Effect of multiple freeze-thaw cycles on hepatitis B virus DNA and hepatitis C virus RNA quantification as measured with branched-DNA technology

被引:46
作者
Krajden, M
Minor, JM
Rifkin, O
Comanor, L
机构
[1] Toronto Hosp, Dept Lab Med & Pathol, Toronto, ON M5T 2S8, Canada
[2] Toronto Med Labs, Toronto, ON, Canada
[3] Chiron Diagnost Corp, Walpole, MA USA
关键词
D O I
10.1128/JCM.37.6.1683-1686.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Quantification of hepatitis B virus (HBV) DNA and hepatitis C virus (HCV) RNA often is performed in specimens that have been frozen and thawed more than once. To ensure optimal therapeutic and prognostic value, it is important to establish whether viral load measurements are affected by repeated freeze-thaw (FT) cycles. We therefore evaluated the effect of multiple FT cycles on HBV DNA and HCV RNA quantification by testing serum specimens subjected to one (baseline), two, four, and eight PT cycles with the appropriate Chiron Quantiplex assay. Linear regression analysis showed minor increases of 1.7% per FT cycle for both HBV DNA and HCV RNA. The rise in HCV RNA levels was more pronounced among low-concentration samples, since further analysis revealed an increase of 3.2% per FT cycle among samples with 0.2 to 3.86 Meg of HCV RNA per mi. Given that the coefficient of variation for the Quantiplex assays is generally 10 to 15%, the minor increases in HBV DNA and HCV RNA levels with progressive FT cycles for the specimens tested were recognized only because analysis of variance revealed a statistically significant trend (P < 0.05). Due to the minor statistical trend, the clinical impact for individual patient specimens is likely to be limited, but it may deserve further study. In conclusion, the concentration of HBV DNA and HCV RNA in serum specimens subjected to up to eight short-term FT cycles was stable.
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页码:1683 / 1686
页数:4
相关论文
共 17 条
[1]   Comparison of four methods for quantitative measurement of hepatitis B viral DNA [J].
Butterworth, LA ;
Prior, SL ;
Buda, PJ ;
Faoagali, JL ;
Cooksley, WGE .
JOURNAL OF HEPATOLOGY, 1996, 24 (06) :686-691
[2]   PREPARATION AND CHARACTERIZATION OF RNA STANDARDS FOR USE IN QUANTITATIVE BRANCHED DNA HYBRIDIZATION ASSAYS [J].
COLLINS, ML ;
ZAYATI, C ;
DETMER, JJ ;
DALY, B ;
KOLBERG, JA ;
CHA, TA ;
IRVINE, BD ;
TUCKER, J ;
URDEA, MS .
ANALYTICAL BIOCHEMISTRY, 1995, 226 (01) :120-129
[3]   Stability of hepatitis C virus RNA during specimen handling and storage prior to NASBA amplification [J].
Damen, M ;
Sillekens, P ;
Sjerps, M ;
Melsert, R ;
Frantzen, I ;
Reesink, HW ;
Lelie, PN ;
Cuypers, HTM .
JOURNAL OF VIROLOGICAL METHODS, 1998, 72 (02) :175-184
[4]  
DAVIS GL, 1994, HEPATOLOGY, V19, P1337, DOI 10.1002/hep.1840190603
[5]   Accurate quantification of hepatitis C virus (HCV) RNA from all HCV genotypes by using branched-DNA technology [J].
Detmer, J ;
Lagier, R ;
Flynn, J ;
Zayati, C ;
Kolberg, J ;
Collins, M ;
Urdea, M ;
SanchezPescador, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (04) :901-907
[6]  
FONG TL, 1993, ARCH PATHOL LAB MED, V117, P150
[7]   Impact of various handling and storage conditions on quantitative detection of hepatitis C virus RNA [J].
Halfon, P ;
Khiri, H ;
Gerolami, V ;
Bourliere, M ;
Feryn, JM ;
Reynier, P ;
Gauthier, A ;
Cartouzou, G .
JOURNAL OF HEPATOLOGY, 1996, 25 (03) :307-311
[8]  
HENDRICKS DA, 1995, AM J CLIN PATHOL, V104, P537
[9]   The treatment of chronic viral hepatitis [J].
Hoofnagle, JH ;
DiBisceglie, AM .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (05) :347-356
[10]   Assessment of hepatitis B virus DNA stability in serum by the chiron quantiplex branched-DNA assay [J].
Krajden, M ;
Comanor, L ;
Rifkin, O ;
Grigoriew, A ;
Minor, JM ;
Kapke, GF .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (02) :382-386