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Updated: Jan 20, 2026
Cofactors, Coenzymes and Vitamins
Fetal coenzyme Q10 deficiency in intrahepatic cholestasis of pregnancy
Manuela Romina Martinefski1, Silvina Ema Cocucci2, María Beatriz Di Carlo2
1Departamento de Tecnología Farmacéutica, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, 5(th) Floor, CABA, Buenos Aires, Argentina.
Insights
Intrahepatic cholestasis of pregnancy (ICP) is linked to lower coenzyme Q10 (CoQ10) levels in newborns, increasing fetal oxidative stress. This finding suggests CoQ10 may be a potential therapeutic target for ICP complications.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Biochemistry
Background:
- Intrahepatic cholestasis of pregnancy (ICP) poses significant risks to fetal health due to increased oxidative stress from bile acid accumulation.
- Coenzyme Q10 (CoQ10), a vital mitochondrial antioxidant, has been found to be decreased in pregnant women with ICP.
Purpose of the Study:
- To investigate and compare coenzyme Q10 (CoQ10) levels in umbilical cord blood of normal pregnancies versus those complicated by ICP.
- To assess CoQ10 levels in relation to maternal serum bile acid levels.
Main Methods:
- Coenzyme Q10 (CoQ10) and bile acid levels were measured in maternal and umbilical cord blood samples.
- Study included 23 normal pregnancies and 13 pregnancies complicated by ICP.
Main Results:
- Neonate CoQ10 levels, adjusted for cholesterol, were significantly lower in ICP pregnancies compared to normal pregnancies (0.069±0.011 vs. 0.105±0.010, P<0.05).
- Total serum bile acid levels were significantly elevated in ICP pregnancies (7.60±2.30 vs. 2.10±0.02, P<0.05).
Conclusions:
- Fetal exposure to oxidative damage is heightened in ICP.
- CoQ10 deficiency in ICP neonates highlights its potential as a therapeutic agent to mitigate oxidative stress and improve fetal outcomes.
Aim:
Intrahepatic cholestasis of pregnancy (ICP) is considered a high-risk condition because it may have serious consequences for the fetus health. ICP is characterized by the accumulation of bile acids in maternal serum which contribute to an imbalance between the production of reactive oxygen species and the antioxidant defenses increasing the oxidative stress experienced by the fetus. Previously, it was reported a significant decrease in plasma coenzyme Q10 (CoQ10) in women with ICP. CoQ10 is a redox substance integrated in the mitochondrial respiratory chain and is recognized as a potent antioxidant playing an intrinsic role against oxidative damage. The objective of the present study was to investigate the levels of CoQ10 in umbilical cord blood during normal pregnancy and in those complicated with ICP, all of them compared to the maternal ones.
Methods:
CoQ10 levels and bile acid levels in maternal and umbilical cord blood levels during normal pregnancies (n=23) and in those complicated with ICP (n=13), were investigated.
Results:
A significant decrease in neonate CoQ10 levels corrected by cholesterol (0.105±0.010 vs. 0.069±0.011, P<0.05, normal pregnancy vs. ICP, respectively), together with an increase of total serum bile acids (2.10±0.02 vs. 7.60±2.30, P<0.05, normal pregnancy vs. ICP, respectively) was observed.
Conclusions:
A fetus from an ICP mother is exposed to a greater risk derived from oxidative damage. The recognition of CoQ10 deficiency is important since it could be the starting point for a new and safe intervention strategy which can establish CoQ10 as a promising candidate to prevent the risk of oxidative stress.
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