Reliability of comparative genomic hybridization to detect chromosome abnormalities in first polar bodies and metaphase II oocytes

BACKGROUND: Preimplantation Genetic Diagnosis (PGD) using FISH to analyze up to nine chromosomes to discard chromosomally abnormal embryos has resulted in an increase of pregnancy rates in certain groups of patients. However, the number of chromosomes that can be analyzed is a clear limitation. We e...

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Veröffentlicht in:Human reproduction (Oxford) 2004-09, Vol.19 (9), p.2118-2125
Hauptverfasser: Gutiérrez-Mateo, Cristina, Wells, Dagan, Benet, Jordi, Sánchez-García, Jorge F., Bermúdez, Mercedes G., Belil, Itziar, Egozcue, Josep, Munné, Santiago, Navarro, Joaquima
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Sprache:eng
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Zusammenfassung:BACKGROUND: Preimplantation Genetic Diagnosis (PGD) using FISH to analyze up to nine chromosomes to discard chromosomally abnormal embryos has resulted in an increase of pregnancy rates in certain groups of patients. However, the number of chromosomes that can be analyzed is a clear limitation. We evaluate the reliability of using comparative genomic hybridization (CGH) to detect the whole set of chromosomes, as an alternative to PGD using FISH. METHODS and RESULTS: We have analysed by CGH both, first polar bodies (1PBs) and metaphase II (MII) oocytes from 30 oocytes donated by 24 women. The aneuploidy rate was 48%. Considering two maternal age groups, a higher number of chromosome abnormalities were detected in the older group of oocytes (23% versus 75%, P
ISSN:0268-1161
1460-2350
1460-2350
DOI:10.1093/humrep/deh367