Center for Depression Research and Clinical Care, and Department of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, Texas.
Int J Neuropsychopharmacol. 2017 Nov 1;20(11):919-927. doi: 10.1093/ijnp/pyx060.
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.
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.
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.
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.
血小板衍生生长因子是维持血脑屏障完整性的重要组成部分,在血脑屏障破坏时会增加,并可能反映神经炎症。基于先前的报告,在炎症生物标志物升高的抑郁患者中,使用多巴胺能抗抑郁药会有更好的结果,我们假设外周血小板衍生生长因子水平升高可以作为选择多巴胺能抗抑郁药的有力生物标志物。
在“联合用药增强抑郁结局试验”的参与者中,作为 Bioplex Pro 人类细胞因子 27- plex 试剂盒的一部分,测量了血小板衍生生长因子、碱性成纤维细胞生长因子和粒细胞集落刺激因子。在基线血浆中(n=166)提供了这些数据的参与者,他们接受了布普啡因-依他普仑、依他普仑-安慰剂或文拉法辛-米氮平治疗。在混合模型分析中,通过治疗组与生物标志物的相互作用测试了整体症状严重程度和快感缺失的差异变化以及副作用。在随后的分析中,根据治疗组对具有显著相互作用的生物标志物进行了分层分析。
抑郁严重程度(P=.03)和快感缺失(P=.008)的治疗组与血小板衍生生长因子的相互作用有显著差异,但副作用(P=.44)没有差异。较高的基线血小板衍生生长因子水平与布普啡因-选择性 5-羟色胺再摄取抑制剂治疗组中抑郁严重程度(效应大小=0.71,P=.015)和快感缺失(效应大小=0.66,P=.02)的更大减轻相关,但在其他两个治疗组中没有相关性。对于其他两个生物标志物,抑郁严重程度和副作用的治疗组与生物标志物的相互作用均无显著差异。
与选择性 5-羟色胺再摄取抑制剂单药治疗或文拉法辛-米氮平相比,布普啡因-依他普仑选择性改善快感缺失,进而导致血小板衍生生长因子水平升高的抑郁患者整体抑郁严重程度改善。