Application of fluorescence in situ hybridization (fish) as a tool to aid cytogenetics in 1,409 fetal samples

Application of fluorescence in situ hybridization (fish) as a tool to aid cytogenetics in 1,409 fetal samples

Autor de Moraes-Malinverni, Andrea C. Autor UNIFESP Google Scholar
Patricio, F. R. S. Autor UNIFESP Google Scholar
Oshima, Celina Tizuko Fujiyama Autor UNIFESP Google Scholar
Moron, Antonio F. Autor UNIFESP Google Scholar
da Silva, I. D. C. G. Autor UNIFESP Google Scholar
de Souza, M. M. Autor UNIFESP Google Scholar
Resumo Aim: To evaluate the technical application of fluorescence in situ hybridization (FISH) as a support to classical cytogenetic in numerical chromosomal aneuploidies studies in samples of amniotic fluid, chorionic villus, and fetal loss. Materials and Methods: The authors performed cytogenetic analyses in 1,409 patients (678 amniocentesis, 512 chorionic villus samples, and 219 spontaneous abortions) during one year. FISH molecular study aided traditional cytogenetic in 90 cases. These cases were indicated based on the diagnostic hypothesis of each patient or when no cellular growth was obtained. The authors standardized the FISH in discoloured slides. Results: They had 85% positive FISH in amniotic fluid, 70% in chorionic villus, and 90% in abortion material using 13, 18, 21 X and Y centromeric probes. It showed 12% of altered FISH in amniotic fluid (100% trisomies), 10% in chorionic villus (50% trisomy and 50% X - monosomy), and 22% in abortion material (50% trisomy, 25% X-monosomy, and 25% triploidy). FISH and cytogenetic analysis confirmed the results. Conclusion: This technique revolutionized clinical and research applications of cytogenetics. In this particular paper, FISH was a valuable and reliable technique to promptly identify rapid detection of aneuploidies in interphase cells, metaphase spread and paraffin-embedded samples. It is hoped that, in the future, the economic viability of array CGH and FISH, with the decreasing cost of testing and their genomics advantages can be incorporated as routine and customized in the approach of prenatal diagnosis.
Assunto Cytogenetic
Fluorescence In Situ Hybridization
Prenatal Diagnosis
Spontaneous AbortionsRapid Prenatal-Diagnosis
Insitu Hybridization
Chromosomal-Abnormalities
Interphase Fish
Aneuploidies
Aberrations
Experience
Amniocytes
Abortions
Europe
Idioma Inglês
Data 2016
Publicado em Clinical And Experimental Obstetrics & Gynecology. Montreal, v. 43, n. 5, p. 685-690, 2016.
ISSN 0390-6663 (Sherpa/Romeo, fator de impacto)
Editor Elsevier Science Inc
Extensão 685-690
Fonte http://dx.doi.org/10.12891/ceog3137.2016
Direito de acesso Acesso restrito
Tipo Artigo
Web of Science WOS:000385211500011
URI http://repositorio.unifesp.br/handle/11600/49386

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