REVAL-Rehabilitation Research Center, Faculty of Rehabilitation Sciences, University of Hasselt, Diepenbeek, Belgium.
Brain Stimulation Laboratory, Department of Psychiatry, Medical University of South Carolina, Charleston, SC, United States of America.
J Neural Eng. 2022 Oct 28;19(5):056045. doi: 10.1088/1741-2552/ac9a78.
. Transcranial electrical stimulation (tES) is a promising method for modulating brain activity and excitability with variable results to date. To minimize electric (E-)field strength variability, we introduce the 2-sample prospective E-field dosing (2-SPED) approach, which uses E-field strengths induced by tES in a first population to individualize stimulation intensity in a second population.. We performed E-field modeling of three common tES montages in 300 healthy younger adults. First, permutation analyses identified the sample size required to obtain a stable group average E-field in the primary motor cortex (M1), with stability being defined as the number of participants where all group-average E-field strengths ± standard deviation did not leave the population's 5-95 percentile range. Second, this stable group average was used to individualize tES intensity in a second independent population (n = 100). The impact of individualized versus fixed intensity tES on E-field strength variability was analyzed.. In the first population, stable group average E-field strengths (V/m) in M1 were achieved at 74-85 participants, depending on the tES montage. Individualizing the stimulation intensity (mA) in the second population resulted in uniform M1 E-field strength (all p < 0.001) and significantly diminished peak cortical E-field strength variability (all p < 0.01), across all montages.. 2-SPED is a feasible way to prospectively induce more uniform E-field strengths in a region of interest. Future studies might apply 2-SPED to investigate whether decreased E-field strength variability also results in decreased physiological and behavioral variability in response to tES.
. 经颅电刺激 (tES) 是一种很有前途的调节大脑活动和兴奋性的方法,但到目前为止,其结果还存在差异。为了最大限度地减少电场 (E-) 强度的可变性,我们引入了两样本前瞻性 E 场剂量 (2-SPED) 方法,该方法使用 tES 在第一人群中产生的 E 场强度来个性化第二人群中的刺激强度。. 我们对 300 名健康年轻成年人进行了三种常见 tES 模式的 E 场建模。首先,通过置换分析确定了在初级运动皮层 (M1) 获得稳定的群体平均 E 场所需的样本量,稳定性定义为所有群体平均 E 场强度 ±标准差都没有超出群体 5-95%百分位数范围的参与者数量。其次,使用稳定的群体平均值来个性化第二独立人群 (n = 100) 的 tES 强度。分析了个性化与固定强度 tES 对 E 场强度可变性的影响。. 在第一人群中,取决于 tES 模式,在 74-85 名参与者中达到了稳定的群体平均 E 场强度 (V/m)。在第二人群中个性化刺激强度 (mA) 导致 M1 的 E 场强度均匀 (所有 p < 0.001),并显著降低了皮质 E 场强度的峰值可变性 (所有 p < 0.01),所有模式均如此。. 2-SPED 是一种可行的方法,可以前瞻性地在感兴趣的区域中产生更均匀的 E 场强度。未来的研究可能会应用 2-SPED 来研究 E 场强度可变性的降低是否也会导致 tES 反应的生理和行为可变性降低。