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Altered somatosensory neurovascular response in patients with Becker muscular dystrophy

INTRODUCTION: Patients with dystrophinopathies show low levels of neuronal nitric oxide synthase (nNOS), due to reduced or absent dystrophin expression, as nNOS is attached to the dystrophin‐associated protein complex. Deficient nNOS function leads to functional ischemia during muscle activity. Dyst...

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Autores principales: Lindberg, Ulrich, Kruuse, Christina, Witting, Nanna, Jørgensen, Stine Lundgaard, Vissing, John, Rostrup, Egill, Larsson, Henrik Bo Wiberg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991560/
https://www.ncbi.nlm.nih.gov/pubmed/30106246
http://dx.doi.org/10.1002/brb3.985
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author Lindberg, Ulrich
Kruuse, Christina
Witting, Nanna
Jørgensen, Stine Lundgaard
Vissing, John
Rostrup, Egill
Larsson, Henrik Bo Wiberg
author_facet Lindberg, Ulrich
Kruuse, Christina
Witting, Nanna
Jørgensen, Stine Lundgaard
Vissing, John
Rostrup, Egill
Larsson, Henrik Bo Wiberg
author_sort Lindberg, Ulrich
collection PubMed
description INTRODUCTION: Patients with dystrophinopathies show low levels of neuronal nitric oxide synthase (nNOS), due to reduced or absent dystrophin expression, as nNOS is attached to the dystrophin‐associated protein complex. Deficient nNOS function leads to functional ischemia during muscle activity. Dystrophin‐like proteins with nNOS attached have also been identified in the brain. This suggests that a mechanism of cerebral functional ischemia with attenuation of normal activation‐related vascular response may cause changes in brain function. METHODS: The aim of this study was to investigate whether the brain response of patients with Becker muscular dystrophy (BMD) is dysfunctional compared to that of healthy controls. To investigate a potential change in brain activation response in patients with BMD, median nerve somatosensory evoked stimulation, with stimulation durations of 2, 4, and 10 s, was performed while recording electroencephalography and blood oxygen level‐dependent (BOLD) functional magnetic resonance imaging. RESULTS: Results in 14 male patients with BMD (36.2 ± 9.9 years) were compared with those of 10 healthy controls (34.4 ± 10.9 years). Compared to controls, the patients with BMD showed sustained cortical electrical activity and a significant smaller BOLD activation in contralateral primary somatosensory cortex and bilaterally in secondary somatosensory cortex. In addition, significant activation differences were found after long duration (10 s) stimuli in thalamus. CONCLUSION: An altered neurovascular response in patients with BMD may increase our understanding of neurovascular coupling and the pathogenesis related to dystrophinopathy and nNOS.
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spelling pubmed-59915602018-06-20 Altered somatosensory neurovascular response in patients with Becker muscular dystrophy Lindberg, Ulrich Kruuse, Christina Witting, Nanna Jørgensen, Stine Lundgaard Vissing, John Rostrup, Egill Larsson, Henrik Bo Wiberg Brain Behav Original Research INTRODUCTION: Patients with dystrophinopathies show low levels of neuronal nitric oxide synthase (nNOS), due to reduced or absent dystrophin expression, as nNOS is attached to the dystrophin‐associated protein complex. Deficient nNOS function leads to functional ischemia during muscle activity. Dystrophin‐like proteins with nNOS attached have also been identified in the brain. This suggests that a mechanism of cerebral functional ischemia with attenuation of normal activation‐related vascular response may cause changes in brain function. METHODS: The aim of this study was to investigate whether the brain response of patients with Becker muscular dystrophy (BMD) is dysfunctional compared to that of healthy controls. To investigate a potential change in brain activation response in patients with BMD, median nerve somatosensory evoked stimulation, with stimulation durations of 2, 4, and 10 s, was performed while recording electroencephalography and blood oxygen level‐dependent (BOLD) functional magnetic resonance imaging. RESULTS: Results in 14 male patients with BMD (36.2 ± 9.9 years) were compared with those of 10 healthy controls (34.4 ± 10.9 years). Compared to controls, the patients with BMD showed sustained cortical electrical activity and a significant smaller BOLD activation in contralateral primary somatosensory cortex and bilaterally in secondary somatosensory cortex. In addition, significant activation differences were found after long duration (10 s) stimuli in thalamus. CONCLUSION: An altered neurovascular response in patients with BMD may increase our understanding of neurovascular coupling and the pathogenesis related to dystrophinopathy and nNOS. John Wiley and Sons Inc. 2018-04-24 /pmc/articles/PMC5991560/ /pubmed/30106246 http://dx.doi.org/10.1002/brb3.985 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Lindberg, Ulrich
Kruuse, Christina
Witting, Nanna
Jørgensen, Stine Lundgaard
Vissing, John
Rostrup, Egill
Larsson, Henrik Bo Wiberg
Altered somatosensory neurovascular response in patients with Becker muscular dystrophy
title Altered somatosensory neurovascular response in patients with Becker muscular dystrophy
title_full Altered somatosensory neurovascular response in patients with Becker muscular dystrophy
title_fullStr Altered somatosensory neurovascular response in patients with Becker muscular dystrophy
title_full_unstemmed Altered somatosensory neurovascular response in patients with Becker muscular dystrophy
title_short Altered somatosensory neurovascular response in patients with Becker muscular dystrophy
title_sort altered somatosensory neurovascular response in patients with becker muscular dystrophy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991560/
https://www.ncbi.nlm.nih.gov/pubmed/30106246
http://dx.doi.org/10.1002/brb3.985
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