Zusammenfassung
Für eine optimale Entwicklung des Fetus ist ein adäquater Austausch von Nährstoffen über die Plazenta unabdingbar. Die Schwangerschaft stellt ein höchst sensitives Zeitfenster dar, in dem Fehlernährung, Adipositas sowie damit einhergehende Stoffwechselveränderungen wie Diabetes mellitus die fetale und kindliche Gesundheit lebenslang prägen können. Eine entscheidende Rolle in diesem Kontext übernimmt die Plazenta, welche als erstes maternofetales Kontaktorgan zum einen die durch mütterliches Übergewicht/Adipositas und/oder Gestationsdiabetes veränderten Nährstoffe an den Fetus weitergibt, zum anderen auf in diesem Zusammenhang veränderte Nährstofftransportmechanismen zurückgreifen muss. Der kindliche Organismus wird durch diese unphysiologischen Bedingungen geprägt. Eine solche Fehlprogrammierung der kindlichen Organfunktionen und Stoffwechselregulationen stellt die Basis für sich später bei den Nachkommen entwickelnde chronische Krankheiten dar wie Adipositas, Diabetes mellitus oder kardiovaskuläre Erkrankungen. In diesem Beitrag wird ein aktueller Überblick über Ernährungsempfehlungen in der Schwangerschaft, Funktion und Nährstofftransport in der Plazenta, maternofetale Transportprozesse sowie Aspekte der plazentaren immunologischen Prozesse gegeben – stets mit speziellem Fokus auf Veränderungen bei Gestationsdiabetes und Adipositas.
Abstract
An adequate exchange of nutrients via the placenta is of particular importance for optimal growth of an unborn fetus. Therefore, pregnancy represents a highly sensitive time frame where an inadequate or unbalanced diet together with overweight/obesity or related metabolic conditions such as gestational diabetes can impact infant health for life. Of particular importance is the placenta as the first fetal–maternal contact organ. Both nutrient availability and placental nutrient transporters are characterized by the obesogenic/diabetic phenotype of the mother and impact fetal development. Disturbed fetal programming of organ function and metabolic processes will increase the risk for later development of chronic diseases such as obesity, type 2 diabetes or cardiovascular disease. In this review, current dietary guidelines during pregnancy, function and nutrient transport in the placenta, fetal–maternal exchange, and aspects involving placental immunological pathways are presented with a particular focus on changes induced by obesity and/or gestational diabetes.
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Literatur
Bandres-Meriz J, Dieberger AM, Hoch D et al (2020) Maternal obesity affects the glucose-insulin axis during the first trimester of human pregnancy. Front Endocrinol (lausanne) 11:566673
Bandres-Meriz J, Majali-Martinez A, Hoch D et al (2021) Maternal C‑peptide and insulin sensitivity, but not BMI, associate with fatty acids in the first trimester of pregnancy. Int J Mol Sci 22(19):10422. https://doi.org/10.3390/ijms221910422
Battaglia FC (1989) An update of fetal and placental metabolism: carbohydrate and amino acids. Biol Neonate 55:347–354
Berry ASF, Pierdon MK, Misic AM et al (2021) Remodeling of the maternal gut microbiome during pregnancy is shaped by parity. Microbiome 9:146
Bianchi DW (2004) Circulating fetal DNA: its origin and diagnostic potential—a review. Placenta Suppl A:S93–S101
Braga A, Neves E, Guimaraes J et al (2022) Th17/Regulatory T cells ratio evolution: A prospective study in a group of healthy pregnant women. J Reprod Immunol 149:103468
Brett KE, Ferraro ZM, Yockell-Lelievre J et al (2014) Maternal-fetal nutrient transport in pregnancy pathologies: the role of the placenta. Int J Mol Sci 15:16153–16185
Burton GJ, Cindrova-Davies T, Turco MY (2020) Review: Histotrophic nutrition and the placental—endometrial dialogue during human early pregnancy. Placenta 102:21–26
Busse M, Campe KJ, Nowak D et al (2019) IL-10 producing B cells rescue mouse fetuses from inflammation-driven fetal death and are able to modulate T cell immune responses. Sci Rep 9:9335
Busse M, Campe KJ, Redlich A et al (2020) Regulatory B cells are decreased and impaired in their function in peripheral maternal blood in pre-term birth. Front Immunol 11:386
Carrasco-Wong I, Moller A, Giachini FR et al (2020) Placental structure in gestational diabetes mellitus. Biochim Biophys Acta Mol Basis Dis 1866:165535
Cervar M, Blaschitz A, Dohr G et al (1999) Paracrine regulation of distinct trophoblast functions in vitro by placental macrophages. Cell Tissue Res 295:297–305
Challier JC, Basu S, Bintein T et al (2008) Obesity in pregnancy stimulates macrophage accumulation and inflammation in the placenta. Placenta 29:274–281
American Diabetes Association Professional Practice Committee, Draznin B, Aroda VR, Bakris G et al (2021) 15. Management of Diabetes in Pregnancy: Standards of Medical Care in Diabetes 2022. Diabetes Care 45:S232–S243
Davidson SJ, Barrett HL, Price SA et al (2021) Probiotics for preventing gestational diabetes. Cochrane Database Syst Rev 4:CD9951
Desoye G (2018) The human placenta in diabetes and obesity: friend or foe? The 2017 Norbert Freinkel award lecture. Diabetes Care 41:1362–1369
Desoye G, Carter AM (2022) Fetoplacental oxygen homeostasis in pregnancies with maternal diabetes mellitus and obesity. Nat Rev Endocrinol 18:593–607
Desoye G, Cervar-Zivkovic M (2020) Diabetes mellitus, obesity, and the placenta. Obstet Gynecol Clin North Am 47:65–79
Desoye G, Herrera E (2021) Adipose tissue development and lipid metabolism in the human fetus: The 2020 perspective focusing on maternal diabetes and obesity. Prog Lipid Res 81:101082
Desoye G, Nolan CJ (2016) The fetal glucose steal: an underappreciated phenomenon in diabetic pregnancy. Diabetologia 59:1089–1094
Desoye G, Shafrir E (1994) Placental metabolism and its regulation in health and diabetes. Mol Aspects Med 15:505–682
Desoye G, Wells JCK (2021) Pregnancies in diabetes and obesity: the capacity-load model of placental adaptation. Diabetes 70:823–830
Deutsche Gesellschaft für Ernährung (DGE), Österreichische Gesellschaft für Ernährung (ÖGE), Schweizerische Gesellschaft für Ernährung (SGE) (Hrsg) (2019) Referenzwerte für die Nährstoffzufuhr, 2. Aufl. Bonn (5. aktualisierte Ausgabe)
Faas MM, De Vos P (2017) Uterine NK cells and macrophages in pregnancy. Placenta 56:44–52
Fettke F, Schumacher A, Canellada A et al (2016) Maternal and fetal mechanisms of B cell regulation during pregnancy: human Chorionic Gonadotropin stimulates B cells to produce IL-10 while Alpha-Fetoprotein drives them into Apoptosis. Front Immunol 7:495
Figueiredo AS, Schumacher A (2016) The T helper type 17/regulatory T cell paradigm in pregnancy. Immunology 148:13–21
Gaccioli F, Lager S (2016) Placental nutrient transport and intrauterine growth restriction. Front Physiol 7:40
Ganal-Vonarburg SC, Fuhrer T, Gomez De Aguero M (2017) Maternal microbiota and antibodies as advocates of neonatal health. Gut Microbes 8:479–485
Institut für Qualität und transparenz im Gesundheitswesen (IQTiG) (2022) Länderbericht Perinatalmedizin: Geburtshilfe. Erfassungsjahr 2021. DEQS_PM-GEBH_2021_LAW_ba_2022-06-30.pdf.
Gil-Sanchez A, Koletzko B, Larque E (2012) Current understanding of placental fatty acid transport. Curr Opin Clin Nutr Metab Care 15:265–272
Gomez De Aguero M, Ganal-Vonarburg SC, Fuhrer T et al (2016) The maternal microbiota drives early postnatal innate immune development. Science 351:1296–1302
Hellmuth C, Lindsay KL, Uhl O et al (2017) Association of maternal prepregnancy BMI with metabolomic profile across gestation. Int J Obes (lond) 41:159–169
Herrera E, Desoye G (2016) Maternal and fetal lipid metabolism under normal and gestational diabetic conditions. Horm Mol Biol Clin Investig 26:109–127
Hirschmugl B, Perazzolo S, Sengers BG et al (2021) Placental mobilization of free fatty acids contributes to altered materno-fetal transfer in obesity. Int J Obes (lond) 45:1114–1123
Illsley NP, Baumann MU (2020) Human placental glucose transport in fetoplacental growth and metabolism. Biochim Biophys Acta Mol Basis Dis 1866:165359
Imai A, Fujimoto E, Tamura K et al (2019) A maternal high-fat diet may accelerate adipo-immunologic aging in offspring. Life Sci 219:100–108
Jansson N, Rosario FJ, Gaccioli F et al (2013) Activation of placental mTOR signaling and amino acid transporters in obese women giving birth to large babies. J Clin Endocrinol Metab 98:105–113
Junge KM, Bauer T, Geissler S et al (2016) Increased vitamin D levels at birth and in early infancy increase offspring allergy risk-evidence for involvement of epigenetic mechanisms. J Allergy Clin Immunol 137:610–613
Junge KM, Leppert B, Jahreis S et al (2018) MEST mediates the impact of prenatal bisphenol A exposure on long-term body weight development. Clin Epigenetics 10:58
Kelly AC, Powell TL, Jansson T (2020) Placental function in maternal obesity. Clin Sci (lond) 134:961–984
Kermack AJ, Finn-Sell S, Cheong YC et al (2015) Amino acid composition of human uterine fluid: association with age, lifestyle and gynaecological pathology. Hum Reprod 30:917–924
Krause JL, Engelmann B, Nunes Da Rocha U et al (2022) MAIT cell activation is reduced by direct and microbiota-mediated exposure to bisphenols. Environ Int 158:106985
Leppert B, Junge KM, Roder S et al (2018) Early maternal perceived stress and children’s BMI: longitudinal impact and influencing factors. Bmc Public Health 18:1211
Leppert B, Strunz S, Seiwert B et al (2020) Maternal paraben exposure triggers childhood overweight development. Nat Commun 11:561
Lindsay KL, Hellmuth C, Uhl O et al (2015) Longitudinal metabolomic profiling of amino acids and lipids across healthy pregnancy. PLoS ONE 10:e145794
Margni RA, Zenclussen AC (2001) During pregnancy, in the context of a Th2-type cytokine profile, serum IL‑6 levels might condition the quality of the synthesized antibodies. Am J Reprod Immunol 46:181–187
Medawar PB (1953) Some immunological and endocrinological problems raised by the evolution of viviparity in vertebrates. Symp Soc Exp Biol 7:320–338
Mijatovic-Vukas J, Capling L, Cheng S et al (2018) Associations of diet and physical activity with risk for gestational diabetes mellitus: a systematic review and meta-analysis. Nutrients 10(6):698. https://doi.org/10.3390/nu10060698
Mor G, Aldo P, Alvero AB (2017) The unique immunological and microbial aspects of pregnancy. Nat Rev Immunol 17:469–482
Nakajima A, Kaga N, Nakanishi Y et al (2017) Maternal high fiber diet during pregnancy and lactation influences regulatory T cell differentiation in offspring in mice. J Immunol 199:3516–3524
Ning F, Liu H, Lash GE (2016) The role of decidual Macrophages during normal and pathological pregnancy. Am J Reprod Immunol 75:298–309
Poloski E, Oettel A, Ehrentraut S et al (2016) JEG‑3 Trophoblast cells producing human Chorionic Gonadotropin promote conversion of human CD4+FOXP3- T cells into CD4+FOXP3+ regulatory T cells and foster T cell suppressive activity. Biol Reprod 94:106
E‑Lacerda RR, Teixeira CJ, Bordin S et al (2019) Maternal obesity in mice exacerbates the allergic inflammatory response in the airways of male offspring. Nutrients 11(12):2902. https://doi.org/10.3390/nu11122902
Rasmussen KM, Yaktine AL (2009) Weight gain during pregnancy: reexamining the guidelines Washington (DC)
Rasmussen L, Poulsen CW, Kampmann U et al (2020) Diet and healthy lifestyle in the management of gestational diabetes mellitus. Nutrients 12(10):3050. https://doi.org/10.3390/nu12103050
Rogers LM, Serezani CH, Eastman AJ et al (2020) Palmitate induces apoptotic cell death and inflammasome activation in human placental macrophages. Placenta 90:45–51
Rolle L, Memarzadeh Tehran M, Morell-Garcia A et al (2013) Cutting edge: IL-10-producing regulatory B cells in early human pregnancy. Am J Reprod Immunol 70:448–453
Schliefsteiner C, Hirschmugl B, Kopp S et al (2017) Maternal gestational diabetes mellitus increases placental and foetal lipoprotein-associated Phospholipase A2 which might exert protective functions against oxidative stress. Sci Rep 7:12628
Schliefsteiner C, Peinhaupt M, Kopp S et al (2017) Human placental Hofbauer cells maintain an anti-inflammatory M2 phenotype despite the presence of gestational diabetes mellitus. Front Immunol 8:888
Schmorl G (1893) Pathologisch-anatomische Untersuchungen über Puerperal-Eklampsie. F.C.W. Vogel, Leipzig
Schumacher A, Sharkey DJ, Robertson SA et al (2018) Immune cells at the fetomaternal interface: how the microenvironment modulates immune cells to foster fetal development. J Immunol 201:325–334
Segura MT, Demmelmair H, Krauss-Etschmann S et al (2017) Maternal BMI and gestational diabetes alter placental lipid transporters and fatty acid composition. Placenta 57:144–151
Simmons D (2019) GDM and nutrition-answered and unanswered questions-there’s more work to do! Nutrients 11(8):1940. https://doi.org/10.3390/nu11081940
Sosenko IR, Kitzmiller JL, Loo SW et al (1979) The infant of the diabetic mother: correlation of increased cord C‑peptide levels with macrosomia and hypoglycemia. N Engl J Med 301:859–862
Vaughan OR, Rosario FJ, Powell TL et al (2017) Regulation of placental amino acid transport and fetal growth. Prog Mol Biol Transl Sci 145:217–251
Workalemahu T, Grantz KL, Grewal J et al (2018) Genetic and environmental influences on fetal growth vary during sensitive periods in pregnancy. Sci Rep 8:7274
Zakaria ZZ, Al-Rumaihi S, Al-Absi RS et al (2022) Physiological changes and interactions between microbiome and the host during pregnancy. Front Cell Infect Microbiol 12:824925
Zenclussen AC, Gerlof K, Zenclussen ML et al (2005) Abnormal T‑cell reactivity against paternal antigens in spontaneous abortion: adoptive transfer of pregnancy-induced CD4+CD25+ T regulatory cells prevents fetal rejection in a murine abortion model. Am J Pathol 166:811–822
Zulu MZ, Martinez FO, Gordon S et al (2019) The elusive role of placental Macrophages: the Hofbauer cell. J Innate Immun 11:447–456
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Junge, K.M., Zenclussen, A.C. & Desoye, G. (Über‑)Ernährung und Einfluss auf die Funktion der Plazenta. Diabetologie 19, 747–757 (2023). https://doi.org/10.1007/s11428-023-01087-4
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DOI: https://doi.org/10.1007/s11428-023-01087-4