Analysis of correlation of quantitative fluorescent detection of HBV DNA and the results of serum marker
Zhu ZiLi
Abstract
Zhu ZiLi
Abstract
Objective To analyze the relationship between the level of HBV DNA and the HBV-M. Methods Serum samples from 1 781 service workers were detected by ELISA and divided into nine groups: HBsAg(+)/HBeAg(+)/HBcAb(+),HBsAg(+)/HBeAb(+)/HBcAb(+),HBsAg(+)/HBcAb(+),HBsAg(+)/HBeAg(+),HBsAb/HBcAb(+),HBeAb(+)/HBcAb(+),HBsAg(+)/HBeAb(+),HBsAb(+) and HBsAg(+).HBV DNA concentration was determined by fluorescent quantitative PCR. Results The positive rate of HBV-DNA in the group of HBsAg(+)/HBeAg(+)/HBcAb(+) was 61.88%(1 102/1 781),the positive rate in the group of HBsAg(+)/HBeAb(+)/HBcAb(+) was 96.15%,the positive rate in the group of HBsAg(+)/HBeAb(+)/HBcAb(+) was 24.38%,the positive rate in the group of HBsAg(+)/HBcAb(+) was 38.41%,90.91% in the group of HBsAg(+)/HBeAg(+),36.36% in the group of HBeAg(+) and the positive rate of HBV-DNA was 0% in the other groups.There significant differences between the different hepatitis B sera positive modes and the result of HBV DNA.The HBV DNA level showed an obvious correlation with the HBeAg content in sera. Conclusion A close correlation exists between these two methods in the detection of HBV markers.The FQ-PCR is a relatively acurate method for detection of HBV-DNA.
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Objective To analyze the relationship between the level of HBV DNA and the HBV-M. Methods Serum samples from 1 781 service workers were detected by ELISA and divided into nine groups: HBsAg(+)/HBeAg(+)/HBcAb(+),HBsAg(+)/HBeAb(+)/HBcAb(+),HBsAg(+)/HBcAb(+),HBsAg(+)/HBeAg(+),HBsAb/HBcAb(+),HBeAb(+)/HBcAb(+),HBsAg(+)/HBeAb(+),HBsAb(+) and HBsAg(+).HBV DNA concentration was determined by fluorescent quantitative PCR. Results The positive rate of HBV-DNA in the group of HBsAg(+)/HBeAg(+)/HBcAb(+) was 61.88%(1 102/1 781),the positive rate in the group of HBsAg(+)/HBeAb(+)/HBcAb(+) was 96.15%,the positive rate in the group of HBsAg(+)/HBeAb(+)/HBcAb(+) was 24.38%,the positive rate in the group of HBsAg(+)/HBcAb(+) was 38.41%,90.91% in the group of HBsAg(+)/HBeAg(+),36.36% in the group of HBeAg(+) and the positive rate of HBV-DNA was 0% in the other groups.There significant differences between the different hepatitis B sera positive modes and the result of HBV DNA.The HBV DNA level showed an obvious correlation with the HBeAg content in sera. Conclusion A close correlation exists between these two methods in the detection of HBV markers.The FQ-PCR is a relatively acurate method for detection of HBV-DNA.
Key concepts: HBsAg, HBeAg, Hepatitis B virus, Hepatitis B, Medicine, Virology, Virus