Characterization of sympathicotonia in post‐covid condition (long covid) and healthy controls using long‐term electrodermal activity (EDA) follow‐up

dc.contributor.authorMustonen, Timo
dc.contributor.authorKytölä, Pasi
dc.contributor.authorLantto, Hanna
dc.contributor.authorLager, Erika
dc.contributor.authorVangelova‐Korpinen, Velina
dc.contributor.authorVirrantaus, Hélène
dc.contributor.authorSulg, Aleksandra
dc.contributor.authorStålnacke, Sanna
dc.contributor.authorPosharina, Tatiana
dc.contributor.authorLuukkonen, Ritva
dc.contributor.authorUusitalo, Arja
dc.contributor.authorPiirilä, Päivi
dc.contributor.authorKanerva, Mari
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.converis.publication-id505611226
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/505611226
dc.date.accessioned2026-01-21T14:32:29Z
dc.date.available2026-01-21T14:32:29Z
dc.description.abstract<h3>Purpose</h3><p>After SARS-CoV-2 infection, some patients develop post-COVID condition (PCC), often associated with sympathicotonia. This study aimed to characterize sympathicotonia in PCC patients using a novel long-term electrodermal activity (EDA) analysis via a smart ring and evaluate its clinical applicability.</p><h3>Methods</h3><p>Seventeen PCC patients were recruited from a Long Covid outpatient clinic, and 18 healthy controls volunteered. PCC patients were divided based on self-reported symptoms into those with or without sympathicotonia. A 14-day EDA monitoring was conducted. Sympathetic nervous system (SNS) activity was expressed as a double normalized index of electrodermal activity (DNE), with higher levels indicating higher SNS activity. Orthostatic tests were performed to identify orthostatic sympathicotonia. DNE levels, representing EDA, were compared to self-reported and orthostatic sympathicotonia.</p><h3>Results</h3><p>DNE levels did not differ between PCC patients with (<em>N</em> = 12) or without (<em>N</em> = 5) self-reported sympathicotonia or compared with nonsympathetic controls. When dividing all participants by orthostatic test results, DNE levels were lower during day (08:00–14:00; <em>p</em> < 0.05) but higher during late night (00:00–02:00; <em>p</em> < 0.05) in those with orthostatic sympathicotonia (<em>N</em> = 21) compared to those without (<em>N</em> = 14), with the 24-h comparison significant (<em>p</em> = 0.022). Among PCC patients, DNE levels were higher in orthostatic nonsympathicotonic (<em>N</em> = 7) than orthostatic sympathicotonic (<em>N</em> = 10) during morning (09:00–12:00; <em>p</em> < 0.05), with the 24-h comparison significant (<em>p</em> = 0.044).</p><h3>Conclusion</h3><p>Self-reported symptoms did not distinguish sympathicotonia. However, individuals with orthostatic test-identified sympathicotonia had heightened EDA, indicating increased sympathetic activity, particularly during late night. PCC was not identifiable by EDA. Long-term EDA monitoring may provide an objective tool for detecting sympathicotonia independently of self-reported symptoms.</p>
dc.identifier.eissn1475-097X
dc.identifier.jour-issn1475-0961
dc.identifier.olddbid213372
dc.identifier.oldhandle10024/196390
dc.identifier.urihttps://www.utupub.fi/handle/11111/55256
dc.identifier.urlhttps://doi.org/10.1111/cpf.70037
dc.identifier.urnURN:NBN:fi-fe202601216474
dc.language.isoen
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherWiley
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumbere70037
dc.relation.doi10.1111/cpf.70037
dc.relation.ispartofjournalClinical Physiology and Functional Imaging
dc.relation.issue6
dc.relation.volume45
dc.source.identifierhttps://www.utupub.fi/handle/10024/196390
dc.titleCharacterization of sympathicotonia in post‐covid condition (long covid) and healthy controls using long‐term electrodermal activity (EDA) follow‐up
dc.year.issued2025

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