首页> 美国卫生研究院文献>Frontiers in Psychiatry >Assessment of Translocator Protein Density as Marker of Neuroinflammation in Major Depressive Disorder: A Pilot Multicenter Comparative Controlled Brain PET Study (INFLADEP Study)
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Assessment of Translocator Protein Density as Marker of Neuroinflammation in Major Depressive Disorder: A Pilot Multicenter Comparative Controlled Brain PET Study (INFLADEP Study)

机译:评估重度抑郁症中作为神经炎症标记的易位蛋白的密度:一项先导多中心比较对照脑PET研究(INFLADEP研究)

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摘要

>Background: Major depressive disorder (MDD) is a serious public health problem with high lifetime prevalence (4.4–20%) in the general population. The monoamine hypothesis is the most widespread etiological theory of MDD. Also, recent scientific data has emphasized the importance of immuno-inflammatory pathways in the pathophysiology of MDD. The lack of data on the magnitude of brain neuroinflammation in MDD is the main limitation of this inflammatory hypothesis. Our team has previously demonstrated the relevance of [18F] DPA-714 as a neuroinflammation biomarker in humans. We formulated the following hypotheses for the current study: (i) Neuroinflammation in MDD can be measured by [18F] DPA-714; (ii) its levels are associated with clinical severity; (iii) it is accompanied by anatomical and functional alterations within the frontal-subcortical circuits; (iv) it is a marker of treatment resistance.>Methods: Depressed patients will be recruited throughout 4 centers (Bordeaux, Montpellier, Tours, and Toulouse) of the French network from 13 expert centers for resistant depression. The patient population will be divided into 3 groups: (i) experimental group—patients with current MDD (n = 20), (ii) remitted depressed group—patients in remission but still being treated (n = 20); and, (iii) control group without any history of MDD (n = 20). The primary objective will be to compare PET data (i.e., distribution pattern of neuroinflammation) between the currently depressed group and the control group. Secondary objectives will be to: (i) compare neuroinflammation across groups (currently depressed group vs. remitted depressed group vs. control group); (ii) correlate neuroinflammation with clinical severity across groups; (iii) correlate neuroinflammation with MRI parameters for structural and functional integrity across groups; (iv) correlate neuroinflammation and peripheral markers of inflammation across groups.>Discussion: This study will assess the effects of antidepressants on neuroinflammation as well as its role in the treatment response. It will contribute to clarify the putative relationships between neuroinflammation quantified by brain neuroimaging techniques and peripheral markers of inflammation. Lastly, it is expected to open innovative and promising therapeutic perspectives based on anti-inflammatory strategies for the management of treatment-resistant forms of MDD commonly seen in clinical practice.Clinical trial registration (reference: ): https://www.clinicaltrials.gov/ct2/show/?term=neuroinflammation&cond=depression&cntry=FR&rank=1
机译:>背景:严重抑郁症(MDD)是一个严重的公共卫生问题,在一般人群中,其终生患病率较高(4.4–20%)。单胺假说是MDD的最广泛的病因学说。同样,最近的科学数据强调了免疫炎症途径在MDD病理生理中的重要性。缺乏关于MDD中脑神经炎症程度的数据是这种炎症假说的主要局限。我们的研究小组先前已证明[18F] DPA-714作为人类神经炎症生物标记物的相关性。我们为当前研究提出了以下假设:(i)MDD中的神经炎症可以通过[18F] DPA-714进行测量; (ii)其水平与临床严重程度有关; (iii)伴随额叶皮层下回路的解剖和功能改变; (iv)它是抗药性的标志。>方法:将在法国网络的4个中心(波尔多,蒙彼利埃,图尔和图卢兹)从13个抗抑郁专家中心招募抑郁症患者。患者人群将分为3组:(i)实验组-当前MDD患者(n = 20),(ii)抑郁症缓解组-缓解但仍在接受治疗的患者(n = 20); (iii)没有MDD病史的对照组(n = 20)。主要目的是比较当前抑郁组和对照组之间的PET数据(即神经炎症分布模式)。次要目标是:(i)比较各组的神经炎症(当前的抑郁症组与缓解的抑郁症组与对照组之间); (ii)将神经炎症与各组的临床严重程度相关联; (iii)将神经炎症与MRI参数相关,以实现跨组的结构和功能完整性; (iv)将神经炎症与各组炎症的周围标志物相关联。>讨论:本研究将评估抗抑郁药对神经炎症的作用及其在治疗反应中的作用。这将有助于阐明通过脑神经影像技术量化的神经炎症与周围炎症标志之间的推测关系。最后,有望基于抗炎策略为临床实践中常见的难治性MDD的治疗方法打开创新的,有希望的治疗前景。临床试验注册(参考:):https://www.clinicaltrials。 gov / ct2 / show /?term = neuroinflammation&cond = depression&cntry = FR&rank = 1

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