Skip to main content

Abstract

Pregnancy is a state of ever-increasing fetal demand for fuel. This demand is met through increased caloric intake, hyperinsulinemia, insulin resistance, and maternal pancreatic islet hypertrophy. In addition, fasting in the pregnant state results in maternal hypoglycemia, elevated plasma lipid concentrations, and hypoaminoacidemia. These maternal adaptive changes serve the unique purpose of self-preservation, with an attempt to use lipid as an alternative fuel in the face of the uninterrupted siphoning of glucose and amino acids to the fetus. The regulation of maternal glucose homeostasis, nutrient flow, and hormonal regulation of maternal and fetal pancreatic function is the subject of this chapter. This discussion of glucose metabolism in pregnancy is divided into three time periods: the first, second, and third trimesters, and a discussion of the postpartum changes is included. For each time period there is a discussion of the normal physiological changes in the pregnant woman and the potential pathological changes in the woman and the fetus.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 74.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Csapo AL, Pulkkinen MO, Wiest WG. Effects of lute-ectomy and progesterone replacement in early pregnant patients. Am J Obstet Gynecol 1973;115:759–765.

    PubMed  CAS  Google Scholar 

  2. Jaffe RB. The endocrinology of pregnancy. In Yen SSC, Jaffee RB, eds: Reproductive Endocrinology: Physiology, Pathophysiology, and Clinical Management. Philadelphia: Saunders, 1978;521–536.

    Google Scholar 

  3. Jovanovic L, Dawood MY, Landesman R, et al. Hormonal profile as a prognostic index of early threatened abortion. Am J Obstet Gynecol 1978; 130:274–276.

    PubMed  CAS  Google Scholar 

  4. Hiriis-Nielsen J, Nielsen V, Molsted-Pedersen L, et al. Effects of pregnancy hormones on pancreatic islets in organ culture. Acta Endocrinol (Copenh) 1986;111:336–341.

    Google Scholar 

  5. Kalkhoff RK, Jacobson M, Lemper D. Progesterone, pregnancy and the augmented plasma insulin response. J Clin Endocrinol Metab 1970;31:24–28.

    PubMed  CAS  Google Scholar 

  6. Barberia JR, Whu-Fadil S, Kletzky OA, et al. Serum prolactin patterns in early human gestation. Am J Obstet Gynecol 1975;121:1107–1110.

    PubMed  CAS  Google Scholar 

  7. Ho Yuen B, Cannon W, Lewis J, et al. A possible role for prolactin in the control of human chorionic gonadotropin and estrogen secretion by the fetoplacental unit. Am J Obstet Gynecol 1980; 136:286.

    PubMed  CAS  Google Scholar 

  8. Michaels RL, Sorenson RL, Parsons JA, et al. Prolactin enhances cell-to-cell communication among beta-cells in pancreatic islets. Diabetes 1987;36:1098–1103.

    PubMed  CAS  Google Scholar 

  9. Josimovich JB. Placental lactogenic hormone. In: Endocrinology of Pregnancy. New York: Harper & Row, 1971;184–196.

    Google Scholar 

  10. Josmovich JB, MacLaren JA. Presence in the human placenta and term serum of a highly lactogenic substance immunologically related to pituitary growth hormone. Endocrinology 1962;71:209–220.

    Google Scholar 

  11. Spellacy WN, Buhi WC, Schram JC, et al. Control of human chorionic somatomammotropin levels during pregnancy. Obstet Gynecol 1971;37:567–573.

    PubMed  CAS  Google Scholar 

  12. Kim YJ, Felig P. Plasma chorionic somatomammotropin levels during starvation in mid-pregnancy. J Clin Endocrinol Metab 1971;32:864–867.

    PubMed  CAS  Google Scholar 

  13. Gaspard VJ, Sandront HM, Luyckx AS, et al. The control of human placental lactogen (HPL) secretion and its interrelation with glucose and lipid metabolism in late pregnancy. In Camerini-Davalos RH, Coles HS, eds: Early Diabetes in Early Life. Orlando: Academic Press, 1975;273–278.

    Google Scholar 

  14. Jovanovic L, Druzin M, Peterson CM. Effect of euglycemia on the outcome of pregnancy in insulin-dependent diabetic women as compared with normal control subjects. Am J Med 1981;71:921–927.

    PubMed  CAS  Google Scholar 

  15. Kuhl C, Hornnes PJ. Endocrine pancreatic function in women with gestational diabetes. Acta Endocrinol [Suppl] (Copenh) 1986;277:19–23.

    CAS  Google Scholar 

  16. Mills JL, Baker L, Goldman A. Malformations in infants of diabetic mothers occur before the seventh gestational week: implications for treatment. Diabetes 1979;23:292–293.

    Google Scholar 

  17. Fuhrmann K, Ruher H, Semmler K, et al. Prevention of congenital malformations in infants of insulin dependent diabetic mothers. Diabetes Care 1983;6: 219–223.

    PubMed  CAS  Google Scholar 

  18. Jovanovic L, Peterson CM, Saxena BB, et al. Feasibility of maintaining normal glucose profiles in insulin-dependent pregnant women. Am J Med 1980;68: 105–112.

    PubMed  CAS  Google Scholar 

  19. Jovanovic L, Peterson CM. Preface. In Jovanovic L, Peterson CM, eds: Diabetes and Pregnancy: Teratology, Toxicology and Treatment. Philadelphia: Praeger, 1985.

    Google Scholar 

  20. Sadler TW, Horton WE. Effects of maternal diabetes on early embryogenesis: the role of insulin and insulin therapy. Diabetes 1983;32:1070–1074.

    PubMed  CAS  Google Scholar 

  21. Miller E, Hare JW, Clogerty JP, et al. Elevated maternal hemoglobin Alc in early pregnancy and major congenital anomalies in infants of diabetic mothers. N Engl J Med 1981;304:1331–1334.

    PubMed  CAS  Google Scholar 

  22. Mills JL, Knopp RH, Simpson JL, et al. Increased malformation rates in infants of diabetic mothers to glycemic control during organogenesis. N Engl J Med 1988;318:671–676.

    PubMed  CAS  Google Scholar 

  23. Castracane VD, Jovanovic L, Mills JL. Effect of normoglycemia before conception on early pregnancy hormone profiles. Diabetes Care 1985;8:473–476.

    PubMed  CAS  Google Scholar 

  24. DeHertogh R, Thomas K, Vanderheyden I. Quantitative determination of sex hormone-binding globulin capacity in the plasma of normal and diabetic pregnancies. J Clin Endocrinol Metab 1976;42:773–777.

    CAS  Google Scholar 

  25. Gibson M, Schiff I, Tulchinsky D, et al. Characterization of hyperandrogenism with insulin-resistant diabetes type A. Fertil Steril 1980;33:501–505.

    PubMed  CAS  Google Scholar 

  26. Szpunar WE, Blair AJ, McCann DS. Plasma androgen concentrations in diabetic women. Diabetes 1977;26: 1125–1129.

    PubMed  CAS  Google Scholar 

  27. Learning AB, Mathur RS, Levine JH. Increased plasma testosterone in streptozotocin-diabetic female rats. Endocrinology 1982;111:1329–1333.

    Google Scholar 

  28. Barbieri RL, Makris A, Ryan KJ. Effects of insulin on steroidogenesis in cultured porcine ovarian theca. Fertil Steril 1983;40:237–241.

    PubMed  CAS  Google Scholar 

  29. Mills JL, Simpson JL, Driscoll SB, et al. Incidence of spontaneous abortion among normal women and insulin dependent diabetic women whose pregnancies were identified within 21 days of conception. N Engl J Med 1988;319:1617–1623.

    PubMed  CAS  Google Scholar 

  30. Peterson CM, Miller N, Walker L, et al. Effect of glipizide on insulin secretion from cultured human fetal pancreatic islets. Diabetes Care 1986;5:556–557.

    Google Scholar 

  31. Weiss PAM. Gestational diabetes —a survey. In Weiss PAM, Coustan DR, eds: Gestational Diabetes. Vien: Springer-Verlag, 1988; 1–58.

    Google Scholar 

  32. Battaglia FC, Meschia G. Principal substrates of fetal metabolism. Physiol Rev 1978;58:499–527.

    PubMed  CAS  Google Scholar 

  33. Meschia G, Battaglia FC, Hay WW, et al. Utilization of substrates by the ovine placenta in vivo. Fed Proc 1980; 39:245–249.

    PubMed  CAS  Google Scholar 

  34. Battaglia FC. Principal substrates of fetal metabolism: fuel and growth requirements of the ovine fetus. Ciba Found Symp 1979;63:57–74.

    CAS  Google Scholar 

  35. Phelps RL, Metzger BE, Freinkel N. Carbohydrate metabolism in pregnancy. XVIII. Diurnal profiles of plasma glucose, insulin, free fatty acids, triglycerides, cholesterol and individual amino acids in late normal pregnancy. Am J Obstet Gynecol 1981;140:730–736.

    PubMed  CAS  Google Scholar 

  36. Hull D, Elphick MG. Evidence for fatty acid transfer across the human placenta. Ciba Found Symp 1979; 63:75–91.

    CAS  Google Scholar 

  37. Steel RB, Mosley JD, Smith CH. Insulin and placenta: degradation and stabilization, binding to microvillous membrane receptors, and amino acid uptake. Am J Obstet Gynecol 1979;135:522.

    PubMed  CAS  Google Scholar 

  38. Heding EG, Persson B, Stangenberg M. B-cell function in newborn infants of diabetic mothers. Dia-betologia 1980;19:427–432.

    CAS  Google Scholar 

  39. Mylvaganam R, Stowers JM, Steel JM, et al. Insulin immunogenicity in pregnancy: maternal and fetal studies. Diabetologia 1983;24:19–25.

    PubMed  CAS  Google Scholar 

  40. Spellacy WN, Goetz FC. Insulin antibodies in pregnancy. Lancet 1963;2:222–224.

    PubMed  CAS  Google Scholar 

  41. Jorgensen KR, Deckert T, Pedersen LM, et al. Insulin antibody and glucose in plasma of newborn infants of diabetic women. Acta Endocrinol (Copenh) 1966;52: 154–167.

    CAS  Google Scholar 

  42. Wright PH. The production of experimental diabetes by insulin antibodies. Am J Med 1961;31:892–900.

    PubMed  CAS  Google Scholar 

  43. Dixon K, Exon PD, Hughes HR. Insulin antibodies in aetiology of labile diabetes. Lancet 1972;1:343–347.

    PubMed  CAS  Google Scholar 

  44. Bauman WA, Yalow RS. Transplacental passage of insulin complexed to antibody. Proc Natl Acad Sci USA 1981;78:4588–4590.

    PubMed  CAS  Google Scholar 

  45. Pedersen J. Hyperglycaemia-hyperinsulinism therapy and birth weight. In: The Pregnant Diabetic and Her Newborn, 2nd ed. Copenhagen: Munksgaard, 1977; 211–217.

    Google Scholar 

  46. Dimario U, Falluca F, Gargiulo P, et al. Insulin-anti-insulin complexes in diabetic women and their neonates. Diabetologia 1984;27:83–86.

    Google Scholar 

  47. Martin FIR, Dahlenburg GW, Russell J, et al. Neonatal hypoglycaemia in infants of insulin-dependent diabetic mothers. Arch Dis Child 1975;50:472–476.

    PubMed  CAS  Google Scholar 

  48. Tamas GY, Befefi D, Gaal O: Insulin antibodies in diabetic pregnancy. Lancet 1975; 1:521 (letter).

    Google Scholar 

  49. Leiper JM, Fineberg SE, Luman CB, et al. Insulin antibodies in the maternal and foetal circulation of pregnant diabetic women treated with human insulin of recombinant DNA origin. Diabetes Res 1984;1: 75–81.

    PubMed  CAS  Google Scholar 

  50. Menon RK, Cohen RM, Sperling MA, et al. Transplacental passage of insulin in pregnant women with insulin-dependent diabetes mellitus. N Engl J Med 1990;323: 309–315.

    PubMed  CAS  Google Scholar 

  51. Jovanovic-Peterson L, Kitzmiller JC, Peterson CM. Lower birthweight and C-peptide response in infants of diabetic pregnant women receiving human versus animal source insulin. Diabetes 1990;39(suppl 1): 1164.

    Google Scholar 

  52. Zwilling E. Micromelia as a direct effect of insulin-evidence from in vitro and in vivo experiments. J Morphol 1959;194:159–179.

    Google Scholar 

  53. Cockrofat DL, Coppola PT. Teratogenic effects of excess glucose on head-fold rat embryos in culture. Teratology 1977;16:141–146.

    Google Scholar 

  54. Van Lancker JL. Molecular and Cellular Mechanisms in Disease. New York: Springer-Verlag, 1976;423–457.

    Google Scholar 

  55. New DAT. Whole embryo culture and the study of mammalian embryos during organogenesis. Biol Rev 1978;53:81–122.

    PubMed  CAS  Google Scholar 

  56. Sadler TW. Culture of early somite mouse embryos during organogenesis. J Embryol Exp Morphol 1979; 49:17–25.

    PubMed  CAS  Google Scholar 

  57. Sadler TW. Effects of maternal diabetes on early embryogenesis. II. Hyperglycemia-induced exenceph-aly. Teratology 1980;21:349–356.

    PubMed  CAS  Google Scholar 

  58. Horton WE, Sadler TW. Effects of maternal diabetes on early embryogenesis alterations in morphogenesis produced by the ketone body β-hydroxybutyrate. Diabetes 1983;32:610–616.

    PubMed  CAS  Google Scholar 

  59. Sadler TW, Horton WE, Warner CW Whole embryo culture: a screening technique for teratogens? Terato-genesis Carcinog Mutagen 1982;2:243–253.

    CAS  Google Scholar 

  60. Cockroft DL, Freinkel N, Phillips LS, et al. Metabolic factors affecting organogenesis in diabetic pregnancy. Clin Res 1981;29:577A.

    Google Scholar 

  61. Gasparo M de, Van Assche FA, Gepts W, et al. The histology of the endocrine pancreas and the insulin content in the microdissected islets of fetal pancreas. Rev Fr Etud Clin Biol 1969;9:904–906.

    Google Scholar 

  62. Van Assche FA, Hoet JJ, Jack PMB. Endocrine pancreas of the pregnant mother, fetus, and newborn. In Beard RW, Nanthanielsz PW, eds: Fetal Physiology and Medicine, 2nd ed. New York: Marcel Dekker, 1984; 127–152.

    Google Scholar 

  63. Fowden AL. Effects of arginine and glucose on the release of insulin in the sheep fetus. J Endocrinol 1980;85:121–129.

    PubMed  CAS  Google Scholar 

  64. Fowden AL. Effects of adrenaline and amino acids on the release of insulin in the sheep fetus. J Endocrinol 1980;87:113–121.

    PubMed  CAS  Google Scholar 

  65. Young M, Horn J, Noakes DL. Protein turnover rate in fetal organs: the influence of insulin. In Visser HKA, ed: Nutrition and Metabolism of the Fetus and Infant. The Hague: Mardrums Nijhoff 1979; 19–27.

    Google Scholar 

  66. Jovanovic-Peterson L. Maternal post prandial glucose levels and infant birth weight: the diabetes in early pregnancy study. Am J Obstet Gynecol 1991; 164: 103–111.

    PubMed  CAS  Google Scholar 

  67. Girard JR. Factors affecting the secretion of insulin and glucagon by the rat fetus. Diabetes 1974;23: 310–317.

    PubMed  CAS  Google Scholar 

  68. Dudek RW, Kawabe T, Brinn JE, et al. Effects of growth hormone on the in vitro maturation of fetal islets. Proc Soc Exp Biol Med 1984;177:69–76.

    PubMed  CAS  Google Scholar 

  69. Jovanovic L, Peterson CM. Screening for gestational diabetes; optimal timing and criteria for retesting. Diabetes 1985;34(suppl 2):21–23.

    PubMed  Google Scholar 

  70. Hollingsworth DR: Alterations of maternal metabolism in normal and diabetic pregnancies: differences in insulin-dependent, non-insulin-dependent, and gestational diabetes. Am J Obstet Gynecol 1983; 146:417–427.

    PubMed  CAS  Google Scholar 

  71. Hadden DR. Geographic, ethnic, & racial variations in the incidence of gestational diabetes. Diabetes 1985; 34(suppl 2):8–12.

    PubMed  Google Scholar 

  72. Metzger BE, Bybec DE, Frienkel NO, et al. Gestational diabetes mellitus: correlations between pheno-typic and genotypic characteristics of the mother and abnormal glucose tolerance during the first year post partum. Diabetes 1985;34(suppl 2):111–115.

    PubMed  Google Scholar 

  73. Nordlander E, Hanson U, Persson B, et al. Pancreatic B-cell function during normal pregnancy. Diabetes Res 1987;6:133–136.

    PubMed  CAS  Google Scholar 

  74. Swenne I. Glucose-stimulated DNA replication of the pancreatic islets during the development of the rat fetus: effects of nutrients, growth hormone, and triiodothyronine. Diabetes 1985;34:803–807.

    PubMed  CAS  Google Scholar 

  75. Hollingsworth DR, Grundy SM. Pregnancy associated hypertriglyceridemia in normal and diabetic women: differences in type I, type II and gestational diabetes. Diabetes 1982;31:1092.

    PubMed  CAS  Google Scholar 

  76. Knopp RH, Warth M. Lipoprotein changes in pregnancy: a distinct endogenous hypertriglyceridemia. J Clin Invest 1973;42:48a.

    Google Scholar 

  77. Ziegler B, Lucke S, Besch W, et al. Pregnancy-associated changes in the endocrine pancreas of normoglycaemic streptozotocin-treated Wistar rats. Diabetologia 1985;28:172–175.

    PubMed  CAS  Google Scholar 

  78. Reusens-Billen B, Remacle C, Daniline J, et al. Cell proliferation in pancreatic islets of rat fetuses and neonates from normal and diabetic mothers: an in vitro and in vivo study. Horm Metab Res 1984;11: 565–571.

    Google Scholar 

  79. Hoet JJ. The etiology of congenital malformations in infants of diabetic mothers: environmental and genetic interaction. In Jovanovic L, Peterson CM, Fuhrmann K, eds: Diabetes and Pregnancy: Teratology, Toxicology, and Treatment. New York: Praeger, 1986;72–82.

    Google Scholar 

  80. Dudek RW, Kawabe T, Brinn JE, et al. Glucose affects in vitro maturation of fetal rat islets. Endocrinology 1984;114:582–587.

    PubMed  CAS  Google Scholar 

  81. Jovanovic L, Peterson CM. Is pregnancy contraindi-cated in women with diabetes mellitus? Diab Nephrop 1984;3:36–38.

    Google Scholar 

  82. Swenne I, Eriksson U. Diabetes in pregnancy: islet cell proliferation in the fetal rat pancreas. Diabetolo-gia 1982;23:525–528.

    CAS  Google Scholar 

  83. Eriksson U, Swenne I. Diabetes in pregnancy: growth of the fetal pancreatic ß cells in the rat. Biol Neonate 1982;42:239–248.

    PubMed  CAS  Google Scholar 

  84. Freinkel N, Metzger BE, Nitzan M, et al. “Accelerated starvation” and mechanism for the conservation of maternal nitrogen during pregnancy. Isr J Med Sci 1972;8:426–439.

    PubMed  CAS  Google Scholar 

  85. Hollingsworth DR. Endocrine and metabolic homeostasis in diabetic pregnancy. Clin Perinatol 1983; 10: 593–614.

    PubMed  CAS  Google Scholar 

  86. Fiore R, Maldonato A, Zicari D, et al. Endocrine pancreatic function in insulin-dependent diabetic pregnant women. Acta Endocrinol [Suppl] (Copenh) 1986; 277:31–36.

    CAS  Google Scholar 

  87. Hull D, Elphick MC. Evidence for fatty acid transfer across the human placenta. Ciba Found Symp 1979; 63:75–91.

    CAS  Google Scholar 

  88. Widdowson EM. Chemical composition of newly born mammals. Nature 1950;166:626–627.

    PubMed  CAS  Google Scholar 

  89. Sparks JW, Girard JR, Battaglia FC. An estimate of the caloric requirements of the human fetus. Biol Neonate 1980;38:113–119.

    PubMed  CAS  Google Scholar 

  90. Roux JF, Myers RE. In vitro metabolism of palmitic acid and glucose in the developing tissue of the rhesus monkey. Am J Obstet Gynecol 1974;118:385–392.

    PubMed  CAS  Google Scholar 

  91. Yoshioka T, Roux JE In vitro metabolism of palmitic acid in human fetal tissues. Pediatr Res 1972;6:675–681.

    PubMed  CAS  Google Scholar 

  92. Robinson AM, Williamson DH. Physiological roles of ketone bodies as substrates and signals in mammalian tissues. Physiol Rev 1980;60:143–189.

    PubMed  CAS  Google Scholar 

  93. Warshaw JB, Terry ML. Cellular energy metabolism during fetal development. II. Fatty acid oxidation by the developing heart. J Cell Biol 1970;44:354–360.

    PubMed  CAS  Google Scholar 

  94. Bailey E, Lockwood E. Some aspects of fatty acid oxidation and ketone body formation and utilization during development of the rat. Enzyme 1973;15:239–253.

    PubMed  CAS  Google Scholar 

  95. McGary JD, Robles-Valdes C, Foster DW. Role of carnitine in hepatic ketogenesis. Proc Natl Acad Sci USA 1975;72:4385–4388.

    Google Scholar 

  96. Schmidt-Sommerfeld E, Penn D, Wolf H. Carnitine deficiency in premature infants receiving total parenteral nutrition: effect of L-carnitine supplementation. J Pediatr 1983;102:931–935.

    PubMed  CAS  Google Scholar 

  97. Coetzee E, Jackson WPU. Diabetes newly diagnosed during pregnancy. S Afr Med J 1979;56:467–474.

    PubMed  CAS  Google Scholar 

  98. Coetzee EJ, Jackson WPU, Berman PA. Ketonuria in pregnancy—with special reference to calorie restricted food intake in obese diabetics. Diabetes 1980; 29:177–180.

    PubMed  CAS  Google Scholar 

  99. Algert S, Shragg P, Hollingsworth DR. Moderate caloric restriction in obese women with gestational diabetes. Obstet Gynecol 1985;65:487–491.

    PubMed  CAS  Google Scholar 

  100. Felig P, Lynch V. Starvation in human pregnancy: hypoglycemia, hypoinsulinemia, and hyperketone-mia. Science 1970;170:990–992.

    PubMed  CAS  Google Scholar 

  101. Churchill JA, Berendes HW Intelligence of children whose mothers have acetonuria in pregnancy. In: Perinatal Factors Affecting Human Development. Scientific Publication 185. Washington, DC: Pan American Health Organization, 1969.

    Google Scholar 

  102. Naeye RL, Chez RA. Effects of maternal acetonuria and low pregnancy weight gain on children’s psychomotor development. Am J Obstet Gynecol 1981; 139: 189–193.

    PubMed  CAS  Google Scholar 

  103. Chez RA, Curcio FD Ketonuria in normal pregnancy. Obstet Gynecol 1987;69:272–274.

    PubMed  CAS  Google Scholar 

  104. Weigensburg M, Sobel R, Garcia-Palmer F, et al. Temporal differences in vulnerability to fuel mediated organ teratogenesis. Diabetes 1988;37(suppl 1):85A.

    Google Scholar 

  105. Riazzo T, Freinkel N, Metzger BE, et al. Fuel mediated behavioral teratogenesis: correlations between maternal metabolism in diabetic pregnancies and Brazelton tests in the newborn. Diabetes 1988;37 (suppl): 86A.

    Google Scholar 

  106. Jovanovic L, Peterson CM. Insulin and glucose requirements during the first stage of labor in insulin-dependent diabetic women. Am J Med 1983;75:607–612.

    PubMed  CAS  Google Scholar 

  107. Bihoreau MT, Ktorza A, Kervran A, et al. Effect of gestational hyperglycemia on insulin secretion in vivo and in vitro by fetal rat pancreas. Am J Physiol 1986; 251:E86-E91.

    PubMed  CAS  Google Scholar 

  108. Cornblath M, Tildon JT, Wapnir RA. Metabolic adaptation in the neonate. Isr J Med Sci 1972;8:453.

    PubMed  CAS  Google Scholar 

  109. Hubinont CJ, Baiasse H, Dufrane SP, et al. Changes in pancreatic ß cell function during late pregnancy, early lactation and postlactation. Gynecol Obstet Invest 1988;25:89–95.

    PubMed  CAS  Google Scholar 

  110. Botto RM, Sinagra D, Donatelli M, et al. Evaluation of β-cell secretion and peripheral insulin resistance during pregnancy and after delivery in gestational diabetes mellitus with obesity. Acta Diabetol Lat 1988; 25:81–88.

    Google Scholar 

  111. Ward WK, Johnston CL, Beard JC, et al. Abnormalities of islet β-cell function, insulin action, and fat distribution in women with histories of gestational diabetes: relation to obesity. J Clin Endocrinol Metab 1985;61:1039–1045.

    PubMed  CAS  Google Scholar 

  112. Mestman JH, Anderson CV, Guadalupe V. Followup of 360 subjects with abnormal carbohydrate metabolism during pregnancy. Obstet Gynecol 1972;39: 421–425.

    PubMed  CAS  Google Scholar 

  113. O’Sullivan JB. Body weight and subsequent diabetes mellitus. JAMA 1982;248:949.

    PubMed  Google Scholar 

  114. Marynissen G, Malaisse WJ, Van-Assche FA. Influence of lactation on morphometric and secretory variables in pancreatic beta-cell of mildly diabetic rats. Diabetes 1987;36:883–891.

    PubMed  CAS  Google Scholar 

  115. Marynissen G, Aerts L, Van Assche FA. The endocrine pancreas during pregnancy and lactation in the rat. J Dev Physiol 1983;5:373–381.

    PubMed  CAS  Google Scholar 

  116. Marynissen G, Malaisse WJ, Van Assche FA. Ultra-structural changes of the pancreatic beta-cell and the insulin secretion by islets from lactating and non-lactating rats. J Dev Physiol 1985;7:17–23.

    PubMed  CAS  Google Scholar 

  117. Hubinont CJ, Dufrane SP, Garcia MP, et al. Influence of lactation upon pancreatic islet function. Endocrinology 1986;118:687–694.

    PubMed  CAS  Google Scholar 

  118. Jovanovic-Peterson L, Peterson CM. Insulin requirements for nursing mothers. Diabetes Professional 1988; summer:7.

    Google Scholar 

  119. Jovanovic-Peterson L, Peterson CM. Maternal milk and plasma glucose and insulin levels: studies in normal and diabetic subjects. J Am Coll Nutr 1989;125–131.

    Google Scholar 

  120. Jovanovic-Peterson L, Peterson CM. Pregnancy and the endocrine pancreas. In Samois E, ed: The Endocrine Pancreas. New York: Raven Press, 1991;229–252.

    Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1991 Springer-Verlag New York Inc.

About this chapter

Cite this chapter

Jovanovic-Peterson, L., Peterson, C.M. (1991). Glucose Metabolism in Pregnancy. In: Cowett, R.M. (eds) Principles of Perinatal-Neonatal Metabolism. Springer, New York, NY. https://doi.org/10.1007/978-1-4684-0400-5_8

Download citation

  • DOI: https://doi.org/10.1007/978-1-4684-0400-5_8

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4684-0402-9

  • Online ISBN: 978-1-4684-0400-5

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics