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Assessing corneal dendritic cells in glucose dysregulation small‐fibre neuropathy

Background and Aims Small‐fibre neuropathy (SFN) is associated with glucose dysregulation, including impaired glucose tolerance (IGT) and type 2 diabetes (T2D). Corneal confocal microscopy (CCM) offers a non‐invasive tool to assess corneal nerve damage and dendritic cell density (DCD). In this study...

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Published in:Journal of the peripheral nervous system 2024-12, Vol.29 (4), p.400-405
Main Authors: Idiaquez, Juan Francisco, Barnett‐Tapia, Carolina, Perkins, Bruce A., Bril, Vera
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creator Idiaquez, Juan Francisco
Barnett‐Tapia, Carolina
Perkins, Bruce A.
Bril, Vera
description Background and Aims Small‐fibre neuropathy (SFN) is associated with glucose dysregulation, including impaired glucose tolerance (IGT) and type 2 diabetes (T2D). Corneal confocal microscopy (CCM) offers a non‐invasive tool to assess corneal nerve damage and dendritic cell density (DCD). In this study, we investigated corneal DCD in patients with SFN and glucose dysregulation, defined as IGT or T2D. Methods We enrolled 38 patients with SFN + glucose dysregulation, 51 with SFN + non‐glucose dysregulation and 20 healthy controls. All participants underwent neurological examination, neurophysiology and CCM. Results Individuals with SFN and glucose dysregulation had higher DCD compared with healthy controls (p = .01), and mature DCD was higher in IGT SFN patients than in T2D patients. Interpretation Higher DCD in IGT compared with controls and patients with established T2D may suggest that DCD is a biomarker of early neuropathy.
doi_str_mv 10.1111/jns.12671
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Corneal confocal microscopy (CCM) offers a non‐invasive tool to assess corneal nerve damage and dendritic cell density (DCD). In this study, we investigated corneal DCD in patients with SFN and glucose dysregulation, defined as IGT or T2D. Methods We enrolled 38 patients with SFN + glucose dysregulation, 51 with SFN + non‐glucose dysregulation and 20 healthy controls. All participants underwent neurological examination, neurophysiology and CCM. Results Individuals with SFN and glucose dysregulation had higher DCD compared with healthy controls (p = .01), and mature DCD was higher in IGT SFN patients than in T2D patients. 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Corneal confocal microscopy (CCM) offers a non‐invasive tool to assess corneal nerve damage and dendritic cell density (DCD). In this study, we investigated corneal DCD in patients with SFN and glucose dysregulation, defined as IGT or T2D. Methods We enrolled 38 patients with SFN + glucose dysregulation, 51 with SFN + non‐glucose dysregulation and 20 healthy controls. All participants underwent neurological examination, neurophysiology and CCM. Results Individuals with SFN and glucose dysregulation had higher DCD compared with healthy controls (p = .01), and mature DCD was higher in IGT SFN patients than in T2D patients. 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subjects Adult
Aged
Cell density
Confocal microscopy
Cornea
Cornea - diagnostic imaging
Cornea - innervation
Cornea - pathology
corneal confocal microscopy
corneal dendritic cells
Dendritic Cells
Diabetes mellitus (non-insulin dependent)
Diabetes Mellitus, Type 2 - complications
Diabetic Neuropathies - diagnosis
Diabetic Neuropathies - metabolism
Diabetic Neuropathies - pathology
Diabetic Neuropathies - physiopathology
Diabetic neuropathy
Female
Glucose Intolerance - metabolism
Glucose tolerance
Humans
Immunological tolerance
impaired glucose tolerance
Male
Microscopy, Confocal
Middle Aged
Neuropathy
Research Report
Small Fiber Neuropathy - diagnosis
Small Fiber Neuropathy - pathology
Small Fiber Neuropathy - physiopathology
small‐fibre neuropathy
title Assessing corneal dendritic cells in glucose dysregulation small‐fibre neuropathy
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