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Maternal and newborn infants amino acid concentrations in obese women born themselves with normal and small for gestational age birth weight

Published online by Cambridge University Press:  30 April 2015

P. B. Tsyvian*
Affiliation:
Mother and Child Care Research Institute, Russian Ministry of Public Health, Yekaterinburg, Russia Ural State Medical University, Yekaterinburg, Russia Institute of Immunology and Physiology, Ural branch of Russian Academy of Sciences Yekaterinburg, Russia
N. V. Bashmakova
Affiliation:
Mother and Child Care Research Institute, Russian Ministry of Public Health, Yekaterinburg, Russia
O. P. Kovtun
Affiliation:
Ural State Medical University, Yekaterinburg, Russia
L. V. Makarenko
Affiliation:
Mother and Child Care Research Institute, Russian Ministry of Public Health, Yekaterinburg, Russia
L. A. Pestryaeva
Affiliation:
Mother and Child Care Research Institute, Russian Ministry of Public Health, Yekaterinburg, Russia
*
*Address for correspondence: P. B. Tsyvian, Mother and Child Care Research Institute, Repin str 1, 620028, Yekaterinburg, Russia. (Email [email protected])

Abstract

This study was undertaken to compare amino acid concentrations in maternal and newborn infants’ serum in normal pregnancy and two groups of obese women who were born themselves with normal and small for gestational age (SGA) birth weight. Maternal cholesterol, lipoproteins concentrations and maternal and infants amino acid concentrations were evaluated at the time of delivery in 28 normal pregnancies, 46 obese pregnant women with normal birth weight (Ob-AGA group) and 44 obese pregnant women born themselves SGA (Ob-SGA group). Mean birth weight of newborn infants in Ob-SGA group was significantly less than in normal and Ob-AGA groups. Cholesterol and lipoproteins were significantly elevated in obese women (more prominent in Ob-SGA group). Most amino acid concentrations and fetal–maternal amino acid gradients were significantly lower in Ob-SGA group. These data suggest significant changes in placental amino acid transport/synthetic function in obese women who were born themselves SGA.

Type
Original Article
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2015 

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References

1. Drake, A, Reinolds, R. Impact of maternal obesity on offspring obesity and cardiometabolic disease risk. Reproduction. 2010; 140, 387398.Google Scholar
2. Blackmore, HL, Ozanne, SE. Maternal diet-induced obesity and offspring cardiovascular health. J Develop Origins Health Dis. 2013; 4, 338347.Google Scholar
3. Stettler, N, Zemel, BS, Kumanika, S, Stallings, VA. Infant weight gain and childhood overweight status in a multicenter cohort study. Pediatrics. 2002; 109, 194199.Google Scholar
4. Dietz, WH. Overweight in childhood and adolescence. N Engl J Med. 2004; 350, 855857.Google Scholar
5. Barker, DJP, Osmond, C, Forsén, T, Kajantie, E, Eriksson, JG. Trajectories of growth among children who have coronary events as adults. N Engl J Med. 2005; 353, 18021809.Google Scholar
6. Hales, CN, Barker, DJP, Clark, PMS, et al. Fetal and infant growth and impaired glucose tolerance at age 64. BMJ. 1991; 303, 10191022.Google Scholar
7. Lithell, UB, Leon, DA. Relation of size at birth to non-insulin dependent diabetes and insulin concentrations in men aged 50–60 years. BMJ. 1996; 312, 406410.Google Scholar
8. Battaglia, FC, Regnault, TRH. Placental transport and metabolism of amino acids. Placenta. 2001; 22, 145161.Google Scholar
9. Parhofer, KG, Barrett, HR, Bier, DM, Schonfeld, G. Determination of kinetic parameters of apolipoprotein B metabolism using amino acids labeled with stable isotopes. J Lipid Res. 1991; 32, 13111323.Google Scholar
10. Lichtenstein, AH, Cohn, JS, Hachey, DL, et al. Comparison of deuterated leucine, valine, and lysine in the measurement of human apolipoprotein A-I and B-100 kinetics. J Lipid Res. 1990; 31, 16931701.CrossRefGoogle ScholarPubMed
11. Young, M, Prenton, MA. Maternal and fetal plasma amino acid concentrations during gestation and in retarded fetal growth. J Obstet Gynaec Br Commonw. 1969; 76, 333344.Google Scholar
12. Johnson, LW, Smith, CH. Neutral amino acid transport systems of microvillous membrane of human placenta. Am J Physiol. 1988; 254, C773C780.Google Scholar
13. Kalkhoff, RK, Kandaraki, E, Morrow, PG, et al. Relationship between neonatal birth weight and maternal plasma amino acids profiles and lean and obese nondiabetic women and type 1 diabetic pregnant women. Metabolism. 1988; 37, 234239.Google Scholar
14. Evans, RW, Powers, RW, Ness, RB, et al. Maternal and fetal amino acid concentrations and fetal outcomes during pre-eclampsia. Reproduction. 2003; 125, 785790.CrossRefGoogle ScholarPubMed
15. WHO child growth standards based on length/height, weight and age. Acta Paediatrica. 2006; 95(Suppl. S459), 7685.CrossRefGoogle Scholar
16. Ordovas, JM, Pocovi, M, Grande, F. Plasma lipids and cholesterol esterification during pregnancy. Obstet Gynecol. 1984; 63, 2025.Google ScholarPubMed
17. Piechota, W, Staslewski, A. Reference ranges of lipids and apolipoproteins in pregnancy. Eur J Obstet Gynecol Reproduct Biol. 1992; 45, 2735.CrossRefGoogle ScholarPubMed
18. Desoye, G, Schweditsch, MO, Pfeiffer, KP, Zechner, L, Kostmer, GM. Correlation of hormones with lipid and lipoprotein levels during normal pregnancy and postpartum. J Clin Endocrinol Metab. 1987; 64, 704712.Google Scholar
19. Martin, U, Davies, C, Hayavi, S, Hartland, A, Dunne, F. Is normal pregnancy atherogenic? Clin Sci. 1999; 96, 421425.Google Scholar
20. Hachey, DL. Benefits and risks of modifying maternal fat intake in pregnancy and lactation. Am J Clin Nutr. 1994; 59, 454S464S.CrossRefGoogle ScholarPubMed
21. Patterson, BW, Hachey, DL, Cook, GL, et al. Metabolic kinetics of apolipoproteins C using a stable isotope amino acid tracer. Arteriosclerosis. 1989; 9, 757a758a.Google Scholar
22. Cohn, JS, Wagner, DA, Cohn, SD, Millar, JS, Schaefer, EJ. Measurement of very low density and low density lipoprotein apolipoprotein (Apo) B-100 and high density lipoprotein ApoA-1 production in human subjects using deuterated leucine (effect of fasting and feeding). J Clin Invest. 1990; 85, 804811.Google Scholar
23. Bel-Serrat, S, Mouratidou, T, Huybrechts, I, et al. The role of dietary fat on the association between dietary amino acids and serum lipid profile in European adolescents participating in the HELENA Study. Eur J Clin Res. 2014; 68, 464473.Google Scholar
24. Klebanoff, MF, Secher, NJ, Mednick, BR, Schulsinger, S. Maternal size at birth and the development of hypertension during pregnancy. A test of the Barker hypothesis. Arch Intern Med. 1999; 159, 16071612.Google Scholar
25. Napoli, C, D’Armiento, FP, Mancini, FP, et al. Fatty streak formation occurs in human fetal aortas and is greatly enhanced by maternal hypercholesterolemia. Intimal accumulation of low density lipoprotein and its oxidation precede monocyte recruitment into early atherosclerotic lesions. J Clin Invest. 1997; 100, 26802690.Google Scholar
26. Barker, DJP. Maternal nutrition, fetal nutrition, and disease in later life. Nutrition. 1997; 13, 807813.Google Scholar
27. Cetin, I. Amino acid interconversions in the fetal-placental unit: the animal model and human studies in vivo. Pediatr Res. 2001; 49, 148154.Google Scholar
28. Broer, S. Adaptation of plasma membrane amino acid transport mechanisms to physiological demands. Pflugers Archiv Eur J Physiol. 2002; 444, 457466.Google Scholar
29. Desforges, M, Greenwood, SL, Glazier, JD, Westwood, M, Sibley, CP. The contribution of SNAT1 to system A amino acid transporter activity in human placental trophoblast. Biochem Biophys Res Commun. 2010; 398, 130134.Google Scholar
30. Jansson, T, Ylven, K, Wennergren, M, Powell, TL. Glucose transport and system A activity in syncytiotrophoblast microvillous and basal plasma membranes in intrauterine growth restriction. Placenta. 2002; 23, 392399.Google Scholar
31. Economides, DL, Nicolaides, KH, Gahl, WA, Bernardini, I, Evans, MI. Plasma amino acids in appropriate- and small-for-gestational-age fetuses. Amer J Obstet Gynecol. 1989; 161, 12191227.Google Scholar
32. Cetin, I, Corbetta, C, Sereni, L, et al. Umbilical amino acid concentrations in normal and growth-retarded fetuses sampled in utero by cordocentesis. Amer J Obstet Gynecol. 1990; 162, 253261.Google Scholar
33. Marconi, AM, Paolini, CL, Stramare, L. Steady state maternal-fetal leucine enrichment in normal and intrauterine growth-restricted pregnancies. Pediatr Res. 1999; 46, 114119.Google Scholar
34. Paolini, CL, Marconi, AM, Ronzoni, S. Placental transport of leucine, phelalanine, glycine, and proline in intrauterine growth-restricted pregnancies. J Clin Edocrinol Metab. 2001; 86, 54275432.Google Scholar
35. Solomons, NW. Developmental origins of health and disease: concepts, caveats, and consequences for public health nutrition. Nutr Rev. 2009; 67, S12S16.Google Scholar
36. Jansson, T, Powell, TL. Human placental transport in altered fetal growth: does the placenta function as a nutrient sensor? Placenta. 2006; 27, 9197.Google Scholar