TY - JOUR
T1 - Rate of homologous chromosome bivalents in spermatocytes may predict completion of spermatogenesis in azoospermic men
AU - Yogev, Leah
AU - Gamzu, Ronni
AU - Paz, Gedalia
AU - Kleiman, Sandra
AU - Botchan, Amnon
AU - Hauser, Ron
AU - Yavetz, Haim
N1 - Funding Information:
Acknowledgements We would like to thank Mrs. Bella Gore and Marina Ilatov for their excellent technical assistance. The continuous support of the entire staff of the Institute for the Study of Fertility is much appreciated. The expert statistical analysis provided by Dr. Yael Villa is most valued. This study was supported in part by the Chief Scientific Office, Ministry of Health, Israel.
PY - 2002/1
Y1 - 2002/1
N2 - The rate of bivalent formation during meiosis was correlated with the presence and amount of spermatozoa in the testes of azoospermic men. Four pairs of chromosomes, X-Y, 9, 15, and 18, were evaluated. In addition, left and right testes were compared. Three biopsies from each testis were undertaken to extract spermatozoa for intracytoplasmic sperm injection. In addition, one sample from each testis was used for histological definition, spermatozoa count and detection of chromosome bivalents in spermatocytes. A significantly higher rate of bivalents of all homologous chromosomes was found whenever spermatozoa were detected. The rate of bivalent X-Y was found to be the most sensitive predictor for detection of spermatozoa, with a cut-off value of 47%. The R2 was 27% (P=0.003) for the percent of spermatozoa in the minced sample as well as the number of mature spermatids per tubule in the histological section. All pairs of testes were in concord in regard to the likelihood of finding spermatozoa. In the testes where no spermatozoa were found on biopsy, the rate of X-Y bivalent indicated the presence of spermatozoa in the opposite side. Thus, it may be concluded that the rate of X-Y bivalent formation in spermatocytes may predict the presence and amount of spermatozoa in the testicular tissue of azoospermic men. It is suggested that when no spermatozoa are located by testicular fine-needle aspiration, X-Y bivalent evaluation may be conducted if spermatocytes are evinced. A high rate of X-Y bivalents may impel one to continue with testicular open biopsies.
AB - The rate of bivalent formation during meiosis was correlated with the presence and amount of spermatozoa in the testes of azoospermic men. Four pairs of chromosomes, X-Y, 9, 15, and 18, were evaluated. In addition, left and right testes were compared. Three biopsies from each testis were undertaken to extract spermatozoa for intracytoplasmic sperm injection. In addition, one sample from each testis was used for histological definition, spermatozoa count and detection of chromosome bivalents in spermatocytes. A significantly higher rate of bivalents of all homologous chromosomes was found whenever spermatozoa were detected. The rate of bivalent X-Y was found to be the most sensitive predictor for detection of spermatozoa, with a cut-off value of 47%. The R2 was 27% (P=0.003) for the percent of spermatozoa in the minced sample as well as the number of mature spermatids per tubule in the histological section. All pairs of testes were in concord in regard to the likelihood of finding spermatozoa. In the testes where no spermatozoa were found on biopsy, the rate of X-Y bivalent indicated the presence of spermatozoa in the opposite side. Thus, it may be concluded that the rate of X-Y bivalent formation in spermatocytes may predict the presence and amount of spermatozoa in the testicular tissue of azoospermic men. It is suggested that when no spermatozoa are located by testicular fine-needle aspiration, X-Y bivalent evaluation may be conducted if spermatocytes are evinced. A high rate of X-Y bivalents may impel one to continue with testicular open biopsies.
UR - http://www.scopus.com/inward/record.url?scp=0036461079&partnerID=8YFLogxK
U2 - 10.1007/s00439-001-0635-9
DO - 10.1007/s00439-001-0635-9
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AN - SCOPUS:0036461079
SN - 0340-6717
VL - 110
SP - 30
EP - 35
JO - Human Genetics
JF - Human Genetics
IS - 1
ER -