Aneuploidies detection in miscarriages and fetal deaths using multiplex ligation-dependent probe amplification: an alternative for speeding up results?

• Tipo: Artigo em Revista Científica Internacional
• Data: 2010

Autores

carvalho, b (Autor) Outra; doria, s (Autor) FMUP; ramalho, c (Autor) FMUP; brandao, o (Autor) Outra; sousa, m (Autor) ICBAS; matias, a (Autor) FMUP; barros, a (Autor) FMUP; carvalho, f (Autor) FMUP

Revista

Título: European Journal of Obstetrics & Gynecology and Reproductive Biology

Vol. 153

Páginas: 151-155

ISSN: 0301-2115

Editora: Elsevier

Indexação

ISI Web of Knowledge - 20 Citações

Scopus - 25 Citações

Classificação Científica

FOS: Ciências médicas e da saúde > Medicina clínica

Outras Informações

ID Authenticus: P-003-0FB

DOI: 10.1016/j.ejogrb.2010.06.022

Abstract (EN): Objective: The aim of this prospective study was to apply the MLPA technique to products of miscarriages and fetal deaths in order to detect the more frequent chromosome aneuploidies and compare the results to conventional karyotyping. Study design: Multiplex ligation-dependent probe amplification (MLPA) is a relatively new molecular technique for targeted detection of common chromosomal aneuploidies, namely trisomy 13, 18,21 and sex chromosomal abnormalities. The reliability and high accuracy of this technique constitute an alternative for rapid results in large scale testing. In this study, a total of 489 DNA samples from fetal tissue were used for aneuploidy detection of chromosomes 13, 18, 21, X and Y using a commercial MLPA kit (SALSA P095) and were simultaneously subjected to conventional karyotyping. Results: MLPA was the only result available in 33% of the cases. A cytogenetic result was obtained in only 328/489 samples. MLPA detected 7.8% of chromosome aneuploidies. Among the total samples karyotyped, MLPA failed to detect some aneuploidies and the false-negative rate was 0.82%. As expected, ploidy changes and reciprocal translocations were not detected by this technique, but MLPA gave a conclusive result even in cases of mosaicism. Conclusion: The present data confirm that MLPA is a rapid, simple and reliable method for detection of chromosome 13, 18, 21, X and Y abnormalities in fetal tissue.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 5