Limitations and improvements of the quantiplex branched-DNA assay in Hepatitis B virus-infected patients receiving lamivudine

Chung Min Jen, Kung Chia Young, Pin Nan Cheng, Ai Wen Kao, Ting Tsung Chang

研究成果: Article同行評審

2 引文 斯高帕斯(Scopus)

摘要

The branched DNA (bDNA) assay for hepatitis B virus (Chiron Corporation Emerville, USA) was investigated by application to HBV-infected patients in Taiwan, where the B and C genotypes of hepatitis B virus are most prevalent. The study group included sera with hepatitis B surface antigen (HBsAg) and e antigen (HBeAg); Group 1 (n = 70) without treatment; Group 2 (n = 28) lamivudine treatment less than 3 months; Group 3 (n = 73) lamivudine treatment 3-12 months; Group 4 (n = 45) HBeAg-negative sera after 1 year treatment with lamivudine; control group (n = 36) HBsAg-negative sera. Comparison of identical-sample results showed a significantly higher coefficient of variation for low-level HBV DNA ( < 100 MEq/ml) than for high-level ( ≥ 100 MEq/ml), indicating increasing assay inaccuracy uncertainty as the sample HBV DNA concentration decreased. It is thus concluded that low-titered sera should receive special careful pipetting and processing. It was also found that using the relative luminescence of the negative control plus two standard deviations (S.D.) as a new cutoff could promote sensitivity (97.1 → 97.1%, 89.3 → 100%, 76.7 → 84.9%, and 17.8 → 22.2% in Groups 1-4, respectively) and specificity (94.4 → 97.2%). In summary, the bDNA HBV assay showed only moderate assay performance for samples with low HBV DNA levels. This problem can be improved partially by choosing a new cutoff value based on the relative luminescence of the negative controls in the kit.

原文English
頁(從 - 到)203-210
頁數8
期刊Journal of Virological Methods
96
發行號2
DOIs
出版狀態Published - 2001

All Science Journal Classification (ASJC) codes

  • 病毒學

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