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Diabetic embryopathy

Summary

Diabetic embryopathy refers to congenital maldevelopments that are linked to maternal diabetes.[1] Prenatal exposure to hyperglycemia can result in spontaneous abortions, perinatal mortality, and malformations. Type 1 and Type 2 diabetic pregnancies both increase the risk of diabetes induced teratogenicity.[2] The rate of congenital malformations is similar in Type 1 and 2 mothers because of increased adiposity and the age of women with type 2 diabetes.[3] Genetic predisposition and different environmental factors both play a significant role in the development of diabetic embryopathy. Metabolic dysfunction in pregnant mothers also increases the risk of fetal malformations.[4]

Diabetic embryopathy
Fetus of mother with diabetes
Pronunciation
  • embrēˈäpəTHē
Complicationsmajor birth defects and spontaneous abortions
Causesmaternal hyperglycemia

Risk factors edit

Women with pregestational diabetes are at the highest risk for fetal malformations. The risk of congenital malformations in pregestational type 1 diabetes is directly correlated with glucose and glycohemoglobin levels in the blood. It is also inversely related to the gestational age at first exposure. The comorbidities associated with pregestational type 2 diabetes include advanced maternal age, lipid preroxidation and obesity.[5] Overweight women (BMI ≥ 25) who develop gestational diabetes have an intermediate risk for malformations. Pregnant women who have gestational diabetes but don't have prediabetic markers experience perinatal outcomes that are similar to women without diabetes.[6]

Gestational consequences edit

Malformations edit

Type 1 diabetes in pregnant women can result in malformations that affect the musculoskeletal , urogenital, and central nervous systems. Most of these malformations occur within the first 4 weeks of gestation.[7] Caudal dysgenesis is one of the most strongly associated diseases to diabetes.[8] This malformation has the highest risk for diabetic embryopathy. Infants from diabetic mothers usually have several blastogenic malformations. Diabetic embryopathy is therefore an etiological subgroup of defects of blastogenesis that present different monotopic and polytopic developmental defects.[7]

Abortion and perinatal deaths edit

Diabetic embryopathy may result in early or late spontaneous abortion and stillbirth. In maternal diabetes, 90% of pregnancy losses happen in the first trimester due to oxidative stress. Diabetic embryopathy abortions in the second-trimester are most likely due to severe birth defect, maternal metabolic derangement, placental insufficiency and fetal hypoxia due to membrane rupture.[9]

Pathogenesis edit

The development of birth defects associated with maternal hyperglycemia is multi-factorial. Environmental factors and genetic predisposition (paternal, maternal and offspring genome) are important in diabetic embryopathy. The diets of diabetic mothers impacts the rate at which malformations form in their offspring. Furthermore, there is evidence that resistance to certain malformations caused by diabetes is genetic. Epigenetics and its relationship with various environmental factors such as metabolism and diet play a significant role in teratogenesis.[10] Hyperglycemia and associated teratogenic mediators influence DNA methylation, non-coding RNA expression, histone modifications and other epigenetic regulation mechanisms. Research is focused on exploring the impact of diabetic embryopathy on methylation signatures, which could potentially serve as a diagnostic biomarker for the condition.[11]

Prevention edit

Preconception edit

The probability of major birth defects in offspring of mothers with diabetes is 0.7-4.4% for glycohemoglobin levels <7%. For glycohemoglobin levels >10% the probability of major birth defects is 16.1-100% with an average of 26.6%.[5] The National Institute of Health and Clinical Excellence in the UK indicated that glycohemoglobin levels <6.1% are correlated with the lowest risk of malformations while the reproductive risks are higher in women above this threshold and prohibitive for glycohemoglobin levels >10%.[12]

Consumption of folic acid and antioxidant substances before fertilization result in a reduced rate of malformations in the offspring of mothers with diabetes.[12] Antioxidants such as lipoic acid, vitamin C, and vitamin E, increase the probability of favorable prenatal outcomes in offspring of diabetic mothers because oxidative stress is a teratogenic mediator of hyperglycemia in mothers with diabetes.[13][14]

After fertilization edit

Optimal weight and glycemic management encourage good outcomes because diabetes has the potential to influence the mother and fetus during the entire pregnancy. The integrity of embryofetal development and placental function can be monitored by fetal echocardiography and ultrasound scanning.[9]

See also edit

References edit

  1. ^ Eriksson, Ulf J.; Wentzel, Parri (2016). "The status of diabetic embryopathy". Upsala Journal of Medical Sciences. 121 (2): 96–112. doi:10.3109/03009734.2016.1165317. ISSN 0300-9734. PMC 4900070. PMID 27117607.
  2. ^ Balsells, Montserrat; García-Patterson, A.; Gich, I.; Corcoy, R. (2009). "Maternal and fetal outcome in women with type 2 versus type 1 diabetes mellitus: a systematic review and metaanalysis". The Journal of Clinical Endocrinology and Metabolism. 94 (11): 4284–4291. doi:10.1210/jc.2009-1231. ISSN 1945-7197. PMID 19808847.
  3. ^ Rankin, J.; Tennant, P. W. G.; Stothard, K. J.; Bythell, M.; Summerbell, C. D.; Bell, R. (2010). "Maternal body mass index and congenital anomaly risk: a cohort study". International Journal of Obesity. 34 (9): 1371–1380. doi:10.1038/ijo.2010.66. ISSN 1476-5497. PMID 20368710.
  4. ^ Miller, Edith; Hare, John W.; Cloherty, John P.; Dunn, Peter J.; Gleason, Ray E.; Soeldner, J. Stuart; Kitzmiller, John L. (1981-05-28). "Elevated Maternal Hemoglobin A1C in Early Pregnancy and Major Congenital Anomalies in Infants of Diabetic Mothers". New England Journal of Medicine. 304 (22): 1331–1334. doi:10.1056/NEJM198105283042204. ISSN 0028-4793. PMID 7012627.
  5. ^ a b Kitzmiller, John L.; Wallerstein, Robert; Correa, Adolfo; Kwan, Saiyin (2010). "Preconception care for women with diabetes and prevention of major congenital malformations". Birth Defects Research Part A: Clinical and Molecular Teratology. 88 (10): 791–803. doi:10.1002/bdra.20734. ISSN 1542-0760. PMID 20890938.
  6. ^ Correa, Adolfo; Gilboa, Suzanne M.; Besser, Lilah M.; Botto, Lorenzo D.; Moore, Cynthia A.; Hobbs, Charlotte A.; Cleves, Mario A.; Riehle-Colarusso, Tiffany J.; Waller, D. Kim; Reece, E. Albert (2008). "Diabetes mellitus and birth defects". American Journal of Obstetrics and Gynecology. 199 (3): 237.e1–237.e9. doi:10.1016/j.ajog.2008.06.028. ISSN 0002-9378. PMC 4916956. PMID 18674752.
  7. ^ a b Opitz, John M.; Zanni, Ginevra; Reynolds, James F.; Gilbert‐Barness, Enid (2002). "Defects of blastogenesis". American Journal of Medical Genetics. 115 (4): 269–286. doi:10.1002/ajmg.10983. ISSN 1096-8628. PMID 12503120.
  8. ^ Martínez‐Frías, María Luisa (1994). "Epidemiological analysis of outcomes of pregnancy in diabetic mothers: Identification of the most characteristic and most frequent congenital anomalies". American Journal of Medical Genetics. 51 (2): 108–113. doi:10.1002/ajmg.1320510206. ISSN 1096-8628. PMID 8092185.
  9. ^ a b Castori, M. (2013). "Diabetic Embryopathy: A Developmental Perspective from Fertilization to Adulthood". Molecular Syndromology. 4 (1–2): 74–86. doi:10.1159/000345205. ISSN 1661-8769. PMC 3638774. PMID 23653578.
  10. ^ Salbaum, J. Michael; Kappen, Claudia (2010). "Neural Tube Defect Genes and Maternal Diabetes during Pregnancy". Birth Defects Research. Part A, Clinical and Molecular Teratology. 88 (8): 601–611. doi:10.1002/bdra.20680. ISSN 1542-0752. PMC 3509193. PMID 20564432.
  11. ^ Schulze, Katharina V.; Bhatt, Amit; Azamian, Mahshid S.; Sundgren, Nathan C.; Zapata, Gladys E.; Hernandez, Patricia; Fox, Karin; Kaiser, Jeffrey R.; Belmont, John W.; Hanchard, Neil A. (2019-04-17). "Aberrant DNA methylation as a diagnostic biomarker of diabetic embryopathy". Genetics in Medicine. 21 (11): 2453–2461. doi:10.1038/s41436-019-0516-z. ISSN 1530-0366. PMID 30992551.
  12. ^ a b Kitzmiller, John L.; Wallerstein, Robert; Correa, Adolfo; Kwan, Saiyin (2010). "Preconception care for women with diabetes and prevention of major congenital malformations". Birth Defects Research. Part A, Clinical and Molecular Teratology. 88 (10): 791–803. doi:10.1002/bdra.20734. ISSN 1542-0760. PMID 20890938.
  13. ^ Sugimura, Y.; Murase, T.; Kobayashi, K.; Oyama, K.; Hayasaka, S.; Kanou, Y.; Oiso, Y.; Murata, Y. (2009). "Alpha-lipoic acid reduces congenital malformations in the offspring of diabetic mice". Diabetes/Metabolism Research and Reviews. 25 (3): 287–294. doi:10.1002/dmrr.947. ISSN 1520-7560. PMID 19242917. S2CID 5082464.
  14. ^ Gäreskog, Mattias; Eriksson, Ulf J.; Wentzel, Parri (2006). "Combined supplementation of folic acid and vitamin E diminishes diabetes-induced embryotoxicity in rats". Birth Defects Research. Part A, Clinical and Molecular Teratology. 76 (6): 483–490. doi:10.1002/bdra.20278. ISSN 1542-0752. PMID 16933212.

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