Volume 8, Issue 4 (7-2010)                   IJRM 2010, 8(4): 173-178 | Back to browse issues page

XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Nowroozi M R, Radkhah K, Ranjbaran A, Ghaffari S R, Sedighi Gilani M A, Gourabi H. Is karyotyping and Y chromosome microdeletion study necessary in men candidate for ICSI?. IJRM 2010; 8 (4) :173-178
URL: http://ijrm.ir/article-1-194-en.html
1- Urology Research Center, Tehran University of Medical Sciences, Tehran, Iran , mrnowroozi@yahoo.com
2- Urology Research Center, Tehran University of Medical Sciences, Tehran, Iran
3- Department of Genetics, Tehran University of Medical Sciences, Tehran, Iran
4- Department of Urology, Rooyan Institute, Tehran University of Medical Sciences, Tehran, Iran
5- Department of Genetics, Rooyan Institute, Tehran, Iran
Abstract:   (2520 Views)
Background: The sperm count and function may be affected by karyotype abnormalities or microdeletion in Y chromosome. These genetic abnormalities can probably transmit to the children.
Objective: In this study, we tried to determine the frequency of karyotype abnormalities and Y chromosome microdeletions in severe oligospermic or azoospermic men who fathered sons by ICSI.
Materials and Methods: This study comprised of fathers who had at least a son with ICSI due to severe oligospermia or azoospermia. General examinations were done and blood sample were obtained for karyotype and Y chromosome studies.
Results: The total of 60 fathers was evaluated along with their 70 sons. The mean duration of infertility was 8.7 years and the sons were 2.4 years in average at the time of examination. The mean age of neonates at the time of delivery was 33 weeks; 42.9% were delivered prematurely; and 40.5% of them were twins. 8.6% of the sons had hypospadiasis and 7.1% had UDT. Most of the side effects were due to prematurity. In total 6 of fathers had karyotype anomaly, meanwhile 4 of their sons had also karyotype anomaly. Only one son had karyotype anomaly without affected father. No case of Y chromosome microdeletion was found in the fathers.
Conclusion: Y chromosome microdeletion is not prevalent in fathers with successful ICSI and it is not necessary to be analyzed before ICSI performance. Karyotype anomaly may transmit to the sons. All together ICSI is reliable and safe. Most of the complications are the result of premature delivery.
Full-Text [PDF 171 kb]   (468 Downloads) |   |   Full-Text (HTML)  (323 Views)  
Type of Study: Original Article |

References
1. Kent -First MG, Kol S, Muallem A, Ofir R, Manor D, Blazer S, et al. The incidence and possible relevance of Y-Linked microdeletions in babies born after intracytoplasmic sperm injection and their infertile fathers. Mol Hum Repord 1996; 2: 943-950. [DOI:10.1093/molehr/2.12.943]
2. OKutman-Emonts O, Pehlivan S, Tavmergen E, Tavmergen-Goker EN, Ozkinay F. Screening of Y chromosome microdeletion which contions AZF regions in 71 Turkish azoospermic mer. Genet Couns 2004;15:199-205.
3. Hopps CV, Mielnik A, Goldstein M, Palermo GD. Rosenwaks Z, Schlegel PN. Detection of sperm in men whith Y chromosome microdeletion of the AZF a, AzFb, AzFc regions. Hum Reprod 2003; 18:1660-1665. [DOI:10.1093/humrep/deg348]
4. Crugerr DG, Agerholm I, Byriel L fedder J, Bruun - Petersen G. Genetic analysis of males from intracytoplasmic sperm injection couples. Clin Genet 2003; 64: 198 - 203. [DOI:10.1034/j.1399-0004.2003.00128.x]
5. Katz MG, Chu B, McLachlan R, Alexopoulos NI, de Kretser DM, Cram DS. Genetic follow-up of male offspring born by ICSI, using a multiplex fluorescent PCR-based test for Yq deletions. Mol Hum Reprod 2002; 8: 589-595. [DOI:10.1093/molehr/8.6.589]
6. Cram DS, Ma K, Bhasin S, Arias J, Pandjaitan M, Chu B, et al. Y chromosome analysis of infertile men and their sons conceived through intracytoplasmic sperm injection: vertical transmission of deletions and rarity of de novo deletions. Fertil Steril 2000; 74: 909-915. [DOI:10.1016/S0015-0282(00)01568-5]
7. Katagiri Y, Neri QV, Takeuchi T, Schlegel PN, Megid WA, Kent-First M, et al. Y chromosome assessment and its implications for the development of ICSI children. Reprod Biomed Online 2004; 8: 307 - 318. [DOI:10.1016/S1472-6483(10)60911-X]
8. Zhu XB, Li Z, Guo AL, Cao XR, Liu Y, Gong DM, et al. Study on the vertical transmission of Y chromosome microdeletions from father to son. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2007; 24: 203-205.
9. Lee SH, Ahn SY, Lee KW, Kwack K, Jun HS, Cha KY. Intracytoplasmic sperm injection may lead to vertical transmission, expansion, and de novo occurrence of Y-chromosome microdeletions in male fetuses. Fertil Steril 2006; 85: 1512-1515. [DOI:10.1016/j.fertnstert.2005.10.034]
10. Bonduelle M, Van Assche E, Joris H, Keymolen K, Devroey P, Van Steirteghem A, et al. Prenatal testing in ICSI pregnancies: incidence of chromosomal anomalies in 1586 karyotypes and relation to sperm parameters. Hum Reprod 2002; 17: 2600 - 2614. [DOI:10.1093/humrep/17.10.2600]
11. Georgiou I, Syrrou M, Pardalidis N, Karakitsios K, Mantzavinos T, Giotitsas N, et al. Genetic and epigenetic risks of intracytoplasmic sperm injection method. Asian J Androl 2006; 8: 643-673. [DOI:10.1111/j.1745-7262.2006.00231.x]
12. Aknin-Seifer IE, Touraine RL, Lejeune H, Laurent JL, Lauras B, Levy R. A simple, low cost and non-invasive method for screening Y-chromosome microdeletions in infertile men. Hum Reprod 2003; 18: 257-261. [DOI:10.1093/humrep/deg067]
13. Verma RS, Babu A. Human chromosomes. Manual of Basic techniques. 2nd ed. McGrow-Hill: New York; 1995.
14. ISCN. An International System for Human Cytogenetic Namenclauter. Mitelman F, editor. Karger: Basal; 1995.
15. Miharu N. Chromosome abnormalities in sperm from infertile men with normal somatic karyotypes: oligozoospermia. Cytogenet Genome Res 2005; 111: 347-351. [DOI:10.1159/000086909]
16. Nagvenkar P, Desai K, Hinduja I, Zaveri K. Chromosomal studies in infertile men with oligozoospermia and non-obstructive azoospermia. Indian J Med Res 2005; 122:34-42.
17. Fedder J, Gabrielsen A, Humaidan P, Erb K, Ernst E, Loft A. Malformation rate and sex ratio in 412 children conceived with epididymal or testicular sperm. Hum Reprod 2007; 22:1080-1085. [DOI:10.1093/humrep/del488]
18. Ericson A, Källén B. Congenital malformations in infants born after IVF: a population-based study. Hum Reprod 2001; 16: 504-509. [DOI:10.1093/humrep/16.3.504]
19. Wennerholm UB, Bergh C, Hamberger L, Lundin K, Nilsson L, Wikland M, et al. Incidence of congenital malformations in children born after ICSI. Hum Reprod 2000; 15: 944-948. [DOI:10.1093/humrep/15.4.944]
20. Bonduelle M, Legein J, Derde MP, Buysse A, Schietecatte J, Wisanto A, et al. Comparative follow-up study of 130 children born after intracytoplasmic sperm injection and 130 children born after in-vitro fertilization. Hum Reprod 1995; 10: 3327-3331. [DOI:10.1093/oxfordjournals.humrep.a135914]
21. Källén B, Finnström O, Nygren KG, Olausson PO. In vitro fertilization (IVF) in Sweden: risk for congenital malformations after different IVF methods. Birth Defects Res A Clin Mol Teratol 2005; 73:162-169. [DOI:10.1002/bdra.20107]
22. Lie RT, Lyngstadaas A, Ørstavik KH, Bakketeig LS, Jacobsen G, Tanbo T. Birth defects in children conceived by ICSI compared with children conceived by other IVF-methods; a meta-analysis. Int J Epidemiol 2005; 34:696-701. [DOI:10.1093/ije/dyh363]
23. Pinborg A, Loft A, Nyboe Andersen A. Neonatal outcome in a Danish national cohort of 8602 children born after in vitro fertilization or intracytoplasmic sperm injection: the role of twin pregnancy. Acta Obstet Gynecol Scand 2004; 83:1071-1078. [DOI:10.1111/j.0001-6349.2004.00476.x]
24. Ristanović M, Bunjevacki V, Tulić C, Novaković I, Ille T, Radojković D, et al. Y chromosome microdeletions in infertile male candidates for microfertilization. Srp Arh Celok Lek 2008; 136:126-130. [DOI:10.2298/SARH0804126R]
25. Marchina E, Imperadori L, Speziani M, Omodei U, Tombesi S, Barlati S. Chromosome abnormalities and Yq microdeletions in infertile italian couples referred for assisted reproductive technique. Sex Dev 2007; 1: 347-352. [DOI:10.1159/000111766]
26. Feng C, Wang LQ, Dong MY, Huang HF. Assisted reproductive technology may increase clinical mutation detection in male offspring. Fertil Steril 2008; 90: 92-96. [DOI:10.1016/j.fertnstert.2007.06.004]
27. Ristanovic M, Bunjevacki V, Tulic C, Novakovic I, Perovic V, Lukovic LJ, et al. Prevalence of Y chromosome microdeletions in infertile men with severe oligozoospermia in Serbia. Genet Couns 2007; 18: 337-342.
28. Spinner NB, Saitta SC, Delaney DP, Colliton R, Zderic SA, Ruchelli E, et al. Intracytoplasmic sperm injection (ICSI) with transmission of a ring(Y) chromosome and ovotesticular disorder of sex development in offspring. Am J Med Genet A 2008; 146A: 1828-1831. [DOI:10.1002/ajmg.a.32358]
29. Arnedo N, Nogués C, Bosch M, Templado C. Mitotic and meiotic behavior of a naturally transmitted ring Y chromosome: reproductive risk evaluation. Hum Reprod 2005; 20: 462-468. [DOI:10.1093/humrep/deh598]
30. Minor A, Wong EC, Harmer K, Ma S. Molecular and cytogenetic investigation of Y chromosome deletions over three generations facilitated by intracytoplasmic sperm injection. Prenat Diagn 2007; 27: 743-747. [DOI:10.1002/pd.1772]

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Designed & Developed by : Yektaweb