Proteomic profile determination of autosomal aneuploidies by mass spectrometry on amniotic fluids

<p>Abstract</p> <p>Background</p> <p>Prenatal diagnosis of chromosomal abnormalities by cytogenetic analysis is time-consuming, expensive, and requires highly qualified technicians. Rapid diagnosis of aneuploidies followed by reassurance of women with normal results can...

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Main Authors: Desmetz Caroline, Mange Alain, Bellet Virginie, Molinari Nicolas, Maudelonde Thierry, Solassol Jerome
Format: Article
Language:English
Published: BMC 2008-01-01
Series:Proteome Science
Online Access:http://www.proteomesci.com/content/6/1/1
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spelling doaj-5e55b46413e84d8e80249687f205dc6d2020-11-24T23:15:52ZengBMCProteome Science1477-59562008-01-0161110.1186/1477-5956-6-1Proteomic profile determination of autosomal aneuploidies by mass spectrometry on amniotic fluidsDesmetz CarolineMange AlainBellet VirginieMolinari NicolasMaudelonde ThierrySolassol Jerome<p>Abstract</p> <p>Background</p> <p>Prenatal diagnosis of chromosomal abnormalities by cytogenetic analysis is time-consuming, expensive, and requires highly qualified technicians. Rapid diagnosis of aneuploidies followed by reassurance of women with normal results can be performed by molecular analysis of uncultured foetal cells. In the present study, we developed a proteomic fingerprinting approach coupled with a statistical classification method to improve diagnosis of aneuploidies, including trisomies 13, 18, and 21, in amniotic fluid samples.</p> <p>Results</p> <p>The proteomic spectra obtained from 52 pregnant women were compiled, normalized, and mass peaks with mass-to-charge ratios between 2.5 and 50 kDa identified. Peak information was combined together and analysed using univariate statistics. Among the 208 expressed protein peaks, 40 differed significantly between aneuploid and non aneuploid samples, with AUC diagnostic values ranging from 0.71 to 0.91. Hierarchical clustering, principal component analysis and support vector machine (SVM) analysis were performed. Two class predictor models were defined from the training set, which resulted in a prediction accuracy of 92.3% and 96.43%, respectively. Using an external and independent validation set, diagnostic accuracies were maintained at 87.5% and 91.67%, respectively.</p> <p>Conclusion</p> <p>This pilot study demonstrates the potential interest of protein expression signature in the identification of new potential biological markers that might be helpful for the rapid clinical management of high-risk pregnancies.</p> http://www.proteomesci.com/content/6/1/1
collection DOAJ
language English
format Article
sources DOAJ
author Desmetz Caroline
Mange Alain
Bellet Virginie
Molinari Nicolas
Maudelonde Thierry
Solassol Jerome
spellingShingle Desmetz Caroline
Mange Alain
Bellet Virginie
Molinari Nicolas
Maudelonde Thierry
Solassol Jerome
Proteomic profile determination of autosomal aneuploidies by mass spectrometry on amniotic fluids
Proteome Science
author_facet Desmetz Caroline
Mange Alain
Bellet Virginie
Molinari Nicolas
Maudelonde Thierry
Solassol Jerome
author_sort Desmetz Caroline
title Proteomic profile determination of autosomal aneuploidies by mass spectrometry on amniotic fluids
title_short Proteomic profile determination of autosomal aneuploidies by mass spectrometry on amniotic fluids
title_full Proteomic profile determination of autosomal aneuploidies by mass spectrometry on amniotic fluids
title_fullStr Proteomic profile determination of autosomal aneuploidies by mass spectrometry on amniotic fluids
title_full_unstemmed Proteomic profile determination of autosomal aneuploidies by mass spectrometry on amniotic fluids
title_sort proteomic profile determination of autosomal aneuploidies by mass spectrometry on amniotic fluids
publisher BMC
series Proteome Science
issn 1477-5956
publishDate 2008-01-01
description <p>Abstract</p> <p>Background</p> <p>Prenatal diagnosis of chromosomal abnormalities by cytogenetic analysis is time-consuming, expensive, and requires highly qualified technicians. Rapid diagnosis of aneuploidies followed by reassurance of women with normal results can be performed by molecular analysis of uncultured foetal cells. In the present study, we developed a proteomic fingerprinting approach coupled with a statistical classification method to improve diagnosis of aneuploidies, including trisomies 13, 18, and 21, in amniotic fluid samples.</p> <p>Results</p> <p>The proteomic spectra obtained from 52 pregnant women were compiled, normalized, and mass peaks with mass-to-charge ratios between 2.5 and 50 kDa identified. Peak information was combined together and analysed using univariate statistics. Among the 208 expressed protein peaks, 40 differed significantly between aneuploid and non aneuploid samples, with AUC diagnostic values ranging from 0.71 to 0.91. Hierarchical clustering, principal component analysis and support vector machine (SVM) analysis were performed. Two class predictor models were defined from the training set, which resulted in a prediction accuracy of 92.3% and 96.43%, respectively. Using an external and independent validation set, diagnostic accuracies were maintained at 87.5% and 91.67%, respectively.</p> <p>Conclusion</p> <p>This pilot study demonstrates the potential interest of protein expression signature in the identification of new potential biological markers that might be helpful for the rapid clinical management of high-risk pregnancies.</p>
url http://www.proteomesci.com/content/6/1/1
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