Published online Nov 30, 2018. doi: 10.5493/wjem.v8.i3.18
Peer-review started: October 15, 2018
First decision: November 1, 2018
Revised: November 5, 2018
Accepted: November 15, 2018
Article in press: November 15, 2018
Published online: November 30, 2018
Processing time: 61 Days and 17.6 Hours
Oxidative stress stemming from tissue exposure to constant hyperglycemia is one of the major pathogenetic pathways of diabetic macro- and microvascular complications. Diabetic polyneuropathy, commonly manifesting as distal, symmetrical sensorimotor polyneuropathy, is characterized by progressive severity of symptoms, with rates analogous to the quality of glycemic control achieved by the patients and physicians. Palliative care with analgesics and aggressive glycemic control often improve quality of life in the absence of causative treatment. Currently, there is a growing body of evidence indicating the role of microRNAs in the pathogenesis of diabetic complications, with emphasis on diabetic nephropathy and neuropathy. Therefore, in this review, we aim to explore the role of microRNAs and their polymorphisms in the pathophysiology of diabetic polyneuropathy, as well as, the possibility of novel diagnostic and therapeutic applications by epigenetic profiling and manipulation.
Core tip: In this review, we aim to create a concise overview of the epigenetics underlining the pathogenesis of diabetic neuropathy with emphasis on the altered microRNA expression patterns identified on both animal and human subjects, while, exploring the manner by which they could be manipulated and utilized as novel therapeutic targets.