Searched over 200M research papers for "prediabetes drugs"
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These studies suggest that various drugs, including metformin, linagliptin, exenatide, thiazolidinediones, -glucosidase inhibitors, acarbose, and GLP-1 receptor agonists, are effective in managing prediabetes by improving insulin secretion, reducing the risk of complications, and increasing the odds of regression to normal blood sugar levels.
20 papers analyzed
Prediabetes is a condition characterized by blood glucose levels that are higher than normal but not yet high enough to be classified as diabetes. It is a critical stage where intervention can prevent the progression to type 2 diabetes (T2D). Approximately 70% of individuals with prediabetes will eventually develop diabetes if left untreated . This condition is also associated with an increased risk of cardiovascular diseases and other complications.
Metformin is widely recognized as the first-line pharmacological treatment for prediabetes. It enhances insulin action in the liver and skeletal muscle, thereby improving glycemic control. Studies have shown that metformin can significantly reduce the risk of developing T2D and is generally well-tolerated and safe for long-term use. In a randomized controlled trial, metformin monotherapy was associated with a 25.1% reduction in the risk of small fiber peripheral neuropathy (SFPN) and a lower decrease in kidney function compared to placebo .
Combining metformin with other glucose-lowering drugs like linagliptin has shown promising results. A study demonstrated that the combination of metformin and linagliptin significantly reduced the risk of SFPN and preserved kidney function better than placebo . Another trial found that this combination, along with lifestyle modifications, improved glucose tolerance and pancreatic β-cell function, and reduced the incidence of T2D more effectively than metformin alone.
Exenatide, a GLP-1 receptor agonist, has also been studied in combination with metformin. In patients with polycystic ovary syndrome (PCOS) and prediabetes, the combination of exenatide and metformin achieved a higher remission rate of prediabetes compared to metformin alone. This combination improved postprandial insulin secretion, which is crucial for maintaining normoglycemia.
A meta-analysis revealed that thiazolidinediones and α-glucosidase inhibitors significantly increased the odds of regressing from prediabetes to normoglycemia. Thiazolidinediones, in particular, were associated with a 2.33-fold increase in the odds of achieving normoglycemia.
Acarbose, the first FDA-approved anti-prediabetes agent, has shown limited efficacy when used alone. However, combining acarbose with Oroxylum indicum seed extract (OISE) significantly improved its effectiveness. This combination reduced the risk of developing diabetes by 75%, improved glucose tolerance, lipid metabolism, and reduced oxidative stress and tissue damage.
Pharmacotherapy for prediabetes is evolving, with several drugs showing promise in preventing the progression to T2D. Metformin remains the cornerstone of treatment, but combination therapies, particularly those involving linagliptin and exenatide, offer enhanced benefits. Other agents like thiazolidinediones, α-glucosidase inhibitors, and innovative combinations like acarbose with OISE also show potential. As research continues, these pharmacological strategies could play a crucial role in managing prediabetes and preventing its complications.
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