Development and validation of a ζ-globin-specific ELISA for carrier screening of the (−−SEA) α thalassaemia deletion. Issue 2 (29th January 2009)
- Record Type:
- Journal Article
- Title:
- Development and validation of a ζ-globin-specific ELISA for carrier screening of the (−−SEA) α thalassaemia deletion. Issue 2 (29th January 2009)
- Main Title:
- Development and validation of a ζ-globin-specific ELISA for carrier screening of the (−−SEA) α thalassaemia deletion
- Authors:
- Tang, L
Zhu, P
Zhou, W J
Zheng, J
Zhou, Y Q
Fu, N
Xu, X M - Abstract:
- Abstract : Aims: The Southeast Asian (SEA) deletion (−− SEA ) represents the most common determinant causing α thalassaemia in Southeast Asian countries. The embryonic ζ-globin chain has been defined as a marker for the detection of this deletion in adults. The aim of this study was to develop an appropriate low-cost ELISA for ζ-globin chain detection as a routine screening test for (−− SEA ) α thalassaemia deletion. Methods: A sandwich ELISA system for ζ-globin chains was established with a pair of ζ-globin-specific monoclonal antibodies prepared in-house, and locally made products. Against a gap-PCR method that was taken as the standard, this assay was validated in a cohort study testing a total of 526 individuals comprising patients scheduled for haemoglobinopathy diagnostic analysis and normal individuals. Routine screening of the (−− SEA ) deletion in 300 random student volunteers was conducted using the assay. Results: While the cut-off point was set at a percentage positive value of 30, the sensitivity and specificity of this ELISA method were 100% and 99.24%, respectively. The mean intra-assay and inter-assay coefficients of variation among the different concentrations in the optimised ELISA conditions were 2.1–11.4% and 4.3–13.2%, respectively. Seventeen of the 300 volunteers sampled were determined by the ELISA to have the (−− SEA ) deletion; these results were in 100% agreement with the gap-PCR results. Conclusions: This study validates the ELISA method describedAbstract : Aims: The Southeast Asian (SEA) deletion (−− SEA ) represents the most common determinant causing α thalassaemia in Southeast Asian countries. The embryonic ζ-globin chain has been defined as a marker for the detection of this deletion in adults. The aim of this study was to develop an appropriate low-cost ELISA for ζ-globin chain detection as a routine screening test for (−− SEA ) α thalassaemia deletion. Methods: A sandwich ELISA system for ζ-globin chains was established with a pair of ζ-globin-specific monoclonal antibodies prepared in-house, and locally made products. Against a gap-PCR method that was taken as the standard, this assay was validated in a cohort study testing a total of 526 individuals comprising patients scheduled for haemoglobinopathy diagnostic analysis and normal individuals. Routine screening of the (−− SEA ) deletion in 300 random student volunteers was conducted using the assay. Results: While the cut-off point was set at a percentage positive value of 30, the sensitivity and specificity of this ELISA method were 100% and 99.24%, respectively. The mean intra-assay and inter-assay coefficients of variation among the different concentrations in the optimised ELISA conditions were 2.1–11.4% and 4.3–13.2%, respectively. Seventeen of the 300 volunteers sampled were determined by the ELISA to have the (−− SEA ) deletion; these results were in 100% agreement with the gap-PCR results. Conclusions: This study validates the ELISA method described here as a simple, rapid and cost-effective assay that is potentially adaptable for application in large-scale population screening for this prevalent disorder in SEA areas such as southern China. … (more)
- Is Part Of:
- Journal of clinical pathology. Volume 62:Issue 2(2009)
- Journal:
- Journal of clinical pathology
- Issue:
- Volume 62:Issue 2(2009)
- Issue Display:
- Volume 62, Issue 2 (2009)
- Year:
- 2009
- Volume:
- 62
- Issue:
- 2
- Issue Sort Value:
- 2009-0062-0002-0000
- Page Start:
- 147
- Page End:
- 151
- Publication Date:
- 2009-01-29
- Subjects:
- Pathology -- Periodicals
Pathology, Molecular -- Periodicals
616.0705 - Journal URLs:
- http://jcp.bmjjournals.com ↗
http://jcp.bmjjournals.com/content/by/year ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=162&action=archive ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/jcp.2008.059477 ↗
- Languages:
- English
- ISSNs:
- 0021-9746
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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