2013-11-01
Decreased excitability of the distal motor nerve of young patients with type 1 diabetes mellitus
Publication
Publication
Pediatric Diabetes (Print) , Volume 2013 - Issue 14 p. 519- 525
Abstract
Objective: The compound muscle action potential (CMAP) scan is a novel
neurophysiological technique that appears more sensitive in detecting
peripheral motor neuropathy than conventional methods. This study explores
the value of the CMAP scan for the detection of subclinical diabetic peripheral
motor neuropathy.
Methods: In this cross-sectional pilot study, CMAP scanning of the peroneal
nerve was performed in (i) 13 well-controlled patients (8–25 yr old) with type 1
diabetes mellitus (T1DM) duration between 2.5 and 5 yr; (ii) 17 patients
(10–25 yr old) with a duration of T1DM of at least 10 yr, poorly controlled
and/or with microvascular complications and (iii) 13 adults with T1DM and
established clinical diabetic peripheral neuropathy (DPN). Various CMAP
scan variables, including measures of axonal excitability and axonal loss and
reinnervation, were compared between patients and healthy controls.
Results: Axonal excitability was significantly decreased in the young patient
groups as compared to their controls. The CMAP scan measures of axonal
loss and reinnervation differed only between patients with clinical DPN and
their controls.
Conclusions: Motor nerve axonal excitability seems to be reduced early in
T1DM, even in well-controlled young patients, and probably before
(irreversible) axonal damage occurs. These changes can be measured by the
CMAP scan, which makes this a promising tool for detecting nerve
dysfunction in T1DM.
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doi.org/10.1111/pedi.12048, hdl.handle.net/1765/50507 | |
Pediatric Diabetes (Print) | |
Organisation | Erasmus School of Health Policy & Management (ESHPM) |
van der Heyden, J., van der Meer, P., Birnie, E., de Coo, R., Castro Cabezas, M., Ozcan, B., … Blok, J. (2013). Decreased excitability of the distal motor nerve of young patients with type 1 diabetes mellitus. Pediatric Diabetes (Print), 2013(14), 519–525. doi:10.1111/pedi.12048 |