Progressive Decline in Hippocampal CAI Volume in Individuals at Ultra-High-Risk for Psychosis Who Do Not Remit: Findings from the Longitudinal Youth at Risk Study

被引:65
|
作者
Ho, New Fei [1 ,2 ]
Holt, Daphne J. [3 ,4 ]
Cheung, Mike [5 ]
Iglesias, Juan Eugenio [6 ]
Goh, Alex [1 ]
Wang, Mingyuan [1 ]
Lim, Joseph K. W. [2 ]
de Souza, Joshua [2 ]
Poh, Joann S. [2 ]
See, Yuen Mei [1 ]
Adcock, Alison R. [7 ]
Wood, Stephen J. [8 ]
Chee, Michael W. L. [2 ]
Lee, Jimmy [1 ]
Zhou, Juan [2 ]
机构
[1] Inst Mental Hlth, 10 Buangkok View,Buangkok Green Med Pk, Singapore 539747, Singapore
[2] Duke Natl Univ Singapore, Grad Sch Med, Neurosci & Behav Disorders Program, Ctr Cognit Neurosci, 8 Coll Rd,06-15, Singapore 169857, Singapore
[3] Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02114 USA
[4] Harvard Med Sch, Boston, MA USA
[5] Natl Univ Singapore, Dept Psychol, Singapore, Singapore
[6] UCL, London, England
[7] Duke Univ, Ctr Cognit Neurosci, Durham, NC USA
[8] Univ Birmingham, Sch Psychol, Birmingham, W Midlands, England
基金
英国工程与自然科学研究理事会; 英国医学研究理事会;
关键词
BIPOLAR-SCHIZOPHRENIA NETWORK; CLINICAL HIGH-RISK; STRUCTURAL ABNORMALITIES; CORTICAL THICKNESS; AMYGDALA VOLUMES; MEMORY DEFICITS; YOUNG-ADULTS; BRAIN VOLUME; DISORDER; SEGMENTATION;
D O I
10.1038/npp.2017.5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Most individuals identified as ultra-high-risk (UHR) for psychosis do not develop frank psychosis. They continue to exhibit subthreshold symptoms, or go on to fully remit. Prior work has shown that the volume of CA1, a subfield of the hippocampus, is selectively reduced in the early stages of schizophrenia. Here we aimed to determine whether patterns of volume change of CA1 are different in UHR individuals who do or do not achieve symptomatic remission. Structural MRI scans were acquired at baseline and at 1-2 follow-up time points (at 12-month intervals) from 147 UHR and healthy control subjects. An automated method (based on an ex vivo atlas of ultra-highresolution hippocampal tissue) was used to delineate the hippocampal subfields. Over time, a greater decline in bilateral CA1 subfield volumes was found in the subgroup of UHR subjects whose subthreshold symptoms persisted (n= 40) and also those who developed clinical psychosis (n = 12), compared with UHR subjects who remitted (n= 41) and healthy controls (n= 54). No baseline differences in volumes of the overall hippocampus or its subfields were found among the groups. Moreover, the rate of volume decline of CA1, but not of other hippocampal subfields, in the non-remitters was associated with increasing symptom severity over time. Thus, these findings indicate that there is deterioration of CA1 volume in persistently symptomatic UHR individuals in proportion to symptomatic progression.
引用
收藏
页码:1361 / 1370
页数:10
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