Literature DB >> 28807814

Development of a Chromosomal Microarray Test for the Detection of Abnormalities in Formalin-Fixed, Paraffin-Embedded Products of Conception Specimens.

Troy J Gliem1, Umut Aypar2.   

Abstract

Testing the products of conception (POCs) provides information about the cause of fetal loss and helps determine the recurrence risk of future losses and chromosome abnormalities in subsequent pregnancies. Historically, the Mayo Clinic Cytogenetics Laboratory performed targeted fluorescent in situ hybridization (FISH) testing to identify aneuploidy of only certain chromosomes in formalin-fixed, paraffin-embedded (FFPE) POC samples. Chromosomal microarray studies using the Affymetrix OncoScan FFPE Assay can detect copy number changes across the genome. We validated the utility of the OncoScan assay using 25 archival FFPE POC specimens with previous FISH results (five normal, 12 trisomy, six triploidy, two monosomy). Of the five normal samples, four had no clinically relevant findings, and one sample was found to have trisomy 9, which is not detectable by the FISH test. For the 20 samples with abnormal FISH results, the OncoScan assay identified all reported abnormalities along with additional findings. A sample with trisomy 22 was also found to have trisomy 7. Another sample reported as triploidy was found to have four copies of chromosome 16. In conclusion, we verified the performance characteristics of OncoScan on FFPE POC specimens and found it acceptable for clinical use. Additional information was identified in 3 of 25 cases (12%) that would explain the pregnancy loss or provide recurrence risk for the family.
Copyright © 2017 American Society for Investigative Pathology and the Association for Molecular Pathology. Published by Elsevier Inc. All rights reserved.

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Year:  2017        PMID: 28807814     DOI: 10.1016/j.jmoldx.2017.07.001

Source DB:  PubMed          Journal:  J Mol Diagn        ISSN: 1525-1578            Impact factor:   5.568


  4 in total

1.  High-resolution genomic alterations in Barrett's metaplasia of patients who progress to esophageal dysplasia and adenocarcinoma.

Authors:  Jorge L Sepulveda; Elena V Komissarova; Sarawut Kongkarnka; Richard A Friedman; Jon M Davison; Brynn Levy; Diana Bryk; Vaidehi Jobanputra; Armando Del Portillo; Gary W Falk; Joshua R Sonett; Charles J Lightdale; Julian A Abrams; Timothy C Wang; Antonia R Sepulveda
Journal:  Int J Cancer       Date:  2019-05-02       Impact factor: 7.396

2.  Optical Genome Mapping and Single Nucleotide Polymorphism Microarray: An Integrated Approach for Investigating Products of Conception.

Authors:  Nikhil Shri Sahajpal; Ashis K Mondal; Sudha Ananth; Chetan Pundkar; Kimya Jones; Colin Williams; Timothy Fee; Amanda Weissman; Giuseppe Tripodi; Eesha Oza; Larisa Gavrilova-Jordan; Nivin Omar; Alex R Hastie; Barbara R DuPont; Lawrence Layman; Alka Chaubey; Ravindra Kolhe
Journal:  Genes (Basel)       Date:  2022-04-03       Impact factor: 4.141

3.  Copy number variation sequencing combined with quantitative fluorescence polymerase chain reaction in clinical application of pregnancy loss.

Authors:  Lin Chen; Li Wang; Feng Tang; Yang Zeng; Daishu Yin; Cong Zhou; Hongmei Zhu; Linping Li; Lili Zhang; Jing Wang
Journal:  J Assist Reprod Genet       Date:  2021-05-30       Impact factor: 3.357

4.  Polymorphous Low-Grade Neuroepithelial Tumor of the Young (PLNTY): Molecular Profiling Confirms Frequent MAPK Pathway Activation.

Authors:  Cristiane M Ida; Derek R Johnson; Asha A Nair; Jaime Davila; Thomas M Kollmeyer; Kay Minn; Numrah M Fadra; Jessica R Balcom; Kar-Ming A Fung; Dong Kun Kim; Timothy J Kaufmann; Benjamin R Kipp; Kevin C Halling; Robert B Jenkins; Caterina Giannini
Journal:  J Neuropathol Exp Neurol       Date:  2021-09-27       Impact factor: 3.685

  4 in total

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