Differential trajectories of corticostriatal structural connectivity in individuals at clinical high risk for psychosis according to functional outcome.

IF 6.2 1区 医学 Q1 PSYCHIATRY
Eugenie Choe, Hyungyou Park, Jiseon Jang, Minah Kim, Jun Soo Kwon
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Abstract

Dysconnectivity in the corticostriatal pathway, which is central to psychosis pathophysiology, is also known to be present in individuals at clinical high risk for psychosis (CHR-P). Considering that the corticostriatal pathway actively matures until adulthood and that neuroanatomical maturation is suggested to be related to functional outcomes in individuals at CHR-P, longitudinal studies on the corticostriatal structural pathway in individuals at CHR-P are warranted. To characterize the longitudinal trajectory of corticostriatal structural connectivity, diffusion-weighted images were collected from 23 individuals at CHR-P and 20 healthy controls (HCs) at baseline and at a 2-year follow-up visit. Probabilistic tractography was performed to segment the pathways between seven cortical regions and the striatum. The relative connectivity between each cortical region and associated striatal subregion was calculated. The CHR-P group was divided into subgroups according to the functional outcome of the modified Global Assessment of Functioning score at follow-up. A significant group‒time interaction between the left orbitofrontal cortex and its associated striatal subregion was found, with a negative slope in the CHR-P group and positive slope in the HC group. In the left orbitofrontal corticostriatal relative connectivity, the group‒time interaction between HCs and individuals at CHR-P with poor functional outcomes at follow-up was statistically significant, whereas that between HCs and individuals at CHR-P with good functional outcomes at follow-up was not. These findings indicate abnormal white matter maturation of the orbitofrontal corticostriatal pathway in individuals at CHR-P. Abnormal neuroanatomical maturation of the orbitofrontal corticostriatal pathway may reflect prognosis for functional outcomes in these individuals.

Abstract Image

Abstract Image

根据功能结果,临床精神病高风险个体的皮质纹状体结构连接的差异轨迹。
皮质纹状体通路的连接障碍是精神病病理生理学的核心,也存在于临床精神病高危人群(chrp)中。考虑到皮质纹状体通路在成年前积极成熟,并且神经解剖学的成熟被认为与chrp患者的功能结局有关,因此有必要对chrp患者的皮质纹状体结构通路进行纵向研究。为了描述皮质纹状体结构连通性的纵向轨迹,在基线和2年随访期间收集了23名chrp患者和20名健康对照(hc)的弥散加权图像。在7个皮质区域和纹状体之间进行了概率神经束造影。计算每个皮质区和相关纹状体亚区之间的相对连通性。根据随访时改良的整体功能评估评分将chrp组分为亚组。左侧眶额皮质与其相关纹状体亚区之间存在显著的组时相互作用,chrp组斜率为负,HC组斜率为正。在左眼窝额叶皮质纹状体相对连通性方面,hcc与随访时功能预后较差的chrp患者之间的组时间相互作用具有统计学意义,而hcc与随访时功能预后较好的chrp患者之间的组时间相互作用无统计学意义。这些结果表明,chrp患者眼窝额叶皮质纹状体通路白质成熟异常。眶额皮质纹状体通路的异常神经解剖学成熟可能反映了这些个体的功能预后。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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