Long-term follow-up of hepatitis B virus and hepatitis C virus replicative levels in chronic hepatitis patients coinfected with both viruses

1995 ◽  
Vol 46 (3) ◽  
pp. 258-264 ◽  
Author(s):  
Kazuyoshi Ohkawa ◽  
Norio Hayashi ◽  
Nobukazu Yuki ◽  
Manabu Masuzawa ◽  
Michio Kato ◽  
...  
2005 ◽  
Vol 12 (2) ◽  
pp. 154-159 ◽  
Author(s):  
M. Natsuizaka ◽  
S. Hige ◽  
Y. Ono ◽  
K. Ogawa ◽  
M. Nakanishi ◽  
...  

Kanzo ◽  
1984 ◽  
Vol 25 (11) ◽  
pp. 1394-1405 ◽  
Author(s):  
Kiyohiko KURAI ◽  
Shiro IINO ◽  
Hiroshi SUZUKI ◽  
Keiji MITAMURA ◽  
Naomi TANAKA ◽  
...  

Kanzo ◽  
1988 ◽  
Vol 29 (3) ◽  
pp. 294-300
Author(s):  
Toshihide SHIMA ◽  
Yoshifumi SETO ◽  
Yoshikuni SAKAMOTO ◽  
Toshikazu NAKAJIMA ◽  
Toshiaki NAKASHIMA ◽  
...  

2013 ◽  
Vol 62 (8) ◽  
pp. 1235-1238 ◽  
Author(s):  
Inmaculada Castillo ◽  
Javier Bartolomé ◽  
Juan Antonio Quiroga ◽  
Vicente Carreño

Hepatitis C virus (HCV) infection in the absence of detectable antibodies against HCV and of viral RNA in serum is called occult HCV infection. Its prevalence and clinical significance in chronic hepatitis B virus (HBV) infection is unknown. HCV RNA was tested for in the liver samples of 52 patients with chronic HBV infection and 21 (40 %) of them were positive for viral RNA (occult HCV infection). Liver fibrosis was found more frequently and the fibrosis score was significantly higher in patients with occult HCV than in negative ones, suggesting that occult HCV infection may have an impact on the clinical course of HBV infection.


2018 ◽  
Vol 67 (3) ◽  
pp. 681-685 ◽  
Author(s):  
Ali Sobhy ◽  
Mohammed Fakhry M. ◽  
Haitham A Azeem ◽  
Ahmed M Ashmawy ◽  
Hamed Omar Khalifa

Several studies were performed to evaluate the degree of liver fibrosis by non-invasive markers. We aimed to assess the diagnostic value of both biglycan (BGN) and osteopontin (OPN) as non-invasive markers of hepatic fibrosis in patients with chronic hepatitis B (CHB) and chronic hepatitis C (CHC). This study was performed on 100 patients with CHB virus, 100 patients with CHC virus and 100 normal controls. All participants were subjected to the following laboratory tests: hemoglobin, platelet, alanine aminotransferase, aspartate aminotransferase, albumin, international normalized ratio, HBs Ag, hepatitis C virus (HCV) antibody, hepatitis B virus DNA, HCV RNA, liver biopsy, BGN and OPN. We found that BGN level was significantly increased in the CHB group compared with the controls (p<0.001), but the level was not different between the CHC group and the controls (p<0.96). OPN was increased in both the CHB and CHC groups compared with the controls (p<0.001). Positive correlation was found between fibrosis stages and BGN level of the CHB group (r=0.64; p<0.001) and between fibrosis stages and OPN level of the CHB (r=0.63; p<0.001) and CHC (r=0.59; p<0.03) groups. The area under the curve (AUC), sensitivity and specificity of BGN were 1.0, 100% and 100% in predicting fibrosis in patients with CHB, and 0.50, 26% and 78% in predicting fibrosis in patients with CHC. OPN had an AUC of 0.997, sensitivity of 96% and specificity of 100% in predicting fibrosis in patients with CHB, and 0.974, 96.5% and 100% in predicting fibrosis in patients with CHC. In conclusion, BGN and OPN could be considered non-invasive markers for liver fibrosis assessment.


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