Neural variability reliably and selectively encodes pain discriminability

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The paper examined how neural variability relates to pain, especially pain discriminability, using five large EEG datasets (total N = 489) from healthy participants and patients with postherpetic neuralgia who received painful versus nonpainful sensory stimuli. Across datasets, the authors found robust, replicable correlations between neural variability and interindividual pain discriminability, with the effect being pain-selective because no significant correlations were seen in nonpain modalities. They also reported that the correlations were clinically relevant since they were partly disrupted in the PHN patients, and that neural variability and EEG signal amplitude were mutually independent with distinct temporal and oscillatory profiles. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract Neural activity varies dramatically across time. While such variability has been associated with cognition, its relationship with pain remains largely unexplored. Here, we systematically investigated the relationship between neural variability and pain, particularly pain discriminability, in five large electroencephalography (EEG) datasets (total N = 489), collected from healthy individuals (Datasets 1–4) and patients with postherpetic neuralgia (PHN; Dataset 5) who had received painful or nonpainful sensory stimuli. We found robust correlations between neural variability and interindividual pain discriminability. These correlations were (1) replicable in multiple datasets, (2) pain selective, as no significant correlations were observed in nonpain modalities, and (3) clinically relevant, as they were partly disrupted in patients with PHN. Importantly, variability and amplitude of EEG signals were mutually independent and had distinct temporal and oscillatory profiles in encoding pain discriminability. These findings demonstrate that neural variability is a replicable and selective indicator of pain discriminability above and beyond amplitude, thereby enhancing the understanding of neural encoding of pain discriminability and underscoring the value of neural variability in pain studies. Competing Interest Statement The authors have declared no competing interest.

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europepmc
last seen: 2026-05-20T01:45:00.602351+00:00
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License: CC-BY-4.0