MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis
The analysis of circulating nucleic acids has revealed applications in the noninvasive diagnosis, monitoring, and prognostication of many clinical conditions. Circulating fetal-specific sequences have been detected and constitute a fraction of the total DNA in maternal plasma. The diagnostic reliabi...
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th-cmuir.6653943832-39822014-08-30T02:35:32Z MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis Ding C. Chiu R.W.K. Lau T.K. Leung T.N. Chan L.C. Chan A.Y.Y. Charoenkwan P. Ng I.S.L. Law H.-Y. Ma E.S.K. Xu X. Wanapirak C. Sanguansermsri T. Liao C. Tan Jin Ai M.A. Chui D.H.K. Cantor C.R. Lo Y.M.D. The analysis of circulating nucleic acids has revealed applications in the noninvasive diagnosis, monitoring, and prognostication of many clinical conditions. Circulating fetal-specific sequences have been detected and constitute a fraction of the total DNA in maternal plasma. The diagnostic reliability of circulating DNA analysis depends on the fractional concentration of the targeted sequence, the analytical sensitivity, and the specificity. The robust discrimination of single-nucleotide differences between circulating DNA species is technically challenging and demands the adoption of highly sensitive and specific analytical systems. We have developed a method based on single-allele base extension reaction and MS, which allows for the reliable detection of fetal-specific alleles, including point mutations and single-nucleotide polymorphisms, in maternal plasma. The approach was applied to exclude the fetal inheritance of the four most common Southeast Asian β-thalassemia mutations in at-risk pregnancies between weeks 7 and 21 of gestation. Fetal genotypes were correctly predicted in all cases studied. Fetal haplotype analysis based on a single-nucleotide polymorphism linked to the β-globin locus, HBB, in maternal plasma also was achieved. Consequently, noninvasive prenatal diagnosis in a mother and father carrying identical β-thalassemia mutations was accomplished. These advances will help in catalyzing the clinical applications of fetal nucleic acids in maternal plasma. This analytical approach also will have implications for many other applications of circulating nucleic acids in areas such as oncology and transplantation. 2014-08-30T02:35:32Z 2014-08-30T02:35:32Z 2004 Article 00278424 10.1073/pnas.0403962101 15247415 PNASA http://www.scopus.com/inward/record.url?eid=2-s2.0-3242703837&partnerID=40&md5=1682349cfcbd800a0fbe16b7bb84f251 http://cmuir.cmu.ac.th/handle/6653943832/3982 English |
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The analysis of circulating nucleic acids has revealed applications in the noninvasive diagnosis, monitoring, and prognostication of many clinical conditions. Circulating fetal-specific sequences have been detected and constitute a fraction of the total DNA in maternal plasma. The diagnostic reliability of circulating DNA analysis depends on the fractional concentration of the targeted sequence, the analytical sensitivity, and the specificity. The robust discrimination of single-nucleotide differences between circulating DNA species is technically challenging and demands the adoption of highly sensitive and specific analytical systems. We have developed a method based on single-allele base extension reaction and MS, which allows for the reliable detection of fetal-specific alleles, including point mutations and single-nucleotide polymorphisms, in maternal plasma. The approach was applied to exclude the fetal inheritance of the four most common Southeast Asian β-thalassemia mutations in at-risk pregnancies between weeks 7 and 21 of gestation. Fetal genotypes were correctly predicted in all cases studied. Fetal haplotype analysis based on a single-nucleotide polymorphism linked to the β-globin locus, HBB, in maternal plasma also was achieved. Consequently, noninvasive prenatal diagnosis in a mother and father carrying identical β-thalassemia mutations was accomplished. These advances will help in catalyzing the clinical applications of fetal nucleic acids in maternal plasma. This analytical approach also will have implications for many other applications of circulating nucleic acids in areas such as oncology and transplantation. |
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Ding C. Chiu R.W.K. Lau T.K. Leung T.N. Chan L.C. Chan A.Y.Y. Charoenkwan P. Ng I.S.L. Law H.-Y. Ma E.S.K. Xu X. Wanapirak C. Sanguansermsri T. Liao C. Tan Jin Ai M.A. Chui D.H.K. Cantor C.R. Lo Y.M.D. |
spellingShingle |
Ding C. Chiu R.W.K. Lau T.K. Leung T.N. Chan L.C. Chan A.Y.Y. Charoenkwan P. Ng I.S.L. Law H.-Y. Ma E.S.K. Xu X. Wanapirak C. Sanguansermsri T. Liao C. Tan Jin Ai M.A. Chui D.H.K. Cantor C.R. Lo Y.M.D. MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis |
author_facet |
Ding C. Chiu R.W.K. Lau T.K. Leung T.N. Chan L.C. Chan A.Y.Y. Charoenkwan P. Ng I.S.L. Law H.-Y. Ma E.S.K. Xu X. Wanapirak C. Sanguansermsri T. Liao C. Tan Jin Ai M.A. Chui D.H.K. Cantor C.R. Lo Y.M.D. |
author_sort |
Ding C. |
title |
MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis |
title_short |
MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis |
title_full |
MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis |
title_fullStr |
MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis |
title_full_unstemmed |
MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis |
title_sort |
ms analysis of single-nucleotide differences in circulating nucleic acids: application to noninvasive prenatal diagnosis |
publishDate |
2014 |
url |
http://www.scopus.com/inward/record.url?eid=2-s2.0-3242703837&partnerID=40&md5=1682349cfcbd800a0fbe16b7bb84f251 http://cmuir.cmu.ac.th/handle/6653943832/3982 |
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1681420151388372992 |