Department of Psychiatry and Behavioral Sciences, The Johns Hopkins University School of Medicine, Baltimore, MD, United States; Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, United States; F. M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD, United States.
J Affect Disord. 2021 Jan 15;279:417-425. doi: 10.1016/j.jad.2020.10.011. Epub 2020 Oct 7.
Magnetic resonance spectroscopy (MRS) methods have quantified changes in levels of neurotransmitters and neurometabolites in patients with major depression across the lifespan. The application of 7T field strengths and greater have not been a major focus of study in patients with late-life depression (LLD).
Nine LLD patients who met DSM-IV criteria for a current major depressive episode and nine non-depressed, healthy, age-matched controls underwent clinical and neuropsychological assessment and single-voxel 7T H-MRS at baseline and after 10-12 weeks of antidepressant treatment (Citalopram; patients only). Spectra were acquired from two brain regions implicated in both depressive symptoms and neuropsychological deficits in LLD, the anterior (ACC) and posterior cingulate (PCC). Levels of γ-aminobutyric acid (GABA), glutamate (Glu), glutathione (GSH), N-acetylaspartylglutamate (NAAG), N-acetylaspartate (NAA), and myo-inositol (mI) were quantified relative to total creatine (tCr) using linear-combination modeling.
Baseline Glu/tCr levels were not significantly different between groups. Decreased Glu/tCr levels after Citalopram treatment were observed in a subset of LLD patients. Exploratory analyses showed that LLD patients had lower NAA levels in the PCC relative to controls. Higher levels of ml in the LLD patients relative to the controls and decreases after Citalopram treatment had large effect sizes but were not statistically significant. Further, decreases in PCC Glu/tCr and increases in ACC GSH/tCr were associated with improvement in depressive symptoms.
Sample size.
These preliminary results suggest a role of neurochemicals and neurometabolites in the neurobiology of LLD and antidepressant treatment response.
磁共振波谱(MRS)方法已经定量检测了一生中患有重度抑郁症的患者的神经递质和神经代谢物水平的变化。在老年抑郁症(LLD)患者中,应用 7T 场强或更高场强尚未成为主要研究焦点。
9 名符合 DSM-IV 标准的当前重度抑郁发作的 LLD 患者和 9 名非抑郁、健康、年龄匹配的对照者接受了临床和神经心理学评估,以及基线和抗抑郁治疗(西酞普兰;仅患者)后 10-12 周的单体素 7T H-MRS。采集了两个与 LLD 中的抑郁症状和神经心理学缺陷都有关的脑区(ACC)和后扣带回(PCC)的光谱。使用线性组合模型,相对于总肌酸(tCr)对γ-氨基丁酸(GABA)、谷氨酸(Glu)、谷胱甘肽(GSH)、N-乙酰天冬氨酸谷氨酸(NAAG)、N-乙酰天冬氨酸(NAA)和肌醇(mI)的水平进行了量化。
基线时两组间 Glu/tCr 水平无显著差异。在一组 LLD 患者中观察到西酞普兰治疗后 Glu/tCr 水平降低。探索性分析表明,与对照组相比,LLD 患者的 PCC 中的 NAA 水平较低。与对照组相比,LLD 患者的 ml 水平较高,西酞普兰治疗后降低,具有较大的效应量,但无统计学意义。此外,PCC 的 Glu/tCr 降低和 ACC 的 GSH/tCr 增加与抑郁症状的改善相关。
样本量。
这些初步结果表明神经化学物质和神经代谢物在 LLD 的神经生物学和抗抑郁治疗反应中起作用。