Guest guest Posted February 8, 2008 Report Share Posted February 8, 2008 Role of genotype and precore/basal core promoter mutations of hepatitis B virus in patients with chronic hepatitis B with acute exacerbation Authors: Wei-Lun Tsai ab; Gin-Ho Lo ab; Ping-I Hsu ab; Kwok-Hung Lai ab; Chiun-Ku Lin ab; Hoi-Hung Chan ab; Wen-Chi Chen ab; Jin-Shiung Cheng ab; Yung-Ching Liu bc; Tsi-Shu Huang bc; Luo-Ping Ger d; Hsi-Hsun Lin e Affiliations: a Division of Gastroenterology, Department of Internal Medicine, Kaohsiung, Taiwan b School of Medicine, National Yang Ming University, Taipei, Taiwan c Division of Microbiology and Infectious Diseases, Department of Internal Medicine, Kaohsiung, Taiwan d Department of Research and Education, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan e Division of Microbiology and Infectious Diseases, E-Da Hospital, Kaohsiung, Taiwan DOI: 10.1080/00365520701745693 Publication Frequency: 12 issues per year Published in: Scandinavian Journal of Gastroenterology, Volume 43, Issue 2 2008 , pages 196 - 201 Subjects: Gastroenterology; Gastrointestinal & Abdominal Surgery; Formats available: HTML (English) : PDF (English) Article Requests: Order Reprints : Request Permissions Abstract Objctive. The results of long-term, follow-up studies show that the severity and frequency of acute exacerbation of chronic hepatitis B virus (HBV) are associated with the development of liver cirrhosis in chronic HBV infection. The aim of this study was to investigate the relationship between virological factors of HBV and the severity of acute exacerbation. Material and methods. Fifty-one chronic hepatitis B patients with symptomatic acute exacerbation without antiviral therapy were enrolled in the study. Genotype of HBV was determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Precore (A1896) and basal core promoter (BCP) mutations (T1762 & A1764) were determined by PCR and direct sequencing. Results. Thirty-nine patients had genotype B, 11 patients had genotype C, and 1 patient had an unclassified genotype. Thirty-two patients had precore mutation and 24 patients had BCP mutation. After adjusting for age, gender, aspartate aminotransferase (ASAT) level, albumin level, and platelet count by multiple logistic regression test, precore mutation had a protective effect on the occurrence of hepatic decompensation (p=0.046), and genotype and BCP mutations were not associated with the occurrence of hepatic decompensation. Conclusions. HBV precore mutation may confer less severe liver disease during acute exacerbation of chronic HBV. Genotype and BCP mutations did not have a significant association with the occurrence of hepatic decompensation. http://www.informaworld.com/smpp/content~content=a789980950~db=all~order=page _________________________________________________________________ Climb to the top of the charts! Play the word scramble challenge with star power. http://club.live.com/star_shuffle.aspx?icid=starshuffle_wlmailtextlink_jan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2008 Report Share Posted February 8, 2008 Role of genotype and precore/basal core promoter mutations of hepatitis B virus in patients with chronic hepatitis B with acute exacerbation Authors: Wei-Lun Tsai ab; Gin-Ho Lo ab; Ping-I Hsu ab; Kwok-Hung Lai ab; Chiun-Ku Lin ab; Hoi-Hung Chan ab; Wen-Chi Chen ab; Jin-Shiung Cheng ab; Yung-Ching Liu bc; Tsi-Shu Huang bc; Luo-Ping Ger d; Hsi-Hsun Lin e Affiliations: a Division of Gastroenterology, Department of Internal Medicine, Kaohsiung, Taiwan b School of Medicine, National Yang Ming University, Taipei, Taiwan c Division of Microbiology and Infectious Diseases, Department of Internal Medicine, Kaohsiung, Taiwan d Department of Research and Education, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan e Division of Microbiology and Infectious Diseases, E-Da Hospital, Kaohsiung, Taiwan DOI: 10.1080/00365520701745693 Publication Frequency: 12 issues per year Published in: Scandinavian Journal of Gastroenterology, Volume 43, Issue 2 2008 , pages 196 - 201 Subjects: Gastroenterology; Gastrointestinal & Abdominal Surgery; Formats available: HTML (English) : PDF (English) Article Requests: Order Reprints : Request Permissions Abstract Objctive. The results of long-term, follow-up studies show that the severity and frequency of acute exacerbation of chronic hepatitis B virus (HBV) are associated with the development of liver cirrhosis in chronic HBV infection. The aim of this study was to investigate the relationship between virological factors of HBV and the severity of acute exacerbation. Material and methods. Fifty-one chronic hepatitis B patients with symptomatic acute exacerbation without antiviral therapy were enrolled in the study. Genotype of HBV was determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Precore (A1896) and basal core promoter (BCP) mutations (T1762 & A1764) were determined by PCR and direct sequencing. Results. Thirty-nine patients had genotype B, 11 patients had genotype C, and 1 patient had an unclassified genotype. Thirty-two patients had precore mutation and 24 patients had BCP mutation. After adjusting for age, gender, aspartate aminotransferase (ASAT) level, albumin level, and platelet count by multiple logistic regression test, precore mutation had a protective effect on the occurrence of hepatic decompensation (p=0.046), and genotype and BCP mutations were not associated with the occurrence of hepatic decompensation. Conclusions. HBV precore mutation may confer less severe liver disease during acute exacerbation of chronic HBV. Genotype and BCP mutations did not have a significant association with the occurrence of hepatic decompensation. http://www.informaworld.com/smpp/content~content=a789980950~db=all~order=page _________________________________________________________________ Climb to the top of the charts! Play the word scramble challenge with star power. http://club.live.com/star_shuffle.aspx?icid=starshuffle_wlmailtextlink_jan Quote Link to comment Share on other sites More sharing options...
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