Prevalence of Dual-Positivity for Both Hepatitis B e Antigen and Hepatitis B e Antibody Among Hospitalized Patients with Chronic Hepatitis B Virus Infection.

hepatitis B e antibody hepatitis B e antigen

Journal

International journal of general medicine
ISSN: 1178-7074
Titre abrégé: Int J Gen Med
Pays: New Zealand
ID NLM: 101515487

Informations de publication

Date de publication:
2021
Historique:
received: 09 07 2021
accepted: 25 08 2021
entrez: 24 9 2021
pubmed: 25 9 2021
medline: 25 9 2021
Statut: epublish

Résumé

The detection of dual-positivity for both hepatitis B e antigen (HBeAg) and hepatitis B e antibody (anti-HBe) is not typically performed for patients with hepatitis B virus (HBV). This cross-sectional study was designed to figure out the prevalence of dual-positivity for both HBeAg and anti-HBe (DEP) among hospitalized patients with chronic hepatitis B virus infection (C-HBVI). Data from 2820 cases with C-HBVI from two centers in China were retrospectively analyzed. Univariate and multivariate logistic regression analyses were undertaken to identify the risk factors for liver fibrosis (LF) and acute-on-chronic liver failure (ACLF). There were 165 (5.9%), 688, and 1903 patients in DEP, HBeAg+/anti-HBe-, and HBeAg-/anti-HBe+ groups, respectively. The DEP patients' median age was 43.6 years old and 71.5% of them were male. They had higher levels of alanine transaminase, total bilirubin, and international normalized ratio. Furthermore, DEP cases had a higher proportion of liver cirrhosis, and it was associated with non-invasive testing of LF, including aspartate transaminase (AST)-to-platelet ratio index (APRI) >1.5 (odds ratio (OR) = 1.96, 95% confidence interval (CI): 1.27-3.03, DEP cases are at higher risks of LF and ACLF than other patients with HBV infection. A fast diagnosis and an active monitoring of liver diseases for DEP patients are extremely vital.

Identifiants

pubmed: 34557028
doi: 10.2147/IJGM.S328714
pii: 328714
pmc: PMC8454426
doi:

Types de publication

Journal Article

Langues

eng

Pagination

5759-5770

Informations de copyright

© 2021 Liu et al.

Déclaration de conflit d'intérêts

The authors declare that there is no conflict of interest.

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Auteurs

Yuanyuan Liu (Y)

Department of Infectious Diseases, State Key Laboratory of Organ Failure Research, Guangdong Provincial Key Laboratory of Viral Hepatitis Research, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, People's Republic of China.
Department of Infectious Diseases, Dongguan People's Hospital, Dongguan, Guangdong, People's Republic of China.

Songmei He (S)

Department of Infectious Diseases, Dongguan People's Hospital, Dongguan, Guangdong, People's Republic of China.

Sichun Yin (S)

Department of Infectious Diseases, Dongguan People's Hospital, Dongguan, Guangdong, People's Republic of China.

Qingyang Zhong (Q)

Department of Infectious Diseases, Dongguan People's Hospital, Dongguan, Guangdong, People's Republic of China.

Jianbo Zhong (J)

Department of Infectious Diseases, Dongguan People's Hospital, Dongguan, Guangdong, People's Republic of China.

Xiaoyong Zhang (X)

Department of Infectious Diseases, State Key Laboratory of Organ Failure Research, Guangdong Provincial Key Laboratory of Viral Hepatitis Research, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, People's Republic of China.

Rong Fan (R)

Department of Infectious Diseases, State Key Laboratory of Organ Failure Research, Guangdong Provincial Key Laboratory of Viral Hepatitis Research, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, People's Republic of China.

Jinlin Hou (J)

Department of Infectious Diseases, State Key Laboratory of Organ Failure Research, Guangdong Provincial Key Laboratory of Viral Hepatitis Research, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, People's Republic of China.
Hepatology Unit, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangdong, People's Republic of China.

Classifications MeSH