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Characterization of lipoproteins and associated lipidome in very preterm infants: a pilot study
Alice Küster1,2, Mikael Croyal3,4,5, Thomas Moyon1
1Nantes University INRAe, UMR 1280 PhAN, CHU Nantes, CRNH Ouest, IMAD, 44000, Nantes, France.
Insights
Very preterm infants born with very low birth weight exhibit altered lipid profiles, including reduced docosahexaenoic acid (DHA) and increased cholesterol. These changes may contribute to neurodevelopmental and cardiometabolic risks later in life.
Area of Science:
- Perinatology
- Neonatology
- Lipidomics
- Cardiovascular Science
Background:
- Preterm birth, especially very preterm birth, is linked to long-term neurodevelopmental and cardiometabolic issues.
- Altered lipid supply between mother and fetus is a potential contributing factor to these risks.
- This study investigated lipidome and apolipoprotein profiles in very preterm infants with very low birth weight (VLBW).
Purpose of the Study:
- To compare lipidome and apolipoprotein profiles in very preterm infants (VLBW) versus term infants.
- To identify specific lipid alterations in umbilical cord blood and maternal plasma.
- To explore the potential implications of these alterations for infant health outcomes.
Main Methods:
- Analysis of maternal and umbilical cord (vein and artery) plasma from 7 VLBW preterm infants (<32 weeks gestational age) and 8 term infants.
- Lipoprotein isolation using Fast Protein Liquid Chromatography (FPLC).
- Quantification of cholesterol, triglycerides, and apolipoproteins (ApoA-I) using LC-MS/MS and lipidomic analysis.
Main Results:
- VLBW infants showed higher cholesterol and VLDL-cholesterol in umbilical vessels (UV and UA).
- Lower apolipoprotein A-I (ApoA-I) was observed in HDL2 within the UV of preterm neonates.
- Increased phosphatidylcholine (PC) with saturated/monounsaturated fatty acids and specific sphingomyelins were found in UV and UA, while DHA-containing PC was reduced in the UV.
Conclusions:
- Reduced DHA-PC in VLBW infants suggests lower DHA bioavailability, potentially impacting neurodevelopment.
- Altered HDL-2, VLDL, and sphingomyelin profiles indicate increased atherogenic and metabolic risks in adulthood.
- These findings highlight the need for targeted nutritional strategies, focusing on fatty acid composition, for infants born very prematurely.
Background:
Preterm birth is associated with higher risks of suboptimal neurodevelopment and cardiometabolic disease later in life. Altered maternal-fetal lipid supply could play a role in such risks. Our hypothesis was that very preterm infants born with very low birth weight (VLBW) have altered lipidome and apolipoprotein profiles, compared with term infants.
Methods:
Seven mothers of VLBW infants born at <32 GA and 8 full-term mother-infant dyads were included. Cholesterol and triglycerides in lipoproteins were determined in maternal plasma and in the two blood vessels of the umbilical cord (vein (UV) and artery (UA)) following FPLC isolation. Apolipoprotein concentrations in lipoproteins and plasma lipidomic analysis were performed by LC-MS/MS.
Results:
We found higher cholesterol and VLDL-cholesterol in UV and UA and lower apolipoprotein A-I in HDL2 in UV in preterm neonates. Phosphatidylcholine (PC) containing saturated and monounsaturated fatty acids and specific sphingomyelin species were increased in UV and UA, whereas PC containing docosahexaenoic acid (DHA) was reduced in UV of VLBW neonates.
Conclusions:
Lower DHA-PC suggests a lower DHA bioavailability and may contribute to the impaired neurodevelopment. Altered HDL-2, VLDL, and sphingomyelin profile reflect an atherogenic risk and increased metabolic risk at adulthood in infants born prematurely.
Impact:
Lower ApoA-I in HDL2, and increased specific sphingomyelin and phosphatidylcholine containing saturated and monounsaturated fatty acid could explain the accumulation of cholesterol in umbilical vein in VLBW preterm neonates. Decreased phosphatidylcholine containing DHA suggest a reduced DHA availability for brain development in VLBW preterm infants. Characterization of alterations in fetal lipid plasma and lipoprotein profiles may help to explain at least in part the causes of the elevated cardiovascular risk known in people born prematurely and may suggest that a targeted nutritional strategy based on the composition of fatty acids carried by phosphatidylcholine may be promising in infants born very early.
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