Aberrant regional homogeneity in multiple frequency bands in patients with alcohol use disorder

TL;DR

This study found abnormal brain activity patterns in alcohol use disorder patients across multiple frequency bands, which could help understand the condition's underlying mechanisms.

Contribution

The study reveals distinct neural oscillation patterns in AUD patients across multiple frequency bands using regional homogeneity.

Findings

Decreased ReHo values were found in the left IPL and right MFG in two frequency bands.

ReHo differences showed high diagnostic efficiency with sensitivities up to 90.0% and specificities up to 86.7%.

Clinical scale scores were not significantly correlated with ReHo values in specific brain areas.

Abstract

It is unclear whether the alterations in neural oscillations in patients with alcohol use disorder (AUD) are specific to different frequency bands. We applied the regional homogeneity (ReHo) approach to examine intrinsic functional connectivity variations in various frequency bands in AUD patients.

Thirty-three AUD patients and 29 healthy controls (HCs) were enrolled in this study. The ReHo values in six frequency bands (conventional frequency band, 0.01–0.08 Hz; slow-2, 0.198–0.25 Hz; slow-3, 0.073–0.198 Hz; slow-4, 0.027–0.073 Hz; slow-5, 0.01–0.027 Hz; and slow-6, 0–0.01 Hz) were calculated and compared between the two groups. The performance of the ReHo on distinguishing AUD patients from HCs was examined using a receiver operating characteristic (ROC) curve. The correlation of functional changes in the network and alcohol dependence was evaluated.

Decreased ReHo values were detected in two frequency bands, and the areas of decreased ReHo values were mainly located in the left inferior parietal lobule (IPL) and right middle frontal gyrus (MFG); the diagnostic efficiency of the ReHo differences in brain areas was respectively 0.876 and 0.868, with sensitivities of 90.0% and 76.7% and specificities of 70.0% and 86.7%. The clinical scale scores were not significantly correlated with the ReHo values in specific brain areas.

Our findings demonstrate that the widespread abnormal brain activity in AUD patients is characterized by distinct patterns of neural oscillatory power across multiple frequency bands. This exploration may provide an objective imaging basis for understanding the pathophysiological mechanisms of AUD.

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