4.6 Article

Multivariate machine learning distinguishes cross-network dynamic functional connectivity patterns in state and trait neuropathic pain

期刊

PAIN
卷 159, 期 9, 页码 1764-1776

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/j.pain.0000000000001264

关键词

Ankylosing spondylitis; Pain; Dynamic functional connectivity; Machine learning

资金

  1. Canadian Institute of Health Research
  2. Canadian Chronic Pain Network
  3. Mayday Fund
  4. Canadian Institute of Health Research Doctoral Research Award
  5. Banting fellowship from Canadian Institute of Health Research

向作者/读者索取更多资源

Communication within the brain is dynamic. Chronic pain can also be dynamic, with varying intensities experienced over time. Little is known of how brain dynamics are disrupted in chronic pain, or relates to patients' pain assessed at various timescales (eg, short-term state vs long-term trait). Patients experience pain traits indicative of their general condition, but also pain states that vary day to day. Here, we used network-based multivariate machine learning to determine how patterns in dynamic and static brain communication are related to different characteristics and timescales of chronic pain. Our models were based on resting-state dynamic functional connectivity (dFC) and static functional connectivity in patients with chronic neuropathic pain (NP) or non-NP. The most prominent networks in the models were the default mode, salience, and executive control networks. We also found that cross-network measures of dFC rather than static functional connectivity were better associated with patients' pain, but only in those with NP features. These associations were also more highly and widely associated with measures of trait rather than state pain. Furthermore, greater dynamic connectivity with executive control networks was associated with milder NP, but greater dynamic connectivity with limbic networks was associated with greater NP. Compared with healthy individuals, the dFC features most highly related to trait NP were also more abnormal in patients with greater pain. Our findings indicate that dFC reflects patients' overall pain condition (ie, trait pain), not just their current state, and is impacted by complexities in pain features beyond intensity.

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