Clinical Significance of Hepatitis B Virus Precore and Core Promoter Variants in Korean Patients With Chronic Hepatitis B. Issue 1 (January 2015)
- Record Type:
- Journal Article
- Title:
- Clinical Significance of Hepatitis B Virus Precore and Core Promoter Variants in Korean Patients With Chronic Hepatitis B. Issue 1 (January 2015)
- Main Title:
- Clinical Significance of Hepatitis B Virus Precore and Core Promoter Variants in Korean Patients With Chronic Hepatitis B
- Authors:
- Yim, Sun Young
Um, Soon Ho
Young Jung, Jin
Kim, Tae Hyung
Kim, Jin Dong
Keum, Bora
Seo, Yeon Seok
Yim, Hyung Joon
Jeen, Yoon Tae
Lee, Hong Sik
Chun, Hoon Jai
Kim, Chang Duck
Ryu, Ho Sang - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Background/Aim:</title> <p>We aimed to clarify the clinical significance of precore (preC)/core promoter (CP) variants of hepatitis B virus (HBV) in chronic hepatitis B (CHB) patients.</p> </sec> <sec> <title>Methods:</title> <p>We assessed serum HBeAg, HBV DNA levels, alanine transferase (ALT) levels, and progression of liver fibrosis in 226 Korean CHB patients, presumed to be infected with genotype C HBV, to analyze HBV variants in the preC region (G1896A) and CP regions (A1762T, G1764A).</p> </sec> <sec> <title>Results:</title> <p>CP and preC variants were more frequently found in HBeAg-negative patients than in HBeAg-positive patients (<italic>P</italic>&lt;0.05). HBeAg-positive patients with CP variants had higher ALT levels and more advanced fibrosis scores (all <italic>P</italic>&lt;0.01) than those without variants; those with preC variant had lower HBV DNA levels (<italic>P</italic>=0.009), with no significant difference in ALT levels and fibrosis scores. However, no significant correlation was found between HBV variants and clinicopathologic findings in HBeAg-negative patients. Furthermore, multivariate analysis revealed that (1) progression of liver fibrosis (≥F2) was associated with older age in both HBeAg-positive and HBeAg-negative patients (<italic>P&lt;</italic>0.05) and with CP variants in the HBeAg-positive group (<italic>P</italic>=0.007), and (2) HBV DNA levels were positively<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Background/Aim:</title> <p>We aimed to clarify the clinical significance of precore (preC)/core promoter (CP) variants of hepatitis B virus (HBV) in chronic hepatitis B (CHB) patients.</p> </sec> <sec> <title>Methods:</title> <p>We assessed serum HBeAg, HBV DNA levels, alanine transferase (ALT) levels, and progression of liver fibrosis in 226 Korean CHB patients, presumed to be infected with genotype C HBV, to analyze HBV variants in the preC region (G1896A) and CP regions (A1762T, G1764A).</p> </sec> <sec> <title>Results:</title> <p>CP and preC variants were more frequently found in HBeAg-negative patients than in HBeAg-positive patients (<italic>P</italic>&lt;0.05). HBeAg-positive patients with CP variants had higher ALT levels and more advanced fibrosis scores (all <italic>P</italic>&lt;0.01) than those without variants; those with preC variant had lower HBV DNA levels (<italic>P</italic>=0.009), with no significant difference in ALT levels and fibrosis scores. However, no significant correlation was found between HBV variants and clinicopathologic findings in HBeAg-negative patients. Furthermore, multivariate analysis revealed that (1) progression of liver fibrosis (≥F2) was associated with older age in both HBeAg-positive and HBeAg-negative patients (<italic>P&lt;</italic>0.05) and with CP variants in the HBeAg-positive group (<italic>P</italic>=0.007), and (2) HBV DNA levels were positively correlated with ALT levels, irrespective of HBeAg (<italic>P</italic>&lt;0.05), whereas they were negatively correlated with the presence of preC variant in the HBeAg-positive group (<italic>P</italic>=0.004).</p> </sec> <sec> <title>Conclusions:</title> <p>In HBeAg-positive CHB patients infected with genotype C HBV, preC variant was associated with enhanced host immune response with lower HBV DNA levels, whereas CP variants were associated with severe liver damage and liver fibrosis progression.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of clinical gastroenterology. Volume 49:Issue 1(2015)
- Journal:
- Journal of clinical gastroenterology
- Issue:
- Volume 49:Issue 1(2015)
- Issue Display:
- Volume 49, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 49
- Issue:
- 1
- Issue Sort Value:
- 2015-0049-0001-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-01
- Subjects:
- Gastroenterology -- Periodicals
Digestive organs -- Diseases -- Periodicals
Gastroenterology -- Periodicals
Digestive organs -- Diseases
Gastroenterology
Periodicals
Periodicals
616.33005 - Journal URLs:
- http://journals.lww.com/jcge/Pages/default.aspx ↗
http://www.jcge.com ↗
http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&PAGE=toc&D=ovft&AN=00004836-000000000-00000 ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/MCG.0000000000000052 ↗
- Languages:
- English
- ISSNs:
- 0192-0790
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4958.470000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4376.xml