Literature DB >> 23301121

Frontiers in research on maternal diabetes-induced neural tube defects: Past, present and future.

Shyamasundar Sukanya1, Boon Huat Bay, Samuel Sam Wah Tay, S Thameem Dheen.   

Abstract

Diabetes mellitus rightly regarded as a silent-epidemic is continually on the rise and estimated to have a global prevalence of 6.4 % as of 2010. Diabetes during pregnancy is a well known risk factor for congenital anomalies in various organ systems that contribute to neonatal mortality, including cardiovascular, gastrointestinal, genitourinary and neurological systems, among which the neural tube defects are frequently reported. Over the last two to three decades, several groups around the world have focussed on identifying the molecular cues and cellular changes resulting in altered gene expression and the morphological defects and in diabetic pregnancy. In recent years, the focus has gradually shifted to looking at pre-programmed changes and activation of epigenetic mechanisms that cause altered gene expression. While several theories such as oxidative stress, hypoxia, and apoptosis triggered due to hyperglycemic conditions have been proposed and proven for being the cause for these defects, the exact mechanism or the link between how high glucose can alter gene expression/transcriptome and activate epigenetic mechanisms is largely unknown. Although preconceptual control of diabetes, (i.e., managing glucose levels during pregnancy), and in utero therapies has been proposed as an effective solution for managing diabetes during pregnancy, the impact that a fluctuating glycemic index can have on foetal development has not been evaluated in detail. A tight glycemic control started before pregnancy has shown to reduce the incidence of congenital abnormalities in diabetic mothers. On the other hand, a tight glycemic control after organogenesis and embryogenesis have begun may prove insufficient to prevent or reverse the onset of congenital defects. The importance of determining the extent to which glycemic levels in diabetic mothers should be regulated is critical as foetal hypoglycemia has also been shown to be teratogenic. Finally, the major question remaining is if this whole issue is negligible and not worthy of investigation as the efficient management of diabetes during pregnancy is well in place in many countries.

Entities:  

Keywords:  Congenital anomalies; Epigenetics; Epigenome; Hyperglycemia; Hypoxia; Maternal diabetes; Neural stem cells; Neural tube defects; Oxidative stress

Year:  2012        PMID: 23301121      PMCID: PMC3538985          DOI: 10.4239/wjd.v3.i12.196

Source DB:  PubMed          Journal:  World J Diabetes        ISSN: 1948-9358


  63 in total

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Authors:  O Langer; D L Conway
Journal:  J Matern Fetal Med       Date:  2000 Jan-Feb

2.  Antioxidants diminish developmental damage induced by high glucose and cyclooxygenase inhibitors in rat embryos in vitro.

Authors:  P Wentzel; U J Eriksson
Journal:  Diabetes       Date:  1998-04       Impact factor: 9.461

3.  Free radical scavenging enzymes in fetal dysmorphogenesis among offspring of diabetic rats.

Authors:  E Sivan; Y C Lee; Y K Wu; E A Reece
Journal:  Teratology       Date:  1997-12

4.  Evidence that elevated glucose causes altered gene expression, apoptosis, and neural tube defects in a mouse model of diabetic pregnancy.

Authors:  E L Fine; M Horal; T I Chang; G Fortin; M R Loeken
Journal:  Diabetes       Date:  1999-12       Impact factor: 9.461

Review 5.  Development of the choroid plexus.

Authors:  K M Dziegielewska; J Ek; M D Habgood; N R Saunders
Journal:  Microsc Res Tech       Date:  2001-01-01       Impact factor: 2.769

6.  Significance of glutathione-dependent antioxidant system in diabetes-induced embryonic malformations.

Authors:  H Sakamaki; S Akazawa; M Ishibashi; K Izumino; H Takino; H Yamasaki; Y Yamaguchi; S Goto; Y Urata; T Kondo; S Nagataki
Journal:  Diabetes       Date:  1999-05       Impact factor: 9.461

Review 7.  Genotoxicity and diabetic embryopathy: impaired expression of developmental control genes as a cause of defective morphogenesis.

Authors:  T I Chang; M R Loeken
Journal:  Semin Reprod Endocrinol       Date:  1999

Review 8.  Spontaneous abortions and major malformations in women with diabetes mellitus.

Authors:  M F Greene
Journal:  Semin Reprod Endocrinol       Date:  1999

9.  Prenatal dietary choline supplementation decreases the threshold for induction of long-term potentiation in young adult rats.

Authors:  G K Pyapali; D A Turner; C L Williams; W H Meck; H S Swartzwelder
Journal:  J Neurophysiol       Date:  1998-04       Impact factor: 2.714

Review 10.  Pregnancy in diabetes.

Authors:  E A Ryan
Journal:  Med Clin North Am       Date:  1998-07       Impact factor: 5.456

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  9 in total

1.  Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype.

Authors:  Karen L Soldano; Melanie E Garrett; Heidi L Cope; J Michael Rusnak; Nathen J Ellis; Kaitlyn L Dunlap; Marcy C Speer; Simon G Gregory; Allison E Ashley-Koch
Journal:  Birth Defects Res B Dev Reprod Toxicol       Date:  2013-12-09

2.  Oxidative stress-induced miR-27a targets the redox gene nuclear factor erythroid 2-related factor 2 in diabetic embryopathy.

Authors:  Yang Zhao; Daoyin Dong; E Albert Reece; Ashley R Wang; Peixin Yang
Journal:  Am J Obstet Gynecol       Date:  2017-11-01       Impact factor: 8.661

3.  Influence of Glucose Concentration on Colony-Forming Efficiency and Biological Performance of Primary Human Tissue-Derived Progenitor Cells.

Authors:  Venkata P Mantripragada; Ryan Kaplevatsky; Wes A Bova; Cynthia Boehm; Nancy A Obuchowski; Ronald J Midura; George F Muschler
Journal:  Cartilage       Date:  2020-02-26       Impact factor: 3.117

4.  Activated ClC-2 Inhibits p-Akt to Repress Myelination in GDM Newborn Rats.

Authors:  Feixiang He; Yuchen Peng; Zhi Yang; Zilu Ge; Yanping Tian; Teng Ma; Hongli Li
Journal:  Int J Biol Sci       Date:  2017-01-15       Impact factor: 6.580

5.  Identification of histone malonylation in the human fetal brain and implications for diabetes-induced neural tube defects.

Authors:  Qin Zhang; Tanxi Cai; Zonghui Xiao; Dan Li; Chunlei Wan; Xiaodai Cui; Baoling Bai
Journal:  Mol Genet Genomic Med       Date:  2020-07-15       Impact factor: 2.183

6.  High glucose environment inhibits cranial neural crest survival by activating excessive autophagy in the chick embryo.

Authors:  Xiao-Yu Wang; Shuai Li; Guang Wang; Zheng-Lai Ma; Manli Chuai; Liu Cao; Xuesong Yang
Journal:  Sci Rep       Date:  2015-12-16       Impact factor: 4.379

7.  High glucose suppresses embryonic stem cell differentiation into cardiomyocytes : High glucose inhibits ES cell cardiogenesis.

Authors:  Penghua Yang; Xi Chen; Sunjay Kaushal; E Albert Reece; Peixin Yang
Journal:  Stem Cell Res Ther       Date:  2016-12-09       Impact factor: 6.832

8.  Prevalence of Congenital Anomalies in the Japan Environment and Children's Study.

Authors:  Hidetoshi Mezawa; Ai Tomotaki; Kiwako Yamamoto-Hanada; Kazue Ishitsuka; Tadayuki Ayabe; Mizuho Konishi; Mayako Saito; Limin Yang; Narufumi Suganuma; Fumiki Hirahara; Shoji F Nakayama; Hirohisa Saito; Yukihiro Ohya
Journal:  J Epidemiol       Date:  2018-09-22       Impact factor: 3.211

9.  High glucose alters the DNA methylation pattern of neurodevelopment associated genes in human neural progenitor cells in vitro.

Authors:  Deepika Kandilya; Sukanya Shyamasundar; Dhiraj Kumar Singh; Avijit Banik; Manoor Prakash Hande; Walter Stünkel; Yap Seng Chong; S Thameem Dheen
Journal:  Sci Rep       Date:  2020-09-24       Impact factor: 4.379

  9 in total

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