Searched over 200M research papers for "simvastatin simvastatin"
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These studies suggest simvastatin has mixed effects, including impairing cardiorespiratory fitness, reducing cholesterol and cardiovascular risk, and improving liver perfusion and diabetic cardiomyopathy, while not significantly affecting COPD exacerbations or delirium duration.
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Simvastatin, a commonly prescribed statin, has been shown to impair exercise training adaptations in overweight or obese adults with metabolic syndrome. A study found that while exercise alone increased cardiorespiratory fitness by 10%, the addition of simvastatin resulted in only a 1.5% increase. Similarly, skeletal muscle mitochondrial content increased by 13% with exercise alone but decreased by 4.5% when combined with simvastatin.
In a large, multicenter randomized trial, simvastatin did not reduce the rate of exacerbations or the time to the first exacerbation in patients with moderate-to-severe COPD. The study concluded that simvastatin at a daily dose of 40 mg had no significant effect on exacerbation rates or clinical outcomes in these patients.
Simvastatin, while effective in lowering lipid levels, can have serious side effects, especially when used in high doses or in combination with certain drugs. The FDA has issued warnings regarding the safe use of simvastatin, emphasizing the need for physicians to adjust dosages and monitor for potential drug interactions to prevent complications.
A randomized, double-blind, placebo-controlled trial investigated the effects of simvastatin on delirium and coma in critically ill patients. The study found no significant difference in the number of days alive without delirium or coma between the simvastatin and placebo groups, suggesting that simvastatin does not modify the duration of delirium and coma in these patients.
Simvastatin has shown promise in reducing depression-like behavior in rats with traumatic brain injury. The study indicated that simvastatin reduced neuronal apoptosis, microglia activation, and TNF-α expression in the hippocampus, leading to a decrease in depressive-like behavior.
Simvastatin has been extensively studied and has demonstrated significant cardiovascular benefits, including reductions in LDL cholesterol and cardiovascular morbidity and mortality. However, its use is associated with rare but serious side effects such as myopathy and rhabdomyolysis, particularly at high doses or when combined with other drugs.
A pilot study found that high-dose simvastatin improved neutrophil function and clinical outcomes in older adults with community-acquired pneumonia and sepsis. The study reported improvements in neutrophil extracellular trap formation, chemotaxis, and Sequential Organ Failure Assessment scores, suggesting potential benefits of simvastatin as an adjuvant therapy in this population.
Simvastatin has been shown to lower portal pressure and improve liver perfusion in patients with cirrhosis and portal hypertension. Additionally, a study found that adding simvastatin to standard therapy for variceal rebleeding did not reduce rebleeding rates but was associated with increased survival in patients with Child-Pugh class A or B cirrhosis .
In a study on diabetic rats, simvastatin was found to ameliorate diabetic cardiomyopathy by reducing oxidative stress, inflammation, and apoptosis. The treatment improved body weight, attenuated hyperglycemia and hyperlipidemia, and prevented histological alterations in the heart.
Simvastatin is a widely used statin with proven benefits in lowering cholesterol and reducing cardiovascular risk. However, its effects on exercise adaptations, COPD exacerbations, and critical care outcomes are limited. Simvastatin shows promise in specific conditions such as traumatic brain injury, pneumonia, and cirrhosis, but its use must be carefully managed to avoid serious side effects. Further research is needed to fully understand its potential and optimize its therapeutic applications.
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