Movement-related cortical potentials in ALS increase at lower and decrease at higher upper motor neuron burden scores

被引:6
作者
Bizovicar, Natasa [1 ]
Koritnik, Blaz [1 ]
Zidar, Ignac [1 ]
Dreo, Jurij [1 ]
Zidar, Janez [1 ]
机构
[1] Univ Med Ctr, Inst Clin Neurophysiol, Div Neurol, SI-1525 Ljubljana, Slovenia
关键词
Amyotrophic lateral sclerosis; breathing; neuroplasticity; electroencephalography; Bereitschaftspotential; AMYOTROPHIC-LATERAL-SCLEROSIS; REORGANIZATION; DEGENERATION; INVOLVEMENT; DYSFUNCTION; ACTIVATION; PLASTICITY; DISORDERS; CORTEX; BRAIN;
D O I
10.3109/21678421.2012.760604
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Our aim was to investigate changes in movement-related cortical potentials (MRCPs) in ALS patients with different degrees of upper motor neuron (UMN) involvement. Since respiratory failure is the main cause of death in ALS, changes in inspiratory-related(sniffing) potentials were studied in addition to finger-flexion-related potentials. Subjects (21 ALS, 19 controls) performed two self-paced motor tasks while their EEGs were recorded. The first task required flexions of the right index finger and the second, brisk nasal inspirations. The early (BP1), late (BP2) and motor potential (MP) components of MRCPs were evaluated. Results showed that patients generated higher MRCPs than controls. However, this effect was most significant in the subgroup of patients with low UMN burden (LUB). The high UMN burden (HUB) subgroup did not differ from controls, but had significantly lower MP amplitudes than the LUB subgroup. Progressive UMN deterioration was associated with an initial increase, followed by a later decrease, in MP amplitudes in ALS. In conclusion, the increased MRCPs in LUB compared to HUB patients indicate different processes of ALS pathophysiology that force opposing changes in MRCP amplitudes.
引用
收藏
页码:380 / 389
页数:10
相关论文
共 55 条
[51]   Generators of movement-related cortical potentials: fMRI-constrained EEG dipole source analysis [J].
Toma, K ;
Matsuoka, T ;
Immisch, I ;
Mima, T ;
Waldvogel, D ;
Koshy, B ;
Hanakawa, T ;
Shill, H ;
Hallett, M .
NEUROIMAGE, 2002, 17 (01) :161-173
[52]   Evidence of widespread cerebral microglial activation in amyotrophic lateral sclerosis:: an [11C](R)-PK11195 positron emission tomography study [J].
Turner, MR ;
Cagnin, A ;
Turkheimer, FE ;
Miller, CCJ ;
Shaw, CE .
NEUROBIOLOGY OF DISEASE, 2004, 15 (03) :601-609
[53]   Cortical excitability distinguishes ALS from mimic disorders [J].
Vucic, Steve ;
Cheah, Benjamin C. ;
Yiannikas, Con ;
Kiernan, Matthew C. .
CLINICAL NEUROPHYSIOLOGY, 2011, 122 (09) :1860-1866
[54]   Bereitschaftspotential in amyotrophic lateral sclerosis (ALS): lower amplitudes in patients with hyperreflexia (spasticity) [J].
Westphal, KP ;
Heinemann, HA ;
Grozinger, B ;
Kotchoubey, BJ ;
Diekmann, V ;
Becker, W ;
Kornhuber, HH .
ACTA NEUROLOGICA SCANDINAVICA, 1998, 98 (01) :15-21
[55]   Changes in motor cortex inhibition over time in patients with amyotrophic lateral sclerosis [J].
Zanette, G ;
Tamburin, S ;
Manganotti, P ;
Refatti, N ;
Forgione, A ;
Rizzuto, N .
JOURNAL OF NEUROLOGY, 2002, 249 (12) :1723-1728