Prevention and Early Intervention Program for Psychoses (PEPP-Montreal), Douglas Mental Health University Institute, Montreal, Canada.
Schizophr Res. 2011 Jan;125(1):13-20. doi: 10.1016/j.schres.2010.09.021. Epub 2010 Nov 6.
Delay in treatment of psychosis is associated with poor clinical and social outcome and is measured as the duration of untreated psychosis (DUP) prior to treatment of the first episode. It has been suggested that this may be mediated through toxic effects of psychosis on the structure and function of the brain. Equivocal evidence exists regarding association between longer DUP and neuro-anatomical changes such as, reduced grey matter volume in specific regions in the brain and deficits in neurocognitive functions.
To examine if duration of untreated psychosis (DUP) preceding treatment of a first episode of psychosis is associated with structural brain abnormalities and deficits in neurocognitive functions.
We investigated the relationship between DUP and grey matter volume using voxel-based morphometry techniques and with multiple domains of cognition. Eighty patients with a first episode of psychosis were separated into two equal sized groups based on a median split (18 weeks) of their DUP.
Compared to the short-DUP group (mean DUP 7.9 weeks ± 5.6), the long-DUP group (mean 113.7 weeks ± 170 .4) showed significant grey matter volume reductions in orbital-frontal regions (bilateral medial frontal gyrus and bilateral rectal gyrus, BA 11) and parietal regions (postcentral gyrus and superior parietal lobule) as well as a significant reduction in whole brain grey matter volume (p<0.04). For schizophrenia spectrum cases only these findings were confined to left rectal gyrus. There were no differences in white matter or cerebral spinal fluid volumes or on cognitive functions. Results are controlled for antipsychotic medication exposure.
The inherent difficulty in separating slow and insidious onset from long-DUP may limit the interpretation of our results and there may be an overlap between DUP and duration of illness (including the prodrome).
Patients with a longer delay in treatment of psychosis show a significant reduction in overall grey matter volume with specific reductions in the inferior-orbital region. These results provide some support to a possible neurotoxic effect of prolonged untreated psychosis.
精神病治疗的延迟与较差的临床和社会结果相关,并通过治疗首次发作之前未经治疗的精神病持续时间(DUP)来衡量。有人认为,这可能是通过精神病对大脑结构和功能的毒性作用来介导的。关于较长的 DUP 与神经解剖学变化之间的关联,存在不确定的证据,例如大脑特定区域的灰质体积减少和神经认知功能缺陷。
检查未经治疗的精神病持续时间(DUP)在治疗首次精神病发作之前是否与结构脑异常和神经认知功能缺陷相关。
我们使用基于体素的形态计量学技术以及多个认知领域研究了 DUP 与灰质体积之间的关系。将 80 名首发精神病患者根据 DUP 的中位数(18 周)分为两组。
与短 DUP 组(平均 DUP 7.9 周±5.6)相比,长 DUP 组(平均 113.7 周±170.4)在眶额区域(双侧额内侧回和双侧直肠回,BA11)和顶叶区域(中央后回和上顶叶)显示出明显的灰质体积减少,以及整个大脑灰质体积的明显减少(p<0.04)。对于精神分裂症谱病例,这些发现仅限于左侧直肠回。在白质或脑脊髓液体积或认知功能方面没有差异。结果控制了抗精神病药物暴露。
将缓慢和隐匿性发作与长 DUP 分开的固有困难可能限制了我们结果的解释,并且 DUP 和疾病持续时间(包括前驱期)之间可能存在重叠。
精神病治疗延迟时间较长的患者表现出整体灰质体积明显减少,下眶区域特异性减少。这些结果为延长未经治疗的精神病可能产生的神经毒性作用提供了一些支持。