脳の臨界性と人間の認知に遺伝的関連を発見(New Study Reveals Genetic Link Between Brain Criticality and Human Cognition)

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2025-06-24 中国科学院(CAS)

脳の臨界性と人間の認知に遺伝的関連を発見(New Study Reveals Genetic Link Between Brain Criticality and Human Cognition)Schematic diagram of the heritability estimation pipeline for critical dynamics (Image by LIU Ning’s group)

中国科学院の生物物理研究所・自動化研究所の共同研究チームは、脳のクリティカリティ(神経興奮と抑制の動的均衡)が遺伝的要因によって強く影響されることを明らかにしました。ヒト・コネクトーム・プロジェクトのrs-fMRIデータと遺伝的類似性の異なる双子・非双子個体の比較により、初期感覚皮質において特に遺伝の影響が強いことが確認されました。さらに、脳内の遺伝子発現パターンとクリティカリティの地域差を照合し、認知機能や脳疾患に関連する生物学的プロセスとの関連性も見出しました。この研究は、脳の最適な情報処理と柔軟性を支えるクリティカルな状態が遺伝により支えられている可能性を示すもので、認知科学や神経疾患の理解に新たな視点を提供します。

<関連情報>

脳臨界への遺伝的寄与とヒト認知機能との関係 Genetic contributions to brain criticality and its relationship with human cognitive functions

Yumeng Xin, Yue Cui, Shan Yu, and Ning Liu
Proceedings of the National Academy of Sciences  Published:June 23, 2025
DOI:https://doi.org/10.1073/pnas.2417010122

Significance

Brain criticality, a state of optimal neural balance between excitation and inhibition, is crucial for efficient cognitive function. Despite its significance, the genetic basis of brain criticality remains largely unexplored. We demonstrate that genetic factors significantly influence brain criticality across various scales, from specific brain regions to large-scale networks, enhancing our understanding of the brain’s operational dynamics. We also identify specific gene expression profiles that elucidate regional critical dynamics. Furthermore, we establish a genetic link between brain criticality and cognitive functions, suggesting a shared genetic foundation. These findings position brain criticality as a biological phenotype, opening broad avenues for exploring its implications in brain function and potential dysfunctions.

Abstract

Recently, extensive evidence has demonstrated that the brain operates close to a critical state, characterized by dynamic patterns known as neuronal avalanches. The critical state, reflecting the delicate balance between neural excitation and inhibition, offers numerous advantages in information processing. However, the role of genetics in shaping brain criticality is not fully understood. Whether there is any shared genetic factor influencing the critical state and cognitive functions remains elusive. Here, we aimed to address these questions by examining the heritability of brain criticality and its relation to cognitive function by analyzing resting-state functional magnetic resonance imaging (rs-fMRI) in 250 monozygotic twins, 142 dizygotic twins, and 437 Not-twin subjects. We found that genetic factors substantially influenced brain criticality across various scales, encompassing brain regions, functional networks, and the whole brain. These genetic influences exhibited heterogeneity, with the criticality of the primary sensory cortex being more strongly influenced by genetic factors compared to that of the association cortex. Furthermore, we combined rs-fMRI data with transcriptional microarray data from the Allen Brain Atlas: Human Brain (ABHB) dataset and found that the organization of regional critical dynamics was highly explained by a specific gene expression profile. Finally, our results showed that the critical state was correlated with total cognition and had a genetic link with it. These findings provide empirical evidence that brain criticality is a biological phenotype and suggest a shared genetic foundation underlying brain criticality and cognitive functions. Our results pave the way toward revealing specific biological mechanisms contributing to critical dynamics and their associations with brain function and dysfunction.

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