3.9 Review

The Role of Biofactors in Diabetic Microvascular Complications

Journal

CURRENT DIABETES REVIEWS
Volume 18, Issue 4, Pages -

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1871527320666210825112240

Keywords

Biofactors; diabetic microvascular complications; diabetic sensorimotor polyneuropathy; cardiovascular autonomic neuropathy; diabetic retinopathy; diabetic nephropathy

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Microvascular complications of diabetes, such as retinopathy, nephropathy, and neuropathy, contribute to significant morbidity, mortality, and healthcare burden. Causal therapies for these complications are limited, thus there is a need for adjunct treatments that can be effective despite ongoing hyperglycemia. Experimental studies have shown promising results in animal models using biofactors to prevent or ameliorate diabetic microvascular complications. These findings, such as the use of alpha-lipoic acid and benfotiamine, could further be translated into clinical trials, particularly for diabetic polyneuropathy. Long-term clinical trials are necessary to confirm the potential benefits of these compounds in modifying the natural history of these complications. Ultimately, biofactors have the potential to expand the therapeutic options for these common and debilitating complications of diabetes.
Microvascular complications are responsible for a major proportion of the burden associated with diabetes contributing to substantial morbidity, mortality, and healthcare burden in people with diabetes. Retinopathy, nephropathy, and neuropathy constitute the leading causes of blindness, end-stage renal disease, and lower-extremity amputations, respectively. Since the efficacy of causal therapies of diabetic microvascular complications is limited, especially in type 2 diabetes, there is an unmet need for adjunct treatments which should be effective despite ongoing hyperglycemia. Experimental studies have indicated that diabetic microvascular complications can be prevented or ameliorated by various biofactors in animal models by interfering with the pathophysiology of the underlying condition. Some of the findings related to biofactors, like alpha-lipoic acid and benfotiamine, could be translated into the clinical arena and confirmed in clinical trials, especially in those focusing on diabetic polyneuropathy. Given the micronutrient nature of these compounds, their safety profile is excellent. Thus, they have the potential to favorably modify the natural history of the underlying complication, but long-term clinical trials are required to confirm this notion. Ultimately, biofactors should expand our therapeutic armamentarium against these common, debilitating, and even life-threatening sequelae of diabetes.

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