Department of Psychiatry, The University of Hong Kong, 2/F New Clinical Building, Queen Mary Hospital, Pokfulam Road, Pokfulam, Hong Kong, China.
The State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.
Psychopharmacology (Berl). 2022 Jul;239(7):2133-2141. doi: 10.1007/s00213-022-06088-7. Epub 2022 Feb 25.
How striatal dopamine synthesis capacity (DSC) contributes to the pathogenesis of negative symptoms in first-episode schizophrenia (SZ) and delusional disorder (DD) has seldom been explored. As negative symptoms during active psychotic episodes can be complicated by secondary influences, such as positive symptoms, longitudinal investigations may help to clarify the relationship between striatal DSC and negative symptoms and differentiate between primary and secondary negative symptoms.
A longitudinal study was conducted to examine whether baseline striatal DSC would be related to negative symptoms at 3 months in first-episode SZ and DD patients.
Twenty-three first-episode age- and gender-matched patients (11 DD and 12 SZ) were consecutively recruited through an early intervention service for psychosis in Hong Kong. Among them, 19 (82.6%) patients (9 DD and 10 SZ) were followed up at 3 months. All patients received an F-DOPA PET/MR scan at baseline.
Baseline striatal DSC (K) was inversely associated with negative symptoms at 3 months in first-episode SZ patients (r = - 0.80, p = 0.010). This association remained in SZ patients even when controlling for baseline negative, positive, and depressive symptoms, as well as cumulative antipsychotic dosage (β = - 0.69, p = 0.012). Such associations were not observed in first-episode DD patients. Meanwhile, the severity of negative symptoms at 3 months was associated with more positive symptoms in DD patients (r = 0.74, p = 0.010) and not in SZ patients.
These findings highlight the role of striatal DSC in negative symptoms upon resolution of active psychotic episodes among first-episode SZ patients. Baseline striatal dopamine activity may inform future symptom expression with important treatment implications.
纹状体多巴胺合成能力(DSC)如何导致首发精神分裂症(SZ)和妄想障碍(DD)的阴性症状的发病机制,这方面的研究很少。由于阳性症状等继发性影响可能会使活动期精神病性发作期间的阴性症状复杂化,因此纵向研究可能有助于阐明纹状体 DSC 与阴性症状之间的关系,并区分原发性和继发性阴性症状。
进行了一项纵向研究,以检验首发SZ 和 DD 患者的基线纹状体 DSC 是否与发病 3 个月时的阴性症状有关。
通过香港的精神病早期干预服务,连续招募了 23 名年龄和性别匹配的首发患者(11 名 DD 和 12 名 SZ)。其中,19 名(82.6%)患者(9 名 DD 和 10 名 SZ)在 3 个月时进行了随访。所有患者均在基线时接受了 F-DOPA PET/MR 扫描。
首发 SZ 患者的基线纹状体 DSC(K)与发病 3 个月时的阴性症状呈负相关(r=-0.80,p=0.010)。即使在控制基线阴性、阳性和抑郁症状以及累积抗精神病药物剂量后,这种相关性仍然存在(β=-0.69,p=0.012)。在首发 DD 患者中没有观察到这种相关性。同时,DD 患者发病 3 个月时的阴性症状严重程度与更多的阳性症状相关(r=0.74,p=0.010),而与 SZ 患者无关。
这些发现强调了纹状体 DSC 在首发 SZ 患者活动期精神病性发作缓解后对阴性症状的作用。基线纹状体多巴胺活性可能为未来的症状表现提供信息,具有重要的治疗意义。