Exploring the false discovery rate in multichannel NIRS

被引:328
作者
Singh, Archana K.
Dan, Ippeita
机构
[1] Natl Food Res Inst, Tsukuba, Ibaraki 3058642, Japan
[2] Univ Tsukuba, Dept Comp Sci, Tsukuba, Ibaraki 3058573, Japan
关键词
optical topography; diffused optical imaging; statistical testing; familywise error;
D O I
10.1016/j.neuroimage.2006.06.047
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Near infrared spectroscopy (NIRS), an emerging non-invasive tool for functional neuroimaging, has evolved as a multichannel technique allowing simultaneous measurements through many channels ranging from below ten to above hundred. Simultaneous testing of such a large number of channels escalates the risk of Type I error, therefore multiplicity correction is unavoidable. To date, only a few studies have considered this issue using Bonferroni correction, which is an effective conservative solution, but may be too severe for neuroimaging. Its power varies in inverse proportion of the number of channels, which varies among NIRS studies depending on selected region of interest (1101), thereby leading to a subjective inference. This problem may be well circumvented by a more contemporary approach, called false discovery rate (FDR) that is widely being adopted in functional neuroimaging. An FDR-based procedure controls the expected proportion of erroneously rejected hypotheses among the rejected hypotheses, which offers a more objective, powerful, and consistent measure of Type I error than Bonferroni correction and maintains a better balance between power and specificity. In this technical note, we examine FDR approach using examples from simulated and real NIRS data. The FDR-based procedure could yield 52% more power than Bonferroni correction in a 172-channel real NIRS study and proved to be more robust against the changing number of channels. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:542 / 549
页数:8
相关论文
共 37 条
[1]  
Benjamini Y, 2001, ANN STAT, V29, P1165
[2]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[3]   COGNITION-ACTIVATED LOW-FREQUENCY MODULATION OF LIGHT-ABSORPTION IN HUMAN BRAIN [J].
CHANCE, B ;
ZHUANG, Z ;
UNAH, C ;
ALTER, C ;
LIPTON, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3770-3774
[4]   On the statistical significance of event-related EEG desynchronization and synchronization in the time-frequency plane [J].
Durka, PJ ;
Zygierewicz, J ;
Klekowicz, H ;
Ginter, J ;
Blinowska, KJ .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2004, 51 (07) :1167-1175
[5]  
Friston K.J., 1994, Human Brain Mapping, V2, P189, DOI DOI 10.1002/HBM.460020402
[6]   Thresholding of statistical maps in functional neuroimaging using the false discovery rate [J].
Genovese, CR ;
Lazar, NA ;
Nichols, T .
NEUROIMAGE, 2002, 15 (04) :870-878
[7]   A SHARPER BONFERRONI PROCEDURE FOR MULTIPLE TESTS OF SIGNIFICANCE [J].
HOCHBERG, Y .
BIOMETRIKA, 1988, 75 (04) :800-802
[8]  
HOLM S, 1979, SCAND J STAT, V6, P65
[9]   DYNAMIC MULTICHANNEL NEAR-INFRARED OPTICAL IMAGING OF HUMAN BRAIN ACTIVITY [J].
HOSHI, Y ;
TAMURA, M .
JOURNAL OF APPLIED PHYSIOLOGY, 1993, 75 (04) :1842-1846
[10]   Differences in the hemodynamic response to event-related motor and visual paradigms as measured by near-infrared spectroscopy [J].
Jasdzewski, G ;
Strangman, G ;
Wagner, J ;
Kwong, KK ;
Poldrack, RA ;
Boas, DA .
NEUROIMAGE, 2003, 20 (01) :479-488