Negative correlation between viral load and HBsAg levels in chronic HBV-infected patients

被引:37
作者
Ozdil, Burhan [1 ]
Cosar, Arif M. [2 ]
Akkiz, Hikmet [1 ]
Sandikci, Macit U. [1 ]
Kece, Can [3 ]
机构
[1] Cukurova Univ, Dept Gastroenterol, Fac Med, TR-01330 Adana, Turkey
[2] Res Hosp Trabzon, Dept Gastroenterol, Trabzon, Turkey
[3] Res Hosp Trabzon, Dept Surg Gastroenterol, Trabzon, Turkey
关键词
HEPATITIS-B-VIRUS; SURFACE-ANTIGEN HBSAG; MONOCLONAL-ANTIBODIES; C VIRUS; DETERMINANT; PREVALENCE; POLYMERASE; MUTATIONS; VARIANTS; GENOMES;
D O I
10.1007/s00705-009-0474-x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The objective of this study is to reveal the relationship between viral load (as HBV DNA) and HBsAg levels. Ninety-two chronically HBV-infected patients were included in the study. The patients were divided in two different groups: the cirrhotic group (n = 32) and the non-cirrhotic group (n = 60). The correlation between study groups was also examined with regard to HBeAg status. Hepatitis B viral markers (HBsAg, HBeAg, Anti-HBs, anti-HBc and anti-HBe) and HBV viral load of the patients were measured. A significant negative correlation between HBV DNA and HBsAg levels was found in the non-cirrhotic group (p < 0.01). The anti-HBc level was higher in the non-cirrhotic group than in the cirrhotic group (p < 0.016). The viral load was significantly higher in HBeAg (+) patients in comparison with HBeAg (-) cases (p < 0.0001). The HBsAg level was low in HBeAg (+) patients, whereas it was higher in HBeAg (-) cases (p < 0.001). In conclusion, a significant negative correlation between viral load and HBsAg levels was detected in the non-cirrhotic chronically HBV-infected group. Therefore, concomitantly low HBsAg and HBV DNA levels may indicate a better prognosis compared to high HBsAg and low HBV DNA levels.
引用
收藏
页码:1451 / 1455
页数:5
相关论文
共 26 条
[1]   Sequential changes in full-length genomes of hepatitis B virus accompanying acute exacerbation of chronic hepatitis B [J].
Asahina, Y ;
Enomoto, N ;
Ogura, Y ;
Kurosaki, M ;
Sakuma, I ;
Izumi, N ;
Marumo, F ;
Sato, C .
JOURNAL OF HEPATOLOGY, 1996, 25 (06) :787-794
[2]   IMMUNE-RESPONSE TO SYNTHETIC PEPTIDE ANALOGS OF HEPATITIS-B SURFACE-ANTIGEN SPECIFIC FOR THE ALPHA-DETERMINANT [J].
BHATNAGAR, PK ;
PAPAS, E ;
BLUM, HE ;
MILICH, DR ;
NITECKI, D ;
KARELS, MJ ;
VYAS, GN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (14) :4400-4404
[3]  
BROWN JL, 1992, HEPATOLOGY, V15, P141
[4]  
CALDWELL SH, 1993, AM J GASTROENTEROL, V88, P1016
[5]  
Carman WF, 1997, HEPATOLOGY, V26, P1658, DOI 10.1002/hep.510260640
[6]  
Chen WN, 2000, AM J GASTROENTEROL, V95, P1098
[7]   Characterization of the reactivity pattern of murine monoclonal antibodies against wild-type hepatitis B surface antigen to G145R and other naturally occurring "a" loop escape mutations [J].
Cooreman, MP ;
van Roosmalen, VH ;
Morsche, RT ;
Sünnen, CMG ;
Schoondermark-Van de Ven, EME ;
Jansen, JBMJ ;
Tytgat, GNJ ;
de Wit, PLM ;
Paulij, WP .
HEPATOLOGY, 1999, 30 (05) :1287-1292
[8]   Quantitation of hepatitis B surface antigen by an automated chemiluminescent microparticle immunoassay [J].
Deguchi, M ;
Yamashita, N ;
Kagita, M ;
Asari, S ;
Iwatani, Y ;
Tsuchida, T ;
Iinuma, K ;
Mushahwar, IK .
JOURNAL OF VIROLOGICAL METHODS, 2004, 115 (02) :217-222
[9]  
FELDMAN M, 1998, HEPATITIS B D, V2, P1130
[10]  
HONGYUAN H, 1997, HEPATOLOGY, V26, P786