Su Qiao, Xuekelaiti Zaimina, Ma Hongyun, Qiu Yuying, Sun Xiaoxiao, Bi Fuyou, Li Meijuan, Li Jie
Tianjin Anding Hospital, Mental Health Center of Tianjin Medical University, Tianjin, China.
Tianjin Anding Hospital, Mental Health Center of Tianjin Medical University, Tianjin, China.
Schizophr Res. 2024 Dec;274:113-120. doi: 10.1016/j.schres.2024.09.011. Epub 2024 Sep 16.
Cognitive impairment is a core feature of schizophrenia with unclear mechanisms, particularly neurocognition. The objective of this study was to investigate the association between duration of untreated psychosis (DUP) and neurocognition, as well as potential biological mechanisms.
A total of 219 patients were recruited in this study. DUP was measured in years, reflecting the untreated period. Neurocognition was assessed by the MATRICS Consensus Cognitive Battery (MCCB). The plasma concentrations of three growth factors, vascular endothelial growth factor (VEGF), brain-derived neurotrophic factor (BDNF), and epidermal Growth Factor (EGF) were detected by enzyme-linked immunosorbent assay in 128 patients. Multiple linear regression analysis was used to analyze the association between DUP, growth factors, and neurocognition.
Our findings showed that DUP was significantly negatively correlated with speed of processing and reasoning and problem-solving in all patients (N = 219, P < 0.05). Five years was defined as cut-off point for long and short DUP group in the present study. Only in the short DUP patients, DUP was strongly associated with visual learning and neurocognition (P < 0.05). In patients with growth factor (N = 128), DUP was independently associated with speed of processing, verbal learning, and neurocognition (P < 0.05). Further, plasma concentrations of VEGF, BDNF, and EGF were all significantly correlated with neurocognition (P < 0.05). Additionally, we found a potential trend of correlation between DUP and BDNF (P = 0.061).
Our study provides insights into a negative correlation between DUP and neurocognition, and BDNF may serve as a potential biological mechanism.
认知障碍是精神分裂症的核心特征,其机制尚不清楚,尤其是神经认知方面。本研究的目的是探讨未治疗精神病持续时间(DUP)与神经认知之间的关联以及潜在的生物学机制。
本研究共招募了219名患者。DUP以年为单位进行测量,反映未治疗期。通过MATRICS共识认知成套测验(MCCB)评估神经认知。采用酶联免疫吸附测定法检测了128名患者血浆中三种生长因子,即血管内皮生长因子(VEGF)、脑源性神经营养因子(BDNF)和表皮生长因子(EGF)的浓度。采用多元线性回归分析来分析DUP、生长因子与神经认知之间的关联。
我们的研究结果表明,在所有患者中(N = 219,P < 0.05),DUP与加工速度、推理及解决问题能力显著负相关。在本研究中,将5年定义为长DUP组和短DUP组的分界点。仅在短DUP患者中,DUP与视觉学习及神经认知密切相关(P < (此处原文有误,推测为P < 0.05))。在有生长因子数据的患者中(N = 128),DUP与加工速度、言语学习及神经认知独立相关(P < 0.05)。此外,VEGF、BDNF和EGF的血浆浓度均与神经认知显著相关(P < 0.05)。另外,我们发现DUP与BDNF之间存在潜在的相关性趋势(P = 0.061)。
我们的研究揭示了DUP与神经认知之间的负相关,并且BDNF可能是一种潜在的生物学机制。