Table 2.
The factors involved in metabolic reprogramming in GDM.
Factor | Author | Research object | Main conclusion | References |
---|---|---|---|---|
NGR 4 | Attique H et al | Pregnant women in the 24th to 28th week of pregnancy | NGR4 levels were significantly lower in GDM subjects and may be a potential biomarker of GDM. | (8) |
Angptl 8 | HuangY et al | Pregnant women in the 12th to 16th week of pregnancy | The level of Angptl8 in early pregnancy is associated with the risk of GDM in pregnancy, which may be used to predict the onset of GDM. | (90) |
Smad 4 | Li L et al | The htr-8/svneo cells | Deficiency of Smad4 significantly increased GDM insulin sensitivity and attenuated inflammation in insulin-resistant cell models. | (91) |
SIRT 1 | Ulubasoglu H et al | Pregnant women in the 24th to 28th week of pregnancy | Low SIRT1 levels in the second trimester are associated with GDM. It may be a diagnostic marker for GDM. | (92) |
WWOX/HIF1 | BarylaI et al | Pregnant women in the 24th to 28th week of pregnancy and 3 months postpartum and 1 year postpartum | The decreased WWOX expression in GDM, especially the decreased WWOX/HIF1A ratio, suggests that WWOX regulates HIF1α activity in normal tissues, gene expression of proteins involved in glycolysis, and may lead to changes in glucose metabolism in GDM. | (93) |
HK 2 | Song T R et al | Pregnant woman | Upregulation of HK2 can lead to glucose metabolism disturbance in GDM patients. | (94) |
Mir-143 | Muralimanoharan S et al | Newly delivered mother | Downregulation of miR-143 mediates a metabolic shift from OXPHOS to aerobic glycolysis in GDM placenta. | (95) |
CMPF | Yi J et al | Pregnant women in the 24th to 28th week of pregnancy | Elevated serum CMPF levels are not conducive to the occurrence of hyperglycemia and pancreatic β-cell failure in GDM patients, which may affect the occurrence and development of GDM. | (96) |