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Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics
PURPOSE: The metaphase karyotype is often used as a diagnostic tool in the setting of early miscarriage; however this technique has several limitations. We evaluate a new technique for karyotyping that uses single nucleotide polymorphism microarrays (SNP). This technique was compared in a blinded, p...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293871/ https://www.ncbi.nlm.nih.gov/pubmed/22403611 http://dx.doi.org/10.1371/journal.pone.0031282 |
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author | Lathi, Ruth B. Loring, Megan Massie, Jamie A. M. Demko, Zachary P. Johnson, David Sigurjonsson, Styrmir Gemelos, George Rabinowitz, Matthew |
author_facet | Lathi, Ruth B. Loring, Megan Massie, Jamie A. M. Demko, Zachary P. Johnson, David Sigurjonsson, Styrmir Gemelos, George Rabinowitz, Matthew |
author_sort | Lathi, Ruth B. |
collection | PubMed |
description | PURPOSE: The metaphase karyotype is often used as a diagnostic tool in the setting of early miscarriage; however this technique has several limitations. We evaluate a new technique for karyotyping that uses single nucleotide polymorphism microarrays (SNP). This technique was compared in a blinded, prospective fashion, to the traditional metaphase karyotype. METHODS: Patients undergoing dilation and curettage for first trimester miscarriage between February and August 2010 were enrolled. Samples of chorionic villi were equally divided and sent for microarray testing in parallel with routine cytogenetic testing. RESULTS: Thirty samples were analyzed, with only four discordant results. Discordant results occurred when the entire genome was duplicated or when a balanced rearrangement was present. Cytogenetic karyotyping took an average of 29 days while microarray-based karytoyping took an average of 12 days. CONCLUSIONS: Molecular karyotyping of POC after missed abortion using SNP microarray analysis allows for the ability to detect maternal cell contamination and provides rapid results with good concordance to standard cytogenetic analysis. |
format | Online Article Text |
id | pubmed-3293871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32938712012-03-08 Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics Lathi, Ruth B. Loring, Megan Massie, Jamie A. M. Demko, Zachary P. Johnson, David Sigurjonsson, Styrmir Gemelos, George Rabinowitz, Matthew PLoS One Research Article PURPOSE: The metaphase karyotype is often used as a diagnostic tool in the setting of early miscarriage; however this technique has several limitations. We evaluate a new technique for karyotyping that uses single nucleotide polymorphism microarrays (SNP). This technique was compared in a blinded, prospective fashion, to the traditional metaphase karyotype. METHODS: Patients undergoing dilation and curettage for first trimester miscarriage between February and August 2010 were enrolled. Samples of chorionic villi were equally divided and sent for microarray testing in parallel with routine cytogenetic testing. RESULTS: Thirty samples were analyzed, with only four discordant results. Discordant results occurred when the entire genome was duplicated or when a balanced rearrangement was present. Cytogenetic karyotyping took an average of 29 days while microarray-based karytoyping took an average of 12 days. CONCLUSIONS: Molecular karyotyping of POC after missed abortion using SNP microarray analysis allows for the ability to detect maternal cell contamination and provides rapid results with good concordance to standard cytogenetic analysis. Public Library of Science 2012-03-05 /pmc/articles/PMC3293871/ /pubmed/22403611 http://dx.doi.org/10.1371/journal.pone.0031282 Text en Lathi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lathi, Ruth B. Loring, Megan Massie, Jamie A. M. Demko, Zachary P. Johnson, David Sigurjonsson, Styrmir Gemelos, George Rabinowitz, Matthew Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics |
title | Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics |
title_full | Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics |
title_fullStr | Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics |
title_full_unstemmed | Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics |
title_short | Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics |
title_sort | informatics enhanced snp microarray analysis of 30 miscarriage samples compared to routine cytogenetics |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293871/ https://www.ncbi.nlm.nih.gov/pubmed/22403611 http://dx.doi.org/10.1371/journal.pone.0031282 |
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