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Platelet-Derived Growth Factor as an Antidepressant Treatment Selection Biomarker: Higher Levels Selectively Predict Better Outcomes with Bupropion-SSRI Combination.
Jha, Manish K; Minhajuddin, Abu; Gadad, Bharathi S; Trivedi, Madhukar H.
Afiliação
  • Jha MK; Center for Depression Research and Clinical Care, and Department of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Minhajuddin A; Center for Depression Research and Clinical Care, and Department of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Gadad BS; Center for Depression Research and Clinical Care, and Department of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Trivedi MH; Center for Depression Research and Clinical Care, and Department of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, Texas.
Int J Neuropsychopharmacol ; 20(11): 919-927, 2017 11 01.
Article em En | MEDLINE | ID: mdl-29016822
ABSTRACT

Background:

Platelet derived growth factor is integral to maintenance of blood brain barrier, increases in response to blood brain barrier disruption, and may reflect neuroinflammation. Based on previous reports of better outcomes with dopaminergic antidepressants in depressed patients with elevated inflammatory biomarkers, we hypothesize that elevated peripheral platelet derived growth factor levels can serve as a powerful biomarker for selecting dopaminergic antidepressants.

Methods:

Platelet derived growth factor, basic fibroblast growth factor, and granulocyte colony stimulating factor were measured as part of Bioplex Pro human cytokine 27-plex kit in participants of the Combining Medications to Enhance Depression Outcomes trial who provided baseline plasma (n=166) and were treated with either bupropion-plus-escitalopram, escitalopram-plus-placebo, or venlafaxine-plus-mirtazapine. Differential changes in overall symptom severity and anhedonia as well as side effects were tested with a treatment-arm-by-biomarker interaction in mixed model analyses. Effect of biomarkers with significant interaction was calculated in subsequent analyses stratified by treatment arm.

Results:

There was a significant treatment-arm-by-platelet derived growth factor interaction for depression severity (P=.03) and anhedonia (P=.008) but not for side effects (P=.44). Higher baseline platelet derived growth factor level was associated with greater reduction in depression severity (effect size=0.71, P=.015) and anhedonia (effect size=0.66, P=.02) in the bupropion- selective serotonin reuptake inhibitor but not the other two treatment arms. There was no significant treatment-arm-by-biomarker interaction for both depression severity and side effects with the other two biomarkers.

Conclusion:

As compared with selective serotonin reuptake inhibitor monotherapy or venlafaxine-plus-mirtazapine, bupropion-plus-escitalopram selectively improves anhedonia, which in turn results in improved overall depression severity in depressed patients with elevated platelet derived growth factor levels.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fator de Crescimento Derivado de Plaquetas / Resultado do Tratamento / Bupropiona / Inibidores Seletivos de Recaptação de Serotonina / Depressão / Antidepressivos Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Neuropsychopharmacol Assunto da revista: NEUROLOGIA / PSICOFARMACOLOGIA Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fator de Crescimento Derivado de Plaquetas / Resultado do Tratamento / Bupropiona / Inibidores Seletivos de Recaptação de Serotonina / Depressão / Antidepressivos Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Neuropsychopharmacol Assunto da revista: NEUROLOGIA / PSICOFARMACOLOGIA Ano de publicação: 2017 Tipo de documento: Article