Literature DB >> 28847712

Corrections for multiple comparisons in voxel-based lesion-symptom mapping.

Daniel Mirman1, Jon-Frederick Landrigan2, Spiro Kokolis2, Sean Verillo2, Casey Ferrara3, Dorian Pustina4.   

Abstract

Voxel-based lesion-symptom mapping (VLSM) is an important method for basic and translational human neuroscience research. VLSM leverages modern neuroimaging analysis techniques to build on the classic approach of examining the relationship between location of brain damage and cognitive deficits. Testing an association between deficit severity and lesion status in each voxel involves very many individual tests and requires statistical correction for multiple comparisons. Several strategies have been adapted from analysis of functional neuroimaging data, though VLSM faces a more difficult trade-off between avoiding false positives and statistical power (missing true effects). We used simulated and real deficit scores from a sample of approximately 100 individuals with left hemisphere stroke to evaluate two such permutation-based approaches. Using permutation to set a minimum cluster size identified a region that systematically extended well beyond the true region, making it ill-suited to identifying brain-behavior relationships. In contrast, generalizing the standard permutation-based family-wise error correction approach provided a principled way to balance false positives and false negatives. Comparison with the widely-used parametric false discovery rate (FDR) correction showed that FDR produces anti-conservative results at smaller sample sizes (N = 30-60). An implementation of the continuous permutation-based FWER correction method described here is included in the lesymap package for lesion-symptom mapping (https://dorianps.github.io/LESYMAP/).
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Cluster size correction; Family-wise error correction; Multiple comparisons; Permutation tests; VLSM; Voxel-based lesion-symptom mapping

Mesh:

Year:  2017        PMID: 28847712      PMCID: PMC5826816          DOI: 10.1016/j.neuropsychologia.2017.08.025

Source DB:  PubMed          Journal:  Neuropsychologia        ISSN: 0028-3932            Impact factor:   3.139


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