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Peripheral nerve ultrasound in amyotrophic lateral sclerosis phenotypes
Authors:Grazyna Debska‐Vielhaber PhD  Judith Machts MSc  Verena Dannhardt‐Stieger MD  Helmut Feistner MD  Andreas Oldag MD  Michael Goertler MD  Susanne Petri MD  Katja Kollewe MD  Siegfried Kropf PhD  Frank Schreiber MSc  Hans‐Jochen Heinze MD  Reinhard Dengler MD  Peter J. Nestor MD  Stefan Vielhaber MD
Affiliation:1. Department of Neurology, Otto‐von‐Guericke University, Germany;2. German Center for Neurodegenerative Diseases, Helmholtz Association, Magdeburg, Germany;3. Clinic for Neurology, Hannover Medical School, Hannover, Germany;4. Institute of Biometry and Medical Informatics, Otto‐von‐Guericke University, Magdeburg, Germany;5. Institute of Control Engineering, Technical University Braunschweig, Braunschweig, Germany
Abstract:Introduction: In this study we sought to determine the cross‐sectional area (CSA) of peripheral nerves in patients with distinct subtypes of amyotrophic lateral sclerosis (ALS). Methods: Ulnar and median nerve ultrasound was performed in 78 ALS patients [classic, n = 21; upper motor neuron dominant (UMND), n = 14; lower motor neuron dominant (LMND), n = 20; bulbar, n = 15; primary lateral sclerosis (PLS), n = 8] and 18 matched healthy controls. Results: Compared with controls, ALS patients had significant, distally pronounced reductions of ulnar CSA (forearm/wrist level) across all disease groups, except for PLS. Median nerve CSA (forearm/wrist level) did not differ between controls and ALS. Conclusion: Ulnar nerve ultrasound in ALS subgroups revealed significant differences in distal CSA values, which suggests it has value as a marker of LMN involvement. Its potential was particularly evident in the UMND and PLS groups, which can be hard to separate clinically, yet their accurate separation has major prognostic implications. Muscle Nerve 51 :669–675, 2015
Keywords:ALS  median nerve  PLS  ulnar nerve  ultrasound
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