High frequency of gr/gr chromosome Y deletions in consecutive oligospermic ICSI candidates

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Abstract

Background: The Y chromosome gr/gr microdeletion eliminates two copies of the DAZ gene and several additional transcriptional units and has been associated as a risk factor for infertility. Our objective was to study the presence of the gr/gr deletion in ICSI candidates in our population and to determine whether the laboratory, clinical and ICSI outcome were different in the gr/gr deleted patients. Methods: Two hundred and eighty-three ICSI candidates were studied. Semen analysis, serum FSH, LH, testosterone, inhibin B, karyotype and detection of sequence tagged sites in the Y chromosome were performed. Results: gr/gr deletions were detected in 11 (5.07%) of 217 oligospermic and in one (1.52%) of 66 azoospermic consecutive ICSI candidates, but in none of 232 controls (P = 0.002). The fertility rate was not different in the four patients of the gr/gr deleted group treated by ICSI (64.38%; 47/73) as compared to average results at our center (65.49%; 2393/3654). Conclusios: gr/gr deletions are a risk factor for spermatogenic failure at our population, but the prognosis of the four patients of the gr/gr deleted group treated by ICSI is not different from that of other ICSI patients. © European Society of Human Reproduction and Embryology 2004; all rights reserved.

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de Llanos, M., Ballescà, J. L., Gázquez, C., Margarit, E., & Oliva, R. (2005). High frequency of gr/gr chromosome Y deletions in consecutive oligospermic ICSI candidates. Human Reproduction, 20(1), 216–220. https://doi.org/10.1093/humrep/deh582

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