Bardouille Timothy, Power Lindsey, Lalancette Marc, Bishop Ronald, Beyea Steven, Taylor Margot J, Dunkley Benjamin T
Department of Physics and Atmospheric Science, Dalhousie University, 6310 Coburg Road, Halifax, NS, B3H 4R2, Canada; Biomedical Translational Imaging Centre (BIOTIC), IWK Health Centre, 5980 University Street, Halifax, NS, B3K 6R8, Canada; Department of Diagnostic Radiology, Dalhousie University, Room 319, Victoria Building, 1276 South Park St, Halifax, NS B3H 2Y9, Canada.
Biomedical Translational Imaging Centre (BIOTIC), IWK Health Centre, 5980 University Street, Halifax, NS, B3K 6R8, Canada.
Clin Neurol Neurosurg. 2018 Aug;171:63-69. doi: 10.1016/j.clineuro.2018.05.018. Epub 2018 May 26.
Magnetoencephalography (MEG) provides functional neuroimaging data for pre-surgical planning in patients with epilepsy or brain tumour. For mapping the primary somatosensory cortex (S1), MEG data are acquired while a patient undergoes median nerve stimulation (MNS) to localize components of the somatosensory evoked field (SEF). In clinical settings, only one MEG imaging session is usually possible due to limited resources. As such, it is important to have an a priori estimate of the expected variability in localization. Variability in S1 localization between mapping sessions using the same MEG system has been previously measured as 8 mm. There are different types of MEG systems available with varied hardware and software, and it is not known how using a different MEG system will impact on S1 localization.
In our study, healthy participants underwent the MNS procedure with two different MEG systems (Vector View and CTF). We compared the location, amplitude and latency of SEF components between data from each system to quantify variability and bias between MEG systems.
We found 8-11 mm variability in S1 localization between the two MEG systems, and no evidence for a systematic bias in location, amplitude or latency between the two systems.
These findings suggest that S1 localization is not biased by the type of MEG system used, and that differences between the two systems are not a major contributor to variability in localization.
脑磁图(MEG)可为癫痫或脑肿瘤患者的术前规划提供功能性神经影像数据。为了绘制初级体感皮层(S1),在患者接受正中神经刺激(MNS)以定位体感诱发电场(SEF)的成分时采集MEG数据。在临床环境中,由于资源有限,通常只能进行一次MEG成像检查。因此,对预期的定位变异性进行先验估计很重要。此前已测得,使用同一MEG系统在不同测绘时段之间S1定位的变异性为8毫米。市面上有不同类型的MEG系统,其硬件和软件各不相同,尚不清楚使用不同的MEG系统会如何影响S1定位。
在我们的研究中,健康参与者使用两种不同的MEG系统(Vector View和CTF)接受了MNS程序。我们比较了每个系统数据之间SEF成分的位置﹑幅度和潜伏期,以量化MEG系统之间的变异性和偏差。
我们发现,两种MEG系统之间S1定位的变异性为8 - 11毫米,且没有证据表明两个系统在位置、幅度或潜伏期方面存在系统性偏差。
这些发现表明,S1定位不受所用MEG系统类型的影响,且两个系统之间的差异不是定位变异性的主要因素。