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对不明原因复发性自然流产病例的甲基化分析显示,正常精子个体的 H19 ICR 存在异常印迹。

Methylation analysis of idiopathic recurrent spontaneous miscarriage cases reveals aberrant imprinting at H19 ICR in normozoospermic individuals.

机构信息

Department of Neuroendocrinology, National Institute for Research in Reproductive Health, Mumbai, India.

出版信息

Fertil Steril. 2012 Nov;98(5):1186-92. doi: 10.1016/j.fertnstert.2012.07.1143. Epub 2012 Sep 6.

Abstract

OBJECTIVE

To study H19 ICR methylation levels in association with sperm parameters routinely analyzed in idiopathic recurrent spontaneous miscarriage cases.

DESIGN

Case-control study.

SETTING

Academic research setting.

PATIENT(S): Male partners of couples with a history of idiopathic recurrent spontaneous miscarriage (RSM group) and male partners of couples with proven fertility (control group).

INTERVENTION(S): None.

MAIN OUTCOME MEASURE(S): Paternal age, sperm concentration, motility, chromatin compaction status, morphology, and H19 ICR methylation were assessed in control and idiopathic RSM group participants.

RESULT(S): Paternal age and basic semen parameters analyzed did not show any significant difference between the two groups; however H19 ICR methylation levels were reduced significantly in the idiopathic RSM group compared with the control group.

CONCLUSION(S): Significant reduction in the H19 ICR methylation without significant difference in the sperm parameters demonstrates aberrant imprinting to be associated with idiopathic RSM.

摘要

目的

研究特发性复发性自然流产病例中与常规分析精子参数相关的 H19 ICR 甲基化水平。

设计

病例对照研究。

设置

学术研究环境。

患者

有特发性复发性自然流产(RSM 组)病史的夫妇的男性伴侣和有明确生育能力的夫妇的男性伴侣(对照组)。

干预措施

无。

主要观察指标

评估对照组和特发性 RSM 组参与者的父亲年龄、精子浓度、活力、染色质致密状态、形态和 H19 ICR 甲基化。

结果

两组间的父亲年龄和基本精液参数分析无显著差异;然而,与对照组相比,特发性 RSM 组的 H19 ICR 甲基化水平显著降低。

结论

H19 ICR 甲基化的显著降低而精子参数无显著差异表明异常印迹与特发性 RSM 相关。

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