A retrospective study of accuracy and usefulness of electrophysiological exercise tests

dc.contributor.authorPeriviita Vesa
dc.contributor.authorJokela Manu
dc.contributor.authorPalmio Johanna
dc.contributor.authorUdd Bjarne
dc.contributor.organizationfi=kliiniset neurotieteet|en=Clinical Neurosciences|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code2607314
dc.converis.publication-id182392739
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/182392739
dc.date.accessioned2025-08-27T21:40:06Z
dc.date.available2025-08-27T21:40:06Z
dc.description.abstract<p>Objectives<br>This study aimed to determine the usefulness of electrophysiological exercise tests. The significance of slightly abnormal exercise tests was also examined.</p><p>Methods<br>We identified all the patients who had undergone exercise testing between February 2007 to June 2022 in Tampere University Hospital, Finland. Their medical records after diagnostic workup and exercise test reports were reviewed. A binary logistic regression was performed to evaluate the association between positive test result in short exercise test, long exercise test, or short exercise test with cooling and genetically confirmed skeletal muscle channelopathy or myotonic disorder.</p><p>Results<br>We identified 256 patients. 27 patients were diagnosed with nondystrophic myotonia, periodic paralysis, myotonic dystrophy type 1, myotonic dystrophy type 2, or other specified myopathy. 14 patients were suspected to have a skeletal muscle channelopathy, but pathogenic variants could not be identified. The remaining 215 patients were diagnosed with other conditions than skeletal muscle channelopathy or myotonic disorder. The combined sensitivity of exercise tests was 59.3% and specificity 99.1%. Abnormal exercise test result was associated with increased risk of skeletal muscle channelopathy or myotonic disorder (OR 164.3, 95% CI 28.3–954.6, p < 0.001).</p><p>Conclusions<br>Electrophysiological exercise test is not optimal to exclude skeletal muscle channelopathy. It may be useful if a skeletal muscle channelopathy is suspected and genetic testing is negative or indeterminate and further evidence is required. Slightly abnormal exercise test results are possible in various conditions and result from different aetiologies. There is a demand for neurophysiological studies with higher sensitivity to detect skeletal muscle channelopathies.</p><p><br></p>
dc.identifier.eissn1432-1459
dc.identifier.jour-issn0340-5354
dc.identifier.olddbid200847
dc.identifier.oldhandle10024/183874
dc.identifier.urihttps://www.utupub.fi/handle/11111/47270
dc.identifier.urlhttp://dx.doi.org/10.1007%2Fs00415%2D023%2D12110%2D5
dc.identifier.urnURN:NBN:fi-fe2025082789255
dc.language.isoen
dc.okm.affiliatedauthorJokela, Manu
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3112 Neurosciencesen_GB
dc.okm.discipline3112 Neurotieteetfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSpringer Nature
dc.publisher.countryGermanyen_GB
dc.publisher.countrySaksafi_FI
dc.publisher.country-codeDE
dc.relation.doi10.1007/s00415-023-12110-5
dc.relation.ispartofjournalJournal of Neurology
dc.source.identifierhttps://www.utupub.fi/handle/10024/183874
dc.titleA retrospective study of accuracy and usefulness of electrophysiological exercise tests
dc.year.issued2023

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