青少年早期内化、外化和思维障碍的常见和障碍特异性皮层厚度变化:一项青少年大脑和认知发展研究。

IF 4.1 2区 医学 Q2 NEUROSCIENCES Journal of Psychiatry & Neuroscience Pub Date : 2023-09-06 Print Date: 2023-09-01 DOI:10.1503/jpn.220202
Gechang Yu, Zhaowen Liu, Xinran Wu, Benjamin Becker, Kai Zhang, Huaxin Fan, Songjun Peng, Nanyu Kuang, Jujiao Kang, Guiying Dong, Xing-Ming Zhao, Gunter Schumann, Jianfeng Feng, Barbara J Sahakian, Trevor W Robbins, Lena Palaniyappan, Jie Zhang
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引用次数: 0

摘要

背景:越来越多的神经影像学研究报告了成年人精神障碍中常见的神经异常。然而,尽管疾病之间存在重叠,但尚不清楚不同的疾病特异性机制是否在青春期发挥作用。方法:我们研究了来自青少年大脑和认知发展队列的11000多名青春期前(9-10岁)儿童。我们采用了一种重组方法来比较健康对照组(n=4041)与外化组(n=1182)、内化组(n=1959)和思维障碍组(n=347)之间的皮层厚度(CT)变化和纵向变化。对4468名不相关的欧洲青年进行了区域CT全基因组关联研究(GWAS)。结果:与对照组相比,患有外化或内化障碍的青年表现出区域CT增加。外部化(p=8×10-4,Cohen d=0.10)和内部化障碍(p=2×10-3,Cohn d=0.08)在左颞叶共有较厚的CT。躯体感觉和初级听觉皮层在外化障碍中受到独特影响,而初级运动皮层和高级视觉联想区域在内化障碍中受到唯一影响。只有患有外化障碍的年轻人在10-12岁时表现出皮质变薄的减速。GWAS在这些区域发现了59个全基因组的显著相关基因变异。常见区域的皮质厚度与谷氨酸能神经元有关,而内化特定区域CT与星形胶质细胞、少突胶质细胞祖细胞和GABA能神经元有关。局限性:GWAS的样本量相对较小。结论:我们的研究为青春期早期外化和内化障碍的CT、发育轨迹和潜在遗传基础的特异性提供了有力的证据。我们的研究结果支持重组方法的神经生物学有效性,该方法可以在未来的临床实践中补充维度方法的使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Common and disorder-specific cortical thickness alterations in internalizing, externalizing and thought disorders during early adolescence: an Adolescent Brain and Cognitive Development study.

Background: A growing body of neuroimaging studies has reported common neural abnormalities among mental disorders in adults. However, it is unclear whether the distinct disorder-specific mechanisms operate during adolescence despite the overlap among disorders.

Methods: We studied a large cohort of more than 11 000 preadolescent (age 9-10 yr) children from the Adolescent Brain and Cognitive Development cohort. We adopted a regrouping approach to compare cortical thickness (CT) alterations and longitudinal changes between healthy controls (n = 4041) and externalizing (n = 1182), internalizing (n = 1959) and thought disorder (n = 347) groups. Genome-wide association study (GWAS) was performed on regional CT across 4468 unrelated European youth.

Results: Youth with externalizing or internalizing disorders exhibited increased regional CT compared with controls. Externalizing (p = 8 × 10-4, Cohen d = 0.10) and internalizing disorders (p = 2 × 10-3, Cohen d = 0.08) shared thicker CT in the left pars opercularis. The somatosensory and the primary auditory cortex were uniquely affected in externalizing disorders, whereas the primary motor cortex and higher-order visual association areas were uniquely affected in internalizing disorders. Only youth with externalizing disorders showed decelerated cortical thinning from age 10-12 years. The GWAS found 59 genome-wide significant associated genetic variants across these regions. Cortical thickness in common regions was associated with glutamatergic neurons, while internalizing-specific regional CT was associated with astrocytes, oligodendrocyte progenitor cells and GABAergic neurons.

Limitations: The sample size of the GWAS was relatively small.

Conclusion: Our study provides strong evidence for the presence of specificity in CT, developmental trajectories and underlying genetic underpinnings among externalizing and internalizing disorders during early adolescence. Our results support the neurobiological validity of the regrouping approach that could supplement the use of a dimensional approach in future clinical practice.

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来源期刊
CiteScore
6.80
自引率
2.30%
发文量
51
审稿时长
2 months
期刊介绍: The Journal of Psychiatry & Neuroscience publishes papers at the intersection of psychiatry and neuroscience that advance our understanding of the neural mechanisms involved in the etiology and treatment of psychiatric disorders. This includes studies on patients with psychiatric disorders, healthy humans, and experimental animals as well as studies in vitro. Original research articles, including clinical trials with a mechanistic component, and review papers will be considered.
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