<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chowdhury NS</submitter><funding>NINDS NIH HHS</funding><funding>National Institutes of Health</funding><pagination>109766</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9848447</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>385</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Many pain biomarkers fail to move from discovery to clinical application, attributed to poor reliability and an inability to accurately classify at-risk individuals. Preliminary evidence has shown that high pain sensitivity is associated with slow peak alpha frequency (PAF), and depression of corticomotor excitability (CME), potentially due to impairments in ascending sensory and descending motor pathway signalling respectively NEW METHOD: The present study evaluated the reliability of PAF and CME responses during sustained pain. Specifically, we determined whether, over several days of pain, a) PAF remains stable and b) individuals show two stable and distinct CME responses: facilitation and depression. Participants were given an injection of nerve growth factor (NGF) i</pubmed_abstract><journal>Journal of neuroscience methods</journal><pubmed_title>The reliability of two prospective cortical biomarkers for pain: EEG peak alpha frequency and TMS corticomotor excitability.</pubmed_title><pmcid>PMC9848447</pmcid><funding_grant_id>R61 NS113269</funding_grant_id><pubmed_authors>Schabrun SM</pubmed_authors><pubmed_authors>Millard SK</pubmed_authors><pubmed_authors>Chiang AKI</pubmed_authors><pubmed_authors>Chowdhury NS</pubmed_authors><pubmed_authors>Si E</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Furman AJ</pubmed_authors><pubmed_authors>Seminowicz DA</pubmed_authors><pubmed_authors>Skippen P</pubmed_authors></additional><is_claimable>false</is_claimable><name>The reliability of two prospective cortical biomarkers for pain: EEG peak alpha frequency and TMS corticomotor excitability.</name><description>&lt;h4>Background&lt;/h4>Many pain biomarkers fail to move from discovery to clinical application, attributed to poor reliability and an inability to accurately classify at-risk individuals. Preliminary evidence has shown that high pain sensitivity is associated with slow peak alpha frequency (PAF), and depression of corticomotor excitability (CME), potentially due to impairments in ascending sensory and descending motor pathway signalling respectively NEW METHOD: The present study evaluated the reliability of PAF and CME responses during sustained pain. Specifically, we determined whether, over several days of pain, a) PAF remains stable and b) individuals show two stable and distinct CME responses: facilitation and depression. Participants were given an injection of nerve growth factor (NGF) i</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-26T11:53:23.036Z</modification><creation>2025-02-19T04:59:54.476Z</creation></dates><accession>S-EPMC9848447</accession><cross_references><pubmed>36495945</pubmed><doi>10.1016/j.jneumeth.2022.109766</doi></cross_references></HashMap>