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Impairment of the Lipid Metabolism in Newborns in the Early Neonatal Period

https://doi.org/10.15360/1813-9779-2018-2-13-24

Abstract

The purpose of the study. To study parameters of the lipid metabolism in newborn infants to identify general patterns depending on the gestational age.

Materials and methods. The course of pregnancy and its outcome was analyzed in 286 women who gave birth to 323 infants; 89 of them were born in multiple pregnancies. The infants were divided into 4 groups depending on the gestational age. Levels of cholesterol (C), triglycerides (TG), low-density lipoproteins (LDL) and high-density lipoproteins (HDL) were tested in the central venous blood immediately after birth and on the 5th day of life.

Results. Hypotriglyceridemia below 0.2 mmol/l was typical for 31.3% of the newborns; a TG level within the range of 0.21—0.5 mmol/l was found in 43.3% of infants, i.e. the perinatal production of TG was decreased in 76.6% of infants. The perinatal TG production depended on the infant's gestational age: the smaller it was, the lower TG blood level was in infants at birth. At the gestational age of 25—33 weeks, the perinatal TG production was low in most newborns. The perinatal production of the lipid metabolism parameter was increased with the increase of the gestational age. The TG blood level increased rapidly at the gestational age of 37 weeks. The postnatal TG production in the blood of newborn babies had no dependence on the gestational age strating from the gestational age of 31 weeks and more. Hypercholesterolemia and lower both LDL and HDL levels were found in newborns of all groups at birth; no significant intergroup differences in concentration of C, HDL or LDL were observed (P>0.01).

Conclusion. The state of the lipid metabolism in the newborns in the perinatal period depends on the gestational age and the birth weight. Low TG production is typical for small premature infants with a low and extremely low birth weight due to physiological immaturity of organs and systems. The peculiarities of the prenatal morphogenesis make an adequate lipid metabolism possible by the full-term gestational age only. An abnormal course of pregnancy impairs normal triglyceride, C, LDL and HDL production. The greatest changes of the tested parameters are typical for small immature infants with a gestational age of 25—31 weeks. This age is associated with a high incidence of the respiratory distress syndrome. Deficiency of buffer bases affects the TG production at birth; the pH value and blood oxygen tension at birth affect the C level. The production of lipid metabolism parameters increases with the increase of the gestational age. There are certain individual characteristics in newborns who may have perinatal disorders of the lipid metabolism at the full-term gestational age. 

About the Author

S. A. Perepelitsa
V. A. Negovsky Research Institute of General Reanimatology, Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology; Imannuel Kant Baltic Federal University
Russian Federation

25 Petrovka Str., Build. 2, 107031 Moscow;

14 Aleksandr Nevsky Str., 236041 Kaliningrad



References

1. Herrera E., Amusquivar E. Lipid metabolism in the fetus and the newborn. Diabetes Metab. Res. Rev. 2000; 16 (3): 202-210. DOI: 10.1002/1520- 7560(200005/06)16:3%3C202::AID-DMRR116%3E3.3.CO;2-R. PMID: 10867720

2. Magnusson-Olsson A.L., Lager S., Jacobsson B., Jansson T., Powell T.L. Effect of maternal triglycerides and free fatty acids on placental LPL in cultured primary trophoblast cells and in a case of maternal LPL deficiency. Am. J. Physiol. Endocrinol. Metab. 2007; 293 (1): 24-30. DOI: 10.1152/ajpendo.00571.2006. PMID: 17299085

3. Herrera E., Amusquivar E., López-Soldado I., Ortega H. Maternal lipid metabolism and placental lipid transfer. Horm. Res. 2006; 65 (Suppl 3): 59-64. DOI: 10.1159/000091507. PMID: 16612115

4. Woollett L.A. Review: transport of maternal cholesterol to the fetal circulation. Placenta. 2011; 32 (Suppl 2): S218-S221. DOI: 10.1016/j.placenta.2011.01.011. PMID: 21300403

5. Sfefuji J., Panzenboeck U., Becker T., Hirschmugl B., Schweinzer C., Lang I., Marsche G., Sadjak A., Lang U., Desoye G., Wadsack C. Human endothelial cells of the placental barrier efficiently deliver cholesterol to the fetal circulation via ABCA1 and ABCG1. Circ. Res. 2009; 104 (5): 600–608. DOI: 10.1161/CIRCRESAHA.108.185066. PMID: 19168441

6. Sales W.B., Silleno Junior J.D., Kroll C., Mastroeni S.S., Silva J.C., Mastroeni M.F.. Influence of altered maternal lipid profile on the lipid profile of the newborn. Arch. Endocrinol. Metab. 2015; 59 (2): 123-128. DOI: 10.1590/2359-3997000000024. PMID: 25993674

7. Fielding B.A., Frayn K.N. Lipoprotein lipase and the disposition of dietary fatty acids. Br. J. Nutr. 1998; 80 (6): 495–502. DOI: 10.1017/S000711 4598001585. PMID: 10211047

8. Waterman I.J., Emmison N., Dutta-Roy A.K. Characterisation of triacylglycerol hydrolase ctivities in human placenta. Biochim. Biophys. Acta. 1998; 1394 (2-3): 169–176. PMID: 9795201

9. Waterman I.J., Emmison N., Sattar N., Dutta-Roy A.K. Further characterization of a novel triacylglycerol hydrolase activity (pH 60 optimum) from microvillous membranes from human term placenta. Placenta. 2000; 21 (8): 813–823. DOI: 10.1053/plac.2000.0572. PMID: 11095931

10. Campbell F.M., Bush P.G., Veerkamp J.H., Dutta-Roy A.K. Detection and cellular localization of plasma membrane-associated and cytoplasmic fatty acid-binding proteins in human placenta. Placenta. 1998; 19 (5-6): 409–415. DOI: 10.1016/S0143-4004(98)90081-9. PMID: 9699962

11. Madsen E.M., Lindegaard M.L., Andersen C.B., Damm P., Nielsen L.B. Human placenta secretes apolipoprotein B-100-containing lipoproteins. J. Biol. Chem. 2004; 279 (53): 55271–55276. DOI: 10.1074/jbc.M411404200. PMID: 15504742

12. Tyurina E.P., Kotlova E.V., Vlasov A.P., Ledyaikina L.V., Gordeyeva Yu.V. Change in lipid metabolism of the placenta in pregnant women with gestosis. Meditsinskie Nauki. Klinicheskaya Meditsina. 2011; 4 (20): 89- 96. [In Russ.]

13. Tyurina E.P., Porshina O.V., Kotlova E.V., Gordeyeva Yu.V. Modification of lipid metabolism in pregnant women with gestosis. Vestnik Rossiiskogo Gosudarstvennogo Meditsinskogo Universiteta. 2011; S2: 50-52. [In Russ.]

14. Turkina T.I., Shcherbakova M.Yu. Features of dyslipidemia in children. Ratsionalnaya Farmakoterapiya v Kardiolodii. 2011; 7 (1): 65 – 69. [In Russ.]

15. Perepelitsa S.A. Complex evaluation oxygen status and lipid metabolism indexes in newborns with perinatal hypoxia and hypovolemic shock. Obshchaya Reanimatologiya = General Reanimatology. 2017; 13 (3): 25-34. DOI: 10.15360/1813-9779-2017-3-25-34. [In Russ., In Engl.]

16. Perepelitsa S.A., Alekseyeva S.V., Luchina A.A. The impact of perinatal metabolic disorders choice mode mechanical ventilation in newborns. Anesteziologiya i Reanimatologiya. 2016; 61 (4): 275-280. DOI: 10.18821/0201-7563-2016-61-4-275-280. [In Russ.]

17. Perepelitsa S.A., Sednev O.V. Perinatal triglyceride and cholesterol metabolic disturbances in newborn infants. Obshchaya Reanimatologiya = General Reanimatology. 2015; 11 (6): 28-37. DOI: 10.15360/1813-9779- 2015-6-28-37. [In Russ., In Engl.]

18. Volodin N.N. (red.). Neonatology. National guide. Moscow: GEOTARMedia; 2008: 749. [In Russ.]

19. Ailamazyan E.K., Kulakov V.I., Radzinsky V.E., Savelyeva G.M. (eds.). Obstetrics. National guide. Moscow: GEOTAR-Media; 2009: 1200. [In Russ.]

20. Marshall V.J. Clinical biochemistry. 6th ed. Moscow: BINOM; 2015: 408. [In Russ.]

21. Neary R.H., Kilby M.D., Kumpatula P., Game F.L., Bhatnagar D., Durrington P.N., O’Brien P.M. Fetal and maternal lipoprotein metabolism in human pregnancy. Clin. Sci. (Lond.). 1995; 88 (3): 311–318. DOI: 10.1042/cs0880311. PMID: 7736700

22. Favrais G., Tourneux P.,· Lopez E.,· Durrmeyer X., Gascoin G., Ramful D., Zana-Taieb E., Baud O. Impact of common treatments given in the perinatal period on the developing brain. Neonatology. 2014; 106 (3): 163- 172. DOI: 10.1159/000363492. PMID: 25012048

23. Brizzi P., Tonolo G., Esposito F., Puddu L., Dessole S., Maioli M., Milia S. Lipoprotein metabolism during normal pregnancy. Am. J. Obstet. Gynecol. 1999; 181 (2): 430-434. DOI: 10.1016/S0002-9378(99)70574-0. PMID: 10454696

24. Rodie V.A., Caslake M.J., Stewart F., Sattar N., Ramsay J.E., Greer I.A., Freeman D.J. Fetal cord plasma lipoprotein status in uncomplicated human pregnancies and in pregnancies complicated by pre-eclampsia and intrauterine growth restriction. Atherosclerosis. 2004; 176 (1): 181–187. DOI: 10.1016/j.atherosclerosis.2004.04.026. PMID: 15306192

25. Rozenberg O.A. Pulmonary surfactants for acute and chronic lung diseases (part I). Obshchaya Reanimatologiya = General Reanimatology. 2014; 10 (4): 51-73. DOI: 10.15360/1813-9779-2014-4-51-73. [In Russ., In Engl.]

26. Grebennikov V.A., Milenin O.B., Ryumina I.I. Results of clinical trials of the synthetic surfactant «ExosurfNeonatal» in Russia. Pediatriya. 1995; 3: 65-68. [In Russ.]

27. Hildebran J.N., Goerke J., Clements J.A. Surfactant released in excised rat lung is stimulated by air inflation. J. Appl. Physiol. Respir. Environ. Exerc. Physiol. 1981; 51 (4): 905-910. PMID: 6895369

28. Lewis J.F., Veldhuizen R. The role of exogenous surfactant in the treatment of acute lung injury. Annu. Rev. Physiol. 2003; 65: 613-642. DOI: 10.1146/annurev.physiol.65.092101.142434. PMID: 12517997

29. Orgeig S., Daniels С.В. The roles of cholesterol in pulmonary surfactant: insights from comparative and evolutionary studies. Comp. Biochem. Physiol. A Mol. Integr. Physiol. 2001; 129 (1): 75—89. DOI: 10.1016/S1095-6433(01)00307-5. PMID: 11369535

30. Orgeig S., Daniels C.B., Johnston S.D., Sullivan L.C. The pattern of surfactant cholesterol during vertebrate evolution and development: does ontogeny recapitulate phylogeny? Reprod. Fertil. Dev. 2003; 15 (1-2): 55-73. DOI: 10.1071/RD02087. PMID: 12729504

31. Emmanuilidis G.K., Bailen B.G. Cardiopulmonary distress in newborns. Moscow: Meditsina Publishers; 1994: 400. [In Russ.]

32. Whitsett J.A., Weaver T.E. Alveolar development and disease. Am. J. Respir. Cell Mol. Biol. 2015; 53 (1): 1-7. DOI: 10.1165/rcmb.2015-0128PS. PMID: 25932959


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For citations:


Perepelitsa S.A. Impairment of the Lipid Metabolism in Newborns in the Early Neonatal Period. General Reanimatology. 2018;14(2):13-24. (In Russ.) https://doi.org/10.15360/1813-9779-2018-2-13-24

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