Structural neuroimaging across early-stage psychosis: Aberrations in neurobiological trajectories and implications for the staging model

被引:51
|
作者
Bartholomeusz, Cali F. [1 ,2 ,3 ,4 ]
Cropley, Vanessa L. [3 ,4 ]
Wannan, Cassandra [1 ,2 ,3 ,4 ]
Di Biase, Maria [3 ,4 ]
McGorry, Patrick D. [1 ,2 ]
Pantelis, Christos [3 ,4 ,5 ]
机构
[1] Orygen, 35 Poplar Rd, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Ctr Youth Mental Hlth, Parkville, Vic, Australia
[3] Univ Melbourne, Dept Psychiat, Melbourne Neuropsychiat Ctr, Carlton, Vic, Australia
[4] Melbourne Hlth, Carlton, Vic, Australia
[5] Univ Melbourne, Dept Elect & Elect Engn, Ctr Neural Engn, Carlton, Vic, Australia
来源
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
Neuroimaging; schizophrenia spectrum; longitudinal trajectory; clinical staging; early psychosis; ULTRA-HIGH-RISK; PROGRESSIVE BRAIN CHANGES; GRAY-MATTER VOLUME; 1ST EPISODE PSYCHOSIS; LIKELIHOOD ESTIMATION METAANALYSIS; 1ST-EPISODE AFFECTIVE PSYCHOSIS; SUPERIOR TEMPORAL GYRUS; CLINICAL HIGH-RISK; HEAVY CANNABIS USE; 1-YEAR FOLLOW-UP;
D O I
10.1177/0004867416670522
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: This review critically examines the structural neuroimaging evidence in psychotic illness, with a focus on longitudinal imaging across the first-episode psychosis and ultra-high-risk of psychosis illness stages. Methods: A thorough search of the literature involving specifically longitudinal neuroimaging in early illness stages of psychosis was conducted. The evidence supporting abnormalities in brain morphology and altered neurodevelopmental trajectories is discussed in the context of a clinical staging model. Results: In general, grey matter (and, to a lesser extent, white matter) declines across multiple frontal, temporal (especially superior regions), insular and parietal regions during the first episode of psychosis, which has a steeper trajectory than that of age-matched healthy counterparts. Although the ultra-high-risk of psychosis literature is considerably mixed, evidence indicates that certain volumetric structural aberrations predate psychotic illness onset (e.g. prefrontal cortex thinning), while other abnormalities present in ultra-high-risk of psychosis populations are potentially non-psychosis-specific (e.g. hippocampal volume reductions). Conclusion: We highlight the advantages of longitudinal designs, discuss the implications such studies have on clinical staging and provide directions for future research.
引用
收藏
页码:455 / 476
页数:22
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