A comparison of ejaculated and testicular spermatozoa aneuploidy rates in patients with high sperm DNA damage

被引:49
|
作者
Moskovtsev, Sergey I. [1 ,2 ]
Alladin, Naazish [1 ]
Lo, Kirk C. [3 ]
Jarvi, Keith [3 ]
Mullen, J. Brendan M. [4 ]
Librach, Clifford L. [1 ,2 ,5 ,6 ]
机构
[1] CReATe Fertil Ctr, Toronto, ON M5G 1N8, Canada
[2] Univ Toronto, Dept Obstet & Gynaecol, Toronto, ON, Canada
[3] Mt Sinai Hosp, Dept Surg, Div Urol, Toronto, ON M5G 1X5, Canada
[4] Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON M5G 1X5, Canada
[5] Sunnybrook Hlth Sci Ctr, Dept Obstet & Gynaecol, Div Reprod Endocrinol & Infertil, Toronto, ON M4N 3M5, Canada
[6] Womens Coll Hosp, Toronto, ON M5S 1B2, Canada
关键词
aneuploidy; sperm DNA damage; testicular spermatozoa; TUNEL; CHROMOSOMAL-ABNORMALITIES; OXIDATIVE STRESS; MALE-INFERTILITY; GENETIC-ANALYSIS; GERM-CELLS; FRAGMENTATION; MEN; ICSI; APOPTOSIS; NONDISJUNCTION;
D O I
10.3109/19396368.2012.667504
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Testicular spermatozoa are utilized to achieve pregnancy in couples with severe male factor infertility. Several studies suggest that aneuploidy rates in spermatozoa are elevated at the testicular level in infertile patients compared to ejaculates of normal controls. However, essential data regarding aneuploidy rates between ejaculated and testicular spermatozoa in the same individuals is lacking. The purpose of our study was to compare aneuploidy rates at the testicular and post-testicular level from the same patients with persistently high sperm DNA damage. Ejaculates and testicular biopsies were obtained from eight patients with persistently high DNA damage (>30%). Both ejaculated and testicular samples were analyzed for sperm DNA damage and sperm aneuploidy for chromosomes 13, 18, 21, X, and Y. In addition, semen samples from ten normozoospermic men presenting for fertility evaluation served as a control group. A strong correlation between the alteration of spermatogenesis and chromatin deterioration was observed in our study. In the same individuals, testicular samples showed a significantly lower DNA damage compared to ejaculated spermatozoa (14.9% +/- 5.0 vs. 40.6% +/- 14.8, P < 0.05), but significantly higher aneuploidy rates for the five analyzed chromosomes (12.41% +/- 3.7 vs. 5.77% +/- 1.2, P < 0.05). While testicular spermatozoa appear favourable for ICSI in terms of lower DNA damage, this potential advantage could be offset by the higher aneuploidy rates in testicular spermatozoa.
引用
收藏
页码:142 / 148
页数:7
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