Structural and functional neuroimaging in amyotrophic lateral sclerosis

Abstract. Amyotrophic lateral sclerosis (ALS) is a fatal progressive central nervous system disorder affecting the upper and lower motor neurons. It is important to study the features of the course and progression of neurodegeneration in ALS, since no effective methods for treating this disease have...

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Main Authors: Ilya S. Bakulin, Aleksandr V. Chervyakov, Elena I. Kremneva, Rodion N. Konovalov, Maria N. Zakharova
Format: Article
Language:English
Published: Research Center of Neurology 2017-08-01
Series:Анналы клинической и экспериментальной неврологии
Subjects:
Online Access:https://annaly-nevrologii.com/journal/pathID/article/viewFile/480/370
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author Ilya S. Bakulin
Aleksandr V. Chervyakov
Elena I. Kremneva
Rodion N. Konovalov
Maria N. Zakharova
author_facet Ilya S. Bakulin
Aleksandr V. Chervyakov
Elena I. Kremneva
Rodion N. Konovalov
Maria N. Zakharova
author_sort Ilya S. Bakulin
collection DOAJ
description Abstract. Amyotrophic lateral sclerosis (ALS) is a fatal progressive central nervous system disorder affecting the upper and lower motor neurons. It is important to study the features of the course and progression of neurodegeneration in ALS, since no effective methods for treating this disease have been developed yet. Despite the clear evidence that brain lesions in ALS are of multisystem nature, there are no objective biomarkers of lesions of the upper motor neuron and the extramotor areas of the brain. Structural and functional neuroimaging, such as MR brain morphometry, diffusion tensor imaging, MR spectroscopy, functional MRI, positron emission tomography (PET), etc., have recently been playing a significant role in studying ALS. The results of neuroimaging studies are analyzed in this review in the context of using them to diagnose, predict, and monitor the course of ALS. Diffusion tensor imaging, MR spectroscopy, PET, combination of several neuroimaging methods and their combination with transcranial magnetic stimulation are the most sensitive and specific techniques to be used to diagnose the disease. Diffusion tensor imaging and MR spectroscopy can be used to monitor and predict the disease course. The main limitations and shortcomings of the performed studies, as well as the possible outlook for using neuroimaging in ALS, are discussed.
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spelling doaj.art-edccd417d7de41baae850d5191dbd0842022-12-22T03:29:32ZengResearch Center of NeurologyАнналы клинической и экспериментальной неврологии2075-54732409-25332017-08-01112768710.18454/ACEN.2017.2.11363Structural and functional neuroimaging in amyotrophic lateral sclerosisIlya S. Bakulin0https://orcid.org/0000-0003-0716-3737Aleksandr V. Chervyakov1Elena I. Kremneva2Rodion N. Konovalov3https://orcid.org/0000-0001-5539-245XMaria N. Zakharova4Research Center of NeurologyResearch Center of NeurologyResearch Center of NeurologyResearch Center of NeurologyResearch Center of NeurologyAbstract. Amyotrophic lateral sclerosis (ALS) is a fatal progressive central nervous system disorder affecting the upper and lower motor neurons. It is important to study the features of the course and progression of neurodegeneration in ALS, since no effective methods for treating this disease have been developed yet. Despite the clear evidence that brain lesions in ALS are of multisystem nature, there are no objective biomarkers of lesions of the upper motor neuron and the extramotor areas of the brain. Structural and functional neuroimaging, such as MR brain morphometry, diffusion tensor imaging, MR spectroscopy, functional MRI, positron emission tomography (PET), etc., have recently been playing a significant role in studying ALS. The results of neuroimaging studies are analyzed in this review in the context of using them to diagnose, predict, and monitor the course of ALS. Diffusion tensor imaging, MR spectroscopy, PET, combination of several neuroimaging methods and their combination with transcranial magnetic stimulation are the most sensitive and specific techniques to be used to diagnose the disease. Diffusion tensor imaging and MR spectroscopy can be used to monitor and predict the disease course. The main limitations and shortcomings of the performed studies, as well as the possible outlook for using neuroimaging in ALS, are discussed.https://annaly-nevrologii.com/journal/pathID/article/viewFile/480/370amyotrophic lateral sclerosismotor neuron diseaseneuroimagingmribiomarkers
spellingShingle Ilya S. Bakulin
Aleksandr V. Chervyakov
Elena I. Kremneva
Rodion N. Konovalov
Maria N. Zakharova
Structural and functional neuroimaging in amyotrophic lateral sclerosis
Анналы клинической и экспериментальной неврологии
amyotrophic lateral sclerosis
motor neuron disease
neuroimaging
mri
biomarkers
title Structural and functional neuroimaging in amyotrophic lateral sclerosis
title_full Structural and functional neuroimaging in amyotrophic lateral sclerosis
title_fullStr Structural and functional neuroimaging in amyotrophic lateral sclerosis
title_full_unstemmed Structural and functional neuroimaging in amyotrophic lateral sclerosis
title_short Structural and functional neuroimaging in amyotrophic lateral sclerosis
title_sort structural and functional neuroimaging in amyotrophic lateral sclerosis
topic amyotrophic lateral sclerosis
motor neuron disease
neuroimaging
mri
biomarkers
url https://annaly-nevrologii.com/journal/pathID/article/viewFile/480/370
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AT rodionnkonovalov structuralandfunctionalneuroimaginginamyotrophiclateralsclerosis
AT marianzakharova structuralandfunctionalneuroimaginginamyotrophiclateralsclerosis