Skip Navigation


Hum. Reprod. Advance Access originally published online on April 24, 2008
Human Reproduction 2008 23(7):1679-1683; doi:10.1093/humrep/den126
This Article
Right arrow Full Text
Right arrow Full Text (PDF )
Right arrow All Versions of this Article:
23/7/1679    most recent
den126v1
Right arrow Alert me when this article is cited
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 Kirkpatrick, G.
Right arrow Articles by Ma, S.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kirkpatrick, G.
Right arrow Articles by Ma, S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2008. 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

A comparison of sperm aneuploidy rates between infertile men with normal and abnormal karyotypes

Gordon Kirkpatrick{dagger}, Kyle A. Ferguson{dagger}, Haijun Gao, Steven Tang, Victor Chow, Basil Ho Yuen and Sai Ma1

Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, Canada

1 Correspondence address. Department of Obstetrics and Gynaecology, Room D414B, BC Women's Hospital and Health Centre, University of British Columbia, D6-4500 Oak Street, Vancouver, British Columbia, Canada V6H 3N1. Tel: +1-604-875-2345 ext. 5686; Fax: +1-604-875-2722; E-mail: sai{at}interchange.ubc.ca

BACKGROUND: Abnormal semen parameters in chromosomally normal men are an indicator of an increased risk of sperm aneuploidy. Male carriers of chromosomal rearrangements may also display an increase in sperm aneuploidy for chromosomes not involved in the rearrangement, known as an interchromosomal effect (ICE), and this may be related to the impaired semen parameters of these men.

METHODS: Aneuploidy was examined in ejaculate sperm from 27 men: 8 carriers of chromosomal rearrangements with severe oligoasthenoteratozoospermia (OAT) or severe teratozoospermia; 10 chromosomally normal men with similarly abnormal semen parameters; and 9 proven fertile men with normal semen parameters. Fluorescence in situ hybridization was used to examine aneuploidy for chromosomes 13, 18, 21, X and Y.

RESULTS: We observed evidence of an ICE in three of the eight carriers of chromosomal rearrangements. However, men who were chromosomally normal but had severe OAT more frequently displayed increased disomy rates. Although autosomal disomy rates were only modestly increased in some of these men, increased XY disomy ranged from slight to extreme (up to a 100-fold increase).

CONCLUSIONS: Despite their similar semen parameters, infertile men with normal karyotypes displayed more frequent increases in sperm aneuploidy, particularly involving the sex chromosomes, than infertile men who were carriers of chromosomal rearrangements. The difference in the magnitude and type of sperm aneuploidy between the two infertile groups is likely related to the different causes of infertility.

Key words: interchromosomal effect/sperm aneuploidy/male infertility/chromosomal rearrangements/FISH


{dagger} These authors contributed equally to this work.

Submitted on December 10, 2007; resubmitted on January 28, 2008; accepted on March 21, 2008.


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.