Technical considerations of a game-theoretical approach for lesion symptom mapping

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Technical considerations of a game-theoretical approach for lesion symptom mapping. / Zavaglia, Melissa; Forkert, Nils D; Cheng, Bastian; Gerloff, Christian; Thomalla, Götz; Hilgetag, Claus C.

In: BMC NEUROSCI, Vol. 17, No. 1, 27.06.2016, p. 40.

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@article{44938614f9c049e884bbb7976d181106,
title = "Technical considerations of a game-theoretical approach for lesion symptom mapping",
abstract = "BACKGROUND: Various strategies have been used for inferring brain functions from stroke lesions. We explored a new mathematical approach based on game theory, the so-called multi-perturbation Shapley value analysis (MSA), to assess causal function localizations and interactions from multiple perturbation data. We applied MSA to a dataset composed of lesion patterns of 148 acute stroke patients and their National Institutes of Health Stroke Scale (NIHSS) scores, to systematically investigate the influence of different parameter settings on the outcomes of the approach. Specifically, we investigated aspects of MSA methodology including the choice of the predictor algorithm (typology and kernel functions), training dataset (original versus binary), as well as the influence of lesion thresholds. We assessed the suitability of MSA for processing real clinical lesion data and established the central parameters for this analysis.RESULTS: We derived general recommendations for the analysis of clinical datasets by MSA and showed that, for the studied dataset, the best approach was to use a linear-kernel support vector machine predictor, trained with a binary training dataset, where the binarization was implemented through a median threshold of lesion size for each region. We demonstrated that the results obtained with different MSA variants lead to almost identical results as the basic MSA.CONCLUSIONS: MSA is a feasible approach for the multivariate lesion analysis of clinical stroke data. Informed choices need to be made to set parameters that may affect the analysis outcome.",
keywords = "Journal Article",
author = "Melissa Zavaglia and Forkert, {Nils D} and Bastian Cheng and Christian Gerloff and G{\"o}tz Thomalla and Hilgetag, {Claus C}",
year = "2016",
month = jun,
day = "27",
doi = "10.1186/s12868-016-0275-6",
language = "English",
volume = "17",
pages = "40",
journal = "BMC NEUROSCI",
issn = "1471-2202",
publisher = "BioMed Central Ltd.",
number = "1",

}

RIS

TY - JOUR

T1 - Technical considerations of a game-theoretical approach for lesion symptom mapping

AU - Zavaglia, Melissa

AU - Forkert, Nils D

AU - Cheng, Bastian

AU - Gerloff, Christian

AU - Thomalla, Götz

AU - Hilgetag, Claus C

PY - 2016/6/27

Y1 - 2016/6/27

N2 - BACKGROUND: Various strategies have been used for inferring brain functions from stroke lesions. We explored a new mathematical approach based on game theory, the so-called multi-perturbation Shapley value analysis (MSA), to assess causal function localizations and interactions from multiple perturbation data. We applied MSA to a dataset composed of lesion patterns of 148 acute stroke patients and their National Institutes of Health Stroke Scale (NIHSS) scores, to systematically investigate the influence of different parameter settings on the outcomes of the approach. Specifically, we investigated aspects of MSA methodology including the choice of the predictor algorithm (typology and kernel functions), training dataset (original versus binary), as well as the influence of lesion thresholds. We assessed the suitability of MSA for processing real clinical lesion data and established the central parameters for this analysis.RESULTS: We derived general recommendations for the analysis of clinical datasets by MSA and showed that, for the studied dataset, the best approach was to use a linear-kernel support vector machine predictor, trained with a binary training dataset, where the binarization was implemented through a median threshold of lesion size for each region. We demonstrated that the results obtained with different MSA variants lead to almost identical results as the basic MSA.CONCLUSIONS: MSA is a feasible approach for the multivariate lesion analysis of clinical stroke data. Informed choices need to be made to set parameters that may affect the analysis outcome.

AB - BACKGROUND: Various strategies have been used for inferring brain functions from stroke lesions. We explored a new mathematical approach based on game theory, the so-called multi-perturbation Shapley value analysis (MSA), to assess causal function localizations and interactions from multiple perturbation data. We applied MSA to a dataset composed of lesion patterns of 148 acute stroke patients and their National Institutes of Health Stroke Scale (NIHSS) scores, to systematically investigate the influence of different parameter settings on the outcomes of the approach. Specifically, we investigated aspects of MSA methodology including the choice of the predictor algorithm (typology and kernel functions), training dataset (original versus binary), as well as the influence of lesion thresholds. We assessed the suitability of MSA for processing real clinical lesion data and established the central parameters for this analysis.RESULTS: We derived general recommendations for the analysis of clinical datasets by MSA and showed that, for the studied dataset, the best approach was to use a linear-kernel support vector machine predictor, trained with a binary training dataset, where the binarization was implemented through a median threshold of lesion size for each region. We demonstrated that the results obtained with different MSA variants lead to almost identical results as the basic MSA.CONCLUSIONS: MSA is a feasible approach for the multivariate lesion analysis of clinical stroke data. Informed choices need to be made to set parameters that may affect the analysis outcome.

KW - Journal Article

U2 - 10.1186/s12868-016-0275-6

DO - 10.1186/s12868-016-0275-6

M3 - SCORING: Journal article

C2 - 27349961

VL - 17

SP - 40

JO - BMC NEUROSCI

JF - BMC NEUROSCI

SN - 1471-2202

IS - 1

ER -