Transdiagnostic reduction in cortical choline-containing compounds in anxiety disorders: a 1H-magnetic resonance spectroscopy meta-analysis

IF 10.1 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Richard J. Maddock, Jason Smucny
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Abstract

Background

Anxiety disorders (AnxDs) are highly prevalent and often untreated or unresponsive to treatment. Although proton magnetic resonance spectroscopy (1H-MRS) studies of AnxDs have been conducted for over 25 years, a consensus regarding neurometabolic abnormalities in these conditions is lacking.

Methods

A systematic review and meta-analysis of 1H-MRS studies of AnxDs (social anxiety disorder, generalized anxiety disorder, and panic disorder) identified 25 published datasets meeting inclusion criteria. These compared neurometabolites between 370 patients and 342 controls, including n-acetlyaspartate (NAA), total creatine, total choline (tCho), myo-inositol, glutamate, glutamate+glutamine, GABA, and lactate.

Results

Across AnxDs, tCho was significantly reduced in prefrontal cortex and across all cortical regions. Effect sizes for cortical tCho were significantly more negative in studies with better measurement quality, with Hedges’ g = −0.64 and an 8% mean reduction. NAA was unchanged in prefrontal cortex but reduced across all cortical regions (after exclusions). These abnormalities did not differ between the three disorders. No other neurometabolites differed significantly.

Discussion

Reduced choline-containing compounds in cortical regions is a consistent, transdiagnostic abnormality in AnxDs. Notably, arousal-related neuromodulators, including norepinephrine, alter membrane phospholipid homeostasis and methylation reactions, which influence brain tCho levels. This suggests that chronically elevated arousal in AnxDs may increase neurometabolic demand for choline compounds without a proportionate increase in brain uptake, leading to reduced tCho levels. Reduced cortical NAA suggests compromised neuronal function in AnxDs. Future studies may clarify the clinical significance of reduced cortical tCho and the possibility that appropriate choline supplementation could have therapeutic benefit in anxiety disorders.

Abstract Image

焦虑症中皮质含胆碱化合物的诊断减少:1h磁共振波谱荟萃分析
背景:焦虑障碍(AnxDs)非常普遍,而且经常得不到治疗或对治疗无反应。虽然质子磁共振波谱(1H-MRS)对anxd的研究已经进行了超过25年,但对这些疾病的神经代谢异常缺乏共识。方法对焦虑症(社交焦虑障碍、广泛性焦虑障碍和惊恐障碍)的1H-MRS研究进行系统回顾和荟萃分析,确定了25个符合纳入标准的已发表数据集。他们比较了370名患者和342名对照组的神经代谢物,包括n-乙酰天冬氨酸(NAA)、总肌酸、总胆碱(tCho)、肌醇、谷氨酸、谷氨酸+谷氨酰胺、GABA和乳酸。结果大鼠前额叶皮层和所有皮质区域的tCho均显著降低。在测量质量较好的研究中,皮质tCho的效应量明显更负,Hedges的g = - 0.64,平均降低8%。前额皮质的NAA没有变化,但所有皮质区域的NAA都减少了(排除后)。这些异常在三种疾病之间没有区别。其他神经代谢物无显著差异。讨论皮质区含胆碱化合物减少是一种一致的跨诊断性异常。值得注意的是,觉醒相关的神经调节剂,包括去甲肾上腺素,改变膜磷脂稳态和甲基化反应,从而影响脑tCho水平。这表明,长期升高的anxd唤醒可能会增加对胆碱化合物的神经代谢需求,而大脑摄取却没有成比例的增加,从而导致tCho水平降低。皮质NAA的减少表明神经元功能受损。未来的研究可能会阐明皮质tCho降低的临床意义,以及适当补充胆碱可能对焦虑症有治疗益处的可能性。
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来源期刊
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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