Spermatozoa DNA damage measured by sperm chromatin structure assay (SCSA) and birth characteristics in children conceived by IVF and ICSI

M. Bungum, L. Bungum, K.-F. Lynch, L. Wedlund, P. Humaidan, A. Giwercman
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引用次数: 29

Abstract

High levels of spermatozoa DNA damage hinder fertility in vivo but not in vitro. It is a source of worry that following in vitro fertilization (IVF) spermatozoa DNA damage, if not repaired by the oocyte, might have a negative impact on the offspring. The aim of this study was to assess if a high spermatozoa DNA Fragmentation Index (DFI) is associated with alterations in birthweight (BW) and/or gestational length in IVF children. One hundred and thirty-one singleton pregnancies established by standard IVF or intracytoplasmic sperm injection (ICSI) were included in the study. DFI was measured by sperm chromatin structure assay (SCSA) in semen samples used for fertilization. DFI was categorized as low and high, using 20, 30, 40 and 50% as cut-off levels. Birthweight, gestational age, as well as gestational age adjusted BW score were used in a linear regression model as end points For none of the tested birth characteristics, statistically significant differences between the groups with low and high DFI were seen regardless of whether 20, 30, 40 or 50% were used as cut-off levels, both when the IVF and ICSI data were merged or analysed separately. Spermatozoa DNA damage as assessed by SCSA is not associated with BW or gestational length in IVF and ICSI children.

用精子染色质结构测定法(SCSA)和试管婴儿(IVF)和单胞注射(ICSI)受孕儿童的出生特征测量精子DNA损伤
高水平的精子DNA损伤在体内会阻碍生育,但在体外不会。令人担忧的是,体外受精(IVF)后,精子DNA损伤如果没有被卵母细胞修复,可能会对后代产生负面影响。本研究的目的是评估高精子DNA碎片指数(DFI)是否与IVF儿童出生体重(BW)和/或妊娠长度的改变有关。131例通过标准体外受精或卵浆内单精子注射(ICSI)建立的单胎妊娠包括在研究中。用精子染色质结构测定法(SCSA)测定用于受精的精液样本的DFI。DFI分为低和高,使用20,30,40和50%作为截止水平。在线性回归模型中,出生体重、胎龄以及胎龄调整后的体重评分作为终点。对于所有测试的出生特征,无论将20%、30%、40%或50%作为截止水平,IVF和ICSI数据合并或单独分析时,低DFI组和高DFI组之间的差异都具有统计学意义。在IVF和ICSI儿童中,SCSA评估的精子DNA损伤与体重或妊娠长度无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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6-12 weeks
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