Synaptic Density in Early Stages of Psychosis and Clinical High Risk

IF 22.5 1区 医学 Q1 PSYCHIATRY JAMA Psychiatry Pub Date : 2024-11-13 DOI:10.1001/jamapsychiatry.2024.3608
M. Belen Blasco, Kankana Nisha Aji, Christian Ramos-Jiménez, Ilana Ruth Leppert, Christine Lucas Tardif, Johan Cohen, Pablo M. Rusjan, Romina Mizrahi
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Abstract

ImportanceSynaptic dysfunction is involved in schizophrenia pathophysiology. However, whether in vivo synaptic density is reduced in early stages of psychosis, including its high-risk states, remains unclear.ObjectiveTo investigate whether synaptic density (synaptic vesicle glycoprotein 2A [SV2A] binding potential) is reduced in first-episode psychosis (FEP) and in clinical high risk (CHR) and investigate the effect of cannabis use on synaptic density and examine its relationship with psychotic symptoms and gray matter microstructure across groups.Design, Setting, and ParticipantsThis cross-sectional study was performed in a tertiary care psychiatric hospital from July 2021 to October 2023. Participants were patients with antipsychotic-free or minimally exposed FEP or CHR and healthy controls with a clean urine drug screen (except cannabis).Main Outcomes and MeasuresSynaptic density was quantified with dynamic 90-minute [18F]SynVesT-1 positron emission tomography (PET) scans across prioritized brain regions of interest (ROIs) delineated in individual magnetic resonance images (MRIs). Cannabis use was confirmed with urine drug screens. Gray matter microstructure was assessed using diffusion-weighted MRI to estimate neurite density.ResultsA total of 49 participants were included, including 16 patients with FEP (mean [SD] age, 26.1 [4.6] years; 9 males and 7 females), 17 patients at CHR (mean [SD] age, 21.2 [3.5] years; 8 males and 9 females), and 16 healthy controls (mean [SD] age, 23.4 [3.6] years; 7 males and 9 females). Synaptic density was significantly different between groups (F2,273 = 4.02, P = .02, Cohen F = 0.17; ROI: F5,273 = 360.18, P &amp;lt; .01, Cohen F = 2.55) with a group × ROI interaction (F10,273 = 2.67, P &amp;lt; .01, Cohen F = 0.32). Synaptic density was lower in cannabis users (F1,272 = 5.31, P = .02, Cohen F = 0.14). Lower synaptic density across groups was associated with more negative symptoms (Positive and Negative Syndrome Scale negative scores: F1,81 = 4.31, P = .04, Cohen F = 0.23; Scale of Psychosis-Risk Symptoms negative scores: F1,90 = 4.12, P = .04, Cohen F = 0.21). SV2A binding potential was significantly associated with neurite density index (F1,138 = 6.76, P = .01, Cohen F = 0.22).Conclusions and RelevanceThis study found that synaptic density reductions were present during the early stages of psychosis and its risk states and associated with negative symptoms. The implications of SV2A for negative symptoms in psychosis and CHR warrant further investigation. Future studies should investigate the impact of cannabis use on synaptic density in CHR longitudinally.
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精神病早期和临床高危人群的突触密度
重要性突触功能障碍与精神分裂症的病理生理学有关。目的 研究首发精神病(FEP)和临床高危精神病(CHR)患者的突触密度(突触小泡糖蛋白 2A [SV2A] 结合电位)是否降低,调查使用大麻对突触密度的影响,并研究其与各组精神病症状和灰质微结构的关系。这项横断面研究于 2021 年 7 月至 2023 年 10 月在一家三级精神病医院进行。主要结果和测量突触密度采用 90 分钟动态[18F]SynVesT-1 正电子发射断层扫描(PET)进行量化,扫描范围为单个磁共振图像(MRI)中划定的优先大脑感兴趣区(ROI)。通过尿液药物筛查确认是否吸食大麻。结果 共纳入 49 名参与者,包括 16 名 FEP 患者(平均 [SD] 年龄 26.1 [4.6] 岁;男性 9 名,女性 7 名)、17 名 CHR 患者(平均 [SD] 年龄 21.2 [3.5] 岁;男性 8 名,女性 9 名)和 16 名健康对照组(平均 [SD] 年龄 23.4 [3.6] 岁;男性 7 名,女性 9 名)。突触密度在组间存在明显差异(F2,273 = 4.02,P = .02,Cohen F = 0.17;ROI:F5,273 = 360.18,P &p;amp;lt; .01,Cohen F = 2.55),组与 ROI 之间存在交互作用(F10,273 = 2.67,P &p;amp;lt; .01,Cohen F = 0.32)。大麻使用者的突触密度较低(F1,272 = 5.31,P = .02,Cohen F = 0.14)。各组较低的突触密度与较多的负面症状有关(正负综合征量表负分:F1,81 = 4.31,Cohen F = 0.32):F1,81 = 4.31,P = .04,Cohen F = 0.23;Scale of Psychosis-Risk Symptoms negative scores:F1,90 = 4.12,P = .04,Cohen F = 0.21)。SV2A 结合电位与神经元密度指数显著相关(F1,138 = 6.76,P = .01,Cohen F = 0.22)。SV2A 对精神病和慢性精神障碍患者的阴性症状的影响值得进一步研究。未来的研究应纵向调查使用大麻对 CHR 中突触密度的影响。
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来源期刊
JAMA Psychiatry
JAMA Psychiatry PSYCHIATRY-
CiteScore
30.60
自引率
1.90%
发文量
233
期刊介绍: JAMA Psychiatry is a global, peer-reviewed journal catering to clinicians, scholars, and research scientists in psychiatry, mental health, behavioral science, and related fields. The Archives of Neurology & Psychiatry originated in 1919, splitting into two journals in 1959: Archives of Neurology and Archives of General Psychiatry. In 2013, these evolved into JAMA Neurology and JAMA Psychiatry, respectively. JAMA Psychiatry is affiliated with the JAMA Network, a group of peer-reviewed medical and specialty publications.
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