# Intra-individual structural covariance network in patients with chronic neck and shoulder pain: a longitudinal brain structure analysis

**Authors:** Tianci Liu, Zhiqiang Qiu, Jia Ming, Maojiang Yang, Libing He, Hongjian Li, Xiaoxue Xu

PMC · DOI: 10.3389/fneur.2026.1732732 · 2026-02-20

## TL;DR

This study explores brain structural changes in patients with chronic neck and shoulder pain before and after treatment, identifying potential biomarkers for predicting treatment response.

## Contribution

The study introduces a longitudinal analysis of individual-level structural covariance networks in chronic neck and shoulder pain patients following treatment.

## Key findings

- CNSP patients showed reduced Degree Centrality and Nodal Efficiency in the right inferior frontal gyrus compared to healthy controls.
- Global network metrics like Gamma and Sigma indices were decreased in CNSP patients but did not recover post-intervention.
- Baseline Degree Centrality in the right inferior frontal gyrus correlated negatively with pain score changes, indicating potential prognostic value.

## Abstract

Neuroimaging studies have suggested that the neural mechanisms underlying chronic neck and shoulder pain (CNSP) are associated with morphological alterations in various cortical regions. However, there is a scarcity of research exploring the structural network characteristics of the brain in patients with CNSP. While most existing studies focus on group-level brain structural networks, there is a lack of insight into individual variability. Additionally, longitudinal studies investigating changes in the brain's structural networks following treatment in CNSP patients remain limited.

To address these gaps, this study enrolled 25 patients with CNSP, obtaining structural brain MRI data and clinical measures before treatment and 3 months after a minimally invasive intervention. Individual-level structural covariance networks were constructed for each participant to explore structural network differences between CNSP patients and healthy controls (HCs). Longitudinal changes in these networks were also assessed post-intervention.

Compared to HCs, CNSP patients exhibited significantly reduced Degree Centrality (P = 0.03, FDR corrected) and Nodal Efficiency (P = 0.0082, FDR corrected) in the right inferior frontal gyrus (pars triangularis), with significant structural recovery observed 3 months after the intervention. In terms of global network topology, the CNSP group showed decreased small-world properties, specifically in Gamma (P = 0.0093) and Sigma (P = 0.0301) indices; however, unlike local metrics, no significant recovery was observed in these global metrics 3 months post-intervention. Furthermore, correlation analysis demonstrated a significant negative association between the baseline Degree Centrality of the right inferior frontal gyrus and the percentage change in VAS scores (r = −0.47, P = 0.0168, FDR corrected), suggesting a potential prognostic value.

These findings provide valuable longitudinal data that help elucidate the central mechanisms of pain in CNSP patients. They also identify potential biomarkers that could predict the response to minimally invasive interventions, offering insights into individualized treatment strategies for chronic cervical and shoulder pain.

## Full-text entities

- **Diseases:** chronic low back pain (MESH:D017116), disc herniation (MESH:D007405), CINP (MESH:D019547), neck and shoulder discomfort (MESH:D000070599), cervical spondylosis (MESH:D055009), spinal nerve root inflammation (MESH:D011843), schizophrenia (MESH:D012559), anxiety (MESH:D001007), atrophy (MESH:D001284), Alzheimer's disease (MESH:D000544), neurological or psychiatric disorders (MESH:D001523), CNSP (MESH:D020069), encephalomalacia (MESH:D004678), Pain (MESH:D010146), HL (MESH:C538324), brain tumors (MESH:D001932), chronic (MESH:D002908), cardiac, hepatic, or renal dysfunction (MESH:D006331), spine degeneration (MESH:D009410), depression (MESH:D003866), Chronic pain (MESH:D059350), CWAD (MESH:D014911), chronic pancreatitis (MESH:D050500), cerebral infarction (MESH:D002544), intervertebral disc pathology (MESH:C535531), intracranial abnormalities (MESH:D001927), abnormal (MESH:D000014)
- **Chemicals:** ozone (MESH:D010126), CNSP (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12965628/full.md

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Source: https://tomesphere.com/paper/PMC12965628