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dc.contributor.authorFagermoen, Even
dc.contributor.authorSulheim, Dag
dc.contributor.authorWinger, Anette
dc.contributor.authorAndersen, Anders M
dc.contributor.authorGjerstad, Johannes
dc.contributor.authorGodang, Kristin
dc.contributor.authorRowe, Peter C
dc.contributor.authorSaul, J. P
dc.contributor.authorSkovlund, Eva
dc.contributor.authorWyller, Vegard B
dc.date.accessioned2015-10-20T12:49:33Z
dc.date.available2015-10-20T12:49:33Z
dc.date.issued2015
dc.identifier.citationBMC Pediatrics. 2015 Sep 10;15(1):117
dc.identifier.urihttp://hdl.handle.net/10852/47472
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. Trial registration Clinical Trials ID: NCT01040429 , date of registration 12/28/2009.
dc.language.isoeng
dc.rightsFagermoen et al; licensee BioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleEffects of low-dose clonidine on cardiovascular and autonomic variables in adolescents with chronic fatigue: a randomized controlled trial
dc.typeJournal article
dc.date.updated2015-10-20T12:49:33Z
dc.creator.authorFagermoen, Even
dc.creator.authorSulheim, Dag
dc.creator.authorWinger, Anette
dc.creator.authorAndersen, Anders M
dc.creator.authorGjerstad, Johannes
dc.creator.authorGodang, Kristin
dc.creator.authorRowe, Peter C
dc.creator.authorSaul, J. P
dc.creator.authorSkovlund, Eva
dc.creator.authorWyller, Vegard B
dc.identifier.doihttp://dx.doi.org/10.1186/s12887-015-0428-2
dc.identifier.urnURN:NBN:no-51544
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/47472/1/12887_2015_Article_428.pdf
dc.type.versionPublishedVersion
cristin.articleid117


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