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观点:解决精神病中TSPO PET成像的异质性难题。

Perspective: Solving the Heterogeneity Conundrum of TSPO PET Imaging in Psychosis.

作者信息

De Picker Livia, Morrens Manuel

机构信息

Collaborative Antwerp Psychiatric Research Institute, University of Antwerp, Antwerp, Belgium.

SINAPS, University Psychiatric Hospital Campus Duffel, Duffel, Belgium.

出版信息

Front Psychiatry. 2020 May 1;11:362. doi: 10.3389/fpsyt.2020.00362. eCollection 2020.

Abstract

Positron emission tomography using ligands targeting translocator protein 18 kDa (TSPO PET) is an innovative method to visualize and quantify glial inflammatory responses in the central nervous system . Compared to some other neuropsychiatric disorders, findings of TSPO PET in schizophrenia and related psychotic disorders have been considerably more heterogeneous. Two conflicting meta-analyses have been published on the topic within the last year: one asserting evidence for decreased TSPO uptake, while the other observed increased TSPO uptake in a selection of studies. In this paper, we review and discuss five hypotheses which may explain the observed variability of TSPO PET findings in psychotic illness, namely that (1) an inflammatory phenotype is only present in a subgroup of psychosis patients; (2) heterogeneity is caused by interference of antipsychotic medication; (3) interference of other clinical confounders in the study populations (such as age, sex, BMI, smoking, and substance use); or (4) methodological variability between studies (such as choice of tracer and kinetic model, genotyping, study power, and diurnal effects); and (5) the glial responses underlying changes in TSPO expression are themselves heterogeneous and dynamic. Finally, we propose four key recommendations for future research proposals to mitigate these different causes of heterogeneity.

摘要

使用靶向18 kDa转运蛋白(TSPO PET)的配体进行正电子发射断层扫描是一种用于可视化和量化中枢神经系统中胶质细胞炎症反应的创新方法。与其他一些神经精神疾病相比,TSPO PET在精神分裂症及相关精神障碍中的研究结果差异更大。去年就该主题发表了两项相互矛盾的荟萃分析:一项断言有证据表明TSPO摄取减少,而另一项在部分研究中观察到TSPO摄取增加。在本文中,我们回顾并讨论了五个假设,这些假设可能解释了在精神疾病中观察到的TSPO PET结果的变异性,即:(1)炎症表型仅存在于部分精神病患者中;(2)异质性是由抗精神病药物的干扰引起的;(3)研究人群中其他临床混杂因素(如年龄、性别、体重指数、吸烟和物质使用)的干扰;或(4)研究之间的方法学差异(如示踪剂和动力学模型的选择、基因分型、研究效能和昼夜效应);以及(5)TSPO表达变化背后的胶质细胞反应本身是异质性和动态的。最后,我们为未来的研究建议提出了四项关键建议,以减轻这些不同的异质性原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdf3/7206714/253432c43ae9/fpsyt-11-00362-g001.jpg

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