Journal
CLINICAL LABORATORY
Volume 59, Issue 5-6, Pages 655-660Publisher
CLIN LAB PUBL
DOI: 10.7754/Clin.Lab.2012.120227
Keywords
mitochondrial DNA (mtDNA); placenta; gestational diabetes mellitus; pregnancy; oxidative DNA damage; oxidative stress; 8-hydroxy-2 '-deoxyguanosine (8-OHdG)
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Funding
- National Institutes of Health [R01-HD-055566, R01-HD-32562]
- National Heart, Lung and Blood Institute [K01-HL-103174]
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Background: Available evidence supports the role of reactive oxygen species in the pathogenesis of placental insufficiency, gestational diabetes mellitus (GDM), and other pregnancy complications. Abnormal placental mitochondrial function resulting from reactive oxygen species may also be an important precedent of adverse perinatal outcomes. Methods: We investigated the association of placental oxidative stress with placental mitochondrial DNA (mtDNA) copy number, an indicator of placental mitochondrial density and possible mitochondrial dysfunction, using samples collected from GDM cases and controls. 8-hydroxy-2'-deoxyguanosine (8-OHdG), a marker of oxidative DNA damage, was measured in placentas of 19 GDM cases and 21 controls using a competitive immunoassay. Placental mtDNA copy number was determined using real-time quantitative PCR. Bivariate and multivariable linear regression procedures were used to evaluate associations of these two biomarkers. Results: Placental DNA oxidation was positively associated with mtDNA copy number in both GDM and control placentas. After adjusting for maternal age, pre-pregnancy body mass index and gestational age at delivery, mtDNA copy number increased (beta = 67.0; 95% CI 27.8 - 106.2, p = 0.001) for every 0.1 ng/mu g increase of placental 8-OHdG among GDM cases and controls. Conclusions: These cross sectional data suggest an association of placental mtDNA copy number with oxidative stress. The consequences of placental oxidative stress and mitochondrial dysfunction on the course and outcomes of pregnancy remain to be elucidated in larger prospective studies.
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