Skip to main content
Top
Published in: Current Diabetes Reports 1/2012

01-02-2012 | Diabetes and Pregnancy (CJ Homko, Section Editor)

The Placenta and Gestational Diabetes Mellitus

Authors: M. Gauster, G. Desoye, M. Tötsch, U. Hiden

Published in: Current Diabetes Reports | Issue 1/2012

Login to get access

Abstract

By its location between maternal and fetal bloodstreams the human placenta not only handles the materno-fetal transport of nutrients and gases, but may also be exposed to intrauterine conditions adversely affecting placental and fetal development. Such adverse conditions exist in pregnancies complicated by gestational diabetes mellitus (GDM), and have been associated with alterations in placental anatomy and physiology. These alterations are mainly based on changes on the micro-anatomical and/or even molecular level including aberrant villous vascularization, a disbalance of vasoactive molecules, and enhanced oxidative stress. The consequence thereof may be impaired fetal oxygenation and changes in transplacental nutrient supply. Although transplacental glucose flux is flow limited and independent of glucose transporter availability, transport of essential and nonessential amino acids and expression of genes involved in lipid transport and metabolism are significantly affected by GDM.
Literature
1.
go back to reference Ben-Haroush A, Yogev Y, Hod M. Epidemiology of gestational diabetes mellitus and its association with Type 2 diabetes. Diabet Med. 2004;21:103–13.PubMedCrossRef Ben-Haroush A, Yogev Y, Hod M. Epidemiology of gestational diabetes mellitus and its association with Type 2 diabetes. Diabet Med. 2004;21:103–13.PubMedCrossRef
2.
go back to reference Radaelli T, Varastehpour A, Catalano P, et al. Gestational diabetes induces placental genes for chronic stress and inflammatory pathways. Diabetes. 2003;52:2951–8.PubMedCrossRef Radaelli T, Varastehpour A, Catalano P, et al. Gestational diabetes induces placental genes for chronic stress and inflammatory pathways. Diabetes. 2003;52:2951–8.PubMedCrossRef
3.
go back to reference Segregur J, Bukovic D, Milinovic D, et al. Fetal macrosomia in pregnant women with gestational diabetes. Coll Antropol. 2009;33:1121–7.PubMed Segregur J, Bukovic D, Milinovic D, et al. Fetal macrosomia in pregnant women with gestational diabetes. Coll Antropol. 2009;33:1121–7.PubMed
4.
go back to reference Kuhl C, Hornnes PJ, Andersen O. Etiology and pathophysiology of gestational diabetes mellitus. Diabetes. 1985;34 Suppl 2:66–70.PubMed Kuhl C, Hornnes PJ, Andersen O. Etiology and pathophysiology of gestational diabetes mellitus. Diabetes. 1985;34 Suppl 2:66–70.PubMed
5.
go back to reference Kautzky-Willer A, Prager R, Waldhausl W, et al. Pronounced insulin resistance and inadequate beta-cell secretion characterize lean gestational diabetes during and after pregnancy. Diabetes Care. 1997;20:1717–23.PubMedCrossRef Kautzky-Willer A, Prager R, Waldhausl W, et al. Pronounced insulin resistance and inadequate beta-cell secretion characterize lean gestational diabetes during and after pregnancy. Diabetes Care. 1997;20:1717–23.PubMedCrossRef
6.
go back to reference Xiang AH, Peters RK, Trigo E, et al. Multiple metabolic defects during late pregnancy in women at high risk for type 2 diabetes. Diabetes. 1999;48:848–54.PubMedCrossRef Xiang AH, Peters RK, Trigo E, et al. Multiple metabolic defects during late pregnancy in women at high risk for type 2 diabetes. Diabetes. 1999;48:848–54.PubMedCrossRef
7.
go back to reference Taricco E, Radaelli T, Rossi G, et al. Effects of gestational diabetes on fetal oxygen and glucose levels in vivo. Bjog. 2009;116:1729–35.PubMedCrossRef Taricco E, Radaelli T, Rossi G, et al. Effects of gestational diabetes on fetal oxygen and glucose levels in vivo. Bjog. 2009;116:1729–35.PubMedCrossRef
8.
go back to reference Daskalakis G, Marinopoulos S, Krielesi V, et al. Placental pathology in women with gestational diabetes. Acta Obstet Gynecol Scand. 2008;87:403–7.PubMedCrossRef Daskalakis G, Marinopoulos S, Krielesi V, et al. Placental pathology in women with gestational diabetes. Acta Obstet Gynecol Scand. 2008;87:403–7.PubMedCrossRef
9.
go back to reference Madazli R, Tuten A, Calay Z, et al. The incidence of placental abnormalities, maternal and cord plasma malondialdehyde and vascular endothelial growth factor levels in women with gestational diabetes mellitus and nondiabetic controls. Gynecol Obstet Invest. 2008;65:227–32.PubMedCrossRef Madazli R, Tuten A, Calay Z, et al. The incidence of placental abnormalities, maternal and cord plasma malondialdehyde and vascular endothelial growth factor levels in women with gestational diabetes mellitus and nondiabetic controls. Gynecol Obstet Invest. 2008;65:227–32.PubMedCrossRef
10.
go back to reference Schafer-Graf UM, Dupak J, Vogel M, et al. Hyperinsulinism, neonatal obesity and placental immaturity in infants born to women with one abnormal glucose tolerance test value. J Perinat Med. 1998;26:27–36.PubMedCrossRef Schafer-Graf UM, Dupak J, Vogel M, et al. Hyperinsulinism, neonatal obesity and placental immaturity in infants born to women with one abnormal glucose tolerance test value. J Perinat Med. 1998;26:27–36.PubMedCrossRef
11.
go back to reference Bartha JL, Martinez-Del-Fresno P, Comino-Delgado R. Gestational diabetes mellitus diagnosed during early pregnancy. Am J Obstet Gynecol. 2000;182:346–50.PubMedCrossRef Bartha JL, Martinez-Del-Fresno P, Comino-Delgado R. Gestational diabetes mellitus diagnosed during early pregnancy. Am J Obstet Gynecol. 2000;182:346–50.PubMedCrossRef
12.
go back to reference Meyer WJ, Carbone J, Gauthier DW, et al. Early gestational glucose screening and gestational diabetes. J Reprod Med. 1996;41:675–9.PubMed Meyer WJ, Carbone J, Gauthier DW, et al. Early gestational glucose screening and gestational diabetes. J Reprod Med. 1996;41:675–9.PubMed
13.
go back to reference Cetin I, de Santis MS, Taricco E, et al. Maternal and fetal amino acid concentrations in normal pregnancies and in pregnancies with gestational diabetes mellitus. Am J Obstet Gynecol. 2005;192:610–7.PubMedCrossRef Cetin I, de Santis MS, Taricco E, et al. Maternal and fetal amino acid concentrations in normal pregnancies and in pregnancies with gestational diabetes mellitus. Am J Obstet Gynecol. 2005;192:610–7.PubMedCrossRef
14.
go back to reference Taricco E, Radaelli T, Nobile de Santis MS, et al. Foetal and placental weights in relation to maternal characteristics in gestational diabetes. Placenta. 2003;24:343–7.PubMedCrossRef Taricco E, Radaelli T, Nobile de Santis MS, et al. Foetal and placental weights in relation to maternal characteristics in gestational diabetes. Placenta. 2003;24:343–7.PubMedCrossRef
15.
go back to reference Kucuk M, Doymaz F. Placental weight and placental weight-to-birth weight ratio are increased in diet- and exercise-treated gestational diabetes mellitus subjects but not in subjects with one abnormal value on 100-g oral glucose tolerance test. J Diabetes Complications. 2009;23:25–31.PubMedCrossRef Kucuk M, Doymaz F. Placental weight and placental weight-to-birth weight ratio are increased in diet- and exercise-treated gestational diabetes mellitus subjects but not in subjects with one abnormal value on 100-g oral glucose tolerance test. J Diabetes Complications. 2009;23:25–31.PubMedCrossRef
16.
go back to reference Lao TT, Lee CP, Wong WM. Placental weight to birthweight ratio is increased in mild gestational glucose intolerance. Placenta. 1997;18:227–30.PubMedCrossRef Lao TT, Lee CP, Wong WM. Placental weight to birthweight ratio is increased in mild gestational glucose intolerance. Placenta. 1997;18:227–30.PubMedCrossRef
17.
go back to reference Chan KK, Ho LF, Lao TT. Nutritional intake and placental size in gestational diabetic pregnancies–a preliminary observation. Placenta. 2003;24:985–8.PubMedCrossRef Chan KK, Ho LF, Lao TT. Nutritional intake and placental size in gestational diabetic pregnancies–a preliminary observation. Placenta. 2003;24:985–8.PubMedCrossRef
18.
go back to reference Pathak S, Hook E, Hackett G, et al. Cord coiling, umbilical cord insertion and placental shape in an unselected cohort delivering at term: relationship with common obstetric outcomes. Placenta. 2010;31:963–8.PubMedCrossRef Pathak S, Hook E, Hackett G, et al. Cord coiling, umbilical cord insertion and placental shape in an unselected cohort delivering at term: relationship with common obstetric outcomes. Placenta. 2010;31:963–8.PubMedCrossRef
19.
go back to reference Calderon IM, Damasceno DC, Amorin RL, et al. Morphometric study of placental villi and vessels in women with mild hyperglycemia or gestational or overt diabetes. Diabetes Res Clin Pract. 2007;78:65–71.PubMedCrossRef Calderon IM, Damasceno DC, Amorin RL, et al. Morphometric study of placental villi and vessels in women with mild hyperglycemia or gestational or overt diabetes. Diabetes Res Clin Pract. 2007;78:65–71.PubMedCrossRef
20.
go back to reference al-Okail MS, al-Attas OS. Histological changes in placental syncytiotrophoblasts of poorly controlled gestational diabetic patients. Endocr J. 1994;41:355–60.PubMedCrossRef al-Okail MS, al-Attas OS. Histological changes in placental syncytiotrophoblasts of poorly controlled gestational diabetic patients. Endocr J. 1994;41:355–60.PubMedCrossRef
21.
go back to reference Nadra K, Quignodon L, Sardella C, et al. PPARgamma in placental angiogenesis. Endocrinology. 2010;151:4969–81.PubMedCrossRef Nadra K, Quignodon L, Sardella C, et al. PPARgamma in placental angiogenesis. Endocrinology. 2010;151:4969–81.PubMedCrossRef
23.
go back to reference Khaliq A, Li XF, Shams M, et al. Localisation of placenta growth factor (PIGF) in human term placenta. Growth Factors. 1996;13:243–50. color plates I-II,pre bk cov.PubMedCrossRef Khaliq A, Li XF, Shams M, et al. Localisation of placenta growth factor (PIGF) in human term placenta. Growth Factors. 1996;13:243–50. color plates I-II,pre bk cov.PubMedCrossRef
24.
go back to reference Lang I, Pabst MA, Hiden U, et al. Heterogeneity of microvascular endothelial cells isolated from human term placenta and macrovascular umbilical vein endothelial cells. Eur J Cell Biol. 2003;82:163–73.PubMedCrossRef Lang I, Pabst MA, Hiden U, et al. Heterogeneity of microvascular endothelial cells isolated from human term placenta and macrovascular umbilical vein endothelial cells. Eur J Cell Biol. 2003;82:163–73.PubMedCrossRef
25.
go back to reference Murthi P, Hiden U, Rajaraman G, et al. Novel homeobox genes are differentially expressed in placental microvascular endothelial cells compared with macrovascular cells. Placenta. 2008;29:624–30.PubMedCrossRef Murthi P, Hiden U, Rajaraman G, et al. Novel homeobox genes are differentially expressed in placental microvascular endothelial cells compared with macrovascular cells. Placenta. 2008;29:624–30.PubMedCrossRef
26.
go back to reference Murthi P, So M, Gude NM, et al. Homeobox genes are differentially expressed in macrovascular human umbilical vein endothelial cells and microvascular placental endothelial cells. Placenta. 2007;28:219–23.PubMedCrossRef Murthi P, So M, Gude NM, et al. Homeobox genes are differentially expressed in macrovascular human umbilical vein endothelial cells and microvascular placental endothelial cells. Placenta. 2007;28:219–23.PubMedCrossRef
27.
go back to reference Grissa O, Yessoufou A, Mrisak I, et al. Growth factor concentrations and their placental mRNA expression are modulated in gestational diabetes mellitus: possible interactions with macrosomia. BMC Pregnancy Childbirth. 2010;10:7.PubMedCrossRef Grissa O, Yessoufou A, Mrisak I, et al. Growth factor concentrations and their placental mRNA expression are modulated in gestational diabetes mellitus: possible interactions with macrosomia. BMC Pregnancy Childbirth. 2010;10:7.PubMedCrossRef
28.
go back to reference Hill DJ, Tevaarwerk GJ, Caddell C, et al. Fibroblast growth factor 2 is elevated in term maternal and cord serum and amniotic fluid in pregnancies complicated by diabetes: relationship to fetal and placental size. J Clin Endocrinol Metab. 1995;80:2626–32.PubMedCrossRef Hill DJ, Tevaarwerk GJ, Caddell C, et al. Fibroblast growth factor 2 is elevated in term maternal and cord serum and amniotic fluid in pregnancies complicated by diabetes: relationship to fetal and placental size. J Clin Endocrinol Metab. 1995;80:2626–32.PubMedCrossRef
29.
go back to reference Holdsworth-Carson SJ, Lim R, Mitton A, et al. Peroxisome proliferator-activated receptors are altered in pathologies of the human placenta: gestational diabetes mellitus, intrauterine growth restriction and preeclampsia. Placenta. 2010;31:222–9.PubMedCrossRef Holdsworth-Carson SJ, Lim R, Mitton A, et al. Peroxisome proliferator-activated receptors are altered in pathologies of the human placenta: gestational diabetes mellitus, intrauterine growth restriction and preeclampsia. Placenta. 2010;31:222–9.PubMedCrossRef
30.
go back to reference • Acosta JC, Haas DM, Saha CK et al (2011) Gestational diabetes mellitus alters maternal and neonatal circulating endothelial progenitor cell subsets. Am J Obstet Gynecol 204: 254 e258-254 e215. Circulating endothelial progenitor cells are reduced in an intrauterine GDM environment. This may contribute to endothelial dysfunction in placenta and program the offspring for later disease associated with impaired endothelial function.CrossRef • Acosta JC, Haas DM, Saha CK et al (2011) Gestational diabetes mellitus alters maternal and neonatal circulating endothelial progenitor cell subsets. Am J Obstet Gynecol 204: 254 e258-254 e215. Circulating endothelial progenitor cells are reduced in an intrauterine GDM environment. This may contribute to endothelial dysfunction in placenta and program the offspring for later disease associated with impaired endothelial function.CrossRef
31.
go back to reference Estes ML, Mund JA, Mead LE, et al. Application of polychromatic flow cytometry to identify novel subsets of circulating cells with angiogenic potential. Cytometry A. 2010;77:831–9.PubMed Estes ML, Mund JA, Mead LE, et al. Application of polychromatic flow cytometry to identify novel subsets of circulating cells with angiogenic potential. Cytometry A. 2010;77:831–9.PubMed
32.
go back to reference Jirkovska M, Kubinova L, Janacek J, et al. Topological properties and spatial organization of villous capillaries in normal and diabetic placentas. J Vasc Res. 2002;39:268–78.PubMedCrossRef Jirkovska M, Kubinova L, Janacek J, et al. Topological properties and spatial organization of villous capillaries in normal and diabetic placentas. J Vasc Res. 2002;39:268–78.PubMedCrossRef
33.
go back to reference Babawale MO, Lovat S, Mayhew TM, et al. Effects of gestational diabetes on junctional adhesion molecules in human term placental vasculature. Diabetologia. 2000;43:1185–96.PubMedCrossRef Babawale MO, Lovat S, Mayhew TM, et al. Effects of gestational diabetes on junctional adhesion molecules in human term placental vasculature. Diabetologia. 2000;43:1185–96.PubMedCrossRef
34.
go back to reference Fadda GM, D'Antona D, Ambrosini G, et al. Placental and fetal pulsatility indices in gestational diabetes mellitus. J Reprod Med. 2001;46:365–70.PubMed Fadda GM, D'Antona D, Ambrosini G, et al. Placental and fetal pulsatility indices in gestational diabetes mellitus. J Reprod Med. 2001;46:365–70.PubMed
35.
go back to reference Brown MA, North L, Hargood J. Uteroplacental Doppler ultrasound in routine antenatal care. Aust N Z J Obstet Gynaecol. 1990;30:303–7.PubMedCrossRef Brown MA, North L, Hargood J. Uteroplacental Doppler ultrasound in routine antenatal care. Aust N Z J Obstet Gynaecol. 1990;30:303–7.PubMedCrossRef
36.
go back to reference Pietryga M, Brazert J, Wender-Ozegowska E, et al. Placental Doppler velocimetry in gestational diabetes mellitus. J Perinat Med. 2006;34:108–10.PubMedCrossRef Pietryga M, Brazert J, Wender-Ozegowska E, et al. Placental Doppler velocimetry in gestational diabetes mellitus. J Perinat Med. 2006;34:108–10.PubMedCrossRef
37.
go back to reference Reisenberger K, Egarter C, Kapiotis S, et al. Transfer of erythropoietin across the placenta perfused in vitro. Obstet Gynecol. 1997;89:738–42.PubMedCrossRef Reisenberger K, Egarter C, Kapiotis S, et al. Transfer of erythropoietin across the placenta perfused in vitro. Obstet Gynecol. 1997;89:738–42.PubMedCrossRef
38.
go back to reference Leushner JR, Tevaarwerk GJ, Clarson CL, et al. Analysis of the collagens of diabetic placental villi. Cell Mol Biol. 1986;32:27–35.PubMed Leushner JR, Tevaarwerk GJ, Clarson CL, et al. Analysis of the collagens of diabetic placental villi. Cell Mol Biol. 1986;32:27–35.PubMed
39.
go back to reference Stanley JL, Cheung CC, Rueda-Clausen CF, et al. Effect of gestational diabetes on maternal artery function. Reprod Sci. 2011;18:342–52.PubMedCrossRef Stanley JL, Cheung CC, Rueda-Clausen CF, et al. Effect of gestational diabetes on maternal artery function. Reprod Sci. 2011;18:342–52.PubMedCrossRef
40.
go back to reference Bobadilla RA, van Bree R, Vercruysse L, et al. Placental effects of systemic tumour necrosis factor-alpha in an animal model of gestational diabetes mellitus. Placenta. 2010;31:1057–63.PubMedCrossRef Bobadilla RA, van Bree R, Vercruysse L, et al. Placental effects of systemic tumour necrosis factor-alpha in an animal model of gestational diabetes mellitus. Placenta. 2010;31:1057–63.PubMedCrossRef
41.
go back to reference Mildenberger E, Biesel B, Siegel G, et al. Nitric oxide and endothelin in oxygen-dependent regulation of vascular tone of human umbilical vein. Am J Physiol Heart Circ Physiol. 2003;285:H1730–7.PubMed Mildenberger E, Biesel B, Siegel G, et al. Nitric oxide and endothelin in oxygen-dependent regulation of vascular tone of human umbilical vein. Am J Physiol Heart Circ Physiol. 2003;285:H1730–7.PubMed
42.
go back to reference Boura AL, Walters WA, Read MA, et al. Autacoids and control of human placental blood flow. Clin Exp Pharmacol Physiol. 1994;21:737–48.PubMedCrossRef Boura AL, Walters WA, Read MA, et al. Autacoids and control of human placental blood flow. Clin Exp Pharmacol Physiol. 1994;21:737–48.PubMedCrossRef
43.
go back to reference San Martin R, Sobrevia L. Gestational diabetes and the adenosine/L-arginine/nitric oxide (ALANO) pathway in human umbilical vein endothelium. Placenta. 2006;27:1–10.PubMedCrossRef San Martin R, Sobrevia L. Gestational diabetes and the adenosine/L-arginine/nitric oxide (ALANO) pathway in human umbilical vein endothelium. Placenta. 2006;27:1–10.PubMedCrossRef
44.
go back to reference Schonfelder G, John M, Hopp H, et al. Expression of inducible nitric oxide synthase in placenta of women with gestational diabetes. Faseb J. 1996;10:777–84.PubMed Schonfelder G, John M, Hopp H, et al. Expression of inducible nitric oxide synthase in placenta of women with gestational diabetes. Faseb J. 1996;10:777–84.PubMed
45.
go back to reference Figueroa R, Martinez E, Fayngersh RP, et al. Alterations in relaxation to lactate and H(2)O(2) in human placental vessels from gestational diabetic pregnancies. Am J Physiol Heart Circ Physiol. 2000;278:H706–13.PubMed Figueroa R, Martinez E, Fayngersh RP, et al. Alterations in relaxation to lactate and H(2)O(2) in human placental vessels from gestational diabetic pregnancies. Am J Physiol Heart Circ Physiol. 2000;278:H706–13.PubMed
46.
go back to reference Sobrevia L, Cesare P, Yudilevich DL, et al. Diabetes-induced activation of system y + and nitric oxide synthase in human endothelial cells: association with membrane hyperpolarization. J Physiol. 1995;489(Pt 1):183–92.PubMed Sobrevia L, Cesare P, Yudilevich DL, et al. Diabetes-induced activation of system y + and nitric oxide synthase in human endothelial cells: association with membrane hyperpolarization. J Physiol. 1995;489(Pt 1):183–92.PubMed
47.
go back to reference Sobrevia L, Yudilevich DL, Mann GE. Elevated D-glucose induces insulin insensitivity in human umbilical endothelial cells isolated from gestational diabetic pregnancies. J Physiol. 1998;506(Pt 1):219–30.PubMedCrossRef Sobrevia L, Yudilevich DL, Mann GE. Elevated D-glucose induces insulin insensitivity in human umbilical endothelial cells isolated from gestational diabetic pregnancies. J Physiol. 1998;506(Pt 1):219–30.PubMedCrossRef
48.
go back to reference Vasquez G, Sanhueza F, Vasquez R, et al. Role of adenosine transport in gestational diabetes-induced L-arginine transport and nitric oxide synthesis in human umbilical vein endothelium. J Physiol. 2004;560:111–22.PubMedCrossRef Vasquez G, Sanhueza F, Vasquez R, et al. Role of adenosine transport in gestational diabetes-induced L-arginine transport and nitric oxide synthesis in human umbilical vein endothelium. J Physiol. 2004;560:111–22.PubMedCrossRef
49.
go back to reference De Vriese AS, Verbeuren TJ, Van de Voorde J, et al. Endothelial dysfunction in diabetes. Br J Pharmacol. 2000;130:963–74.PubMedCrossRef De Vriese AS, Verbeuren TJ, Van de Voorde J, et al. Endothelial dysfunction in diabetes. Br J Pharmacol. 2000;130:963–74.PubMedCrossRef
50.
51.
go back to reference Sobrevia L, Mann GE. Dysfunction of the endothelial nitric oxide signalling pathway in diabetes and hyperglycaemia. Exp Physiol. 1997;82:423–52.PubMed Sobrevia L, Mann GE. Dysfunction of the endothelial nitric oxide signalling pathway in diabetes and hyperglycaemia. Exp Physiol. 1997;82:423–52.PubMed
52.
go back to reference • Sobrevia L, Gonzalez M (2009) A role for insulin on L-arginine transport in fetal endothelial dysfunction in hyperglycaemia. Curr Vasc Pharmacol 7: 467–474. Insulin blocks the stimulatory high-glucose effect on L-arginine transport by reducing transcriptional activity of the amino acid transporter through transcription factors specificity protein 1 and nuclear factor-κB. This may contribute to fetal endothelial dysfunction in diabetic pregnancies.PubMedCrossRef • Sobrevia L, Gonzalez M (2009) A role for insulin on L-arginine transport in fetal endothelial dysfunction in hyperglycaemia. Curr Vasc Pharmacol 7: 467–474. Insulin blocks the stimulatory high-glucose effect on L-arginine transport by reducing transcriptional activity of the amino acid transporter through transcription factors specificity protein 1 and nuclear factor-κB. This may contribute to fetal endothelial dysfunction in diabetic pregnancies.PubMedCrossRef
53.
go back to reference •• Lappas M, Hiden U, Froehlich J et al (2011) The Role of Oxidative Stress in the Pathophysiology of Gestational Diabetes Mellitus. Antioxid Redox Signal. This is a comprehensive review on pathogenesis of gestational diabetes and the oxidative and nitrative processes occurring in the placenta in this pathology. •• Lappas M, Hiden U, Froehlich J et al (2011) The Role of Oxidative Stress in the Pathophysiology of Gestational Diabetes Mellitus. Antioxid Redox Signal. This is a comprehensive review on pathogenesis of gestational diabetes and the oxidative and nitrative processes occurring in the placenta in this pathology.
54.
go back to reference Coughlan MT, Vervaart PP, Permezel M, et al. Altered placental oxidative stress status in gestational diabetes mellitus. Placenta. 2004;25:78–84.PubMedCrossRef Coughlan MT, Vervaart PP, Permezel M, et al. Altered placental oxidative stress status in gestational diabetes mellitus. Placenta. 2004;25:78–84.PubMedCrossRef
55.
go back to reference Kwek K, Read MA, Khong TY, et al. Vasoactive effects of 8-epi-prostaglandin F(2alpha)in isolated human placental conduit and resistance blood vessels in vitro. Placenta. 2001;22:526–33.PubMedCrossRef Kwek K, Read MA, Khong TY, et al. Vasoactive effects of 8-epi-prostaglandin F(2alpha)in isolated human placental conduit and resistance blood vessels in vitro. Placenta. 2001;22:526–33.PubMedCrossRef
56.
go back to reference Lappas M, Mitton A, Permezel M. In response to oxidative stress, the expression of inflammatory cytokines and antioxidant enzymes are impaired in placenta, but not adipose tissue, of women with gestational diabetes. J Endocrinol. 2010;204:75–84.PubMedCrossRef Lappas M, Mitton A, Permezel M. In response to oxidative stress, the expression of inflammatory cytokines and antioxidant enzymes are impaired in placenta, but not adipose tissue, of women with gestational diabetes. J Endocrinol. 2010;204:75–84.PubMedCrossRef
57.
go back to reference Singh U, Devaraj S, Jialal I. Vitamin E, oxidative stress, and inflammation. Annu Rev Nutr. 2005;25:151–74.PubMedCrossRef Singh U, Devaraj S, Jialal I. Vitamin E, oxidative stress, and inflammation. Annu Rev Nutr. 2005;25:151–74.PubMedCrossRef
58.
go back to reference Bowen JM, Chamley L, Mitchell MD, et al. Cytokines of the placenta and extra-placental membranes: biosynthesis, secretion and roles in establishment of pregnancy in women. Placenta. 2002;23:239–56.PubMedCrossRef Bowen JM, Chamley L, Mitchell MD, et al. Cytokines of the placenta and extra-placental membranes: biosynthesis, secretion and roles in establishment of pregnancy in women. Placenta. 2002;23:239–56.PubMedCrossRef
59.
go back to reference Marseille-Tremblay C, Ethier-Chiasson M, Forest JC, et al. Impact of maternal circulating cholesterol and gestational diabetes mellitus on lipid metabolism in human term placenta. Mol Reprod Dev. 2008;75:1054–62.PubMedCrossRef Marseille-Tremblay C, Ethier-Chiasson M, Forest JC, et al. Impact of maternal circulating cholesterol and gestational diabetes mellitus on lipid metabolism in human term placenta. Mol Reprod Dev. 2008;75:1054–62.PubMedCrossRef
60.
go back to reference Coughlan MT, Oliva K, Georgiou HM, et al. Glucose-induced release of tumour necrosis factor-alpha from human placental and adipose tissues in gestational diabetes mellitus. Diabet Med. 2001;18:921–7.PubMedCrossRef Coughlan MT, Oliva K, Georgiou HM, et al. Glucose-induced release of tumour necrosis factor-alpha from human placental and adipose tissues in gestational diabetes mellitus. Diabet Med. 2001;18:921–7.PubMedCrossRef
61.
go back to reference Challier JC, Basu S, Bintein T, et al. Obesity in pregnancy stimulates macrophage accumulation and inflammation in the placenta. Placenta. 2008;29:274–81.PubMedCrossRef Challier JC, Basu S, Bintein T, et al. Obesity in pregnancy stimulates macrophage accumulation and inflammation in the placenta. Placenta. 2008;29:274–81.PubMedCrossRef
62.
go back to reference Lager S, Jansson N, Olsson AL, et al. Effect of IL-6 and TNF-alpha on fatty acid uptake in cultured human primary trophoblast cells. Placenta. 2011;32:121–7.PubMedCrossRef Lager S, Jansson N, Olsson AL, et al. Effect of IL-6 and TNF-alpha on fatty acid uptake in cultured human primary trophoblast cells. Placenta. 2011;32:121–7.PubMedCrossRef
63.
go back to reference Magnusson AL, Waterman IJ, Wennergren M, et al. Triglyceride hydrolase activities and expression of fatty acid binding proteins in the human placenta in pregnancies complicated by intrauterine growth restriction and diabetes. J Clin Endocrinol Metab. 2004;89:4607–14.PubMedCrossRef Magnusson AL, Waterman IJ, Wennergren M, et al. Triglyceride hydrolase activities and expression of fatty acid binding proteins in the human placenta in pregnancies complicated by intrauterine growth restriction and diabetes. J Clin Endocrinol Metab. 2004;89:4607–14.PubMedCrossRef
64.
go back to reference • Gauster M, Hiden U, vanPoppel M et al (2011) Dysregulation of placental endothelial lipase in obese women with gestational diabetes mellitus. Diabetes in press. This demonstrates that neither GDM nor obesity alone but only their combination induces changes in a placental key lipase. • Gauster M, Hiden U, vanPoppel M et al (2011) Dysregulation of placental endothelial lipase in obese women with gestational diabetes mellitus. Diabetes in press. This demonstrates that neither GDM nor obesity alone but only their combination induces changes in a placental key lipase.
65.
go back to reference Gauster M, Hiden U, Blaschitz A, et al. Dysregulation of placental endothelial lipase and lipoprotein lipase in intrauterine growth-restricted pregnancies. J Clin Endocrinol Metab. 2007;92:2256–63.PubMedCrossRef Gauster M, Hiden U, Blaschitz A, et al. Dysregulation of placental endothelial lipase and lipoprotein lipase in intrauterine growth-restricted pregnancies. J Clin Endocrinol Metab. 2007;92:2256–63.PubMedCrossRef
66.
go back to reference Varastehpour A, Radaelli T, Minium J, et al. Activation of phospholipase A2 is associated with generation of placental lipid signals and fetal obesity. J Clin Endocrinol Metab. 2006;91:248–55.PubMedCrossRef Varastehpour A, Radaelli T, Minium J, et al. Activation of phospholipase A2 is associated with generation of placental lipid signals and fetal obesity. J Clin Endocrinol Metab. 2006;91:248–55.PubMedCrossRef
67.
go back to reference •• Radaelli T, Lepercq J, Varastehpour A et al (2009) Differential regulation of genes for fetoplacental lipid pathways in pregnancy with gestational and type 1 diabetes mellitus. Am J Obstet Gynecol 201: 209 e201-209 e210. This demonstrates that GDM is a distinct diabetic entity in its effects on the placenta.CrossRef •• Radaelli T, Lepercq J, Varastehpour A et al (2009) Differential regulation of genes for fetoplacental lipid pathways in pregnancy with gestational and type 1 diabetes mellitus. Am J Obstet Gynecol 201: 209 e201-209 e210. This demonstrates that GDM is a distinct diabetic entity in its effects on the placenta.CrossRef
68.
go back to reference Jansson T, Ekstrand Y, Bjorn C, et al. Alterations in the activity of placental amino acid transporters in pregnancies complicated by diabetes. Diabetes. 2002;51:2214–9.PubMedCrossRef Jansson T, Ekstrand Y, Bjorn C, et al. Alterations in the activity of placental amino acid transporters in pregnancies complicated by diabetes. Diabetes. 2002;51:2214–9.PubMedCrossRef
69.
go back to reference Kuruvilla AG, D'Souza SW, Glazier JD, et al. Altered activity of the system A amino acid transporter in microvillous membrane vesicles from placentas of macrosomic babies born to diabetic women. J Clin Invest. 1994;94:689–95.PubMedCrossRef Kuruvilla AG, D'Souza SW, Glazier JD, et al. Altered activity of the system A amino acid transporter in microvillous membrane vesicles from placentas of macrosomic babies born to diabetic women. J Clin Invest. 1994;94:689–95.PubMedCrossRef
70.
71.
go back to reference Hahn T, Barth S, Weiss U, et al. Sustained hyperglycemia in vitro down-regulates the GLUT1 glucose transport system of cultured human term placental trophoblast: a mechanism to protect fetal development? Faseb J. 1998;12:1221–31.PubMed Hahn T, Barth S, Weiss U, et al. Sustained hyperglycemia in vitro down-regulates the GLUT1 glucose transport system of cultured human term placental trophoblast: a mechanism to protect fetal development? Faseb J. 1998;12:1221–31.PubMed
72.
go back to reference Illsley NP, Hall S, Stacey TE. The modulation of glucose transfer across the human placenta by intervillous flow rates: An in vitro perfusion study. Troph Res. 1987;2:535–44. Illsley NP, Hall S, Stacey TE. The modulation of glucose transfer across the human placenta by intervillous flow rates: An in vitro perfusion study. Troph Res. 1987;2:535–44.
73.
go back to reference Osmond DT, King RG, Brennecke SP, et al. Placental glucose transport and utilisation is altered at term in insulin-treated, gestational-diabetic patients. Diabetologia. 2001;44:1133–9.PubMedCrossRef Osmond DT, King RG, Brennecke SP, et al. Placental glucose transport and utilisation is altered at term in insulin-treated, gestational-diabetic patients. Diabetologia. 2001;44:1133–9.PubMedCrossRef
74.
go back to reference Osmond DT, Nolan CJ, King RG, et al. Effects of gestational diabetes on human placental glucose uptake, transfer, and utilisation. Diabetologia. 2000;43:576–82.PubMedCrossRef Osmond DT, Nolan CJ, King RG, et al. Effects of gestational diabetes on human placental glucose uptake, transfer, and utilisation. Diabetologia. 2000;43:576–82.PubMedCrossRef
75.
go back to reference • Colomiere M, Permezel M, Riley C et al (2009) Defective insulin signaling in placenta from pregnancies complicated by gestational diabetes mellitus. Eur J Endocrinol 160: 567–578. This compares the effects of GDM with and without obesity on insulin signaling in the placenta and shows varying effects, thus demonstrating the complexity of GDM-associated changes.PubMedCrossRef • Colomiere M, Permezel M, Riley C et al (2009) Defective insulin signaling in placenta from pregnancies complicated by gestational diabetes mellitus. Eur J Endocrinol 160: 567–578. This compares the effects of GDM with and without obesity on insulin signaling in the placenta and shows varying effects, thus demonstrating the complexity of GDM-associated changes.PubMedCrossRef
Metadata
Title
The Placenta and Gestational Diabetes Mellitus
Authors
M. Gauster
G. Desoye
M. Tötsch
U. Hiden
Publication date
01-02-2012
Publisher
Current Science Inc.
Published in
Current Diabetes Reports / Issue 1/2012
Print ISSN: 1534-4827
Electronic ISSN: 1539-0829
DOI
https://doi.org/10.1007/s11892-011-0244-5

Other articles of this Issue 1/2012

Current Diabetes Reports 1/2012 Go to the issue

Diabetes and Pregnancy (CJ Homko, Section Editor)

Diabetes-Induced Birth Defects: What Do We Know? What Can We Do?

Diabetes and Pregnancy (CJ Homko, Section Editor)

Metabolic Programming, Epigenetics, and Gestational Diabetes Mellitus

Pediatric Type 2 Diabetes (M Freemark, Section Editor)

Determining Genetic Risk Factors for Pediatric Type 2 Diabetes

Diabetes and Pregnancy (CJ Homko, Section Editor)

Gestational Diabetes: Implications for Cardiovascular Health

Diabetes and Pregnancy (CJ Homko, Section Editor)

Management of Diabetes in Pregnancy

Hospital Management of Diabetes (M Korytkowski, Section Editor)

Medical Nutrition Therapy in Hospitalized Patients with Diabetes

Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.