Evidence map›Paper›PMID 42582622›Full record

ArticleBrain communications2026

Stable insular spectral patterns underlie dynamic pain encoding in chronic neuropathic pain.

Chang-Chia Liu, Mark Quigg, Patrick H Finan, Shayan Moosa, W Jeffrey Elias

Abstract read
In one paragraph

Article in Brain communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Chang-Chia LiuDepartment of Neurological Surgery, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.ORCID https://orcid.org/0000-0002-2990-739X
Mark QuiggDepartment of Neurology, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.
Patrick H FinanDepartment of Anesthesiology, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.
Shayan MoosaDepartment of Neurological Surgery, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.
W Jeffrey EliasDepartment of Neurological Surgery, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.

Funding

A staged, comprehensive investigation for developing insular deep brain stimulation to treat refractory chronic painUH3NS123308 · NINDS · UNIVERSITY OF VIRGINIA · PI ELIAS, WILLIAM JEFFREY, LIU, CHANG-CHIA · 2022 to 2025
$3.0M
NINDS NIH HHS UH3 NS123308
6 · The paper itself

Abstract

Chronic neuropathic pain persists for years yet fluctuates markedly from day to day, raising a fundamental question: how do stable neural patterns relate to dynamic pain experience? The insula is a central hub for pain processing, but it remains unclear whether ongoing pain is associated with enduring baseline neural patterns within the insula or day-to-day variation in neural activity. We analysed multiday bilateral intracranial electroencephalography recordings from six individuals with chronic unilateral neuropathic pain, comprising 34 days of resting-state data. Spectral power, peak-derived spectral metrics and intra-insular functional connectivity (coherence and phase-locking value) were quantified across anterior and posterior insular subregions. Linear mixed-effects models were used to distinguish stable within-cohort neural patterns from within-subject, day-to-day pain-related fluctuations in pain intensity and unpleasantness, with explicit control for longitudinal temporal drift. The insula exhibited stable within-cohort spectral organization characterized by an anterior-posterior gradient with lower posterior fast-band power and spectral slowing, together with greater posterior spectral power in the hemisphere contralateral to the chronic pain side. Superimposed on this stable pattern, daily pain intensity was most strongly associated with increased contralateral posterior alpha power, accounting for approximately 33% of within-subject variance. Pain unpleasantness showed its strongest association with increased contralateral posterior beta power, accounting for approximately 19% of within-subject variance. Peak-derived spectral metrics and intra-insular connectivity largely reflected stable baseline patterns, with comparatively modest day-to-day pain-related variation. These exploratory findings suggest that chronic neuropathic pain is associated with stable insular spectral patterns upon which frequency-specific oscillatory variation relates to daily pain experience. Posterior insular alpha and beta oscillations showed partially distinct associations with pain intensity and unpleasantness, respectively, whereas intra-insular connectivity primarily reflected stable network structure. Posterior insular spectral power may therefore provide a candidate physiological signal for tracking pain states.

Indexed as

Chronic neuropathic painInsulaIntracranial EEGPain intensityPain unpleasantness

Identifiers

PMID42582622
PMCPMC13457931

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.