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Altered Functional Connectivity in the Reward Circuit in Betel Quid-Dependent Chewers
Yuegui Cao1, Sisi Chen1, Jiayu Li1
1Department of Radiology, Xiangya Hospital, Central South University, Changsha, China.
Addiction Biology
|August 5, 2026
Summary
Betel quid dependence (BQD) alters brain reward circuit connectivity, particularly between the thalamus and posterior cingulate cortex. This dysfunction is linked to dependence severity and usage dosage, suggesting a potential biomarker for BQD.
Area of Science:
- Neuroimaging
- Addiction Neuroscience
- Public Health
Background:
- Betel quid (BQ) is a Group 1 carcinogen, posing a significant public health risk.
- Betel quid dependence (BQD) is associated with changes in brain reward regions.
- Neural correlates of BQD's reward circuit and its link to clinical features are not well understood.
Purpose of the Study:
- To investigate resting-state functional connectivity (FC) within the reward circuit in individuals with BQD.
- To explore the neural correlates of aberrant FC with clinical features of BQD.
- To identify potential circuit-level biomarkers for BQD.
Main Methods:
- Recruited 53 male BQD chewers and 53 male healthy controls (HCs).
- Utilized resting-state functional magnetic resonance imaging (rs-fMRI) to analyze FC in 11 reward circuit regions (e.g., ventral striatum, VMPFC, ACC, PCC, thalamus).
- Correlated aberrant FC with BQD scales and dosage of BQ use.
Main Results:
- Individuals with BQD showed altered FC in reward circuit regions, including the thalamus and PCC, compared to HCs.
- Decreased FC between the right thalamus and PCC negatively correlated with BQD severity and BQ dosage.
- This study provides the first empirical evidence of aberrant resting-state FC in the reward circuit in BQD.
Conclusions:
- Aberrant resting-state FC in the reward circuit is a key feature of BQD.
- The thalamus-PCC connectivity may serve as a potential circuit-level biomarker for BQD.
- Understanding reward circuit dysfunction is crucial for the pathophysiology of BQD.
