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. 1988 Oct;63(10 Spec No):1119–1121. doi: 10.1136/adc.63.10_spec_no.1119

The fetus of the diabetic mother: growth and malformations.

I Swenne 1
PMCID: PMC1590211  PMID: 3058050

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bhaumick B., Dawson E. P., Bala R. M. The effects of insulin-like growth factor-I and insulin on placental lactogen production by human term placental explants. Biochem Biophys Res Commun. 1987 Apr 29;144(2):674–682. doi: 10.1016/s0006-291x(87)80018-9. [DOI] [PubMed] [Google Scholar]
  2. Brownscheidle C. M., Davis D. L. Diabetes in pregnancy: a preliminary study of the pancreas, placenta and malformations in the BB Wistar rat. Placenta Suppl. 1981;3:203–216. [PubMed] [Google Scholar]
  3. D'Ercole A. J., Applewhite G. T., Underwood L. E. Evidence that somatomedin is synthesized by multiple tissues in the fetus. Dev Biol. 1980 Mar 15;75(2):315–328. doi: 10.1016/0012-1606(80)90166-9. [DOI] [PubMed] [Google Scholar]
  4. Endo A. Teratogenesis in diabetic mice treated with alloxan prior to conception. Arch Environ Health. 1966 Apr;12(4):492–500. doi: 10.1080/00039896.1966.10664415. [DOI] [PubMed] [Google Scholar]
  5. Eriksson U. J., Dahlström V. E., Styrud J. Metabolically determined teratogenesis: malformations and maternal diabetes. Biochem Soc Trans. 1985 Feb;13(1):79–82. doi: 10.1042/bst0130079. [DOI] [PubMed] [Google Scholar]
  6. Eriksson U. J. Importance of genetic predisposition and maternal environment for the occurrence of congenital malformations in offspring of diabetic rats. Teratology. 1988 Apr;37(4):365–374. doi: 10.1002/tera.1420370410. [DOI] [PubMed] [Google Scholar]
  7. Eriksson U., Andersson A., Efendić S., Elde R., Hellerström C. Diabetes in pregnancy: effects on the foetal and newborn rat with particular regard to body weight, serum insulin concentration and pancreatic contents of insulin, glucagon and somatostatin. Acta Endocrinol (Copenh) 1980 Jul;94(3):354–364. doi: 10.1530/acta.0.0940354. [DOI] [PubMed] [Google Scholar]
  8. Eriksson U., Swenne I. Diabetes in pregnancy: growth of the fetal pancreatic B cells in the rat. Biol Neonate. 1982;42(5-6):239–248. doi: 10.1159/000241605. [DOI] [PubMed] [Google Scholar]
  9. Freinkel N., Lewis N. J., Akazawa S., Roth S. I., Gorman L. The honeybee syndrome - implications of the teratogenicity of mannose in rat-embryo culture. N Engl J Med. 1984 Jan 26;310(4):223–230. doi: 10.1056/NEJM198401263100404. [DOI] [PubMed] [Google Scholar]
  10. Hill D. J., Crace C. J., Milner R. D. Incorporation of [3H]thymidine by isolated fetal myoblasts and fibroblasts in response to human placental lactogen (HPL): possible mediation of HPL action by release of immunoreactive SM-C. J Cell Physiol. 1985 Nov;125(2):337–344. doi: 10.1002/jcp.1041250224. [DOI] [PubMed] [Google Scholar]
  11. Hill D. J., Milner R. D. Insulin as a growth factor. Pediatr Res. 1985 Sep;19(9):879–886. doi: 10.1203/00006450-198509000-00001. [DOI] [PubMed] [Google Scholar]
  12. Horton W. E., Jr, Sadler T. W. Effects of maternal diabetes on early embryogenesis. Alterations in morphogenesis produced by the ketone body, B-hydroxybutyrate. Diabetes. 1983 Jul;32(7):610–616. doi: 10.2337/diab.32.7.610. [DOI] [PubMed] [Google Scholar]
  13. Kakita K., Giddings S. J., Rotwein P. S., Permutt M. A. Insulin gene expression in the developing rat pancreas. Diabetes. 1983 Aug;32(8):691–696. doi: 10.2337/diab.32.8.691. [DOI] [PubMed] [Google Scholar]
  14. Kalkhoff R. K., Kandaraki E., Morrow P. G., Mitchell T. H., Kelber S., Borkowf H. I. Relationship between neonatal birth weight and maternal plasma amino acid profiles in lean and obese nondiabetic women and in type I diabetic pregnant women. Metabolism. 1988 Mar;37(3):234–239. doi: 10.1016/0026-0495(88)90101-1. [DOI] [PubMed] [Google Scholar]
  15. Liu L., Russell S. M., Nicoll C. S. Growth and differentiation of transplanted rat embryos in intact, diabetic and hypophysectomized hosts: comparison with their growth in situ. Biol Neonate. 1987;52(6):307–316. doi: 10.1159/000242726. [DOI] [PubMed] [Google Scholar]
  16. Miller E., Hare J. W., Cloherty J. P., Dunn P. J., Gleason R. E., Soeldner J. S., Kitzmiller J. L. Elevated maternal hemoglobin A1c in early pregnancy and major congenital anomalies in infants of diabetic mothers. N Engl J Med. 1981 May 28;304(22):1331–1334. doi: 10.1056/NEJM198105283042204. [DOI] [PubMed] [Google Scholar]
  17. Mills J. L., Knopp R. H., Simpson J. L., Jovanovic-Peterson L., Metzger B. E., Holmes L. B., Aarons J. H., Brown Z., Reed G. F., Bieber F. R. Lack of relation of increased malformation rates in infants of diabetic mothers to glycemic control during organogenesis. N Engl J Med. 1988 Mar 17;318(11):671–676. doi: 10.1056/NEJM198803173181104. [DOI] [PubMed] [Google Scholar]
  18. Milner R. D., Hill D. J. Interaction between endocrine and paracrine peptides in prenatal growth control. Eur J Pediatr. 1987 Mar;146(2):113–122. doi: 10.1007/BF02343214. [DOI] [PubMed] [Google Scholar]
  19. Olofsson P., Liedholm H., Sartor G., Sjöberg N. O., Svenningsen N. W., Ursing D. Diabetes and pregnancy. A 21-year Swedish material. Acta Obstet Gynecol Scand Suppl. 1984;122:3–62. [PubMed] [Google Scholar]
  20. Otonkoski T., Andersson S., Knip M., Simell O. Maturation of insulin response to glucose during human fetal and neonatal development. Studies with perifusion of pancreatic isletlike cell clusters. Diabetes. 1988 Mar;37(3):286–291. doi: 10.2337/diab.37.3.286. [DOI] [PubMed] [Google Scholar]
  21. PEDERSEN J. Weight and length at birth of infants of diabetic mothers. Acta Endocrinol (Copenh) 1954 Aug;16(4):330–342. doi: 10.1530/acta.0.0160330. [DOI] [PubMed] [Google Scholar]
  22. Pedersen J. F., Molsted-Pedersen L. Early fetal growth delay detected by ultrasound marks increased risk of congenital malformation in diabetic pregnancy. Br Med J (Clin Res Ed) 1981 Jul 25;283(6286):269–271. doi: 10.1136/bmj.283.6286.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Pedersen J. F., Mølsted-Pedersen L. Early growth retardation in diabetic pregnancy. Br Med J. 1979 Jan 6;1(6155):18–19. doi: 10.1136/bmj.1.6155.18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Sadler T. W., Horton W. E., Warner C. W. Whole embryo culture: a screening technique for teratogens? Teratog Carcinog Mutagen. 1982;2(3-4):243–253. doi: 10.1002/1520-6866(1990)2:3/4<243::aid-tcm1770020306>3.0.co;2-u. [DOI] [PubMed] [Google Scholar]
  25. Sadler T. W., Hunter E. S., 3rd Hypoglycemia: how little is too much for the embryo? Am J Obstet Gynecol. 1987 Jul;157(1):190–193. doi: 10.1016/s0002-9378(87)80378-2. [DOI] [PubMed] [Google Scholar]
  26. Smith E. P., Sadler T. W., D'Ercole A. J. Somatomedins/insulin-like growth factors, their receptors and binding proteins are present during mouse embryogenesis. Development. 1987 Sep;101(1):73–82. doi: 10.1242/dev.101.1.73. [DOI] [PubMed] [Google Scholar]
  27. Swenne I., Hill D. J., Strain A. J., Milner R. D. Effects of human placental lactogen and growth hormone on the production of insulin and somatomedin C/insulin-like growth factor I by human fetal pancreas in tissue culture. J Endocrinol. 1987 May;113(2):297–303. doi: 10.1677/joe.0.1130297. [DOI] [PubMed] [Google Scholar]
  28. Tallarigo L., Giampietro O., Penno G., Miccoli R., Gregori G., Navalesi R. Relation of glucose tolerance to complications of pregnancy in nondiabetic women. N Engl J Med. 1986 Oct 16;315(16):989–992. doi: 10.1056/NEJM198610163151603. [DOI] [PubMed] [Google Scholar]

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