Exploring the Diet-Gut Microbiota-Epigenetics Crosstalk Relevant to Neonatal Diabetes

被引:6
|
作者
Alsharairi, Naser A. [1 ]
机构
[1] Griffith Univ, Heart Mind & Body Res Grp, POB 4222, Gold Coast, QLD 4222, Australia
关键词
neonatal diabetes; gestational diabetes; gut microbiota; diet; gene expression; epigenetic; THIOREDOXIN-INTERACTING PROTEIN; CHAIN FATTY-ACIDS; DNA METHYLATION; GENE-EXPRESSION; INTRAUTERINE GROWTH; LACTONASE ACTIVITY; ENDOTHELIAL-CELLS; OXIDATIVE STRESS; PARAOXONASE; PPAR-GAMMA;
D O I
10.3390/genes14051017
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Neonatal diabetes (NDM) is a rare monogenic disorder that presents as hyperglycemia during the first six months of life. The link between early-life gut microbiota dysbiosis and susceptibility to NDM remains uncertain. Experimental studies have demonstrated that gestational diabetes mellitus (GDM) could develop into meconium/gut microbiota dysbiosis in newborns, and thus, it is thought to be a mediator in the pathogenesis of NDM. Epigenetic modifications have been considered as potential mechanisms by which the gut microbiota and susceptibility genes interact with the neonatal immune system. Several epigenome-wide association studies have revealed that GDM is associated with neonatal cord blood and/or placental DNA methylation alterations. However, the mechanisms linking diet in GDM with gut microbiota alterations, which may in turn induce the expression of genes linked to NDM, are yet to be unraveled. Therefore, the focus of this review is to highlight the impacts of diet, gut microbiota, and epigenetic crosstalk on altered gene expression in NDM.
引用
收藏
页数:17
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