Decoding the striatum of drug-naive patients with obsessive-compulsive disorder: a transcriptome and longitudinal functional magnetic resonance imaging study.

IF 6.2 1区 医学 Q1 PSYCHIATRY
Yiding Han, Haohao Yan, Xiaoxiao Shan, Huabing Li, Feng Liu, Ping Li, Dongsheng Lv, Jingping Zhao, Wenbin Guo
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Abstract

The striatum's role in obsessive-compulsive disorder (OCD) pathology is recognized. However, the specific contributions of individual striatal subregions (SSs) to OCD pathology are underexplored. We recruited 49 drug-naive OCD patients and 53 healthy controls, conducting clinical assessments and resting-state functional magnetic resonance imaging (rs-fMRI) scans pre- and post-4-week paroxetine treatment. Inter-group comparisons were conducted to investigate baseline and treatment-related changes in the patients' striatum using several fMRI metrics, including amplitude of low-frequency fluctuation, regional homogeneity, and degree centrality (DC). Furthermore, these metrics, along with functional connectivity (FC), and effective connectivity (EC) of SSs, were analyzed. Associations between gene expression patterns and altered information flow patterns in SSs were examined, where information flow was measured using EC, followed by enrichment analysis of relevant genes. While no significant alterations were observed in the patients' striata in whole-brain statistical analyses, significant changes in DC, FC, and EC were identified in SSs pre- and post-treatment. In particular, the EC analysis unveiled an enhanced top-down control and diminished bottom-up regulation in drug-naive OCD patients. Following treatment, bottom-up EC improved, along with an improvement in clinical symptoms. Additionally, information flow alteration-related genes were enriched in various biological processes and pathways. They substantially overlapped between bidirectional information flows among SSs and the rest of brain and between information flows among homotopical SSs and the rest of brain. This study highlights the diverse contributions of each striatal subregion to OCD pathology. Paroxetine may alleviate OCD symptoms by enhancing bottom-up regulation, specifically the normalization of aberrant connectivity. Furthermore, integrating transcriptomic and rs-fMRI findings offer novel insights into the biological substrates underlying the altered EC of SSs in OCD patients.

解码未用药强迫症患者的纹状体:转录组和纵向功能磁共振成像研究。
纹状体在强迫症(OCD)病理中的作用是公认的。然而,个别纹状体亚区(SSs)对强迫症病理的具体贡献尚未得到充分探讨。我们招募了49名未用药的强迫症患者和53名健康对照者,进行了临床评估和静息状态功能磁共振成像(rs-fMRI)扫描,并在帕罗西汀治疗前和后4周进行了扫描。采用多种功能磁共振成像(fMRI)指标,包括低频波动幅度、区域均匀性和程度中心性(DC),进行组间比较,以调查患者纹状体的基线和治疗相关变化。此外,我们还分析了这些指标以及SSs的功能连通性(FC)和有效连通性(EC)。研究了SSs中基因表达模式与改变的信息流模式之间的关系,其中使用EC测量信息流,然后对相关基因进行富集分析。虽然在全脑统计分析中未观察到患者纹状体的显著变化,但在SSs治疗前后发现DC、FC和EC的显著变化。特别地,EC分析揭示了在药物初始的强迫症患者中自上而下的控制增强和自下而上的调节减弱。治疗后,自下而上的EC得到改善,临床症状也有所改善。此外,信息流改变相关基因在各种生物过程和途径中富集。它们在ssss与大脑其余部分之间的双向信息流以及同侧ssss与大脑其余部分之间的信息流之间存在大量重叠。本研究强调了纹状体亚区对强迫症病理的不同贡献。帕罗西汀可能通过增强自下而上的调节,特别是异常连接的正常化来缓解强迫症症状。此外,整合转录组学和rs-fMRI的发现为强迫症患者SSs EC改变的生物学基础提供了新的见解。
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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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