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运用吖啶橙试验对302例不育症患者精子DNA完整性的评估 被引量:3

Evaluation of sperm DNA integrality of 302 patients with infertility using acridine orange staining technique
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摘要 目的探讨吖啶橙试验在精子DNA完整性评估中的应用价值。方法选择男性不育症患者302例。通过吖啶橙试验(AOT)与计算机辅助精液分析(CASA)检测DFI(精子DNA损伤指数,即精液标本中存在DNA损伤的精子所占的比率)和精液常规参数。结果所有302例不育患者中,DFI异常者72例,占23.84%。共260例患者精液常规参数异常,其中DFI异常50例,占19.23%;42例患者精液常规参数正常,DFI异常22例,占52.3 8%。畸形率异常组,DFI异常率为51.06%(24/47);活动率低下组,DFI异常率为38.65%(63/163);精子密度低下组,DFI异常率为36.67%(22/60)。精子活动率和精子密度与DFI均呈负相关,r分别为-0.297,-0.217,P均<0.01;精子畸形率与DFI呈显著正相关,P<0.01,r=0.352。结论评估精子DNA完整性在不育症临床上有重要作用,吖啶橙试验能够满足这一需要,值得推荐。 Objective To evaluate the clinical value of acridine orange staining technique (AOT) for analysis of sperm DNA integrality in male infertility. Methods Semen samples of 302 male infertilite patients were analyzed in the study. Sperm DFI(DNA damage index) was detected by AOT and semen routine parameters by CASA. Results Of all 302 patients, 72 of them (23.81%) had abnormal DFI. Of all 260 patients with abnormal semen parameters, 50 of them(19.23%) had abnormal DFI.Of all 42 patients with normal semen parameters, 22 of them (52.38%) had abnormal DFI.In the group with abnormal malformation rate, motility and density, the rates of abnormal DFI were 51.06% (24/47), 38.65%(63/163) and 36.67% (22/60) respectively. DFI was negatively correlated with sperm motility and density(r=-0.297,-0.217, P〈0.01), positively with the malformation rate(r=0.352, P〈0.01). Conclusion Analysis of of sperm DNA integrality was very important for diagnosis of male infertility in clinic. AO test deserved to be recommended in clinic.
出处 《中国男科学杂志》 CAS CSCD 2010年第8期19-22,共4页 Chinese Journal of Andrology
关键词 男性不育症 精子DNA完整性 吖啶橙试验 male infertility sperm DNA integrality AO Test
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  • 1Tejada RI, Mitchell JC, Norman A, et al. A test for the practical evaluation of male fertility by acridine orange (AO) fluorescence. Fertil Steril 1984; 42(1): 87-91.
  • 2Benchaib M, Braun V, Lornage J, et al. Sperm DNA fragmentation decreases the pregnancy rate in an assisted reproductive technique. Hum Reprod 2003; 18(5): 1023- 1028.
  • 3Duran EH, Morshedi M, Taylor S, et al. Sperm DNA quality predicts intrauterine insemination, outcome: a prospective cohort study. Hum Reprod 2002; 17(12): 3122-3128.
  • 4Tomlinson MJ, Moffatt O, Manicardi GC, et al. Interrelationships between seminal parameters and sperm nuclear DNA damage before and after density gradient centrifugation: implications for assited conception. Hum Reprod 2001; 16(10): 2160-2165.
  • 5Virro MR, Larson-CooK KL, Evenson DP. Sperm chromation structure assay (SCSA) parameters are related to fertilization,blastocyst development,and ongoning pregnancy in in vitro fertilization and intracytoplasmic sperm injection cycles. Fertil Steril 2004; 81(5): 1289-1295.
  • 6Evenson DP, Larson KL, Jost LK. Sperm chromatin structure assay: its clinical use for detecting sperm DNA fragmentation in male infertility and comparisons with the other techniques. J Androl 2002; 23(1): 25-43.
  • 7Agarwal A, Said TM.Role of sperm chromatin abnormalitie and DNA damagage in male infertility. Hum Reprod 2003; 9(4): 331-345.
  • 8Saleh RA, Agarwal A, Nada EA, et al. Negative effects of increased sperm DNA damage in relation to seminal oxidative stress in men with idiopathic and male factor infertility. Fertil Steril 2003; 79: Suppl 3:1597-1605.
  • 9Sergerie M, Laforest G, Boulanger K, et al. Longitudina study of sperm DNA fragmentation as measured by terminal uridine nick end-labelling assay. Hum Reprod 2005; 20(7): 1921-1927.
  • 10Bungum M. Reply to: sperm chromatin structural assay versus hypoosmatic swelling test in predicting the need for in vitro fertilization with intracytoplasmie sperm injection. Hum Reprod 2005; 20(3): 841-842.

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