Alpha-lipoic acid reduces AGEsAlpha-Lipoic Acid Treatment Reduces the Levels of Advanced End Glycation Products in Type 2 Diabetes Patients with Neuropathy.
Direct effect on T2DM neuropathy
We investigated the potential benefits of alpha-lipoic acid (ALA) for patients with type 2 diabetes mellitus (T2DM) suffering from neuropathy. Over six months, we treated 54 patients with a daily dose of 600 mg of ALA while keeping their current oral medications unchanged. We also included a control group of 24 matched individuals who did not experience neuropathy.
Our findings showed a significant decrease in advanced glycation end products (AGEs), which are harmful compounds that can worsen diabetes complications. The levels of AGEs dropped from 11.89 to 10.95 AU/μg, reflecting the positive impact ALA treatment can have. Interestingly, while the levels of soluble receptor for AGEs (sRAGE) and the AGEs/sRAGE ratio did not show changes with ALA treatment, we did observe correlations between the reduction of AGEs and improvements in neuropathic symptoms and endothelial function.
Overall, our study supports the idea that ALA can effectively lower AGEs in T2DM patients with neuropathy, which could help improve their nerve function and overall health. This offers a promising avenue for managing such complications in diabetes.
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Alpha-lipoic acid and neuropathy insightsExpanded Clinical Phenotype and the Role of Untargeted Metabolomics Analysis in Confirming the Diagnosis of Sodium-Dependent Multivitamin Transporter Deficiency.
Moderate relevance to neuropathy treatment
We explored the effects of alpha-lipoic acid in the context of sodium-dependent multivitamin transporter deficiency (SMVTD), a rare condition resulting from loss-of-function variants in the SLC5A6 gene. In a detailed case of a 25-year-old woman, whose symptoms included developmental delays, epilepsy, and neurocognitive challenges, we observed an intriguing combination of treatments.
Alongside alpha-lipoic acid, her therapy incorporated biotin and pantothenic acid, which collectively enhanced her overall metabolic control and neurocognitive function. While our findings do highlight the improvement in her condition, they make it difficult to draw strong conclusions about the isolated effect of alpha-lipoic acid on neuropathy alone.
Ultimately, this case points towards a promising domain for further research. It emphasizes the importance of considering how combined vitamin treatments may yield benefits for individuals affected by neuropathies associated with unique metabolic disorders.
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We examined the complexities of diabetic neuropathy and the role of benfotiamine in its management. Recent findings confirm that benfotiamine can inhibit harmful pathways triggered by high blood sugar, thus helping to promote healthier nerve function. Numerous clinical trials worldwide have shown it to be effective.
Furthermore, benfotiamine works alongside other treatments like alpha-lipoic acid to improve symptoms gradually. By focusing on these new therapeutic approaches, we can better address neuropathy and enhance quality of life for those affected.
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We examined the effects of benfotiamine, a synthetic derivative of vitamin B1, on neuropathy. This compound increases intracellular thiamine diphosphate, which helps combat advanced glycation end products (AGEs) that contribute to nerve damage, particularly in diabetes.
While benfotiamine shows promise due to its anti-AGE properties and potential benefits for diabetic complications like neuropathy, recent studies offer mixed results regarding its overall effectiveness.
Thus, while it may be helpful in some contexts, the results highlight the need for further investigation to confirm its benefits for neuropathy.
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We explored the potential of benfotiamine in alleviating inflammatory and neuropathic pain through a detailed study with rats. By inducing pain through specific methods, we noted significant reductions in pain-related behaviors when benfotiamine was administered at varying doses.
The findings suggest that benfotiamine shows promise in reducing pain from different causes, hinting at its potential benefits for humans suffering from nerve pain. While this research is promising, further studies are needed to fully understand its effects in human trials.
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