Skip Navigation



Hum. Reprod. Advance Access published online on October 22, 2009

Human Reproduction, doi:10.1093/humrep/dep364
This Article
Right arrow Full Text
Right arrow Full Text (PDF )
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 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 arrowRequest Permissions
Google Scholar
Right arrow Articles by Halliday, J. L.
Right arrow Articles by Amor, D.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Halliday, J. L.
Right arrow Articles by Amor, D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2009. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Increased risk of blastogenesis birth defects, arising in the first 4 weeks of pregnancy, after assisted reproductive technologies

Jane L. Halliday1,2,7, Obioha C. Ukoumunne1,2, H.W. Gordon Baker3,4, Sue Breheny5, Alice M. Jaques1, Claire Garrett4, David Healy5,6 and David Amor1,2,3

1 Murdoch Childrens Research Institute, Royal Children's Hospital, Flemington Rd, Parkville, VIC 3052, Australia 2 Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia 3 Melbourne IVF, East Melbourne, VIC, Australia 4 Department of Obstetrics and Gynaecology, University of Melbourne, Royal Women's Hospital, Parkville, VIC, Australia 5 Monash IVF, Richmond, VIC, Australia 6 Department of Obstetrics and Gynaecology, Monash University, Clayton, VIC, Australia

7 Correspondence address. Tel: +61-3-8341-6260; Fax: +61-3-8341-6212; E-mail: janehalliday.h{at}mcri.edu.au

BACKGROUND: The reasons for increased birth defect prevalence following in-vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI) are largely unknown. Classification of birth defects by pathology rather than organ system, and examination of the role of embryo freezing and thawing may provide clues to the mechanisms involved. This study aimed to investigate these two factors.

METHOD: Data on 6946 IVF or ICSI singleton pregnancies were linked to perinatal outcomes obtained from population-based data sets on births and birth defects occurring between 1991 and 2004 in Victoria, Australia. These were compared with 20 838 outcomes for singleton births in the same population, conceived without IVF or ICSI. Birth defects were classified according to pathogenesis.

RESULTS: Overall, birth defects were increased after IVF or ICSI [adjusted odds ratio (OR) 1.36; 95% CI: 1.19–1.55] relative to controls. There was no strong evidence of risk differences between IVF and ICSI or between fresh and thawed embryo transfer. However, a specific group, blastogenesis birth defects, were markedly increased [adjusted OR 2.80, 95% CI: 1.63–4.81], with the increase relative to the controls being significant for fresh embryo transfer (adjusted OR 3.65; 95% CI: 2.02–6.59) but not for thawed embryo transfer (adjusted OR 1.60; 95% CI: 0.69–3.69).

CONCLUSION: Our findings suggest that there is a specific risk of blastogenesis birth defects arising very early in pregnancy after IVF or ICSI and that this risk may be lower with use of frozen-thawed embryo transfer.

Key words: assisted reproduction/birth defects/blastogenesis/embryo transfer/cryopreservation

Submitted on July 24, 2009; resubmitted on September 5, 2009; accepted on September 18, 2009.


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




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.