Assessment of QF-PCR as the First Approach in Prenatal Diagnosis

• Autores: Cèlia Badenas, Laia Rodríguez Revenga Bodi, Carmen Morales, Carmen Mediano, Alberto Plaja, M. Mar Pérez Iribarne, Anna Soler, Núria Clusellas, Antoni Borrell Vilaseca, M.A. Sánchez Duran, Elisabeth Miró, Aurora Sánchez, Montserrat Milà Ricasens, Wladimiro Jiménez
• Localización: The Journal of molecular diagnostics, ISSN 1525-1578, Vol. 12, Nº 6, 2010, págs. 828-834
• Idioma: inglés
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• Resumen

  • Quantitative fluorescent PCR (QF-PCR) has been used by many laboratories for prenatal diagnosis of the most common aneuploidies. QF-PCR is rapid, cost-effective, and suitable for automation and can detect most abnormalities diagnosed by conventional karyotyping. Whether QF-PCR should be used alone in most of the samples and in which karyotyping should also be offered is currently a topic of debate. We evaluated and compared the results obtained from 7679 prenatal samples in which conventional karyotype and QF-PCR had been performed, including 1243 chorionic villi and 6436 amniotic fluid samples. Concordant QF-PCR and karyotype results were obtained in 98.75% of the samples. An abnormal karyotype associated with adverse clinical outcome undetected by QF-PCR was found in 0.05% of samples. Therefore, QF-PCR can be used alone in a large number of samples studied in a prenatal laboratory, thereby reducing both the workload in cytogenetic laboratories and parental anxiety when awaiting results.