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DNA的氧化损伤与妊娠结局

Oxidant damage to DNA and pregnancy outcome.

作者信息

Scholl T O, Stein T P

机构信息

Department of Obstetrics and Gynecology, University of Medicine and Dentistry of New Jersey-School of Osteopathic Medicine, Stratford 08084, USA.

出版信息

J Matern Fetal Med. 2001 Jun;10(3):182-5. doi: 10.1080/714904323.

Abstract

OBJECTIVE

DNA is susceptible to oxidation and is constantly being damaged and repaired in living cells. The most abundant of the nucleoside oxidation products is 8-oxo-7,8 dihydro-2 deoxyguanosine (8 OH-dG). Our objective was to determine whether oxidative damage to DNA, as measured by 8 OH-dG, is increased with poor pregnancy outcome.

METHOD

We utilized a case-control design to study oxidative damage to DNA during an ongoing prospective study. Cases (n = 18) included all women giving birth to a low-birth-weight (< 2500 g) or growth-restricted (< 10th centile) or preterm infant (< 37 completed weeks). Controls (n = 34) were selected at random from women with normal pregnancies. Urine samples were obtained early in the third trimester (28 +/- 2 weeks) and normalized to creatinine. Diet was assessed at three points during pregnancy.

RESULTS

Cases had significant (p < 0.05) increases in maternal urinary 8 OH-dG excretion at week 28, when all cases were considered and when cases were defined as those who delivered a low-birth-weight infant. 8OH-dG excretion, in turn, correlated positively with saturated fat in the maternal diet.

CONCLUSION

This study suggests that gravidas with poor pregnancy outcome have increased oxidative damage to their DNA early in the third trimester of pregnancy.

摘要

目的

DNA易被氧化,在活细胞中不断受到损伤并得到修复。最丰富的核苷氧化产物是8-氧代-7,8-二氢-2'-脱氧鸟苷(8-OH-dG)。我们的目的是确定以8-OH-dG衡量的DNA氧化损伤是否会随着不良妊娠结局而增加。

方法

在一项正在进行的前瞻性研究中,我们采用病例对照设计来研究DNA的氧化损伤。病例组(n = 18)包括所有分娩低体重儿(<2500 g)、生长受限儿(<第10百分位数)或早产儿(<37足周)的女性。对照组(n = 34)从正常妊娠的女性中随机选取。在妊娠晚期早期(28±2周)采集尿样,并以肌酐进行标准化。在孕期三个时间点评估饮食情况。

结果

当将所有病例纳入考虑以及将病例定义为分娩低体重儿的女性时,病例组在第28周时母体尿中8-OH-dG排泄量显著增加(p < 0.05)。反过来,8-OH-dG排泄量与母体饮食中的饱和脂肪呈正相关。

结论

本研究表明,妊娠结局不良的孕妇在妊娠晚期早期其DNA氧化损伤增加。

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