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本文引用的文献

1
Relationship between DNA damage and sperm head birefringence.DNA 损伤与精子头双折射的关系。
Reprod Biomed Online. 2011 Jun;22(6):583-9. doi: 10.1016/j.rbmo.2011.03.017. Epub 2011 Mar 21.
2
Coherence-controlled holographic microscope.相干控制全息显微镜。
Opt Express. 2010 Oct 11;18(21):21990-2003. doi: 10.1364/OE.18.021990.
3
Seminal plasma homocysteine, folate and cobalamin in men with obstructive and non-obstructive azoospermia.精液中同型半胱氨酸、叶酸和钴胺素与梗阻性和非梗阻性无精子症男性。
J Assist Reprod Genet. 2010 Sep;27(9-10):533-8. doi: 10.1007/s10815-010-9458-8. Epub 2010 Jul 31.
4
Ontological evaluation of transcriptional differences between sperm of infertile males and fertile donors using microarray analysis.利用微阵列分析对不育男性和可育供体精子之间转录差异的本体论评估。
J Assist Reprod Genet. 2010 Feb;27(2-3):111-20. doi: 10.1007/s10815-010-9388-5. Epub 2010 Feb 2.
5
New aspects of gamete transport, fertilization, and embryonic development in the oviduct gained by means of live cell imaging.通过活细胞成像获得输卵管配子运输、受精和胚胎发育的新方面。
Theriogenology. 2010 Apr 1;73(6):786-95. doi: 10.1016/j.theriogenology.2009.11.002. Epub 2010 Jan 18.
6
Function of sperm chromatin structural elements in fertilization and development.精子染色质结构元素在受精和发育中的功能。
Mol Hum Reprod. 2010 Jan;16(1):30-6. doi: 10.1093/molehr/gap080. Epub 2009 Sep 11.
7
Proving tumour cells by acute nutritional/energy deprivation as a survival threat: a task for microscopy.证明急性营养/能量剥夺将肿瘤细胞视为生存威胁:显微镜的一项任务。
Anticancer Res. 2009 Jun;29(6):2339-45.
8
Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: report and review.土耳其西部地区179例男性不育患者的细胞遗传学异常:报告与综述
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9
Birefringence characteristics in sperm heads allow for the selection of reacted spermatozoa for intracytoplasmic sperm injection.精子头部的双折射特性可用于选择反应性精子进行胞浆内单精子注射。
Fertil Steril. 2010 Feb;93(3):807-13. doi: 10.1016/j.fertnstert.2008.10.024. Epub 2008 Dec 6.
10
The correlation between male age, sperm quality and sperm DNA fragmentation in 320 men attending a fertility center.320名前往生育中心就诊男性的年龄、精子质量与精子DNA碎片化之间的相关性
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数字全息显微镜在人类精子成像中的应用。

Digital holographic microscopy in human sperm imaging.

机构信息

Department of Gynecology and Obstetrics, Faculty of Medicine, Masaryk University, and Faculty Hospital, Brno, Czech Republic.

出版信息

J Assist Reprod Genet. 2011 Aug;28(8):725-9. doi: 10.1007/s10815-011-9584-y. Epub 2011 Jun 11.

DOI:10.1007/s10815-011-9584-y
PMID:21667103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3170116/
Abstract

PURPOSE

The aim of this study was to use digital holographic microscopy (DHM) in human sperm imaging and compare quantitative phase contrast of sperm heads in normozoospermia (NZ) and oligoasthenozoospermia (OAT).

METHODS

DHM spermatozoa imaging and repeated quantitative phase shift evaluation were used. Five NZ and 5 OAT samples were examined. Semen samples were examined by semen analysis and processed for DHM. Main outcome measures were maximum phase shift value of the sperm heads. Differences of the phase shift and in NZ and OAT samples were statistically tested.

RESULTS

In NZ samples median phase shifts were in the range 2.72-3.21 rad and 2.00-2.15 in OAT samples. Differences among individual samples were statistically significant (p < 0.001) in both groups. Median phase shift according to sperm count was 2.90 rad in NZ samples and 2.00 rad in OAT samples. This difference was statistically significant (p < 0.001).

CONCLUSION

Quantitative evaluation of the phase shift by DHM could provide new information on the exact structure and composition of the sperm head. At present, this technique is not established for clinical utility.

摘要

目的

本研究旨在使用数字全息显微镜(DHM)对人精子进行成像,并比较正常精子症(NZ)和少精子症(OAT)精子头部的定量相位对比。

方法

使用 DHM 精子成像和重复定量相移评估。检查了 5 个 NZ 和 5 个 OAT 样本。精液样本通过精液分析进行检查,并进行 DHM 处理。主要观察指标为精子头部的最大相移值。统计检验了 NZ 和 OAT 样本中相移的差异。

结果

在 NZ 样本中,中位数相移范围为 2.72-3.21 拉德,在 OAT 样本中为 2.00-2.15 拉德。两组中个体样本之间的差异均具有统计学意义(p<0.001)。根据精子计数,NZ 样本中的中位数相移为 2.90 拉德,OAT 样本中的中位数相移为 2.00 拉德。这种差异具有统计学意义(p<0.001)。

结论

DHM 对相移的定量评估可以提供关于精子头的确切结构和组成的新信息。目前,该技术尚未在临床应用中得到确立。