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These studies suggest metformin prescription is associated with various health benefits, including reduced abdominal aortic aneurysm growth, decreased risk of heart failure and stroke in diabetic patients, and potential anti-aging effects.
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Metformin is a widely prescribed oral hypoglycemic agent primarily used to manage type 2 diabetes mellitus (T2DM). It is known for its efficacy in controlling blood glucose levels and has been the cornerstone of diabetes treatment for decades. However, recent studies have highlighted its potential benefits beyond glycemic control, including cardiovascular protection, anti-aging effects, and the management of abdominal aortic aneurysm (AAA) growth.
Several studies have demonstrated that metformin prescription is associated with a significant reduction in the growth rate of AAA. A meta-analysis involving 153,553 patients found that those prescribed metformin had a significantly lower annual AAA growth rate compared to those not on the medication (0.9 mm/year vs. 1.8 mm/year). Another study in a Swedish cohort confirmed these findings, showing that metformin was associated with reduced AAA growth rates and lower chemokine expression, suggesting anti-inflammatory effects. Additionally, metformin was linked to a decreased risk of AAA-related clinical events, such as rupture or the need for surgical repair.
The exact mechanisms by which metformin exerts its effects on AAA are not fully understood. However, it is believed that its anti-inflammatory properties play a crucial role. Metformin has been shown to reduce the expression of various inflammatory chemokines, which are involved in the pathogenesis of AAA. This anti-inflammatory action, along with its ability to improve vascular health, may contribute to the observed reduction in AAA growth and events.
Metformin has also been studied for its effects on heart failure, particularly HFpEF, in patients with T2DM and hypertension. A retrospective study with a 6-year follow-up found that long-term metformin use was associated with a significantly lower incidence of new-onset symptomatic HFpEF compared to non-metformin therapy (6 out of 130 patients vs. 31 out of 260 patients). The study also reported improvements in left ventricular diastolic function and hypertrophy, suggesting that metformin may help delay the progression of HFpEF.
In addition to its benefits for heart failure, metformin has been shown to reduce the risk of stroke in patients with diabetes. A 4-year follow-up study involving 14,856 patients found that those on metformin had a significantly lower incidence of stroke compared to those not on the medication (9.2% vs. 17.5%). The protective effect of metformin remained significant even after adjusting for various confounding factors, highlighting its potential role in stroke prevention.
Metformin has garnered attention for its potential anti-aging properties. Studies have shown that metformin can retard aging in model organisms and reduce the incidence of aging-related diseases such as neurodegenerative diseases and cancer in humans. The drug's mechanisms of action in this context are not entirely clear, but its anti-inflammatory and antioxidant effects are believed to contribute to its anti-aging benefits.
Beyond its traditional use in diabetes management, metformin's non-glycemic effects have opened up new therapeutic possibilities. It has shown promise in weight stabilization, renoprotection, neuroprotection, cardiovascular protection, and even as an adjunct therapy in treating infectious diseases like tuberculosis and viral hepatitis. These pleiotropic effects make metformin a candidate for repurposing in various medical conditions.
Metformin's benefits extend far beyond its role in managing blood glucose levels in patients with T2DM. Its potential to reduce AAA growth, protect against cardiovascular events, prevent stroke, and even combat aging-related diseases makes it a versatile and valuable medication. However, while the current evidence is promising, further randomized controlled trials are needed to confirm these benefits and fully understand the mechanisms behind metformin's diverse effects.
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