比 4.1%,均<0.001)。二元逻辑回归分析显示,HBV 现症感染(比值比[OR] = 7.748;95%可信区间:2.890-20.774;=0.000)或既往感染(OR = 5.525;95%可信区间:3.159-8.739;=0.000)的 WD 患者发生严重肝病的风险显著高于单纯 WD 患者。

结论

WD 患者 HBV 现症感染的总患病率为 2.1%。CHB 患者的 WD 诊断通常被漏诊。HBV 感染是 WD 患者发生严重肝病的独立危险因素。对于某些 CHB 感染患者,应排除 WD 诊断。