Neurophysiological Hallmarks of Axonal Degeneration in CIDP Patients: A Pilot Analysis

In this work, we aim to identify sensitive neurophysiological biomarkers of axonal degeneration in CIDP patients. A total of 16 CIDP patients, fulfilling the clinical and neurophysiological criteria for typical CIDP, treated with subcutaneous immunoglobulin (ScIg) (0.4 g/kg/week) were evaluated at b...

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Published in:Brain Sciences
Main Authors: Dario Ricciardi, Federica Amitrano, Armando Coccia, Vincenzo Todisco, Francesca Trojsi, Gioacchino Tedeschi, Giovanni Cirillo
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2022
Subjects:
EMG
DML
Online Access:https://doi.org/10.3390/brainsci12111510
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spelling ftmdpi:oai:mdpi.com:/2076-3425/12/11/1510/ 2023-08-20T04:06:10+02:00 Neurophysiological Hallmarks of Axonal Degeneration in CIDP Patients: A Pilot Analysis Dario Ricciardi Federica Amitrano Armando Coccia Vincenzo Todisco Francesca Trojsi Gioacchino Tedeschi Giovanni Cirillo 2022-11-07 application/pdf https://doi.org/10.3390/brainsci12111510 EN eng Multidisciplinary Digital Publishing Institute Neuromuscular and Movement Disorders https://dx.doi.org/10.3390/brainsci12111510 https://creativecommons.org/licenses/by/4.0/ Brain Sciences; Volume 12; Issue 11; Pages: 1510 chronic inflammatory demyelinating polyneuropathy EMG axonal degeneration motor unit analysis subcutaneous immunoglobulin Text 2022 ftmdpi https://doi.org/10.3390/brainsci12111510 2023-08-01T07:13:59Z In this work, we aim to identify sensitive neurophysiological biomarkers of axonal degeneration in CIDP patients. A total of 16 CIDP patients, fulfilling the clinical and neurophysiological criteria for typical CIDP, treated with subcutaneous immunoglobulin (ScIg) (0.4 g/kg/week) were evaluated at baseline (before ScIg treatment) and after long-term treatment with ScIg (24 months) by clinical assessment scales, nerve conduction studies (NCS) and electromyography (EMG). Conventional and non-conventional neurophysiological parameters: motor unit potential (MUP) analysis, MUP thickness and size index (SI)] and interference pattern (IP) features were evaluated after long-term treatment (24 months) and compared with a population of 16 healthy controls (HC). An increase of distal motor latency (DML) and reduced compound motor action potential (CMAP) amplitude and area in CIDP patients suggest axonal damage of motor fibers, together with a significant increase of MUP amplitude, duration and area. Analysis of non-conventional MUP parameters shows no difference for MUP thickness; however, in CIDP patients, SI is increased and IP area and amplitude values are lower than HC. Despite clinical and neurophysiological improvement after ScIg treatment, neurophysiological analysis revealed axonal degeneration of motor fibers and motor unit remodeling. Correlation analysis shows that the axonal degeneration process is related to the diagnostic and therapeutic delay. MUP area and SI parameters can detect early signs of axonal degeneration, and their introduction in clinical practice may help to identify patients with the worst outcome. Text DML MDPI Open Access Publishing Brain Sciences 12 11 1510
institution Open Polar
collection MDPI Open Access Publishing
op_collection_id ftmdpi
language English
topic chronic inflammatory demyelinating polyneuropathy
EMG
axonal degeneration
motor unit analysis
subcutaneous immunoglobulin
spellingShingle chronic inflammatory demyelinating polyneuropathy
EMG
axonal degeneration
motor unit analysis
subcutaneous immunoglobulin
Dario Ricciardi
Federica Amitrano
Armando Coccia
Vincenzo Todisco
Francesca Trojsi
Gioacchino Tedeschi
Giovanni Cirillo
Neurophysiological Hallmarks of Axonal Degeneration in CIDP Patients: A Pilot Analysis
topic_facet chronic inflammatory demyelinating polyneuropathy
EMG
axonal degeneration
motor unit analysis
subcutaneous immunoglobulin
description In this work, we aim to identify sensitive neurophysiological biomarkers of axonal degeneration in CIDP patients. A total of 16 CIDP patients, fulfilling the clinical and neurophysiological criteria for typical CIDP, treated with subcutaneous immunoglobulin (ScIg) (0.4 g/kg/week) were evaluated at baseline (before ScIg treatment) and after long-term treatment with ScIg (24 months) by clinical assessment scales, nerve conduction studies (NCS) and electromyography (EMG). Conventional and non-conventional neurophysiological parameters: motor unit potential (MUP) analysis, MUP thickness and size index (SI)] and interference pattern (IP) features were evaluated after long-term treatment (24 months) and compared with a population of 16 healthy controls (HC). An increase of distal motor latency (DML) and reduced compound motor action potential (CMAP) amplitude and area in CIDP patients suggest axonal damage of motor fibers, together with a significant increase of MUP amplitude, duration and area. Analysis of non-conventional MUP parameters shows no difference for MUP thickness; however, in CIDP patients, SI is increased and IP area and amplitude values are lower than HC. Despite clinical and neurophysiological improvement after ScIg treatment, neurophysiological analysis revealed axonal degeneration of motor fibers and motor unit remodeling. Correlation analysis shows that the axonal degeneration process is related to the diagnostic and therapeutic delay. MUP area and SI parameters can detect early signs of axonal degeneration, and their introduction in clinical practice may help to identify patients with the worst outcome.
format Text
author Dario Ricciardi
Federica Amitrano
Armando Coccia
Vincenzo Todisco
Francesca Trojsi
Gioacchino Tedeschi
Giovanni Cirillo
author_facet Dario Ricciardi
Federica Amitrano
Armando Coccia
Vincenzo Todisco
Francesca Trojsi
Gioacchino Tedeschi
Giovanni Cirillo
author_sort Dario Ricciardi
title Neurophysiological Hallmarks of Axonal Degeneration in CIDP Patients: A Pilot Analysis
title_short Neurophysiological Hallmarks of Axonal Degeneration in CIDP Patients: A Pilot Analysis
title_full Neurophysiological Hallmarks of Axonal Degeneration in CIDP Patients: A Pilot Analysis
title_fullStr Neurophysiological Hallmarks of Axonal Degeneration in CIDP Patients: A Pilot Analysis
title_full_unstemmed Neurophysiological Hallmarks of Axonal Degeneration in CIDP Patients: A Pilot Analysis
title_sort neurophysiological hallmarks of axonal degeneration in cidp patients: a pilot analysis
publisher Multidisciplinary Digital Publishing Institute
publishDate 2022
url https://doi.org/10.3390/brainsci12111510
genre DML
genre_facet DML
op_source Brain Sciences; Volume 12; Issue 11; Pages: 1510
op_relation Neuromuscular and Movement Disorders
https://dx.doi.org/10.3390/brainsci12111510
op_rights https://creativecommons.org/licenses/by/4.0/
op_doi https://doi.org/10.3390/brainsci12111510
container_title Brain Sciences
container_volume 12
container_issue 11
container_start_page 1510
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