Feasibility analysis of quantitative detection on serum HBeAg/HBeAb by time-resolved immunofluorescence assay / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 852-855, 2016.
Article
in Zh
| WPRIM
| ID: wpr-814952
Responsible library:
WPRO
ABSTRACT
OBJECTIVE@#To determine whether time-resolved immunofluorescence assay (TRIFA) shares the similar accuracy and specificity with automatic chemiluminescence immunoassay (CMIA) in analyzing HBeAg levels in hepatitis B.
@*METHODS@#A total of 157 serum samples were collected from outpatients with infection of HBV in Xiangya Hospital, Central South University. CMIA and TRIFA were used to analyze HBeAg quantitation and HBeAg/HBeAb qualitative detection, respectively.
@*RESULTS@#The linear regression equation for the two methods was Y=0.72779X-4.0551 (r=0.712, P<0.001). Compared with the CMIA, the sensitivity and specificity in detection of HBeAg by TRIFA were 89.89% and 100%, respectively, and the coincidence rate of HBeAg was 94.27% by two assays. Similarly, the sensitivity and specificity in detection of HBeAb by TRIFA were 100% and 95.45%, respectively. The coincidence rate was 97.45% by two assays.
@*CONCLUSION@#TRIFA has similar accuracy, sensitivity, and specificity with CMIA in quantitative detection of HBeAg, and their coincidence rate in detection of HBeAg/HBeAb is high.
Full text:
1
Index:
WPRIM
Main subject:
Feasibility Studies
/
Hepatitis B virus
/
Fluorescent Antibody Technique
/
Hepatitis B
/
Hepatitis B Antibodies
/
Hepatitis B e Antigens
Type of study:
Diagnostic_studies
/
Qualitative_research
Limits:
Humans
Language:
Zh
Journal:
Journal of Central South University(Medical Sciences)
Year:
2016
Type:
Article