Plasma levels of soluble TNF receptors 1 and 2 after tDCS and sertraline treatment in major depression: Results from the SELECT-TDCS trial
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | BRUNONI, Andre R. | |
dc.contributor.author | MACHADO-VIEIRA, Rodrigo | |
dc.contributor.author | SAMPAIO-JUNIOR, Bernardo | |
dc.contributor.author | VIEIRA, Erica L. M. | |
dc.contributor.author | VALIENGO, Leandro | |
dc.contributor.author | BENSENOR, Isabela M. | |
dc.contributor.author | LOTUFO, Paulo A. | |
dc.contributor.author | CARVALHO, Andre F. | |
dc.contributor.author | CHO, Hyong Jin | |
dc.contributor.author | GATTAZ, Wagner F. | |
dc.contributor.author | TEIXEIRA, Antonio L. | |
dc.date.accessioned | 2015-10-26T16:25:10Z | |
dc.date.available | 2015-10-26T16:25:10Z | |
dc.date.issued | 2015 | |
dc.description.abstract | Background: The cytokine hypothesis of depression postulates that the pathophysiology of this illness incorporates an increased production of pro-inflammatory cytokines, which leads to an over activation of the hypothalamic-pituitary-adrenal axis as well as monoaminergic disturbances. Nevertheless, it remains unclear whether the amelioration of depressive symptoms could decrease cytokine levels. Notwithstanding antidepressant drug therapy might exert anti-inflammatory effects, the effects of non-invasive neuromodulatory approaches like transcranial direct current stimulation (tDCS) on pro-inflammatory cytokine networks are largely unknown. Methods: We evaluated, in the Set-Leanne vs. Eleciric Curreni Therapy for TreaLing Depression Clinical SLudy (SELECT-TDCS) fetal, whether the plasma levels of the soluble TNF recepLors 1 and 2 (sTNFRs) changed tiller anLiclepressanL LreaLmeni in a sample of 73 anLidepressanL-free paLienis with unipolar depressive disorder in an episode of aL leasL mocleraLe inLensiLy. Results: Although boat LDCS and set-Leanne exerLed anLiclepressanL effecfs. the plasma levels of sTNFRs did noi change over Lime regardless of Lhe infervenLion and clinical response. Also, baseline sTNFRs levels did noL predicL anLiclepressanL response. Limitations: Our negative findings could be a type LI error, as this trial did not use an equivalence design. Conclusions: To conclude, in this novel placebo-controlled trial prospectively evaluating the changes of sTNFRs in depressed patients, we found that these molecules are not surrogate biomarkers of treatment I esponse of tDCS, whose antidepressant effects occurred regardless of normalization of immunological activity. | |
dc.description.index | MEDLINE | |
dc.description.sponsorship | FAPESP (Sao Paulo Research Foundation) [2009/05728-7] | |
dc.description.sponsorship | FAPEMIG | |
dc.description.sponsorship | CNPq | |
dc.identifier.citation | JOURNAL OF AFFECTIVE DISORDERS, v.185, p.209-213, 2015 | |
dc.identifier.doi | 10.1016/j.jad.2015.07.006 | |
dc.identifier.eissn | 1573-2517 | |
dc.identifier.issn | 0165-0327 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/11549 | |
dc.language.iso | eng | |
dc.publisher | ELSEVIER SCIENCE BV | |
dc.relation.ispartof | Journal of Affective Disorders | |
dc.rights | restrictedAccess | |
dc.rights.holder | Copyright ELSEVIER SCIENCE BV | |
dc.subject | Major depressive disorder | |
dc.subject | Transcranial direct current sdmulation | |
dc.subject | Sertraline | |
dc.subject | STNFR1 | |
dc.subject | STNFR2 | |
dc.subject.other | electrical-current therapy | |
dc.subject.other | antidepressant treatment | |
dc.subject.other | cytokine production | |
dc.subject.other | metaanalysis | |
dc.subject.other | disorder | |
dc.subject.other | factorial | |
dc.subject.other | il-6 | |
dc.subject.other | pathways | |
dc.subject.other | impact | |
dc.subject.wos | Clinical Neurology | |
dc.subject.wos | Psychiatry | |
dc.title | Plasma levels of soluble TNF receptors 1 and 2 after tDCS and sertraline treatment in major depression: Results from the SELECT-TDCS trial | |
dc.type | article | |
dc.type.category | original article | |
dc.type.version | publishedVersion | |
dspace.entity.type | Publication | |
hcfmusp.affiliation.country | Estados Unidos | |
hcfmusp.affiliation.countryiso | us | |
hcfmusp.author.external | MACHADO-VIEIRA, Rodrigo:NIMH, Expt Therapeut & Pathophysiol Branch, Intramural Res Program, NIH, Bethesda, MD 20892 USA | |
hcfmusp.author.external | VIEIRA, Erica L. M.:Fed Univ Minas Gerais UFMG, Sch Med, Interdisciplinary Lab Med Invest LIIM, Div Neurosci, Belo Horizonte, MG, Brazil | |
hcfmusp.author.external | CARVALHO, Andre F.:Univ Fed Ceara, Dept Clin Med, Fortaleza, Ceara, Brazil; Univ Fed Ceara, Translat Pychiatry Res Grp, Fac Med, Fortaleza, Ceara, Brazil | |
hcfmusp.author.external | CHO, Hyong Jin:Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Cousins Ctr Psychoneuroimmunol, Los Angeles, CA 90024 USA | |
hcfmusp.citation.scopus | 18 | |
hcfmusp.contributor.author-fmusphc | ANDRE RUSSOWSKY BRUNONI | |
hcfmusp.contributor.author-fmusphc | BERNARDO DE SAMPAIO PEREIRA JUNIOR | |
hcfmusp.contributor.author-fmusphc | LEANDRO DA COSTA LANE VALIENGO | |
hcfmusp.contributor.author-fmusphc | ISABELA JUDITH MARTINS BENSEñOR | |
hcfmusp.contributor.author-fmusphc | PAULO ANDRADE LOTUFO | |
hcfmusp.contributor.author-fmusphc | WAGNER FARID GATTAZ | |
hcfmusp.description.beginpage | 209 | |
hcfmusp.description.endpage | 213 | |
hcfmusp.description.volume | 185 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 26241865 | |
hcfmusp.origem.scopus | 2-s2.0-84938319315 | |
hcfmusp.origem.wos | WOS:000359725400030 | |
hcfmusp.publisher.city | AMSTERDAM | |
hcfmusp.publisher.country | NETHERLANDS | |
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hcfmusp.scopus.lastupdate | 2024-05-10 | |
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