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Published on: March 8, 2018
Current concepts in targeted therapies for the pathophysiology of diabetic microvascular complications
Brian C Cumbie1, Kathie L Hermayer
1Division of Endocrinology, Diabetes & Medical Genetics, Department of Medicine, Medical University of South Carolina, Charleston 29425, USA.
Abstract:
Microvascular complications characterized by retinopathy, nephropathy, and neuropathy are highly prevalent among diabetics. Glycemic control has long been the mainstay for preventing progression of these complications; however, such control is not easily achieved. Currently, alternative adjunctive approaches to treating and preventing microvascular damage are being undertaken by targeting the molecular pathogenesis of diabetic complications. This review summarizes the specific pathogenic mechanisms of microvascular complications for which clinical therapies have been developed, including the polyol pathway, advanced glycation end products, protein kinase c, vascular epithelium growth factor, and the superoxide pathway. The review further focuses on therapies for these targets that are currently available or are undergoing late-stage clinical trials.
Insights
Diabetic microvascular complications like retinopathy and neuropathy are common. This review explores targeted therapies beyond glycemic control, focusing on molecular pathways and emerging treatments.
Area of Science:
- Endocrinology and Metabolism
- Diabetology
- Vascular Biology
Background:
- Diabetic microvascular complications, including retinopathy, nephropathy, and neuropathy, significantly impact patient quality of life.
- While glycemic control is primary, it's often insufficient in preventing disease progression.
- Emerging strategies focus on molecular pathways underlying these complications.
Purpose of the Study:
- To review pathogenic mechanisms of diabetic microvascular complications.
- To summarize currently available and late-stage clinical trial therapies targeting these mechanisms.
Main Methods:
- Literature review of pathogenic mechanisms.
- Analysis of clinical therapies for specific molecular targets.
Main Results:
- Key pathways discussed include the polyol pathway, advanced glycation end products (AGEs), protein kinase C (PKC), vascular endothelial growth factor (VEGF), and the superoxide pathway.
- Therapies targeting these pathways are either approved or in advanced clinical trials.
Conclusions:
- Targeting specific molecular pathways offers a promising adjunctive approach to managing diabetic microvascular complications.
- Further research and clinical trials are essential to validate and implement these novel therapeutic strategies.
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