AI Article Synopsis

  • The review highlights the rising prevalence of diabetes and its complications, particularly the incidence of diabetic distal symmetrical polyneuropathy (DPN), which affects about 25% of diabetes patients.
  • Recent findings indicate that factors like gender, clinical characteristics, biomarkers, brain imaging, genetics, and skin biopsies can help differentiate between painful (painful-DPN) and painless DPN, with painful-DPN often linked to female patients and small fiber dysfunction.
  • Further research is needed to better understand the causes of neuropathic pain in DPN, which may lead to new and effective treatments.

Article Abstract

Purpose Of Review: The prevalence of diabetes mellitus and its chronic complications are increasing to epidemic proportions. This will unfortunately result in massive increases in diabetic distal symmetrical polyneuropathy (DPN) and its troublesome sequelae, including disabling neuropathic pain (painful-DPN), which affects around 25% of patients with diabetes. Why these patients develop neuropathic pain, while others with a similar degree of neuropathy do not, is not clearly understood. This review will look at recent advances that may shed some light on the differences between painful and painless-DPN.

Recent Findings: Gender, clinical pain phenotyping, serum biomarkers, brain imaging, genetics, and skin biopsy findings have been reported to differentiate painful- from painless-DPN. Painful-DPN seems to be associated with female gender and small fiber dysfunction. Moreover, recent brain imaging studies have found neuropathic pain signatures within the central nervous system; however, whether this is the cause or effect of the pain is yet to be determined. Further research is urgently required to develop our understanding of the pathogenesis of pain in DPN in order to develop new and effective mechanistic treatments for painful-DPN.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505492PMC
http://dx.doi.org/10.1007/s11892-019-1150-5DOI Listing

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