Novel genetic variants of Hepatitis B Virus in fulminant hepatitis
Fulminant hepatitis (FH) is a life-threatening liver disease characterised by intense immune attack and massive liver cell death. The common precore stop codon mutation of hepatitis B virus (HBV), A1896, is frequently associated with FH, but lacks specificity. This study attempts to uncover all poss...
Saved in:
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi
2017
|
Subjects: | |
Online Access: | http://eprints.sunway.edu.my/871/1/Chook%20JB%202017%20Novel%20Genetic%20variants%20of%20fulminant%20HBV%20J%20Pathog.pdf http://eprints.sunway.edu.my/871/ http://doi.org/10.1155/2017/1231204 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Sunway University |
Language: | English |
id |
my.sunway.eprints.871 |
---|---|
record_format |
eprints |
spelling |
my.sunway.eprints.8712019-04-30T08:24:20Z http://eprints.sunway.edu.my/871/ Novel genetic variants of Hepatitis B Virus in fulminant hepatitis Chook, Jack Bee * Ngeow, Yun Fong Tee, Kok Keng Peh, Suat Cheng * Mohamed, Rosmawati R Medicine (General) Fulminant hepatitis (FH) is a life-threatening liver disease characterised by intense immune attack and massive liver cell death. The common precore stop codon mutation of hepatitis B virus (HBV), A1896, is frequently associated with FH, but lacks specificity. This study attempts to uncover all possible viral nucleotides that are specifically associated with FH through a compiled sequence analysis of FH and non-FH cases from acute infection. We retrieved 67 FH and 280 acute non-FH cases of hepatitis B from GenBank and applied support vector machine (SVM) model to seek candidate nucleotides highly predictive of FH. Six best candidates with top predictive accuracy, 92.5%, were used to build a SVM model; they are C2129 (85.3%), T720 (83.0%), Y2131 (82.4%), T2013 (82.1%),K2048 (82.1%), and A2512 (82.1%). This model gave a high specificity (99.3%), positive predictive value (95.6%), and negative predictive value (92.1%), but only moderate sensitivity (64.2%).We successfully built a SVM model comprising six variants that are highly predictive and specific for FH: four in the core region and one each in the polymerase and the surface regions. These variants indicate that intracellular virion/core retention could play an important role in the progression to FH. Hindawi 2017-12-19 Article PeerReviewed text en http://eprints.sunway.edu.my/871/1/Chook%20JB%202017%20Novel%20Genetic%20variants%20of%20fulminant%20HBV%20J%20Pathog.pdf Chook, Jack Bee * and Ngeow, Yun Fong and Tee, Kok Keng and Peh, Suat Cheng * and Mohamed, Rosmawati (2017) Novel genetic variants of Hepatitis B Virus in fulminant hepatitis. Journal of Pathogens, 2017. pp. 1-6. ISSN 2090-3057 http://doi.org/10.1155/2017/1231204 doi:10.1155/2017/1231204 |
institution |
Sunway University |
building |
Sunway Campus Library |
collection |
Institutional Repository |
continent |
Asia |
country |
Malaysia |
content_provider |
Sunway University |
content_source |
Sunway Institutional Repository |
url_provider |
http://eprints.sunway.edu.my/ |
language |
English |
topic |
R Medicine (General) |
spellingShingle |
R Medicine (General) Chook, Jack Bee * Ngeow, Yun Fong Tee, Kok Keng Peh, Suat Cheng * Mohamed, Rosmawati Novel genetic variants of Hepatitis B Virus in fulminant hepatitis |
description |
Fulminant hepatitis (FH) is a life-threatening liver disease characterised by intense immune attack and massive liver cell death. The common precore stop codon mutation of hepatitis B virus (HBV), A1896, is frequently associated with FH, but lacks specificity. This study attempts to uncover all possible viral nucleotides that are specifically associated with FH through a compiled sequence analysis of FH and non-FH cases from acute infection. We retrieved 67 FH and 280 acute non-FH cases of hepatitis B from GenBank and applied support vector machine (SVM) model to seek candidate nucleotides highly predictive of FH. Six best candidates with top predictive accuracy, 92.5%, were used to build a SVM model; they are C2129 (85.3%), T720 (83.0%), Y2131 (82.4%), T2013 (82.1%),K2048 (82.1%), and A2512 (82.1%). This model gave a high specificity (99.3%), positive predictive value (95.6%), and negative
predictive value (92.1%), but only moderate sensitivity (64.2%).We successfully built a SVM model comprising six variants that are highly predictive and specific for FH: four in the core region and one each in the polymerase and the surface regions. These variants indicate that intracellular virion/core retention could play an important role in the progression to FH. |
format |
Article |
author |
Chook, Jack Bee * Ngeow, Yun Fong Tee, Kok Keng Peh, Suat Cheng * Mohamed, Rosmawati |
author_facet |
Chook, Jack Bee * Ngeow, Yun Fong Tee, Kok Keng Peh, Suat Cheng * Mohamed, Rosmawati |
author_sort |
Chook, Jack Bee * |
title |
Novel genetic variants of Hepatitis B Virus in fulminant hepatitis |
title_short |
Novel genetic variants of Hepatitis B Virus in fulminant hepatitis |
title_full |
Novel genetic variants of Hepatitis B Virus in fulminant hepatitis |
title_fullStr |
Novel genetic variants of Hepatitis B Virus in fulminant hepatitis |
title_full_unstemmed |
Novel genetic variants of Hepatitis B Virus in fulminant hepatitis |
title_sort |
novel genetic variants of hepatitis b virus in fulminant hepatitis |
publisher |
Hindawi |
publishDate |
2017 |
url |
http://eprints.sunway.edu.my/871/1/Chook%20JB%202017%20Novel%20Genetic%20variants%20of%20fulminant%20HBV%20J%20Pathog.pdf http://eprints.sunway.edu.my/871/ http://doi.org/10.1155/2017/1231204 |
_version_ |
1644324422966837248 |