Fetal coenzyme Q10 deficiency in intrahepatic cholestasis of pregnancy

MARTINEFSKI, MANUELA ROMINA; COCUCCI, SILVINA EMA; DI CARLO, MARÍA BEATRIZ; VEGA, HILDA RUDA; LUCANGIOLI, SILVIA EDITH; PERAZZI, BEATRIZ ELIZABETH; TRIPODI, VALERIA PAULA

Clinics and Research in Hepatology and Gastroenterology

Elsevier Masson SAS

Año: 2020 vol. 44 p. 368 - 374

2210-7401

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.