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1.
Rwanda Journal of Medicine and Health Sciences ; 6(2): 199-207, 2023. figures, tables
Article in English | AIM | ID: biblio-1509421

ABSTRACT

Background Hepatitis B virus (HBV) infection among pregnant women has a high rate of vertical transmission and consequential effects on fetal and neonatal outcomes. The aim of this study was to determine the prevalence and associated risk factors of infection among pregnant women attending antenatal care services in Osogbo, Nigeria. Methodology This hospital based cross-sectional study was conducted among pregnant women attending routine antenatal care clinic between April and June 2021. Systematic random sampling technique was used to recruit 240 pregnant women, their data were collected by face to face interview using a pretested questionnaire, while blood sample was collected aseptically to determine hepatitis B surface antigen by enzyme linked immunosorbent assay test kit. Univariate and multivariate logistic regression were used to examine the association between explanatory variables and outcome variable. Results The mean age and seroprevalence of the study population were 27.50 ± 4.4 years and 5.8% respectively. The significant risk factors for HBV infection were tattooing (aOR = 5.22; 95% CI = 0.52­8.01; p = 0.0000), history of multiple sexual partners (aOR = 2.88; 95% CI = 1.92­12.42; p = 0.0044); and past history of contact with HBV patient (aOR = 2.17; 95% CI = 1.21­15.32; p = 0.0310) were significant predictors of HBV infection. Conclusion The seroprevalence of HBV from this study was of intermediate endemicity. We therefore, advocate for continuous health education programs on the mode of HBV transmission, high-risk behaviors and methods of preventions at antenatal care clinics to raise the awareness of mothers and limit the spread of infection.


Subject(s)
Humans , Male , Female , Seroepidemiologic Studies , Hepatitis B virus , Hepatitis B Surface Antigens
2.
Afr. health sci. (Online) ; 22(2): 107-115, 2022. figures, tables
Article in English | AIM | ID: biblio-1400304

ABSTRACT

Background: Hepatitis B virus infection is one of the leading causes of liver diseases which occurs worldwide particularly in developing countries. It is often caused by prenatal transmission from mother to child or household transmission from a close contact during early childhood. It causes different complications like; jaundice, induces premature labor, and prematurity. Objective: The aim of this study was to estimate the sero-prevalence of hepatitis B virus surface antigen and associated factors among women of reproductive age in Bench Maji Zone, South West Ethiopia. Methods: A community-based cross-sectional study was conducted from December 15th, 2016 to February 15th, 2017. Multistage sampling technique was applied to select study participants. Logistic regression analysis was applied and p-values < 0.05 was used to see the significant association between dependent and independent variables. Results: A total of 330 participants were included in this study yielding 98.8% response rate. The sero-prevalence of HBsAg among women of reproductive age was 28(8.5%). Having multiple sexual partners (AOR = 18.73, 95% CI =3.65, 96.21) history of unprotected sex (AOR = 9.39, 95% CI =1.64, 53.77) were found to be significantly associated with sero-prevalence of HBV. Conclusions: The sero-prevalence of HBV infection among women of reproductive age was highly endemic. Hence, behavioral education and communication programs focusing on reduction of risky sexual behaviors should be designed to reduce HBV infection.


Subject(s)
Humans , Male , Female , Hepatitis B virus , Hepatitis B , Hepatitis B Surface Antigens , Obstetric Labor, Premature , Jaundice
3.
African Health Sciences ; 22(1): 496-503, March 2022. Figures, Tables
Article in English | AIM | ID: biblio-1400684

ABSTRACT

Background: Hepatitis B virus infection is one of the leading causes of liver diseases which occurs worldwide particularly in developing countries. It is often caused by prenatal transmission from mother to child or household transmission from a close contact during early childhood. It causes different complications like; jaundice, induces premature labor, and prematurity. Objective: The aim of this study was to estimate the Sero-prevalence of hepatitis B virus surface antigen and associated factors among women of reproductive age in Bench Maji Zone, South West Ethiopia. Methods: A community-based cross-sectional study was conducted from December 15th, 2016, to February 15th, 2017. Multistage sampling technique was applied to select study participants. Logistic regression analysis was applied and p-values < 0.05 was used to see the significant association between dependent and independent variables. Results: A total of 330 participants were included in this study yielding 98.8% response rate. The Sero-prevalence of hbsag among women of reproductive age was 28(8.5%). Having multiple sexual partners (AOR = 18.73, 95% CI = [3.65, 96.21) history of unprotected sex (AOR = 9.39, 95% CI = [1.64, 53.77) were found to be significantly associated with Sero-prevalence of HBV. Conclusions: The Sero-prevalence of HBV infection among women of reproductive age was highly endemic. Hence, behavioral education and communication programs focusing on reduction of risky sexual behaviors should be designed to reduce HBV infection


Subject(s)
Viruses , Hepatitis B , Infections , Liver Diseases , Antigens, Surface , Reproductive Control Agents , Women , Ethiopia
4.
Journal of Clinical Hepatology ; (12): 51-55, 2021.
Article in Chinese | WPRIM | ID: wpr-862544

ABSTRACT

Objective To investigate the noninvasive indicators of indications for antiviral therapy in HBeAg-negative chronic hepatitis B virus (HBV) infection patients with alanine aminotransferase (ALT) ≤40 U/L under the guidance of liver pathology. MethodsA retrospective analysis was performed for the clinical data of 377 HBeAg-negative chronic HBV infection patients with ALT ≤40 U/L who were hospitalized in Affiliated Hospital of Yan’an University, from October 2013 to August 2018 and underwent liver biopsy, among whom the patients with inflammatory activity <A2 and fibrosis stage <F2 were enrolled as non-antiviral therapy group(n=266), and the patients with inflammatory activity ≥A2 or fibrosis stage ≥F2 were enrolled as antiviral therapy group(n=111). The chi-square test was used for comparison of categorical data between two groups; the t-test was used for comparison of normally distributed continuous data between two groups, and the Mann-Whitney U test was used for comparison of non-normally distributed continuous data between two groups; univariate and multivariate binary logistic regression analyses were used to screen out the influencing factors for the initiation of antiviral therapy; the receiver operating characteristic (ROC) curve was plotted to evaluate the diagnostic efficiency of each indicator in determining the need for antiviral therapy in HBeAg-negative chronic HBV infection patients with ALT ≤40 U/L. ResultsOf all 377 patients, 266 (70.6%) did not need antiviral therapy for the time being, and 111 (29.4%) had marked liver damage and thus needed active antiviral therapy. The multivariate analysis showed that liver stiffness measurement (LSM) (odds ratio [HR]=2.003, 95% confidence interval [CI]: 1.647-2.437, P<005), HBsAg (HR=1.563, 95% CI: 1.110-2.200, P<0.05), HBV DNA (HR=1.519, 95% CI: 1173-1.966, P<0.05), and albumin (HR=0.939, 95% CI: 0.884-0.998, P<0.05) were independent influencing factors for the initiation of antiviral therapy. The ROC curve analysis showed that the area under the ROC curve (AUC) was 0.749 (95% CI: 0.699-0799) for LSM, 0642 (95% CI: 0.586-0.699) for HBV DNA, and 0.565 (95% CI: 0.507-0.623) for HBsAg, and the combination of LSM, HBV DNA, and HBsAg had a larger AUC of 0.779 (95% CI: 0.732-0.827). ConclusionThe levels of LSM, HBV DNA, and HBsAg have a reference value in determining the initiation of antiviral therapy in HBeAg-negative chronic HBV infection patients with ALT≤40 U/L.

5.
Hepatología ; 1(2): 116-133, 2020. ilus, tab
Article in Spanish | LILACS, COLNAL | ID: biblio-1396635

ABSTRACT

El virus de la hepatitis delta (VHD) es un virus satélite del virus de la hepatitis B (VHB), dado que requiere el antígeno de superficie del VHB (HBsAg) para la producción de partículas virales infecciosas. Se han caracterizado ocho genotipos del VHD, con una distribución geográfica relacionada con la prevalencia de la infección por VHB. Se estima que aproximadamente el 5% de los pacientes con infección crónica por VHB también están infectados con VHD. Se han descrito dos tipos de infección: la coinfección simultánea por VHB y VHD, y la superinfección con VHD en un paciente previamente infectado por VHB, esta última asociada a una mayor morbilidad y mortalidad por falla hepática aguda. La infección se diagnostica en nuestro medio con la determinación de IgM contra el VHD, acompañada idealmente de la carga viral. Aunque el tratamiento de elección es la terapia con interferón alfa pegilado, en el momento se están evaluando otros medicamentos antivirales en ensayos clínicos, con resultados alentadores, teniendo en cuenta el efecto observado en la carga viral del VHD y/o del VHB en los pacientes. La presente revisión tiene como objetivo incluir temas como la biología del virus, la epidemiología, las características clínicas, el diagnóstico y el tratamiento en la infección por VHD.


Hepatitis delta virus (HDV) is a satellite virus of hepatitis B virus (HBV), as it requires the HBV surface antigen (HBsAg) for the production of infectious viral particles. Eight HDV genotypes have been characterized with a geographic distribution associated with the prevalence of HBV infection. It is estimated that approximately 5% of patients with chronic HBV infection are also infected with HDV. Two types of infection have been described: coinfection, by simultaneously contracting HBV and HDV infection, and superinfection, by contracting HDV when chronically infected with HBV, the latter associated with increased morbidity and mortality from acute liver failure. Anti-HDV IgM is used to diagnose the infection, ideally together with the detection of HDV-RNA. Although the treatment of choice is pegylated interferon alpha, other antiviral drugs are currently being evaluated in clinical trials, with encouraging results, in terms of their effect on HDV and/or HBV viral load in patients. This review aims to include topics such as virus biology, epidemiology, clinical manifestations, diagnosis, and treatment in HDV infection.


Subject(s)
Humans , Hepatitis Delta Virus , Hepatitis B virus , Epidemiology , Diagnosis , Drug Therapy
6.
Chinese Journal of Integrated Traditional and Western Medicine in Intensive and Critical Care ; (6): 62-64, 2019.
Article in Chinese | WPRIM | ID: wpr-754503

ABSTRACT

Objective To observe the clinical efficacy of artificial liver plasma bilirubin adsorption for treatment of patients with severe viral hepatitis B (HBV). Methods A retrospective study was conducted, the 120 patients with severe HBV B and their historical data of having undergone treatment of artificial liver plasma bilirubin adsorption admitted to Department of Respiration of Mianyang Central Hospital from August 2015 to August 2017 were collected, and there were 68 cases in the cirrhotic group and 52 cases in the non-cirrhotic group. The indexes of liver function and coagulation function before and after the treatment of artificial liver plasma bilirubin adsorption were collected; the differences of alanine aminotransferase (ALT), aspartate aminotransferase (AST), glutamine transferase (GGT), alkaline phosphatase (ALP), lactate dehydrogenase (LDH), total protein (TP), albumin (Alb), globulin (Glo), prothrombin time (PT), prothrombin activity (PTA), total bilirubin (TBil) and indirect bilirubin (IBil), total bile acid (TBA), etc were compared between cirrhotic group and the severe hepatitis B non-cirrhotic group. Results The levels of ALT, AST, ALP, LDH after artificial liver plasma bilirubin adsorption therapy were lower than those before the treatment [ALT (U/L): 138.8±26.2 vs. 993.4±185.2, AST (U/L): 121.7±119.9 vs. 798.7±226.8, ALP (U/L): 129.7±8.1 vs. 178.9±14.1, LDH (μmol·L-1·s-1·L-1): 4.50±0.32 vs. 8.15 ±1.75, all P < 0.05], PTA was higher than that before the treatment [(43.2±25.6)% vs. (30.0±16.1)%, P < 0.05]. After the treatment, the decline rate of ALP, TBil, and TBA of non-cirrhotic group was higher than those in cirrhotic group (ALP: 34.20% vs. 17.80%, TBil: 39.10% vs. 18.10%, TBA:30.70% vs. 5.00%, P < 0.05), the elevation rate of PTA in non-cirrhotic group was also higher than that in cirrhotic group (52.50% vs. 25.10%, P < 0.05). Conclusion Artificial liver plasma bilirubin adsorption therapy is effective for treatment of patients with severe HBV B, particularly the effect being good on the early severe viral HBV B non-cirrhotic group.

7.
Rev. nefrol. diál. traspl ; 36(1): 21-25, ene. 2016. ilus
Article in Spanish | LILACS | ID: biblio-1006012

ABSTRACT

INTRODUCCIÓN: La vacunación frente al virus de la hepatitis B (VHB) es más efectiva en prediálisis pero en ocasiones el paciente llega a diálisis de forma no programada sin realizar vacunación completa previa. Pretendemos determinar el grado de respuesta a inmunización frente a VHB con diferentes esquemas en hemodiálisis. MATERIAL Y MÉTODOS: Estudiamos 30 pacientes en hemodiálisis administrando 2 esquemas de vacunación frente a VHB. Un grupo realiza el esquema de 3 dosis (0, 1, 6 meses) (PAUTA 3) y otro de 4 dosis (0, 1, 2, 6 meses) (PAUTA 4). RESULTADOS: El 56.7% hizo pauta 3 con respuesta del 26.7% y el 43.3% hizo pauta 4 con 23.3% de respuesta, sin diferencias significativas entre ambas (p=0.6). La tasa de AcHBs postvacunacional fue significativamente mayor con pauta 4 (p<0.05) así como en las tasas de anticuerpos mantenidas al año; a los 2 años las tasas de anticuerpos no fueron significativamente diferentes entre ambas pautas. En el resto de análisis estadístico, la vacunación realizada en pacientes con más tiempo en diálisis tuvo mayor respuesta con pauta 4 (p<0.05) aunque con respecto a los niveles de anticuerpos no hubo diferencias en los que respondieron con cada pauta. CONCLUSIONES: No existen diferencias en la respuesta inmunológica a vacunación frente VHB en hemodiálisis entre esquemas de 3 y 4 dosis. Hay mayor respuesta con el esquema de 4 dosis en la vacunación en pacientes con mayor tiempo en diálisis. Por ello, aconsejamos realizar la inmunoprofilaxis con el esquema de 3 dosis en pacientes incidentes en hemodiálisis que no han sido vacunados anteriormente


INTRODUCTION: Vaccination against hepatitis B virus (HBV) is more effective in pre-dialysis, but sometimes the patient has to start treatment in an unscheduled way, without full immunization coverage. We try to establish the immune response rate against HBV in hemodialysis with different vaccination schemes. METHODS: We studied 30 patients in hemodialysis program with 2 different vaccination schemes against HBV. One group performed a 3-doses scheme (0, 1 and 6 months) (PATTERN 3) and the other group performed a 4-doses scheme (0, 1, 2 and 6 months) (PATTERN 4). RESULTS: 56.7% performed pattern 3, with immune response of 26.7%. 43.3% performed pattern 4, with immune response of 23.3%, without significant differences between them (p=0.06). Anti-hepatitis B surface antibodies (anti-HBs) rate after vaccination was significantly higher with pattern 4 (p<0.05) as well as the antibodies counts maintained within 1 year. After 2 years, anti-HBs rates were not significantly different between both patterns. In other statical analysis, vaccination carried out in patients who have been for a long time in hemodialysis treatment, was more responsive with pattern 4 (p<0.05) although anti-HBs levels were similar in patients that had response with each pattern. CONCLUSIONS: There are no differences in immune response between 3-doses scheme and 4-doses scheme in HBV vaccination for hemodialysis patients. There is greater response with 4-doses scheme in hemodialysis patients who have not been vaccinated previously


Subject(s)
Humans , Renal Dialysis , Hepatitis B Vaccines/administration & dosage , Hepatitis B , Hepatitis B/prevention & control
8.
The Korean Journal of Gastroenterology ; : 369-375, 2007.
Article in Korean | WPRIM | ID: wpr-192065

ABSTRACT

BACKGROUND/AIMS: Alcohol may be a cocarcinogen in patients with chronic viral hepatitis. We investigated the effect of alcohol on the development of hepatocellular carcinoma (HCC) in liver cirrhosis (LC) caused by hepatitis B virus (HBV). METHODS: All patients with LC or HCC associated with HBV or alcohol, admitted between March 2001 and June 2005, were included. Patients were divided into three groups according to the etiology of LC: Alcohol (AL), HBV, or HBV+alcohol (HBV+AL). Age and laboratory data at the enrollment of study were analyzed. The logistic regression coefficiency for the prevalence of HCC was calculated by using variables such as age, gender, serologic markers, and etiology of LC. RESULTS: In LC patients (n=342), the proportions of AL, HBV, and HBV+AL groups were 44%, 39%, and 17%, respectively. The proportions of HCC in AL, HBV and HBV+AL groups were 17%, 55%, and 76%, respectively. Age at the diagnosis of HCC was younger in HBV+AL than in AL group (p=0.036). In logistic regression analysis for the risk factor of HCC, odds ratio of age was 1.056 (p<0.001). Odds ratios of HBV and HBV+AL group comparing AL were 8.449 (p<0.001) and 17.609 (p<0.001), respectively. Therefore, old age and chronic alcohol intake in patients with HBsAg were the risk factors of HCC. CONCLUSIONS: Chronic alcohol intake may be an additive factor for the development of HCC in patient with LC caused by HBV. However, a prospective cohort study is needed to confirm these findings.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Carcinoma, Hepatocellular/epidemiology , Cross-Sectional Studies , Hepatitis B, Chronic/complications , Hepatitis, Alcoholic/complications , Liver Cirrhosis/complications , Liver Cirrhosis, Alcoholic/complications , Liver Neoplasms/epidemiology , Odds Ratio , Regression Analysis , Retrospective Studies , Risk Factors
9.
Journal of Medical Research ; : 64-69, 2003.
Article in Vietnamese | WPRIM | ID: wpr-4830

ABSTRACT

A study was conducted among 427 HIV-positive patients at Bach Mai hospital in 6 months early 2002. The results showed that: the rate of HIV- positive patients in anti-HCV positive group was 81.03%, the rate of HBsAg in HIV- positive patients was 18.26%. The rate of co-infection of Hepatitis C virus, Hepatitis B virus in HIV- positive patients was 14.9%. The rate of hepatitis C virus infection in HIV- positive persons infected through injecting drug use was 88.5%; in HIV- positive persons infected both through injecting drug use and sex was 83.67%. The rate of HIV- positive in patients infected through sex was 47.44%


Subject(s)
Epidemiology , Hepacivirus , Hepatitis B virus , HIV
10.
Chinese Journal of Bases and Clinics in General Surgery ; (12)2003.
Article in Chinese | WPRIM | ID: wpr-545686

ABSTRACT

Objective To investigate the prevention of HBV reinfection in the perioperative period of liver transplantation on HBV-related diseases.Methods Published papers were collected and reviewed.Results HBV-related diseases were the main indications of liver transplantation.The prevention for HBV reinfection affects the survivals remarkably.Nowadays,a lot of medication have been used in the prevention of HBV reinfection,and the therapeutic regimens were different from each other.Conclusion Liver transplantation is an effective treatment for HBV-related disease.Appropriate prevention of HBV reinfection in the perioperative period of liver transplantation is important for the survivals of patients.

11.
The Korean Journal of Hepatology ; : 371-380, 2002.
Article in Korean | WPRIM | ID: wpr-161717

ABSTRACT

BACKGROUND/AIMS: Hepatitis B virus (HBV) is the etiological factor for hepatocellular carcinoma (HCC). Numerous evidence has indicated a link between chronic infection with HBV and the development of HCC. Among the four proteins encoded by HBV, Hepatitis B virus X gene(HBx), best characterized as a transcriptional transactivator, gained attention owing to its presumptive role in oncogenesis. Further, HBx has been shown to stimulate signal transduction pathways such as Ras-MAPK pathway, NF-kappaB, and Src kinase. The pleiotropic events caused by HBx may be the key to understanding the HBV-mediated oncogenicity. However, the specific roles of HBx in oncogenesis remain largely elusive. To explore the role of HBx in hepatocarcinogenesis, we examined the deregulation of host genes induced by HBx expression. METHODS: HBx was ectopically expressed in HepG2 cells using a recombinant adenovirus to transiently express HBx. Gene expression profiling of HBx was conducted on cDNA microarrays that contained 1,028 cDNAs. RESULTS: A number of oncogenes and genes that are involved in cell growth, DNA repair, cell cycle regulation, and cell motility were deregulated by HBx. CONCLUSIONS: Theses results suggest that HBx regulates transcription in a way that contributes to the proliferation of hepatocytes, a probable early event of HCC.


Subject(s)
Humans , Carcinoma, Hepatocellular/virology , Cell Line, Tumor , English Abstract , Gene Expression Profiling , Gene Expression Regulation , Genes, Viral/physiology , Genetic Vectors , Hepatitis B Antigens/genetics , Hepatitis B virus/genetics , Liver Neoplasms/virology , Oligonucleotide Array Sequence Analysis , Trans-Activators/genetics
12.
Traditional Chinese Drug Research & Clinical Pharmacology ; (6)1993.
Article in Chinese | WPRIM | ID: wpr-572495

ABSTRACT

Objective To investigate the pharmacological actions of Compound Hypericum Perforutum granule(CHPG). Methods Duck models with hepatitis B induced by 2.2.15 cell strain were used to observe the effect of CHPG on the replication of hepatitis B virus(HBV).Mice models of liver injury induced by CCl4,D-aminogalactose and BCG+LPS were applied to observe the protective effect of CHPG on liver and mice immune function.Solid-phase radioimmuoassay, spot-hybridism radiation self-developing method and MTT method were adopted.Results The average inhibitory rate of CHPG 125 ?g/mL was(29.8?2.3)%,(36.5?4.7)%and(30.3?8.8)%for HBsAg,HBeAg and HBV-DNA respectively.In the duckling hepatitis B model,CHPG 4.0,6.0,8.0 g/kg had an obvious effect in inhibiting the replication of DHBV-DNA,CHPG 8.0 g/kg in particular;the effect was weaker but maintained longer time than lamivudine.1.25,2.50,5.00 g/kg of CHPG could decreased serum levels of AST and ALT and protect liver cells mice with liver injury and increased serum hemolysin concentration(HC50).0.01~10 mg/L of CHPG accelerated the proliferation of T lymphocyte of mice in vitro.Conclusion CHPG is effective in reducing the secretion of HBsAg,HBeAg in vitro,inhibiting the replication of DHBV-DNA in duck hepatitis B model.It has effect in protecting liver cells,decreasing ALT and AST levels and regulating immune function.

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