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These studies suggest that metformin improves liver function, body composition, and metabolic parameters in non-alcoholic fatty liver disease patients, both alone and in combination with other treatments, although further research is needed to confirm these findings.
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Non-alcoholic fatty liver disease (NAFLD) is a prevalent liver condition characterized by excessive fat accumulation in the liver, not due to alcohol consumption. Metformin, a common antidiabetic medication, has been explored for its potential benefits in treating NAFLD, particularly in non-diabetic and diabetic populations.
Several studies have investigated the effects of metformin on liver enzymes and body composition in NAFLD patients. A systematic review and meta-analysis of randomized controlled trials (RCTs) involving non-diabetic NAFLD patients found that metformin significantly reduced body mass index (BMI) and serum aspartate aminotransferase (AST) levels. However, its impact on alanine transaminase (ALT) was not statistically significant. This suggests that metformin can improve certain liver function markers and body composition in non-diabetic NAFLD patients.
A study comparing luseogliflozin and metformin in type 2 diabetes (T2D) patients with NAFLD found that luseogliflozin significantly reduced liver fat deposition more than metformin. Additionally, luseogliflozin showed greater improvements in visceral fat area, HbA1c, and BMI. This indicates that while metformin is beneficial, other medications like luseogliflozin might offer superior outcomes in reducing liver fat.
In a randomized trial comparing metformin with vitamin E and a prescriptive diet, metformin showed superior results in improving aminotransferase levels and reducing liver fat, necroinflammation, and fibrosis. The study concluded that metformin was more effective than both vitamin E and dietary interventions in treating NAFLD.
Another study compared the effects of metformin and rosiglitazone on liver fat content and insulin sensitivity in T2D patients. While both drugs improved hepatic insulin sensitivity, rosiglitazone significantly reduced liver fat and increased insulin clearance, unlike metformin. This suggests that rosiglitazone might be more effective in reducing liver fat compared to metformin.
Research on the combination of metformin and malvidin in diabetic rats with NAFLD showed that this combination therapy significantly improved lipid and glucose metabolism and reduced inflammation markers. This combination was more effective than metformin alone in alleviating NAFLD symptoms.
A study investigating the additive effect of ipragliflozin on NAFLD in patients already treated with metformin and pioglitazone found that ipragliflozin significantly reduced hepatic fat content and visceral fat. This combination therapy showed promising results in further ameliorating liver steatosis and reducing excessive fat.
Metformin's beneficial effects on NAFLD are partly attributed to its ability to improve insulin sensitivity and reduce hepatic glucose production. Additionally, metformin has been shown to affect intestinal microbiota and barrier function, which may play a role in its protective effects against NAFLD.
Metformin has demonstrated significant benefits in improving liver function and body composition in NAFLD patients, particularly in non-diabetic populations. While it is effective, other treatments like luseogliflozin and rosiglitazone may offer superior outcomes in certain aspects. Combination therapies involving metformin also show promise in enhancing its therapeutic effects. Further large-scale and well-designed RCTs are needed to confirm these findings and optimize treatment strategies for NAFLD.
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