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Correlation between DNA defect and sperm-head morphology

DNA断裂 精子 染色质 男科 生物 精子活力 卵胞浆内精子注射 精液 碎片(计算) DNA 解剖 胚胎 遗传学 体外受精 医学 细胞凋亡 程序性细胞死亡 生态学
作者
Nino Guy Cassuto,A. Hazout,Ibrahim Hammoud,R. Balet,Dominique Bouret,Yona Barak,Sonia Jellad,Jean Marie Plouchart,J. Selva,Chadi Yazbeck
标识
DOI:10.1016/j.rbmo.2011.10.006
摘要

The utility of sperm DNA testing remains controversial. However, it may be helpful in couples with unexplained failures of multiple assisted reproductive techniques and/or recurrent abortions. This study analysed 10,400 spermatozoa of 26 patients for sperm-head morphology with high-magnification microscopy, DNA fragmentation and sperm chromatin decondensation. A significant negative correlation was demonstrated between sperm-parameters and abnormal sperm-head morphology as assessed by high magnification (score 0 according to this study’s classification): concentration (r = −0.41; P = 0.03), motility (r = −0.42; P = 0.03), morphology (r = −0.63; P = 0.0008). No correlation was found with DNA fragmentation. However, the sperm chromatin-decondensation rate of score-0 spermatozoa was twice as high as the controls (19.5% versus 10.1%; P < 0.0001). This observation suggests that score-0 spermatozoa should not be selected for intracytoplasmic sperm injection.We analysed 10,400 spermatozoa of 26 patients for sperm head morphology at high magnification, DNA fragmentation and sperm chromatin decondensation. We demonstrated a significant negative correlation between sperm parameters: concentration (r = –0.41; P = 0.03), motility (r = −0.42; P = 0.03), morphology (r = –0.63; P = 0.0008) and abnormal sperm head morphology as assessed by high magnification (score 0 according our classification). No correlation was found with DNA fragmentation. The sperm chromatin decondensation rate of score-0 spermatozoa was twice as high as than in controls (19.5% versus 10.1%; P < 0.0001). No significant relationship with sperm DNA fragmentation was observed. We suggest that high-magnification sperm selection could be an important step and a new tool for the clinician, who could decide to discard score-0 spermatozoa with a high risk of abnormal chromatin and select the best sperm cells for intracytoplasmic sperm injection.

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