COMPARISON OF CLINICAL APPLICATION OF THE ABBOTT HBV PCR KIT AND THE VERSANT HBV DNA 3.0 TEST TO MEASURE SERUM HEPATITIS B VIRUS DNA IN TAIWANESE PATIENTS

被引:13
|
作者
Yang, Jeng-Fu [1 ,2 ]
Lin, Ya-Yun [2 ]
Huang, Jee-Fu [1 ,3 ]
Liu, Shu-Fen [1 ]
Chu, Pei-Yu [4 ]
Hsieh, Ming-Yen [1 ]
Lin, Zu-Yau [1 ,3 ]
Chen, Shinn-Cherng [1 ,3 ]
Wang, Liang-Yen [1 ,3 ]
Dai, Chia-Yen [1 ,3 ,5 ]
Chuang, Wan-Long [1 ,3 ]
Yu, Ming-Lung [1 ,2 ,3 ]
机构
[1] Kaohsiung Med Univ Hosp, Dept Internal Med, Hepatobiliary Div, Kaohsiung 807, Taiwan
[2] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Prevent Med, Kaohsiung, Taiwan
[3] Kaohsiung Med Univ, Coll Med, Fac Internal Med, Kaohsiung, Taiwan
[4] Kaohsiung Med Univ, Coll Hlth Sci, Dept Med Lab Sci & Biotechnol, Kaohsiung, Taiwan
[5] Kaohsiung Med Univ Hosp, Dept Occupat & Environm Med, Kaohsiung, Taiwan
来源
KAOHSIUNG JOURNAL OF MEDICAL SCIENCES | 2009年 / 25卷 / 08期
关键词
bDNA; 3.0; assay; HBeAg; HBV DNA PCR Kit; HBV DNA quantification; HBV infection; SIGNAL AMPLIFICATION ASSAY; QUANTITATIVE DETECTION; LIVER-DISEASE; LAMIVUDINE THERAPY; MONITOR TEST; QUANTIFICATION; INFECTION;
D O I
10.1016/S1607-551X(09)70536-4
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
With an estimated 350-400 million people worldwide chronically infected with hepatitis B virus (HBV), and the subsequent serious complications caused by liver damage including cirrhosis, liver failure, and hepatocellular carcinoma, HBV infection remains a global health issue, particularly in Taiwan, an HBV-hyperendemic area. Sensitive and accurate quantification of HBV DNA is necessary to monitor patients with chronic hepatitis B who are receiving antiviral therapy to determine treatment response and adapt therapy. We evaluated and compared the clinical performance of two HBV DNA assays based on different technologies: the RealArt(TM) HBV(TM) PCR Kit (Abbott HBV DNA PCR kit, real-time polymerase chain reaction assay, detection limit: 27 IU/mL) and the VERSANT bDNA 3.0 assay (Bayer, branched DNA signal amplification assay, detection limit: 357IU/mL). Serum levels of HBV DNA in 173 chronic HBV carriers were determined using both the RealArt(TM) HBV(TM) PCR Kit and the VERSANT bDNA 3.0 test. Of the 173 samples analyzed for baseline viral load detection, HBV DNA was quantifiable in 147 patients (82.1%) by the RealArt(TM) HBV(TM) PCR Kit, which was significantly higher than the 92 (53.2%) samples quantified by the VERSANT bDNA 3.0 assay. A total of 86 (49.7%) samples were quantifiable by both assays, whereas 25 (14.5%) were below the detection limit of both assays. The HBV DNA quantification values measured by the RealArt(TM) HBV(TM) PCR Kit and the VERSANT bDNA 3.0 assay were positively correlated (Spearman's rank correlation coefficient r = 0.932, p < 0.001). On average, the results derived from the RealArt(TM) HBV(TM) PCR Kit were 0.67 log lower than those of the VERSANT bDNA 3.0 assay. HBV DNA concentrations were significantly higher in 63 HBV e antigen (HBeAg)seropositive patients than in 110 HBeAg-seronegative patients (5.42 +/- 2.34 logs vs. 3.21 +/- 2.27 logs, p < 0.001). The RealArt(TM) HBV(TM) PCR Kit is more sensitive and has a wider dynamic range than the VERSANT bDNA 3.0 assay in the clinical setting of chronic hepatitis B patients. The sensitivity and wide dynamic range of the PCR assay allow optimal monitoring and timely adaptation of antiviral therapy. Nevertheless, the HBV DNA values measured by the RealArt(TM) HBV(TM) PCR Kit and the VERSANT bDNA 3.0 assay were significantly correlated.
引用
收藏
页码:413 / 421
页数:9
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