Yamamoto Yuki, Kawai Wakana, Hayashi Tatsuya, Uga Minako, Kyutoku Yasushi, Dan Ippeita
Chuo University, Applied Cognitive Neuroscience Laboratory, Faculty of Science and Engineering, Tokyo, Japan.
Yamato University, Department of Information Science, Faculty of Science and Engineering, Osaka, Japan.
Neurophotonics. 2024 Jul;11(3):035004. doi: 10.1117/1.NPh.11.3.035004. Epub 2024 Jul 27.
The advancement of multichannel functional near-infrared spectroscopy (fNIRS) has enabled measurements across a wide range of brain regions. This increase in multiplicity necessitates the control of family-wise errors in statistical hypothesis testing. To address this issue, the effective multiplicity ( ) method designed for channel-wise analysis, which considers the correlation between fNIRS channels, was developed. However, this method loses reliability when the sample size is smaller than the number of channels, leading to a rank deficiency in the eigenvalues of the correlation matrix and hindering the accuracy of calculations.
We aimed to reevaluate the effectiveness of the method for fNIRS data with a small sample size.
In experiment 1, we used resampling simulations to explore the relationship between sample size and values. Based on these results, experiment 2 employed a typical exponential model to investigate whether valid could be predicted from a small sample size.
Experiment 1 revealed that the values were underestimated when the sample size was smaller than the number of channels. However, an exponential pattern was observed. Subsequently, in experiment 2, we found that valid values can be derived from sample sizes of 30 to 40 in datasets with 44 and 52 channels using a typical exponential model.
The findings from these two experiments indicate the potential for the effective application of correction in fNIRS studies with sample sizes smaller than the number of channels.
多通道功能近红外光谱技术(fNIRS)的发展使得能够对广泛的脑区进行测量。这种测量多样性的增加使得在统计假设检验中需要控制族系误差。为了解决这个问题,开发了用于通道级分析的有效多样性( )方法,该方法考虑了fNIRS通道之间的相关性。然而,当样本量小于通道数量时,该方法会失去可靠性,导致相关矩阵的特征值出现秩亏,从而影响 计算的准确性。
我们旨在重新评估对于小样本量的fNIRS数据, 方法的有效性。
在实验1中,我们使用重采样模拟来探索样本量与 值之间的关系。基于这些结果,实验2采用典型的指数模型来研究是否可以从小样本量预测有效的 。
实验1表明,当样本量小于通道数量时, 值被低估。然而,观察到一种指数模式。随后,在实验2中,我们发现使用典型的指数模型,在具有44和52个通道的数据集里,样本量为30至40时可以得出有效的 值。
这两个实验的结果表明,在样本量小于通道数量的fNIRS研究中,有效应用 校正具有潜力。