Impairment of sensory-motor plasticity in mild Alzheimer¡¯s disease

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• 作者：Terranova Carmen^a ; ¹ ; Sant’ ; Angelo Antonino^a ; Morgante Francesca^a ; Rizzo Vincenzo^a ; Allegra Roberta^a ; Arena Maria Grazia^a ; Ricciardi Lucia^a ; Ghilardi Maria Felice^b ; Girlanda Paolo^a ; Quartarone Angelo^a ; ^b ; ^c ; ¹ ; ^{angelo.quartarone@unime.it}
• 关键词：Alzheimer disease ; Associative stimulation ; LTP ; Motor cortex plasticity ; Short afferent inhibition ; TMS
• 刊名：Brain Stimulation
• 出版年：2013
• 出版时间：January, 2013
• 年：2013
• 卷：6
• 期：1
• 页码：62-66
• 全文大小：250 K

文摘

Background

Primary motor cortex (M1) is relatively spared in the early stages of Alzheimer¡¯s disease (AD).

Objective

Aim of the present study was to investigate whether abnormal M1 synaptic plasticity is present at an early stage of AD. We employed an electrophysiological protocol, named rapid paired associative stimulation (rPAS), involving repetitive transcranial magnetic stimulation (rTMS) paired with electrical stimulation of the contralateral median nerve, that modifies corticospinal excitability and short latency afferent inhibition (SAI).

Methods

We studied 10 patients with a diagnosis of probable mild AD according to the Mini Mental State Examination score (minimum 21) and 14 age-matched control subjects. Motor evoked potentials (MEP) amplitudes and short-afferent inhibition (SAI) were measured at baseline before and for up to 60?min after 5Hz-rPAS in abductor pollicis brevis (APB). rPAS consisted of 600 pairs of transcranial magnetic stimuli, at a rate of 5?Hz for 2?min, coupled with electrical median nerve stimulation preceding TMS over the contralateral M1 at an inter-stimulus interval of 25?ms.

Results

Baseline SAI was significantly reduced in AD patients. In the control subjects rPAS induced a significant increase in MEP amplitudes and a decrease of SAI in the APB muscle persistently for up to 1?h. Conversely 5Hz-rPAS did not induce any significant changes in MEP amplitudes and SAI in mild AD patients.

Conclusions

Sensory-motor plasticity is impaired in the motor cortex of AD at an early stage of the disease.