首页> 外文期刊>The Journal of Urology >Ideal culture time for improvement in sperm motility from testicular sperm aspirates of men with azoospermia.
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Ideal culture time for improvement in sperm motility from testicular sperm aspirates of men with azoospermia.

机译:无精症男性睾丸精子抽吸可改善精子活力的理想培养时间。

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PURPOSE: The motility of testicular derived spermatozoa reflects viability and predicts success during intracytoplasmic sperm injection. Although improvements in sperm motility are seen after incubation for extended periods, no guidelines suggest duration or media use for optimal improvement in motility. MATERIALS AND METHODS: Between July 1999 and February 2005 testicular aspirations were performed on 95 men with azoospermia, including 51 with obstructive azoospermia and 44 with nonobstructive azoospermia. Sperm motility was determined at initial collection and following incubation for 24 or 48 hours in processing media or Ham's F10 + protein. A mixed regression model controlling for testis side, media and baseline motility was created to analyze the change in motility between 24 and 48 hours. RESULTS: Mean motility improved from 3% to 20% at 24 hours and 25% at 48 hours for OA cases and from 0% to 5% at 24 hours and 11% at 48 hours for nonobstructive azoospermia cases. The improvement in motility from 24 to 48 hours was significant for obstructive azoospermia cases (p = 0.001). While media was a nonsignificant factor in regression models, when patients were grouped into categories of motility change there was a significantly better response to F10 compared to processing media (p = 0.03). CONCLUSIONS: Incubation in processing media or Ham's F10 + albumin media improves sperm motility with significant improvement noted between 24 and 48 hours for obstructive azoospermia cases. Ham's F10 + albumin media may provide extra benefit for cases of nonobstructive azoospermia or nerve injury. These results suggest the ideal timing of oocyte retrieval for intracytoplasmic sperm injection correlates with 48-hour sperm incubation for obstructive azoospermia cases, and 24 hours for nonobstructive azoospermia and nerve injury cases.
机译:目的:睾丸来源的精子的活力反映出活力,并预测在胞浆内注射精子的过程中是否成功。尽管经过长时间的孵育后,精子的运动能力有所改善,但尚无指导意见建议持续时间或使用培养基以最佳地改善运动能力。材料与方法:1999年7月至2005年2月,对95例无精子症男性进行了睾丸抽吸术,其中包括51例梗阻性无精子症和44例非梗阻性无精子症。在初次采集时以及在加工培养基或Ham's F10 +蛋白质中孵育24或48小时后确定精子活力。建立了控制睾丸侧,中层和基线运动性的混合回归模型,以分析24至48小时之间运动性的变化。结果:对于OA患者,平均运动度在24小时时从3%提高到20%,在48小时时从25%提高到24%,而在非阻塞性无精症患者中则从48%从24%从11%提高到5%。对于阻塞性无精子症患者,从24小时到48小时的运动能力显着改善(p = 0.001)。尽管在回归模型中培养基不是重要因素,但将患者分为运动性改变类别时,与处理培养基相比,对F10的反应明显更好(p = 0.03)。结论:在处理培养基或Ham's F10 +白蛋白培养基中孵育可改善精子运动能力,对于梗阻性无精症病例,可在24至48小时内显着改善。对于非阻塞性无精子症或神经损伤,Ham的F10 +白蛋白培养基可能会提供额外的好处。这些结果表明,对于梗阻性无精子症患者,卵母细胞内注射精子的理想时机与48小时精子孵育有关;对于非梗阻性无精子症和神经损伤病例,则与24小时卵子孵育有关。

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