Novel Strategy: Identifying New Markers for Demyelination in Diabetic Distal Symmetrical Polyneuropathy.
Document Type
Article
Publication Date
4-26-2024
Publication Title
Heliyon
Abstract
OBJECTIVE: To develop a novel strategy for identifying acquired demyelination in diabetic distal symmetrical polyneuropathy (DSP).
BACKGROUND: Motor nerve conduction velocity (CV) slowing in diabetic DSP exceeds expectations for pure axonal loss thus implicating superimposed acquired demyelination.
METHODS: After establishing demyelination confidence intervals by regression analysis of nerve conduction data from chronic inflammatory demyelinating polyneuropathy (CIDP), we prospectively studied CV slowing in 90 diabetic DSP patients with and without at least one motor nerve exhibiting CV slowing (groups A and B) into the demyelination range by American Academy of Neurology (AAN) criteria respectively and 95 amyotrophic lateral sclerosis (ALS) patients. Simultaneously, secretory phospholipase A2 (sPLA2) activity was assessed in both diabetic groups and 46 healthy controls.
RESULTS: No ALS patient exhibited CV slowing in more than two motor nerves based on AAN criteria or the confidence intervals. Group A demonstrated a significantly higher percentage of patients as compared to group B fulfilling the above criteria, with an additional criterion of at least one motor nerve exhibiting CV slowing in the demyelinating range and a corresponding F response in the demyelinating range by AAN criteria (70.3 %
CONCLUSION: A combination of regression analysis of electrodiagnostic data and a urine biological marker of systemic inflammation identifies a subgroup of diabetic DSP with superimposed acquired demyelination that may respond favorably to immunomodulatory therapy.
Volume
10
Issue
9
First Page
e30419
Recommended Citation
Souayah N, Chen H, Chong ZZ, Patel T, Pahwa A, Menkes DL, et al. Novel strategy: identifying new markers for demyelination in diabetic distal symmetrical polyneuropathy. Heliyon. 2024 Apr 26;10(9):e30419. doi: 10.1016/j.heliyon.2024.e30419. PMID: 38765173.
DOI
10.1016/j.heliyon.2024.e30419
ISSN
2405-8440
PubMed ID
38765173