A melting curve analysis--based PCR assay for one-step genotyping of β-thalassemia mutations a multicenter validation

The increasing number of disease-causing mutations demands a simple, direct, and cost-effective diagnostic genotyping technique capable of detecting multiple mutations. This study validated the efficacy of a novel melting curve analysis-based genotyping assay (MeltPro HBB assay) for 24 β-thalassemia...

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Veröffentlicht in:The Journal of molecular diagnostics : JMD 2011-07, Vol.13 (4), p.427-435
Hauptverfasser: Xiong, Fu, Huang, Qiuying, Chen, Xiaoyun, Zhou, Yuqiu, Zhang, Xinhua, Cai, Ren, Chen, Yajun, Xie, Jiansheng, Feng, Shanwei, Wei, Xiaofeng, Xiao, Qizhi, Zhang, Tianlang, Luo, Shiqiang, Yang, Xuehuang, Hao, Ying, Qu, Yanxia, Li, Qingge, Xu, Xiangmin
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Sprache:eng
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Zusammenfassung:The increasing number of disease-causing mutations demands a simple, direct, and cost-effective diagnostic genotyping technique capable of detecting multiple mutations. This study validated the efficacy of a novel melting curve analysis-based genotyping assay (MeltPro HBB assay) for 24 β-thalassemia mutations in the Chinese population. The diagnostic potential of this assay was evaluated in 1022 pretyped genomic DNA samples, including 909 clinical cases of β-thalassemia minor or major, using a double-blind analysis in a multicenter validation study. Reproducibility of the assay was 100%, and the limit of detection was 10 pg per reaction. All 24 β-thalassemia mutations were accurately genotyped, and β-thalassemia genotypes were correctly determined in all 1022 samples, yielding overall sensitivity and specificity of 100%. The concordance rate was 99.4% between this assay and the reference method. It was concluded that the MeltPro HBB assay is useful for reliable genotyping of multiple β-thalassemia mutations in clinical settings and may have potential as a versatile method for rapid genotyping of known mutations because of its high throughput, accuracy, ease of use, and low cost.
ISSN:1525-1578
1943-7811
DOI:10.1016/j.jmoldx.2011.03.005