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dc.rights.licenseopenen_US
hal.structure.identifierCentro de Investigación Biomédica en Red Salud Mental [Madrid] [CIBER-SAM]
dc.contributor.authorNAVINES, Ricard
hal.structure.identifierCentro de Investigación Biomédica en Red Salud Mental [Madrid] [CIBER-SAM]
dc.contributor.authorORIOLO, Giovanni
hal.structure.identifierCentro de Investigación Biomédica en Red Salud Mental [Madrid] [CIBER-SAM]
dc.contributor.authorHORRILLO, Igor
hal.structure.identifierCentro de Investigación Biomédica en Red Salud Mental [Madrid] [CIBER-SAM]
dc.contributor.authorCAVERO, Myriam
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorAOUIZERATE, Bruno
IDREF: 069471851
dc.contributor.authorSCHAEFER, Martin
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorCAPURON, Lucile
IDREF: 167018736
hal.structure.identifierCentro de Investigación Biomédica en Red Salud Mental [Madrid] [CIBER-SAM]
dc.contributor.authorMEANA, J. Javier
hal.structure.identifierCentro de Investigación Biomédica en Red Salud Mental [Madrid] [CIBER-SAM]
dc.contributor.authorMARTIN-SANTOS, Rocio
dc.date.accessioned2023-02-20T15:09:02Z
dc.date.available2023-02-20T15:09:02Z
dc.date.issued2022-02-17
dc.identifier.issn1461-1457en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/172006
dc.description.abstractEnBackground: The relationship between antidepressant response and glial, inflammatory, and metabolic markers is poorly understood in depression. This study assessed the ability of biological markers to predict antidepressant response in major depressive disorder (MDD). Methods: We included 31 MDD outpatients treated with escitalopram or sertraline for 8 consecutive weeks. The Montgomery-Åsberg Depression Rating Scale (MADRS) was administered at baseline and at week 4 and 8 of treatment. Concomitantly, blood samples were collected for the determination of serum S100B, C-reactive protein (CRP), and high-density lipoprotein cholesterol (HDL)-C levels. Treatment response was defined as ≥50% improvement in the MADRS score from baseline to either week 4 or 8. Variables associated with treatment response were included in a linear regression model as predictors of treatment response. Results: Twenty-seven patients (87%) completed 8 weeks of treatment; 74% and 63% were responders at week 4 and 8, respectively. High S100B and low HDL-C levels at baseline were associated with better treatment response at both time points. Low CRP levels were correlated with better response at week 4. Multivariate analysis showed that high baseline S100B levels and low baseline HDL-C levels were good predictors of treatment response at week 4 (R2 = 0.457, P =. 001), while S100B was at week 8 (R2 = 0.239, P =. 011). Importantly, baseline S100B and HDL-C levels were not associated with depression severity and did not change over time with clinical improvement. Conclusions: Serum S100B levels appear to be a useful biomarker of antidepressant response in MDD even when considering inflammatory and metabolic markers. © 2022 The Author(s) 2022.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subject.enS100B protein
dc.subject.enReactive-C protein
dc.subject.enHDL-cholesterol
dc.subject.enMajor depression
dc.subject.enAntidepressant
dc.title.enHigh S100B Levels Predict Antidepressant Response in Patients With Major Depression Even When Considering Inflammatory and Metabolic Markers
dc.typeArticle de revueen_US
dc.identifier.doi10.1093/ijnp/pyac016en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed35176771en_US
bordeaux.journalInternational Journal of Neuropsychopharmacologyen_US
bordeaux.page468-478en_US
bordeaux.volume25en_US
bordeaux.hal.laboratoriesNutriNeurO (Laboratoire de Nutrition et Neurobiologie Intégrée) - UMR 1286en_US
bordeaux.issue6en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINRAEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03997495
hal.version1
hal.date.transferred2023-02-20T15:09:32Z
hal.exporttrue
dc.rights.ccCC BY-NCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=International%20Journal%20of%20Neuropsychopharmacology&rft.date=2022-02-17&rft.volume=25&rft.issue=6&rft.spage=468-478&rft.epage=468-478&rft.eissn=1461-1457&rft.issn=1461-1457&rft.au=NAVINES,%20Ricard&ORIOLO,%20Giovanni&HORRILLO,%20Igor&CAVERO,%20Myriam&AOUIZERATE,%20Bruno&rft.genre=article


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