# MRI assessment of intrinsic neural timescales in male alcohol use disorder patients

**Authors:** Weijian Wang, Xinyu Wang, Yimeng Kang, Wenjing Li, Yichen Guo, Hui Zhang, Jiawen Tian, Longyao Ma, Bohui Mei, Mengzhe Zhang, Yarui Wei, Yong Zhang

PMC · DOI: 10.3389/fpsyt.2026.1736813 · Frontiers in Psychiatry · 2026-02-19

## TL;DR

This study uses MRI to find differences in brain activity timing in people with alcohol use disorder compared to healthy individuals.

## Contribution

The study introduces intrinsic neural timescale analysis to investigate brain activity patterns in alcohol use disorder.

## Key findings

- AUD patients showed significantly longer intrinsic neural timescales in the thalamus.
- AUD patients exhibited significantly shorter intrinsic neural timescales in the calcarine cortex.
- Abnormal intrinsic neural timescales may reflect neural mechanisms underlying alcohol dependence.

## Abstract

Alcohol use disorder (AUD) is a chronic, relapsing condition marked by compulsive drinking, imposing a significant burden on both the individual and their environment. The intrinsic neural timescale (INT) is determined through the assessment of autocorrelation of the brain activity in resting-state functional magnetic resonance imaging, serving to elucidate the diversity of neural timescales.

This study involved 55 alcohol-dependent patients and 33 non-drinking healthy controls (HCs) matched for age, sex, and hand-use habits. We calculated the INT by evaluating the strength of autocorrelation in resting-state brain activity, and subsequently compared between-group differences in INT. We also analyzed the correlation between abnormal INT and clinical characteristics.

The AUD group exhibited significantly longer INT in the left and right thalamus when compared to the HC group. Additionally, significantly shorter INT was observed in the calcarine cortex in the AUD group in comparison to the HC group.

Our study identified abnormalities of the brain activity at the resting state in alcohol-dependent patients by means of an INT approach, which may provide more insight into the neural mechanisms of alcohol dependence.

## Full-text entities

- **Genes:** INTU (inturned planar cell polarity protein) [NCBI Gene 27152] {aka CPLANE4, INT, OFD17, PDZD6, PDZK6, SRTD20}
- **Diseases:** medical diseases (MESH:D000069279), neurological (MESH:D009461), anxiety disorder (MESH:D001008), conduct disorder (MESH:D019955), thalamic (MESH:D013786), Alcohol use disorder (MESH:D000437), autism spectrum disorders (MESH:D000067877), decline in visual (MESH:D014786), addiction (MESH:D019966), psychiatric disorders (MESH:D001523), schizophrenia (MESH:D012559), autism (MESH:D001321), deficits in impulse control (MESH:D007174), obsessive compulsive drinking (MESH:D009771), depression (MESH:D003866), INT abnormalities (MESH:C563242), neurological system (MESH:D009422), cognitive impairment (MESH:D003072), epilepsy (MESH:D004827)
- **Chemicals:** alcohol (MESH:D000438), Dopamine (MESH:D004298)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12960577/full.md

## References

70 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960577/full.md

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Source: https://tomesphere.com/paper/PMC12960577