Laboratory for Molecular Reproduction and Genetics, Department of Anatomy, All India Institute of Medical Science (AIIMS), New Delhi 110029, India.
Arch Gynecol Obstet. 2011 Dec;284(6):1577-84. doi: 10.1007/s00404-011-1990-y. Epub 2011 Jul 22.
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.
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).
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.
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.
大多数反复自然流产(RSA)夫妇的病因仍不清楚。本研究旨在探讨染色体异常、Y 染色体微缺失、氧化应激(OS)和精子 DNA 碎片化在 RSA 夫妇男性伴侣中的作用。
纳入 48 对 RSA 夫妇和 20 名正常生育对照者。将研究对象分为 RSA 夫妇精子参数异常(SA)男性伴侣(N=16)、RSA 夫妇精子参数正常(NS)男性伴侣(N=32)和年龄匹配的正常生育对照者(FC)(N=20)。
48 名男性中,有 1 名(2%)出现 46,XY(1qh-)染色体核型。包括 FC 在内的所有病例均未在 Y 染色体长臂的任何 3 个 AZF 位点缺失。SA 组的精子计数明显低于 NS 组(P<0.0001)和 FC 组(P<0.005)。SA 组的精子前向运动能力明显低于 NS 组和 FC 组(P<0.05)。RSA 夫妇精子参数异常的男性伴侣 ROS 水平(P<0.005)和精子 DNA 损伤(P<0.0001)明显升高,而 RSA 夫妇精子参数正常的男性伴侣仅精子 DNA 损伤升高(P<0.0001)。
除染色体异常外,精子 DNA 碎片化和精液 OS 可能是 RSA 的潜在病理机制,因此筛查精液 ROS 水平和 DNA 碎片化具有诊断和预后能力。