Di Lazzaro V, Oliviero A, Pilato F, Saturno E, Dileone M, Marra C, Ghirlanda S, Ranieri F, Gainotti G, Tonali P
Institute of Neurology, Università Cattolica, L.go A. Gemelli 8, 00168 Rome, Italy.
J Neurol Neurosurg Psychiatry. 2005 Aug;76(8):1064-9. doi: 10.1136/jnnp.2004.051334.
In vivo evaluation of cholinergic circuits of the human brain has recently been introduced using a transcranial magnetic stimulation (TMS) protocol based on coupling peripheral nerve stimulation with motor cortex TMS (short latency afferent inhibition, SAI). SAI is reduced in Alzheimer's disease (AD) and drugs enhancing cholinergic transmission increase SAI.
We evaluated whether SAI testing, together with SAI test-retest, after a single dose of the acetylcholinesterase (AChE) inhibitor rivastigmine, might be useful in predicting the response after 1 year treatment with rivastigmine in 16 AD patients.
Fourteen AD patients had pathologically reduced SAI. SAI was increased after administration of a single oral dose of rivastigmine in AD patients with abnormal baseline SAI, but individual responses to rivastigmine varied widely, with SAI change ranging from an increase in inhibition of approximately 50% of test size to no change. Baseline SAI and the increase in SAI after a single dose of rivastigmine were correlated with response to long term treatment. A normal SAI in baseline conditions, or an abnormal SAI in baseline conditions that was not greatly increased by a single oral dose of rivastigmine, were invariably associated with poor response to long term treatment, while an abnormal SAI in baseline conditions in conjunction with a large increase in SAI after a single dose of rivastigmine was associated with good response to long term treatment in most of the patients.
Evaluation of SAI may be useful for identifying AD patients likely to respond to treatment with AChE inhibitors.
最近引入了一种基于将外周神经刺激与运动皮层经颅磁刺激(TMS)相结合的经颅磁刺激(TMS)方案(短潜伏期传入抑制,SAI),用于对人脑胆碱能回路进行体内评估。在阿尔茨海默病(AD)中SAI降低,而增强胆碱能传递的药物可增加SAI。
我们评估了在16例AD患者中,单剂量乙酰胆碱酯酶(AChE)抑制剂卡巴拉汀治疗后进行SAI测试以及SAI重测,是否有助于预测卡巴拉汀治疗1年后的反应。
14例AD患者的SAI病理性降低。基线SAI异常的AD患者口服单剂量卡巴拉汀后SAI增加,但个体对卡巴拉汀的反应差异很大,SAI变化范围从抑制增加约50%的测试大小到无变化。基线SAI和单剂量卡巴拉汀后SAI的增加与长期治疗反应相关。基线条件下SAI正常,或基线条件下SAI异常但单剂量口服卡巴拉汀后未大幅增加,均与长期治疗反应不佳相关,而基线条件下SAI异常且单剂量卡巴拉汀后SAI大幅增加,在大多数患者中与长期治疗反应良好相关。
SAI评估可能有助于识别可能对AChE抑制剂治疗有反应的AD患者。