Skip Navigation


Hum. Reprod. Advance Access originally published online on April 7, 2004
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF ) Freely available
Right arrow All Versions of this Article:
19/5/1163    most recent
deh162v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (22)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Magli, M.C.
Right arrow Articles by Fasolino, M.C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Magli, M.C.
Right arrow Articles by Fasolino, M.C.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol. 19, No. 5, 1163-1169, May 2004
© 2004 European Society of Human Reproduction and Embryology

The combination of polar body and embryo biopsy does not affect embryo viability

M.Cristina Magli, Luca Gianaroli1, Anna P. Ferraretti, Marco Toschi, Francesca Esposito and M.Carmen Fasolino

S.I.S.Me.R., Reproductive Medicine Unit, Via Mazzini 12, 40138 Bologna, Italy

1 To whom correspondence should be addressed. e-mail: sismer{at}sismer.it

BACKGROUND: The biopsy of both polar bodies and a blastomere from the same embryo was investigated as an approach aimed at increasing the quantity of DNA available for genetic analysis in preimplantation embryos. METHODS: In 113 cycles, preimplantation genetic diagnosis (PGD) was performed for aneuploidy: 19 cycles underwent polar body biopsy, 32 cycles had both polar body and blastomere biopsy done, and the remaining 62 cycles underwent blastomere biopsy. The chromosomal analysis was performed in a two-round fluorescence in situ hybridization (FISH) protocol with probes specific for the chromosomes X, Y, 13, 15, 16, 18, 21 and 22. RESULTS: The morphological evaluation of the analysed embryos demonstrated similar rates of development irrespective of the biopsy procedure. Accordingly, the implantation rate did not differ significantly in the three biopsy groups and was 15% after polar body biopsy, 26% after the combined biopsy procedures of polar bodies and blastomeres, and 25% after blastomere biopsy. CONCLUSIONS: The removal of a blastomere subsequent to polar body biopsy does not seem to have negative effects on embryo viability. This approach could be especially valuable for a combined diagnosis of aneuploidy and single-gene disorders in preimplantation embryos generated by couples at high reproductive risk.

Key words: aneuploidy/blastomere biopsy/embryo viability/polar body biopsy/preimplantation genetic diagnosis


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol. Cell. ProteomicsHome page
Y. Yu, J. Wu, Y. Fan, Z. Lv, X. Guo, C. Zhao, R. Zhou, Z. Zhang, F. Wang, M. Xiao, et al.
Evaluation of Blastomere Biopsy Using a Mouse Model Indicates the Potential High Risk of Neurodegenerative Disorders in the Offspring
Mol. Cell. Proteomics, July 1, 2009; 8(7): 1490 - 1500.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
V. Goossens, M. De Rycke, A. De Vos, C. Staessen, A. Michiels, W. Verpoest, A. Van Steirteghem, C. Bertrand, I. Liebaers, P. Devroey, et al.
Diagnostic efficiency, embryonic development and clinical outcome after the biopsy of one or two blastomeres for preimplantation genetic diagnosis
Hum. Reprod., March 1, 2008; 23(3): 481 - 492.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
C. M.H. Combelles
What are the trade-offs between one-cell and two-cell biopsies of preimplantation embryos?
Hum. Reprod., March 1, 2008; 23(3): 493 - 498.
[Full Text] [PDF]


Home page
ReproductionHome page
A. Pujol, J. Benet, C. Staessen, E. Van Assche, M. Campillo, J. Egozcue, and J. Navarro
The importance of aneuploidy screening in reciprocal translocation carriers.
Reproduction, June 1, 2006; 131(6): 1025 - 1035.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
J. Cohen and S. Munne
Comment 2 on Staessen et al. (2004). Two-cell biopsy and PGD pregnancy outcome
Hum. Reprod., August 1, 2005; 20(8): 2363 - 2364.
[Full Text] [PDF]


Home page
Hum ReprodHome page
C. Staessen, P. Platteau, E. Van Assche, A. Michiels, H. Tournaye, M. Camus, P. Devroey, I. Liebaers, and A.C. Van Steirteghem
Reply to Comments on Staessen et al. (2004)
Hum. Reprod., August 1, 2005; 20(8): 2364 - 2365.
[Full Text] [PDF]


Home page
Mol Hum ReprodHome page
J. F. Sanchez-Garcia, J. Benet, C. Gutierrez-Mateo, J. Luis Seculi, E. Monros, and J. Navarro
Multiple mutation analysis of the cystic fibrosis gene in single cells
Mol. Hum. Reprod., June 1, 2005; 11(6): 463 - 468.
[Abstract] [Full Text] [PDF]


Home page
J. Histochem. Cytochem.Home page
L. Gianaroli, M. C. Magli, and A. P. Ferraretti
Sperm and Blastomere Aneuploidy Detection in Reproductive Genetics and Medicine
J. Histochem. Cytochem., March 1, 2005; 53(3): 261 - 267.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.