Literature DB >> 35068784

Epidemiology, Genotyping, Mutational and Phylogenetic Analysis of Hepatitis B Virus Infection in North-east India.

Premashis Kar1, Bhabadev Goswami2, Jagdish Mahanta3, Thngam Bhimo4, Anup K Das5, Manab Deka6, Kyrshanlang G Lynrah7, Mool R Kotwal8, Pradip Bhaumik9, Moji Jini10, Rahul Karna1, Vijay K Karra11, Harpreet Kaur11.   

Abstract

BACKGROUND/
OBJECTIVE: Hepatitis B virus (HBV) infection is a major public health problem globally. Northeast India is home to indigenous tribes with different ethnicity and high rates of drug abuse and HIV infection. The study was designed to estimate the burden of HBV infection across various spectrums of liver diseases from this region. HBV genotypes and subgenotypes play a role in the chronicity of disease, response to treatment and its progression. As very limited data are available from this region, we tried to elucidate the role of HBV genotypes, HBV mutants and their phylogenetic analysis.
METHOD: We designed a prospective multicentric study, and included 7464 liver disease cases, 7432 blood donors and 650 health care workers, who were screened for HBV infection. HBV DNA positive patients were genotyped and subjected to surface protein, precore and core mutation and phylogenetic analysis.
RESULTS: The prevalence of HBV infection with respect to different types of liver diseases, blood donors and health care workers was 9.9% (1550/15,546). 49.5% (768/1550) cases were found to be HBV DNA positive. The most common genotype was found to be genotype D 74.2% (570/768), followed by genotype C 6.5% (50/768), A 4.4% (34/768) and I 0.9% (7/768).
CONCLUSION: This study highlights the high hepatitis B burden in Northeast India, reflecting lacunae in health care needs of the region. Also, the different genotype distribution and presence of mutations may translate into different rates of liver disease progression, prognosis and ultimately, clinical significance. However, further prospective cohort study from Northeast India is warranted, to elucidate the clinical significance of multiple genotypes and mutation in this unique population.
© 2021 Indian National Association for Study of the Liver. Published by Elsevier B.V.

Entities:  

Keywords:  AFP, alpha fetoprotein; ALT, alanine transaminase; AVH, acute viral hepatitis; BCP, basal core promoter mutations; CAH: chronic active hepatitis, CHB: chronic hepatitis B; CLD, chronic liver disease; DNA, deoxyribose nucleic acid; EASL, European Association for the study of the liver; FHF, fulminant hepatic failure; FNAC, fine needle aspiration cytology; HBV; HBV, hepatitis B virus; HBcAg, icosahedral core; HBsAg, surface proteins; HCC, hepatocellular carcinoma; PCR, polymerase chain reaction; RT, reverse transcriptase; SGOT, serum glutamic oxaloacetic transaminase; SGPT, serum glutamic pyruvic transaminase; SHB, small hepatitis B surface antigen; ULN, upper limit of normal; epidemiology; evolution; genotype; mutation

Year:  2021        PMID: 35068784      PMCID: PMC8766538          DOI: 10.1016/j.jceh.2021.04.002

Source DB:  PubMed          Journal:  J Clin Exp Hepatol        ISSN: 0973-6883


  43 in total

1.  A case-control study for clinical and molecular biological differences between hepatitis B viruses of genotypes B and C. Japan HBV Genotype Research Group.

Authors:  E Orito; M Mizokami; H Sakugawa; K Michitaka; K Ishikawa; T Ichida; T Okanoue; H Yotsuyanagi; S Iino
Journal:  Hepatology       Date:  2001-01       Impact factor: 17.425

2.  Virus evolution: the importance of being erroneous.

Authors:  Sebastian Bonhoeffer; Paul Sniegowski
Journal:  Nature       Date:  2002-11-28       Impact factor: 49.962

3.  [The discrepancy of HBsAg titre and HBV DNA in patients with chronic hepatitis B, HBV-related liver cirrhosis and hepatocellular carcinoma].

Authors:  Yan-zhen Pei; Tao Han; Xiao-yan Ma; Ying Li; Jing Xing; Zuo-li Song
Journal:  Zhonghua Gan Zang Bing Za Zhi       Date:  2011-10

4.  Correlation between quantitative serum HBsAg and HBV DNA test in Korean patients who showed high level of HBsAg.

Authors:  Jong-Han Lee; Sue Jung Kim; Sang Hoon Ahn; Jinhwa Lee; Yongjung Park; Hyon-Suk Kim
Journal:  J Clin Pathol       Date:  2010-09-23       Impact factor: 3.411

5.  Influence of genotypes and precore mutations on fulminant or chronic outcome of acute hepatitis B virus infection.

Authors:  Atsushi Ozasa; Yasuhito Tanaka; Etsuro Orito; Masaya Sugiyama; Jong-Hon Kang; Shuhei Hige; Tomoyuki Kuramitsu; Kazuyuki Suzuki; Eiji Tanaka; Shunichi Okada; Hajime Tokita; Yasuhiro Asahina; Kazuaki Inoue; Shinichi Kakumu; Takeshi Okanoue; Yoshikazu Murawaki; Keisuke Hino; Morikazu Onji; Hiroshi Yatsuhashi; Hiroshi Sakugawa; Yuzo Miyakawa; Ryuzo Ueda; Masashi Mizokami
Journal:  Hepatology       Date:  2006-08       Impact factor: 17.425

6.  Wild-type levels of pregenomic RNA and replication but reduced pre-C RNA and e-antigen synthesis of hepatitis B virus with C(1653) --> T, A(1762) --> T and G(1764) --> A mutations in the core promoter.

Authors:  S Günther; N Piwon; H Will
Journal:  J Gen Virol       Date:  1998-02       Impact factor: 3.891

7.  Acute liver failure: a management challenge for the practicing gastroenterologist.

Authors:  Dawn McDowell Torres; Robert D Stevens; Ahmet Gurakar
Journal:  Gastroenterol Hepatol (N Y)       Date:  2010-07

8.  A novel hepatitis B virus genotyping system by using restriction fragment length polymorphism patterns of S gene amplicons.

Authors:  Guo-Bing Zeng; Shu-Juan Wen; Zhan-Hui Wang; Li Yan; Jian Sun; Jin-Lin Hou
Journal:  World J Gastroenterol       Date:  2004-11-01       Impact factor: 5.742

Review 9.  Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures.

Authors:  D Lavanchy
Journal:  J Viral Hepat       Date:  2004-03       Impact factor: 3.728

10.  Hepatitis B virus genotypes and serotypes in western India: lack of clinical significance.

Authors:  Swati S Gandhe; Mandeep S Chadha; Vidya A Arankalle
Journal:  J Med Virol       Date:  2003-03       Impact factor: 2.327

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