Cengiz Bülent, Boran H Evren, Alaydın Halil Can, Tankisi Hatice, Samusyte Gintaute, Howells James, Koltzenburg Martin, Bostock Hugh
Department of Neurology, Gazi University Faculty of Medicine, Beşevler, 06500, Ankara, Turkey.
Department of Clinical Neurophysiology, Aarhus University Hospital, Aarhus, Denmark.
Exp Brain Res. 2022 Apr;240(4):1241-1247. doi: 10.1007/s00221-022-06327-5. Epub 2022 Feb 22.
Short-latency afferent inhibition (SAI), which is conventionally measured as a reduction in motor evoked potential amplitude (A-SAI), is of clinical interest as a potential biomarker for cognitive impairment. Since threshold-tracking has some advantages for clinical studies of short-interval cortical inhibition, we have compared A-SAI with a threshold-tracking alternative method (T-SAI). In the T-SAI method, inhibition was calculated by tracking the required TMS intensity for the targeted MEP amplitude (200 uV) both for the test (TMS only) and paired (TMS and peripheral stimulation) stimuli. A-SAI and T-SAI were recorded from 31 healthy subjects using ten stimuli at each of 12 inter-stimulus intervals, once in the morning and again in the afternoon. There were no differences between morning and afternoon recordings. When A-SAI was normalized by log conversion it was closely related to T-SAI. Between subjects, variability was similar for the two techniques, but within-subject variability was significantly smaller for normalized A-SAI. Conventional amplitude measurements appear more sensitive for detecting changes within-subjects, such as in interventional studies, but threshold-tracking may be as sensitive as detecting abnormal SAI in a patient.
短潜伏期传入抑制(SAI),传统上通过运动诱发电位幅度的降低(A-SAI)来测量,作为认知障碍的潜在生物标志物具有临床意义。由于阈值跟踪在短间隔皮质抑制的临床研究中有一些优势,我们将A-SAI与一种阈值跟踪替代方法(T-SAI)进行了比较。在T-SAI方法中,通过跟踪测试(仅TMS)和配对(TMS和外周刺激)刺激下达到目标运动诱发电位幅度(200 μV)所需的经颅磁刺激(TMS)强度来计算抑制。使用12个刺激间隔中的每一个间隔的10个刺激,从31名健康受试者中记录A-SAI和T-SAI,上午记录一次,下午再记录一次。上午和下午的记录之间没有差异。当通过对数转换对A-SAI进行标准化时,它与T-SAI密切相关。在受试者之间,两种技术的变异性相似,但标准化A-SAI的受试者内变异性明显较小。传统的幅度测量在检测受试者内部的变化(如在干预研究中)时似乎更敏感,但阈值跟踪在检测患者异常SAI方面可能同样敏感。