脳損傷が他人の影響を受けやすくする仕組み(Focal brain damage leaves people more open to being influenced by impulsive others)

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2025-04-29 バーミンガム大学

バーミンガム大学、オックスフォード大学、ヴュルツブルク大学の研究チームは、前頭前野内側部(mPFC)の損傷が、自己の衝動性を高めるだけでなく、他者の衝動的な行動に影響されやすくなることを明らかにしました。この研究では、mPFCに局所的な損傷を持つ33人、他の部位に損傷を持つ17人、健常者71人の計121人を対象に、報酬選択課題を実施。その結果、mPFC損傷者は、他者が衝動的な選択をする場合に特に影響を受けやすいことが判明しました。また、mPFCの背内側部の損傷は社会的影響による衝動性の増加と関連し、腹内側部の損傷は一般的な衝動性の増加と関連していました。これらの結果は、他者の行動が自己の意思決定に与える影響に特定の神経基盤が存在することを示唆しており、誤情報の拡散や金融判断への影響など、社会的意思決定の理解に重要な示唆を提供します。

<関連情報>

前頭前皮質背内側および内側前野の病変は、社会的影響と時間的割引に異なる影響を及ぼす Dorsomedial and ventromedial prefrontal cortex lesions differentially impact social influence and temporal discounting

Zhilin Su ,Mona M. Garvert,Lei Zhang,Todd A. Vogel,Jo Cutler,Masud Husain,Sanjay G. Manohar,Patricia L. Lockwood
PLOS Biology  Published: April 28, 2025
DOI:https://doi.org/10.1371/journal.pbio.3003079

脳損傷が他人の影響を受けやすくする仕組み(Focal brain damage leaves people more open to being influenced by impulsive others)

Abstract

The medial prefrontal cortex (mPFC) has long been associated with economic and social decision-making in neuroimaging studies. Several debates question whether different ventral mPFC (vmPFC) and dorsal mPFC (dmPFC) regions have specific functions or whether there is a gradient supporting social and nonsocial cognition. Here, we tested an unusually large sample of rare participants with focal damage to the mPFC (N = 33), individuals with lesions elsewhere (N = 17), and healthy controls (N = 71) (total N = 121). Participants completed a temporal discounting task to estimate their baseline discounting preferences before learning the preferences of two other people, one who was more temporally impulsive and one more patient. We used Bayesian computational models to estimate baseline discounting and susceptibility to social influence after learning others’ economic preferences. mPFC damage increased susceptibility to impulsive social influence compared to healthy controls and increased overall susceptibility to social influence compared to those with lesions elsewhere. Importantly, voxel-based lesion-symptom mapping (VLSM) of computational parameters showed that this heightened susceptibility to social influence was attributed specifically to damage to the dmPFC (area 9; permutation-based threshold-free cluster enhancement (TFCE) p < 0.025). In contrast, lesions in the vmPFC (areas 13 and 25) and ventral striatum were associated with a preference for seeking more immediate rewards (permutation-based TFCE p < 0.05). We show that the dmPFC is causally implicated in susceptibility to social influence, with distinct ventral portions of mPFC involved in temporal discounting. These findings provide causal evidence for sub-regions of the mPFC underpinning fundamental social and cognitive processes.

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