Neuroimaging alterations and relapse in early-stage psychosis

被引:0
|
作者
Mihaljevic, Marina [1 ]
Nagpal, Anisha [1 ]
Etyemez, Semra [1 ]
Narita, Zui [1 ]
Ross, Anna [1 ]
Schaub, Rebecca
Cascella, Nicola G. [1 ]
Coughlin, Jennifer M. [1 ]
Nestadt, Gerald [1 ]
Nucifora, Frederik C. [1 ]
Sedlak, Thomas W. [1 ]
Calhoun, Vince D. [6 ]
Faria, Andreia V. [2 ]
Yang, Kun [1 ,7 ]
Sawa, Akira [1 ,3 ,4 ,5 ,7 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD USA
[2] Johns Hopkins Univ, Sch Med, Dept Radiol & Radiol Sci, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Phamarchol, Baltimore, MD USA
[4] Johns Hopkins Univ, Sch Med, Dept Genet Med, Baltimore, MD USA
[5] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Mental Hlth, Baltimore, MD USA
[6] Emory Univ, Georgia State Univ, Georgia Inst Technol, Triinst Ctr Translat Res Neuroimaging & Data Sci T, Atlanta, GA USA
[7] Johns Hopkins Univ Hosp, 600 N Wolfe St, Baltimore, MD 21287 USA
来源
JOURNAL OF PSYCHIATRY & NEUROSCIENCE | 2024年 / 49卷 / 02期
基金
美国国家卫生研究院;
关键词
1ST EPISODE PSYCHOSIS; FUNCTIONAL CONNECTIVITY; SCHIZOPHRENIA; NETWORK;
D O I
10.1503/jpn.230115
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Recent reports have indicated that symptom exacerbation after a period of improvement, referred to as relapse, in early-stage psychosis could result in brain changes and poor disease outcomes. We hypothesized that substantial neuroimaging alterations may exist among patients who experience relapse in early-stage psychosis. Methods: We studied patients with psychosis within 2 years after the first psychotic event and healthy controls. We divided patients into 2 groups, namely those who did not experience relapse between disease onset and the magnetic resonance imaging (MRI) scan (no-relapse group) and those who did experience relapse between these 2 timings (relapse group). We analyzed 3003 functional connectivity estimates between 78 regions of interest (ROIs) derived from resting-state functional MRI data by adjusting for demographic and clinical confounding factors. Results: We studied 85 patients, incuding 54 in the relapse group and 31 in the no-relapse group, along with 94 healthy controls. We observed significant differences in 47 functional connectivity estimates between the relapse and control groups after multiple comparison corrections, whereas no differences were found between the no-relapse and control groups. Most of these pathological signatures (64%) involved the thalamus. The Jonckheere-Terpstra test indicated that all 47 functional connectivity changes had a significant cross-group progression from controls to patients in the no-relapse group to patients in the relapse group. Limitations: Longitudinal studies are needed to further validate the involvement and pathological importance of the thalamus in relapse. Conclusion: We observed pathological differences in neuronal connectivity associated with relapse in early-stage psychosis, which are more specifically associated with the thalamus. Our study implies the importance of considering neurobiological mechanisms associated with relapse in the trajectory of psychotic disorders.
引用
收藏
页码:E135 / E142
页数:8
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