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阿尔茨海默病患者皮质结构和功能连接中断:弥散张量成像和经颅磁刺激的联合研究。

Structural and functional cortical disconnection in Alzheimer's disease: a combined study using diffusion tensor imaging and transcranial magnetic stimulation.

机构信息

DZNE, German Centre for Neurodegenerative Diseases, Rostock, Germany.

出版信息

Psychiatry Res. 2013 Jun 30;212(3):192-200. doi: 10.1016/j.pscychresns.2012.04.008. Epub 2012 Nov 11.

Abstract

We investigated the functional consequences of compromised white matter integrity in Alzheimer's disease by combining Diffusion Tensor Imaging (DTI) and Transcranial Magnetic Stimulation (TMS) in 19 patients with AD (Alzheimer's disease) and 19 healthy controls. We used a region of interest approach and correlated the ipsilateral silent period (iSP) and the resting motor threshold (RMT) from TMS with fractional anisotropy (FA) and mean diffusivity (MD) values of the corpus callosum and corticospinal tract. AD patients showed significant reductions of FA in intracortical projecting fibre tracts compared to controls and widespread increases in MD. TMS data showed increased latency of iSP in AD patients and a decreased RMT, indicating decreased motor cortical inhibition. Although both TMS and DTI metrics were prominently altered in AD patients, impaired white matter integrity was not associated with increased iSP latency or reduced RMT, as correlation of TMS parameters with FA and MD values in the a priori defined regions showed no significant effects. Therefore, we argue that beside the direct degeneration of the underlying fibre tracts, other pathophysiological mechanisms may account for the observation of decreased transcallosal inhibition and increased motor excitability in AD.

摘要

我们通过对 19 例 AD(阿尔茨海默病)患者和 19 例健康对照者进行弥散张量成像(DTI)和经颅磁刺激(TMS)联合研究,探讨了 AD 患者白质完整性受损的功能后果。我们采用了感兴趣区方法,并将 TMS 的同侧静息期(iSP)和静息运动阈值(RMT)与胼胝体和皮质脊髓束的各向异性分数(FA)和平均弥散度(MD)值相关联。与对照组相比,AD 患者皮质内投射纤维束的 FA 值显著降低,MD 值广泛升高。TMS 数据显示 AD 患者 iSP 的潜伏期延长,RMT 降低,表明运动皮质抑制减弱。尽管 AD 患者的 TMS 和 DTI 指标均明显改变,但白质完整性受损与 iSP 潜伏期延长或 RMT 降低无关,因为 TMS 参数与预先定义区域的 FA 和 MD 值的相关性没有显示出显著影响。因此,我们认为除了潜在纤维束的直接变性外,其他病理生理机制可能解释了 AD 患者观察到的跨胼胝体抑制减弱和运动兴奋性增加。

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