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Some studies suggest type 2 diabetes progresses faster in children and young people compared to type 1 diabetes, while other studies indicate no better perinatal outcomes for women with type 2 diabetes during pregnancy than those with type 1.
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Type 1 diabetes (T1D) and type 2 diabetes (T2D) are chronic conditions characterized by high blood sugar levels due to the body's inability to produce or effectively use insulin. While both types share some similarities, they differ significantly in their pathophysiology, progression, and complications.
In pregnant women, glycemic disturbance is generally less severe in those with T2D compared to those with T1D. However, despite this milder glycemic disturbance, women with T2D do not necessarily experience better perinatal outcomes. Studies have shown that women with T2D have a higher risk of perinatal mortality compared to those with T1D, although there are no significant differences in the rates of major congenital malformations, stillbirth, and neonatal mortality. Additionally, women with T2D experience less diabetic ketoacidosis and fewer cesarean sections compared to those with T1D.
T2D progresses more rapidly in children and young people compared to T1D in the same age group and T2D in adults. This rapid progression is evident in the faster deterioration of beta-cell function and the quicker onset of complications such as nephropathy, neuropathy, and cardiovascular issues. Youth with T2D also exhibit a worse cardiovascular risk profile and a faster progression to cardiovascular death compared to those with T1D. This highlights the aggressive nature of T2D in younger populations and underscores the need for urgent interventions.
Both T1D and T2D are associated with significant alterations in plasma metabolites, including glucose, fructose, amino acids, and lipids. These changes can be identified using metabolomic techniques and are crucial for understanding the pathophysiological pathways of both types of diabetes. The identification of these metabolites can help in creating effective interventions for managing T1D and T2D.
There is evidence of shared genetic components between T1D and T2D, particularly in the HLA class II locus. Certain alleles that are protective against T1D also offer protection against T2D, while others increase the risk for both diseases. This suggests that the genetic architecture of T1D and T2D might share common elements, which could have implications for developing therapeutic strategies that target both conditions .
While T1D and T2D have distinct characteristics, both conditions present significant health challenges. T2D, particularly in younger populations, can progress more rapidly and lead to severe complications. Despite milder glycemic disturbances, T2D in pregnancy does not result in better outcomes compared to T1D. Understanding the shared genetic and metabolic pathways can aid in developing comprehensive treatment strategies for both types of diabetes.
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