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Updated: Aug 4, 2026

HPLC Measurement of the DNA Oxidation Biomarker, 8-oxo-7,8-dihydro-2’-deoxyguanosine, in Cultured Cells and Animal Tissues
Published on: August 1, 2015
Oxidant damage to DNA and pregnancy outcome
1Department of Obstetrics and Gynecology, University of Medicine and Dentistry of New Jersey-School of Osteopathic Medicine, Stratford 08084, USA. scholl@umdnj.edu
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.
Insights
Maternal urinary 8-oxo-7,8 dihydro-2 deoxyguanosine (8 OH-dG), a marker of DNA oxidative damage, was significantly increased in pregnancies with poor outcomes, correlating with dietary saturated fat intake.
Area of Science:
- Biochemistry
- Obstetrics
- Genetics
Background:
- DNA is susceptible to oxidative damage, with 8-oxo-7,8 dihydro-2 deoxyguanosine (8 OH-dG) being the most prevalent nucleoside oxidation product.
- Cellular DNA repair mechanisms are constantly active to counteract oxidative stress.
Purpose of the Study:
- To investigate if oxidative DNA damage, quantified by urinary 8 OH-dG levels, is elevated in pregnancies resulting in adverse outcomes.
- To explore the relationship between maternal diet and DNA oxidative damage during pregnancy.
Main Methods:
- A case-control study design was employed within a prospective cohort.
- Urine samples were collected in the third trimester (28 +/- 2 weeks) from women with normal pregnancies (controls, n=34) and those with poor pregnancy outcomes (cases, n=18), including low birth weight, growth restriction, or preterm delivery.
- Dietary intake was assessed at multiple points during pregnancy.
Main Results:
- Maternal urinary 8 OH-dG excretion was significantly higher (p < 0.05) in cases compared to controls at 28 weeks gestation.
- Elevated 8 OH-dG levels were particularly noted in women delivering low-birth-weight infants.
- Urinary 8 OH-dG levels showed a positive correlation with saturated fat consumption in the maternal diet.
Conclusions:
- Increased oxidative DNA damage, as indicated by urinary 8 OH-dG, is associated with poor pregnancy outcomes early in the third trimester.
- Maternal diet, specifically saturated fat intake, may play a role in modulating DNA oxidative damage during pregnancy.
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