Brain activity, regional gray matter loss, and decision-making in multiple sclerosis

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Brain activity, regional gray matter loss, and decision-making in multiple sclerosis. / Weygandt, Martin; Wakonig, Katharina; Behrens, Janina; Meyer-Arndt, Lil; Söder, Eveline; Brandt, Alexander U; Bellmann-Strobl, Judith; Ruprecht, Klemens; Gold, Stefan M; Haynes, John-Dylan; Paul, Friedemann.

In: MULT SCLER J, Vol. 24, No. 9, 08.2018, p. 1163-1173.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Weygandt, M, Wakonig, K, Behrens, J, Meyer-Arndt, L, Söder, E, Brandt, AU, Bellmann-Strobl, J, Ruprecht, K, Gold, SM, Haynes, J-D & Paul, F 2018, 'Brain activity, regional gray matter loss, and decision-making in multiple sclerosis', MULT SCLER J, vol. 24, no. 9, pp. 1163-1173. https://doi.org/10.1177/1352458517717089

APA

Weygandt, M., Wakonig, K., Behrens, J., Meyer-Arndt, L., Söder, E., Brandt, A. U., Bellmann-Strobl, J., Ruprecht, K., Gold, S. M., Haynes, J-D., & Paul, F. (2018). Brain activity, regional gray matter loss, and decision-making in multiple sclerosis. MULT SCLER J, 24(9), 1163-1173. https://doi.org/10.1177/1352458517717089

Vancouver

Weygandt M, Wakonig K, Behrens J, Meyer-Arndt L, Söder E, Brandt AU et al. Brain activity, regional gray matter loss, and decision-making in multiple sclerosis. MULT SCLER J. 2018 Aug;24(9):1163-1173. https://doi.org/10.1177/1352458517717089

Bibtex

@article{3d5ca218c2244791bf9dd7c1555b926b,
title = "Brain activity, regional gray matter loss, and decision-making in multiple sclerosis",
abstract = "BACKGROUND: Decision-making (DM) abilities deteriorate with multiple sclerosis (MS) disease progression which impairs everyday life and is thus clinically important.OBJECTIVE: To investigate the underlying neurocognitive processes and their relation to regional gray matter (GM) loss induced by MS.METHODS: We used a functional magnetic resonance imaging (fMRI) Iowa Gambling Task to measure DM-related brain activity in 36 MS patients and 21 healthy controls (HC). From this activity, we determined neural parameters of two cognitive stages, a deliberation ({"}choice{"}) period preceding a choice and a post-choice ({"}feedback{"}) stage reporting decision outcomes. These measures were related to DM separately in intact and damaged GM areas as determined by a voxel-based morphometry analysis.RESULTS: Severely affected patients (with high lesion burden) showed worse DM-learning than HC ( t = -1.75, p = 0.045), moderately affected (low lesion burden) did not. Activity in the choice stage in intact insular ( t = 4.60, pFamily-Wise Error [FWE] corrected = 0.034), anterior cingulate ( t = 4.50, pFWE = 0.044), and dorsolateral prefrontal areas ( t = 4.43, pFWE = 0.049) and in insular areas with GM loss ( t = 3.78, pFWE = 0.011) was positively linked to DM performance across patients with severe tissue damage and HC. Furthermore, activity in intact orbitofrontal areas was positively linked to DM-learning during the feedback stage across these participants ( t = 4.49, pFWE = 0.032). During none of the stages, moderately affected patients showed higher activity than HC, which might have indicated preserved DM due to compensatory activity.CONCLUSION: We identified dysregulated activity linked to impairment in specific cognitive stages of reward-related DM. The link of brain activity and impaired DM in areas with MS-induced GM loss suggests that this deficit might be tightly coupled to MS neuropathology.",
keywords = "Journal Article",
author = "Martin Weygandt and Katharina Wakonig and Janina Behrens and Lil Meyer-Arndt and Eveline S{\"o}der and Brandt, {Alexander U} and Judith Bellmann-Strobl and Klemens Ruprecht and Gold, {Stefan M} and John-Dylan Haynes and Friedemann Paul",
year = "2018",
month = aug,
doi = "10.1177/1352458517717089",
language = "English",
volume = "24",
pages = "1163--1173",
journal = "MULT SCLER J",
issn = "1352-4585",
publisher = "SAGE Publications",
number = "9",

}

RIS

TY - JOUR

T1 - Brain activity, regional gray matter loss, and decision-making in multiple sclerosis

AU - Weygandt, Martin

AU - Wakonig, Katharina

AU - Behrens, Janina

AU - Meyer-Arndt, Lil

AU - Söder, Eveline

AU - Brandt, Alexander U

AU - Bellmann-Strobl, Judith

AU - Ruprecht, Klemens

AU - Gold, Stefan M

AU - Haynes, John-Dylan

AU - Paul, Friedemann

PY - 2018/8

Y1 - 2018/8

N2 - BACKGROUND: Decision-making (DM) abilities deteriorate with multiple sclerosis (MS) disease progression which impairs everyday life and is thus clinically important.OBJECTIVE: To investigate the underlying neurocognitive processes and their relation to regional gray matter (GM) loss induced by MS.METHODS: We used a functional magnetic resonance imaging (fMRI) Iowa Gambling Task to measure DM-related brain activity in 36 MS patients and 21 healthy controls (HC). From this activity, we determined neural parameters of two cognitive stages, a deliberation ("choice") period preceding a choice and a post-choice ("feedback") stage reporting decision outcomes. These measures were related to DM separately in intact and damaged GM areas as determined by a voxel-based morphometry analysis.RESULTS: Severely affected patients (with high lesion burden) showed worse DM-learning than HC ( t = -1.75, p = 0.045), moderately affected (low lesion burden) did not. Activity in the choice stage in intact insular ( t = 4.60, pFamily-Wise Error [FWE] corrected = 0.034), anterior cingulate ( t = 4.50, pFWE = 0.044), and dorsolateral prefrontal areas ( t = 4.43, pFWE = 0.049) and in insular areas with GM loss ( t = 3.78, pFWE = 0.011) was positively linked to DM performance across patients with severe tissue damage and HC. Furthermore, activity in intact orbitofrontal areas was positively linked to DM-learning during the feedback stage across these participants ( t = 4.49, pFWE = 0.032). During none of the stages, moderately affected patients showed higher activity than HC, which might have indicated preserved DM due to compensatory activity.CONCLUSION: We identified dysregulated activity linked to impairment in specific cognitive stages of reward-related DM. The link of brain activity and impaired DM in areas with MS-induced GM loss suggests that this deficit might be tightly coupled to MS neuropathology.

AB - BACKGROUND: Decision-making (DM) abilities deteriorate with multiple sclerosis (MS) disease progression which impairs everyday life and is thus clinically important.OBJECTIVE: To investigate the underlying neurocognitive processes and their relation to regional gray matter (GM) loss induced by MS.METHODS: We used a functional magnetic resonance imaging (fMRI) Iowa Gambling Task to measure DM-related brain activity in 36 MS patients and 21 healthy controls (HC). From this activity, we determined neural parameters of two cognitive stages, a deliberation ("choice") period preceding a choice and a post-choice ("feedback") stage reporting decision outcomes. These measures were related to DM separately in intact and damaged GM areas as determined by a voxel-based morphometry analysis.RESULTS: Severely affected patients (with high lesion burden) showed worse DM-learning than HC ( t = -1.75, p = 0.045), moderately affected (low lesion burden) did not. Activity in the choice stage in intact insular ( t = 4.60, pFamily-Wise Error [FWE] corrected = 0.034), anterior cingulate ( t = 4.50, pFWE = 0.044), and dorsolateral prefrontal areas ( t = 4.43, pFWE = 0.049) and in insular areas with GM loss ( t = 3.78, pFWE = 0.011) was positively linked to DM performance across patients with severe tissue damage and HC. Furthermore, activity in intact orbitofrontal areas was positively linked to DM-learning during the feedback stage across these participants ( t = 4.49, pFWE = 0.032). During none of the stages, moderately affected patients showed higher activity than HC, which might have indicated preserved DM due to compensatory activity.CONCLUSION: We identified dysregulated activity linked to impairment in specific cognitive stages of reward-related DM. The link of brain activity and impaired DM in areas with MS-induced GM loss suggests that this deficit might be tightly coupled to MS neuropathology.

KW - Journal Article

U2 - 10.1177/1352458517717089

DO - 10.1177/1352458517717089

M3 - SCORING: Journal article

C2 - 28657480

VL - 24

SP - 1163

EP - 1173

JO - MULT SCLER J

JF - MULT SCLER J

SN - 1352-4585

IS - 9

ER -