Medication-Naïve首发精神病患者结构和功能默认模式网络连通性与抗精神病药物治疗反应。

Schizophrenia Bulletin Open Pub Date : 2021-07-16 eCollection Date: 2021-01-01 DOI:10.1093/schizbullopen/sgab032
Jose O Maximo, Nina V Kraguljac, Boone G Rountree, Adrienne C Lahti
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引用次数: 4

摘要

只有少数研究在结构和功能水平上全面描述了默认模式网络(DMN)的病理特征,由于抗精神病药物暴露和疾病的慢性性,无法得出明确的结论。本研究的目的是表征medication-naïve首发精神病(FEP)患者的DMN病理特征,并确定DMN结构和功能连通性(FC)是否具有作为后续抗精神病治疗反应预测因子的潜在效用。方法:分析42例对照组和52例FEP患者的弥散成像和静息状态FC数据。然后患者接受16周的抗精神病药物治疗。利用兴趣区分析,我们量化了DMN的FC和支持DMN功能的白质束的结构完整性。然后,我们对DMN结构和FC指数与抗精神病药物治疗反应进行了线性回归。结果:与对照组相比,我们检测到FEP的DMN分数各向异性和轴向扩散率降低。未发现DMN FC异常,也未发现DMN结构与FC之间的相关性。最后,DMN分数各向异性和径向扩散率与治疗反应有关。结论:我们的研究强调了DMN在病理生理学中的关键作用,表明FEP患者可能已经存在轴突损伤。我们还证明DMN病理学与临床相关,因为DMN结构改变越大,抗精神病药物的临床反应越差。
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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Structural and Functional Default Mode Network Connectivity and Antipsychotic Treatment Response in Medication-Naïve First Episode Psychosis Patients.

Introduction: Only a few studies have comprehensively characterized default mode network (DMN) pathology on a structural and functional level, and definite conclusions cannot be drawn due to antipsychotic medication exposure and illness chronicity. The objective of this study was to characterize DMN pathology in medication-naïve first episode psychosis (FEP) patients, and determine if DMN structural and functional connectivity (FC) have potential utility as a predictor for subsequent antipsychotic treatment response.

Methods: Diffusion imaging and resting state FC data from 42 controls and 52 FEP were analyzed. Patients then received 16 weeks of antipsychotic treatment. Using region of interest analyses, we quantified FC of the DMN and structural integrity of the white matter tracts supporting DMN function. We then did linear regressions between DMN structural and FC indices and antipsychotic treatment response.

Results: We detected reduced DMN fractional anisotropy and axial diffusivity in FEP compared to controls. No DMN FC abnormalities nor correlations between DMN structural and FC were found. Finally, DMN fractional anisotropy and radial diffusivity were associated with response to treatment.

Conclusion: Our study highlights the critical role of the DMN in the pathophysiology suggesting that axonal damage may already be present in FEP patients. We also demonstrated that DMN pathology is clinically relevant, as greater structural DMN alterations were associated with a less favorable clinical response to antipsychotic medications.

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