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dc.contributor.authorFagermoen, Evenen_US
dc.contributor.authorSulheim, Dagen_US
dc.contributor.authorWinger, Anetteen_US
dc.contributor.authorAndersen, Anders M.en_US
dc.contributor.authorGjerstad, Johannesen_US
dc.contributor.authorGodang, Kristinen_US
dc.contributor.authorRowe, Peter C.en_US
dc.contributor.authorSaul, J. Philipen_US
dc.contributor.authorSkovlund, Evaen_US
dc.contributor.authorWyller, Vegard Bruunen_US
dc.date.accessioned2015-10-07T09:10:13Z
dc.date.available2015-10-07T09:10:13Z
dc.date.issued2015-10-09en_US
dc.identifier.citationFagermoen, E., Sulheim, D., Winger, A., Andersen, A.M., Gjerstad, J., Godang, K. ... Wyller, V.B. (2015). Effects of low-dose clonidine on cardiovascular and autonomic variables in adolescents with chronic fatigue: a randomized controlled trial. BMC Pediatrics, 15:117, doi: 10.1186/s12887-015-0428-2en_US
dc.identifier.issn1471-2431en_US
dc.identifier.otherFRIDAID 1263937en_US
dc.identifier.urihttps://hdl.handle.net/10642/2744
dc.description.abstractBackground: Chronic Fatigue Syndrome (CFS) is a common and disabling condition in adolescence with few treatment options. A central feature of CFS is orthostatic intolerance and abnormal autonomic cardiovascular control characterized by sympathetic predominance. We hypothesized that symptoms as well as the underlying pathophysiology might improve by treatment with the alpha2A–adrenoceptor agonist clonidine. Methods: A total of 176 adolescent CFS patients (12–18 years) were assessed for eligibility at a single referral center recruiting nation-wide. Patients were randomized 1:1 by a computer system and started treatment with clonidine capsules (25 μg or 50 μg twice daily, respectively, for body weight below/above 35 kg) or placebo capsules for 9 weeks. Double-blinding was provided. Data were collected from March 2010 until October 2012 as part of The Norwegian Study of Chronic Fatigue Syndrome in Adolescents: Pathophysiology and Intervention Trial (NorCAPITAL). Effect of clonidine intervention was assessed by general linear models in intention-to-treat analyses, including baseline values as covariates in the model. Results: A total of 120 patients (clonidine group n = 60, placebo group n = 60) were enrolled and started treatment. There were 14 drop-outs (5 in the clonidine group, 9 in the placebo group) during the intervention period. At 8 weeks, the clonidine group had lower plasma norepinephrine (difference = 205 pmol/L, p = 0.05) and urine norepinephrine/ creatinine ratio (difference = 3.9 nmol/mmol, p = 0.002). During supine rest, the clonidine group had higher heart rate variability in the low-frequency range (LF-HRV, absolute units) (ratio = 1.4, p = 0.007) as well as higher standard deviation of all RR-intervals (SDNN) (difference = 12.0 ms, p = 0.05); during 20° head-up tilt there were no statistical differences in any cardiovascular variable. Symptoms of orthostatic intolerance did not change during the intervention period. Conclusions: Low-dose clonidine reduces catecholamine levels in adolescent CFS, but the effects on autonomic cardiovascular control are sparse. Clonidine does not improve symptoms of orthostatic intolerance.en_US
dc.language.isoengen_US
dc.publisherBioMed Centralen_US
dc.relation.ispartofseriesBMC Pediatrics;15:117en_US
dc.subjectChronic Fatigue Syndromeen_US
dc.subjectAdolescentsen_US
dc.subjectLow-dose clonidineen_US
dc.titleEffects of low-dose clonidine on cardiovascular and autonomic variables in adolescents with chronic fatigue: a randomized controlled trialen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
dc.identifier.doihttp://dx.doi.org/10.1186/s12887-015-0428-2


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