Rogeau Antoine, Boer Anne Jetske, Guedj Eric, Sala Arianna, Sommer Iris E, Veronese Mattia, van der Weijden-Germann Monique, Fraioli Francesco
Department of Nuclear Medicine, Lille University Hospital, Lille, France.
Department of Neuroscience, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Eur J Nucl Med Mol Imaging. 2025 Feb;52(3):876-899. doi: 10.1007/s00259-024-06987-1. Epub 2024 Nov 22.
There is a need for biomarkers in psychiatry to improve diagnosis, prognosis and management, and with confirmed value in follow-up care. Radionuclide imaging, given its molecular imaging characteristics, is well-positioned for translation to the clinic. This systematic review lays the groundwork for integrating PET and SPECT imaging in the clinical management of schizophrenia-spectrum disorders.
Systematic search of PubMed, Embase, Web of Science and Cochrane library databases was conducted from the earliest date available until February 2024. The focus was on longitudinal studies evaluating PET or SPECT imaging in individuals with a schizophrenia-spectrum or another psychotic disorders. Quality assessment was done using the Newcastle-Ottawa Scale (NOS), NIH scale for before-after studies and Cochrane Risk of Bias tool version 2 (Cochrane RoB2). Studies were further categorised into three groups: preclinical and diagnosis, predicting disease course or personalising treatment.
Fifty-six studies were included in the systematic review investigating in total 1329 patients over a median of 3 months. Over two-thirds used PET tracers, whereas the remaining studies employed SPECT tracers. The most frequently investigated system was dopaminergic transmission, followed by cerebral metabolism and blood flow. [F]FDOPA demonstrated large effect size in predicting conversion of subjects at risk and treatment response. Additionally, treatment dosage could be optimised to reduce side effects using [I]IBZM or [C]raclopride.
Molecular imaging holds significant promise for real-life application in schizophrenia, with two particularly encouraging avenues being the prediction of conversion/response to antipsychotic medication and the improved management of antipsychotic dosage. Further longitudinal studies and clinical trials will be essential for validating both the clinical effectiveness and economic sustainability, as well as for exploring new applications.
精神病学领域需要生物标志物来改善诊断、预后和管理,并在后续护理中具有确证价值。放射性核素成像因其分子成像特性,在转化应用于临床方面具有优势。本系统评价为将正电子发射断层扫描(PET)和单光子发射计算机断层扫描(SPECT)成像整合到精神分裂症谱系障碍的临床管理中奠定了基础。
从可获取的最早日期至2024年2月,对PubMed、Embase、科学网和考克兰图书馆数据库进行系统检索。重点是评估PET或SPECT成像在精神分裂症谱系或其他精神障碍个体中的纵向研究。使用纽卡斯尔-渥太华量表(NOS)、美国国立卫生研究院(NIH)前后研究量表和考克兰偏倚风险工具第2版(考克兰RoB2)进行质量评估。研究进一步分为三组:临床前与诊断、预测疾病进程或个性化治疗。
该系统评价纳入了56项研究,共调查了1329例患者,中位随访时间为3个月。超过三分之二的研究使用PET示踪剂,其余研究使用SPECT示踪剂。研究最频繁的系统是多巴胺能传递,其次是脑代谢和血流。[F]氟多巴在预测有风险个体的转化和治疗反应方面显示出较大的效应量。此外,使用[I]碘苄胍或[C]雷氯必利可以优化治疗剂量以减少副作用。
分子成像在精神分裂症的实际应用中具有重大前景,两个特别令人鼓舞的方向是预测对抗精神病药物的转化/反应以及改善抗精神病药物剂量的管理。进一步的纵向研究和临床试验对于验证临床有效性和经济可持续性以及探索新应用至关重要。