alexa Hepatitis B Viral Load (HBV-DNA) with Age and Sex Stratifications in Bangladeshi People | OMICS International
ISSN: 2161-0703
Journal of Medical Microbiology & Diagnosis
Like us on:
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Hepatitis B Viral Load (HBV-DNA) with Age and Sex Stratifications in Bangladeshi People

Moyen Uddin Pk1*, Rabby A2, Nahar Begum SMK3, Kabir Y2, Rahman M4 and Absar N4

1Department of Biochemistry, Primeasia University, Dhaka-1213, Bangladesh

2Department of Biochemistry & Molecular Biology, Dhaka University, Bangladesh

3Department of pathology, Anwer Khan Modern Medical College & Hospital Ltd., Bangladesh

4Department of Biochemistry & Molecular Biology, Rajshahi University, Bangladesh

*Corresponding Author:
Moyen Uddin PK
Department of Biochemistry, Primeasia University
Dhaka-1213, Bangladesh
Tel: +88029822133
E-mail: [email protected]

Received Date: June 25, 2014; Accepted Date: June 29, 2014; Published Date: July 01, 2014

Citation: Moyen Uddin PK, Rabby A, Nahar Begum SMK, Kabir Y, Rahman M, et al. (2014) Hepatitis B Viral Load (HBV-DNA) with Age and Sex Stratifications in Bangladeshi People. J Med Microb Diagn 3:144. doi: 10.4172/2161-0703.1000144

Copyright: © 2014 Moyen Uddin PK, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Journal of Medical Microbiology & Diagnosis

Abstract

Background: Hepatitis B virus surface antigen (HBsAg) is used for the detection of Hepatitis B virus (HBV) infection and to predict disease progression.

Objectives: The main objective of this study was to observe the pattern of HBV viral load levels among people in terms of age and sex distribution in Bangladesh.

Method: Blood specimen was collected from 585 objects with HBsAg Positive and assayed for the quantity of hepatitis B virus using PCR based technique.

Results: It is found from the study that the mean viral load was 353,500,000 DNA copies/ml for 20-35 age group, 249,300,000 DNA copies/ml for 35-50 age group and 104,800,000 DNA copies/ml for 50-65 age group. The median HBV viral loads for male and female were 58,494 and 103,287 DNA copies/ml, respectively.

Conclusion: High viral load was observed in the 21-35 and 36-50 age group while females are at most risk due to HBV infection as their viral load is higher compared to male.

Keywords

Viral load; HBV infection; HBV DNA; Bangladesh

Introduction

Hepatitis B virus (HBV) infection is considered as a serious public health concern worldwide since more than 350 million people are chronic carriers of HBV [1]. Persistent HBV infection is a risk factor for the development of Hepatocellular Carcinoma (HCC) [2]. According to Liver Foundation of Bangladesh incidence of Hepatitis-B infection in Bangladesh is about 4%-7% of total population. About 3.5% of pregnant mothers in Bangladesh are the carriers of the hepatitis B virus. Among them those are HBeAg positive (about 90%) will transmit the virus to their offspring [3]. According to a study published in 1996, 36% of the Hepatocellular carcinoma is associated with hepatitis B infection in Bangladesh [4]. Influence of age and sex on the development of HBV carrier state has been studied and a consistent relation was found [5].

Hepatitis B Virus surface Antigen (HBsAg) is an important marker for the detection of HBV infection and also it can be used to predict disease progression [6]. In Bangladesh although there is setup for quantitative detection of HBV viral load but these tests are quite expensive and rare [7]. It should be also consider that co-infections and super-infections with other hepatitis viruses (e.g. HCV) may also occur [8]. Therefore, person's disease history, age, sex, vaccination status and previous tests results should be considered to guide appropriate testing. The purpose of our study was to present the pattern of HBV viral load levels among people in terms of age and sex distribution in Bangladesh.

Materials and Methods

All samples were collected from six different metropolitan city of Bangladesh. Metropolitan cities have supply water system for drinking purpose and also sewage system parallel, most of the slum area have no proper sanitation system especially in the slum are of Dhaka city and hospitals do not have legitimate waste management system.
 

Specimen collection and processing

A bio-data was raised for each of the 585 subjects containing details of their age and sex. All subjects were informed about this study and only included if they permitted to use their data. Inclusion criteria for the subjects were age from 12 to 80 years old and HBsAg Positive. Only the first test carried out by a patient was included in this study. The specimen of choice for the diagnosis of HBV infection was blood. In brief, 5 ml of blood was collected from each individual into EDTA treated tubes and centrifuged for 10 minutes. The plasma was separated and stored at -20°C until analyzed. Patients had been previously confirmed as HBsAg positive and well aware about their inclusion in this study, prior to assessing the HBV viral load test.

HBV DNA viral load assay

Samples were assayed for the quantity of hepatitis B virus according to the SMART CYCLER HBV monitor test Version 2.0, a PCR based technique. The HBV viral load results were expressed in DNA copies/ml.

Statistical analyses

Graph Pad Prism 5 was used for statistical analysis and test of significance was done using Kruskal-Wall is statistical packages [9]. Differences of p<0.05 were taken to be statistically significant at 95% confidence interval.

Results

In brief, HBV viral load is found minimum 256 and maximum 15,645,417,077 DNA copies/ml among the participants sample. The mean value of the viral load is observed using statistical analysis 263,000,000 DNA copies/ml with 95% Confidence Interval (CI) (lower mean: 157,100,000; upper mean: 368,900,000). Mean Value at 75% Percentile is calculated 6,169,000 DNA copies/ml.

The participant’s age range was from 20 to 65 Years. We have equally classified the age range into three categories: 20-35, 36-50 and 51-65 years of old (Table 1). As the life expectancy of Bangladeshi people is 69.8 years [10]; therefore this age distribution is covered the entire population of Bangladesh except younger population and children. The mean viral load found 353,500,000 DNA copies/ml for 20-35 age group, while it was 249,300,000 DNA copies/ml for 35-50 age group and 104,800,000 DNA copies/ml for 50-65 age group. The median HBV viral loads for male and female were 58,494 and 103,287 DNA copies/ml, respectively (P>0.005) (Table 2). Male to female ratio was 2:1.

Values\Age Distribution (Years) <20 20-35 36-50 51-65 >65
Mean 1,562,000 273,800,000 228,100,000 104,000,000 20,334
Median 21,546 28,749 57,646 54,823 22,565
Lower 95% CI of mean -793,239 120,400,000 77,820,000 -5,926,000 -23,054
Upper 95% CI of mean 3,918,000 427,200,000 378,300,000 214,000,000 63,723

Table 1: The age distribution of the HBV viral load

Values/Sex Distribution Male Female
Mean 218,800,000 209,800,000
Median 36,627 36,548
Lower 95% CI of mean 113,300,000 57,840,000
Upper 95% CI of mean 324,300,000 361,700,000

Table 2: The sex distribution of the HBV viral load

Discussion

Infection with HBV is under control in developed countries, but it is still a serious public health problem in developing countries like Bangladesh. In this study we examined the viral load pattern of those assessing laboratory services at our site, being the only laboratory at present where HBV viral load is carried out commercially within the country. As such samples were received from a wide range of localities across the country. There was a wide age range observed by the patients, with the highest prevalence being between 30-39 years (Figure 1).

medical-microbiology-diagnosis-viral-load

Figure 1: Prevalence of HBV viral load among different age group. Age group below 20 years has minimum viral load as people above 65 years old. On the contrary, People between 36 to 65 years old has highest risk of HBV infection.

Infection with HBV is a serious public health concern in Bangladesh like other developing countries. According to WHO [11], 2–5% of the general population in the Indian subcontinent is chronically infected with HBV. In this study viral load pattern was examined in the blood sample collected from various site of the country. In the wide age range of patients highest prevalence was observed between 36-50 years (29.47% of the population). Males have relatively higher prevalace than female. Country like Bangladesh males are the main work resourse; they travel to the different part of the country for business or job purpose, drink unhygienic resturant water or supply water from roadside small tea shop. Therefore males are likely to be exposed to the contamination rather than females. The lower and upper limit of viral load found in the analysis for the Hepatitis B monitor assay is 128,300,000 and 301,900,000 DNA copies/ml respectively.

HBV viral load is important for clinical monitoring and treatment of individual with high HBV viral load as it is an indepenednt predictor of liver cancer lisk. Measurements of HBV viral load and genotype may help to define which male HBV carriers aged 30 years or older are at high risk for HCC [12]. our study showed that HBV is more prevalent in male group and in the 36-50 age group. According to a Taiwanises study the risk of HCC is closely associated with HBV. They also showed that HBV DNA levels were persistently elevated in patients at highest risk of liver cancer [13]. Another study in the Gambia, West Africa showed that High-level HBV DNA (>10,000 copies/ml) was strongly associated with both HCC and cirrhosis (17- and 39-fold increased risk); even Lower level HBV viremia (200–10,000 copies/ml) confer a significant risk of HCC [14]. Though Antiviral treatment is the only way to reduce morbidity and mortality from chronic HBV infection but The implementation of mass immunization programs, which have been recommended by the World Health Organization since 1991, have dramatically decreased the incidence of HBV infection among infants, children, and adolescents in many countries [15].

However regular/routine screening of the HBV can alter that morbidity rate in Bangladesh and also the risk could be minimized if the National programme on immunization (NPI) scheme for HBV vaccination is implemented.

Conclusion

In conclusion, high viral load observed in the 21-35 and 36-50 age group where risk of HCC is involved. There were no study performed to compare the HBV viral load of metropolitopn population with rural poulation. Also it would be nice if geographical distribusion can be shown by further study. However, it is recommended that there should be health education for public and health care providers and also screening and vaccination of all special risk groups. National vaccination program and mass awareness about HBV infection can reduce the risk of viral infection and other associated disease.

Acknowledgements

We are thankful to Anwer Khan Modern Medical College & Hospital Ltd, Dhaka, Bangladesh for their providing opportunity of sample collection and help to carry out the research work.

Conflict of Interest

There is no conflict of interest

References

Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Relevant Topics

Recommended Conferences

  • 10th World Congress on Alzheimers Disease & Dementia
    May 30-31, 2018 Osaka, Japan
  • 4th World Congress and Exhibition on Antibiotics and Antibiotic Resistance
    June 14-15, 2018 Barcelona, Spain
  • 4th Annual Congress on Infectious Diseases  
    September 17-18, 2018 San Diego, USA
  • 13th World Congress on Virology
    September 26-27, 2018 Montreal, Canada

Article Usage

  • Total views: 12215
  • [From(publication date):
    September-2014 - Dec 16, 2017]
  • Breakdown by view type
  • HTML page views : 8435
  • PDF downloads : 3780
 

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

Agri & Aquaculture Journals

Dr. Krish

[email protected]

1-702-714-7001Extn: 9040

Biochemistry Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Business & Management Journals

Ronald

[email protected]

1-702-714-7001Extn: 9042

Chemistry Journals

Gabriel Shaw

[email protected]

1-702-714-7001Extn: 9040

Clinical Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Engineering Journals

James Franklin

[email protected]

1-702-714-7001Extn: 9042

Food & Nutrition Journals

Katie Wilson

[email protected]

1-702-714-7001Extn: 9042

General Science

Andrea Jason

[email protected]

1-702-714-7001Extn: 9043

Genetics & Molecular Biology Journals

Anna Melissa

[email protected]

1-702-714-7001Extn: 9006

Immunology & Microbiology Journals

David Gorantl

[email protected]

1-702-714-7001Extn: 9014

Materials Science Journals

Rachle Green

[email protected]

1-702-714-7001Extn: 9039

Nursing & Health Care Journals

Stephanie Skinner

[email protected]

1-702-714-7001Extn: 9039

Medical Journals

Nimmi Anna

[email protected]

1-702-714-7001Extn: 9038

Neuroscience & Psychology Journals

Nathan T

[email protected]

1-702-714-7001Extn: 9041

Pharmaceutical Sciences Journals

Ann Jose

[email protected]

1-702-714-7001Extn: 9007

Social & Political Science Journals

Steve Harry

[email protected]

1-702-714-7001Extn: 9042

 
© 2008- 2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version