首页> 外文期刊>Archives of gynecology and obstetrics. >Cytogenetic, Y chromosome microdeletion, sperm chromatin and oxidative stress analysis in male partners of couples experiencing recurrent spontaneous abortions.
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Cytogenetic, Y chromosome microdeletion, sperm chromatin and oxidative stress analysis in male partners of couples experiencing recurrent spontaneous abortions.

机译:反复自然流产的夫妻的男性伴侣的细胞遗传学,Y染色体微缺失,精子染色质和氧化应激分析。

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PURPOSE: Etiology in majority of couples experiencing recurrent spontaneous abortions (RSA) is still unknown. The aim of the study was to find the role of cytogenetic abnormalities, Y chromosome microdeletion, oxidative stress (OS) and sperm DNA fragmentation in male partners of couples experiencing RSA. METHODS: Forty-eight couples with history of RSA and 20 fertile controls were included in the study. The study subjects were divided into male partners of RSA couples with abnormal sperm parameters (SA) (N = 16), male partners of RSA couples with normal sperm parameters (NS) (N = 32) and age-matched fertile controls with normal sperm parameters (FC) (N = 20). RESULTS: One of 48 men (2%) showed 46, XY (1qh-) chromosomal complement. None of the cases including FC showed deletion in any of the 3 AZF loci on Y chromosome long arm. Sperm count was found be significantly lower in SA cases as compared to group NS cases (P < 0.0001) and FC (P < 0.005). Sperm forward motility was found to be significantly (P < 0.05) lower in SA cases as compared to NS and FC. Male partners of RSA couples with abnormal sperm parameters had higher reactive oxygen species (ROS) levels (P < 0.005) and sperm DNA damage (P < 0.0001), however, in male partners of RSA couples with normal sperm parameters had only increased (P < 0.0001) sperm DNA damage. CONCLUSION: Other than chromosomal anomalies, sperm DNA fragmentation and seminal OS may be the underlying pathology in RSA, thus screening for seminal ROS levels and DNA fragmentation has diagnostic and prognostic capabilities.
机译:目的:大多数复发性自然流产(RSA)的病因尚不清楚。该研究的目的是发现细胞遗传异常,Y染色体微缺失,氧化应激(OS)和精子DNA片段化在经历RSA的夫妻中的作用。方法:四十八对有RSA病史的夫妇和20名可育对照者纳入研究。研究对象分为精子参数异常(SA)(N = 16)的RSA夫妇的男性伴侣,精子参数正常(NS)(N = 32)的RSA夫妇的男性伴侣和精子正常的年龄匹配的可育对照参数(FC)(N = 20)。结果:48名男性中的一名(占2%)显示出46个XY(1qh-)染色体补体。包括FC在内的所有病例均未在Y染色体长臂的3个AZF基因座中显示出缺失。与NS组(P <0.0001)和FC(P <0.005)组相比,SA组的精子数量明显降低。与NS和FC相比,SA患者的精子向前运动明显降低(P <0.05)。具有异常精子参数的RSA伴侣的男性伴侣具有较高的活性氧(ROS)水平(P <0.005)和精子DNA损伤(P <0.0001),但是,具有正常精子参数的RSA伴侣的男性伴侣仅增加(P <0.0001)精子DNA损伤。结论:除了染色体异常外,精子DNA片段化和精子OS可能是RSA的潜在病理,因此筛选精子ROS水平和DNA片段具有诊断和预后的能力。

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