Martin Pastre, Bob-Valéry Occéan, Vincent Boudousq, Ismael Conejero, Pascale Fabbro-Peray, Laurent Collombier, Luc Mallet, Jorge Lopez-Castroman
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引用次数: 0
Abstract
Obsessive-compulsive disorder (OCD) is a frequent and disabling condition, with many patients being treatment-resistant. Improved understanding of its neurobiology is vital for better therapies. Evidence is still conflicting regarding specific serotonergic-related dysfunctions in OCD. We systematically reviewed the literature to provide a quantitative assessment of the role of serotonin (5-HT) in patients with untreated OCD through imaging. We searched for neuroimaging studies investigating central 5-HT tonus in unmedicated patients with OCD, excluding studies comprising treated patients to prevent bias from antidepressant-induced changes in serotonergic tonus. We also conducted a meta-analysis using a homogeneous group of positron emission tomography and single photon emission computed tomography articles that compared 5-HT transporter (SERT) and 5-HT2A receptor (HT2AR) binding potential in different brain regions of patients with untreated OCD and healthy controls. The systematic review encompassed 18 articles, with 13 included in the subsequent meta-analysis. Risk of bias was assessed by a revised form of the Newcastle-Ottawa Scale. We provided standardized mean difference (SMD) values for SERT and 5-HT2AR binding potential measures across 15 different brain regions. Patients with OCD showed lower SERT binding potential in the brainstem (SMD = -1.13, 95% CI [-1.81 to -0.46]), midbrain (SMD = -0.54, 95% CI [-0.92 to -0.16]), and thalamus/hypothalamus regions (SMD = -0.58, 95% CI [-0.99 to -0.18]) with neglectable to moderate heterogeneity. By combining results from 2 decades of molecular imaging studies, we show that individuals with OCD exhibit lower SERT binding potential in specific brain regions, providing compelling evidence of a 5-HT system dysfunction. However, the exact mechanisms underlying this phenotype remain elusive. The limitations include heterogeneity across studies in populations, imaging techniques, and radiotracer usage.
强迫症(OCD)是一种常见的致残性疾病,许多患者对治疗具有抗药性。要想获得更好的治疗方法,就必须加深对其神经生物学的了解。关于强迫症中与血清素能相关的特定功能障碍,目前仍存在相互矛盾的证据。我们系统地回顾了相关文献,通过影像学对未经治疗的强迫症患者体内血清素(5-HT)的作用进行了定量评估。我们搜索了对未接受治疗的强迫症患者的中枢 5-HT 调强进行调查的神经影像学研究,排除了包括接受治疗的患者的研究,以防止因抗抑郁药引起的血清素能调强变化而产生偏差。我们还利用一组同质的正电子发射计算机断层扫描和单光子发射计算机断层扫描文章进行了荟萃分析,这些文章比较了未经治疗的强迫症患者和健康对照者不同脑区的 5-HT 转运体(SERT)和 5-HT2A 受体(HT2AR)结合电位。系统综述包括 18 篇文章,其中 13 篇被纳入随后的荟萃分析。偏倚风险通过纽卡斯尔-渥太华量表的修订版进行评估。我们提供了15个不同脑区的SERT和5-HT2AR结合电位测量的标准化平均差(SMD)值。强迫症患者在脑干(SMD = -1.13,95% CI [-1.81 to -0.46])、中脑(SMD = -0.54,95% CI [-0.92 to -0.16])和丘脑/下丘脑区域(SMD = -0.58,95% CI [-0.99 to -0.18])的SERT结合电位较低,异质性可忽略至中等。通过综合20年来的分子成像研究结果,我们发现强迫症患者在特定脑区表现出较低的SERT结合电位,为5-HT系统功能障碍提供了令人信服的证据。然而,这种表型的确切机制仍然难以捉摸。研究的局限性包括不同研究在人群、成像技术和放射性示踪剂使用方面的异质性。
期刊介绍:
PCN (Psychiatry and Clinical Neurosciences)
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Published 12 online issues a year by JSPN
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