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DOI 10.1002/1531-8257(200011)15:6<1210::aid-mds1022>3.0.co;2-r

Медицинская библиотека · Movement disorders : official journal of the Movement Disorder Society · 2000

Abnormalities of motor cortical excitability are not correlated with clinical features in atypical parkinsonism.

Marchese R, Trompetto C, Buccolieri A, Abbruzzese G

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVE

To evaluate the specificity of motor cortical excitability changes in parkinsonian syndromes and their relevance to the pathophysiology of cardinal parkinsonian features.

METHODS

Paired transcranial magnetic stimulation (TMS) was used to assess cortico-cortical inhibition (CCI) and facilitation (CCF) in the opponens pollicis muscle of patients with atypical, non-L-dopa- (LD) responsive parkinsonism.

RESULTS

Compared with age-matched normal control subjects, CCI (interstimulus interval [ISI], 3 ms) was significantly reduced in 10 patients with predominantly parkinsonian multiple system atrophy (MSA-P) and in seven with vascular parkinsonism (VP), but not in four with predominantly cerebellar MSA. No significant change of CCF (ISI, 12 ms) was observed. No correlation was found between the amount of CCI and clinical status as evaluated with the Unified Parkinson's Disease Rating Scale (UPDRS). In 10 patients (5 MSA-P, 5 VP), CCI was significantly increased by LD acute administration without concurrent clinical changes.

CONCLUSIONS

Abnormalities of CCI are not peculiar to idiopathic Parkinson's disease and seem unlikely to underlie any specific parkinsonian feature, but rather possibly reflect a nonspecific imbalance of inhibitory and facilitatory motor cortical circuits.

Для цитирования: Marchese R, Trompetto C, Buccolieri A, Abbruzzese G. Abnormalities of motor cortical excitability are not correlated with clinical features in atypical parkinsonism.. Movement disorders : official journal of the Movement Disorder Society. 2000. DOI: 10.1002/1531-8257(200011)15:6<1210::aid-mds1022>3.0.co;2-r.

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