Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1, OgawaHigashi, Kodaira, Tokyo 187-8502, Japan; Department of Physiology, Yonsei University College of Medicine, 50-1, Yonsei-ro, Seodaemun-gu, Seoul 120-752, South Korea.
Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1, OgawaHigashi, Kodaira, Tokyo 187-8502, Japan; Translational Medical Center, National Center of Neurology and Psychiatry, Kodaira, Tokyo 187-8502, Japan.
J Affect Disord. 2018 May;232:134-138. doi: 10.1016/j.jad.2018.02.039. Epub 2018 Feb 21.
Cocaine- and amphetamine-regulated transcript (CART) peptide is a candidate neuropeptide as a biomarker for major depressive disorder (MDD) because of its effects on emotion and distribution covering brain areas involved in the pathophysiology of MDD symptoms. However, it is unknown whether CART peptide levels are altered in the cerebrospinal fluid (CSF) of patients with MDD patients and are correlated with MDD symptoms.
Subjects were 24 patients with MDD and 25 healthy controls matched for age, gender and ethnicity (Japanese). We measured CSF CART levels by a commercially available immunoassay kit and analyzed the relationships of the levels with antidepressant dose and symptoms assessed with the 21 item Hamilton Depression Rating Scale (HAMD-21).
CSF CART levels were significantly decreased in the patients than in the controls (p < 0.05). In MDD patient group, the CART levels had a negative correlation with antidepressant dose (imipramine-equivalent dose) (ρ = -0.55, p < 0.01) and significantly decreased in antidepressant-treated group (AD-treated group) compared to controls (p < 0.05). CSF CART levels showed significant negative correlations with psychomotor retardation, somatic anxiety, and general somatic symptoms (all p < 0.05) and a positive correlation with obsessive and compulsive symptoms (p < 0.05).
In our analysis, all classes of antidepressants were combined together and the effects of medication use in a longitudinal manner did not confirm.
We report for the first time that CSF CART peptide levels are reduced in patients with MDD compared with healthy controls. The CART levels showed negative correlations with antidepressant dose and some symptoms, supporting the possibility that CART peptide is involved in the development of depressive symptoms.
可卡因和安非他命调节转录物 (CART) 肽是一种候选神经肽,可作为重度抑郁症 (MDD) 的生物标志物,因为它对情绪有影响,并且分布在涉及 MDD 症状病理生理学的大脑区域。然而,目前尚不清楚 CART 肽水平是否在 MDD 患者的脑脊液 (CSF) 中改变,以及是否与 MDD 症状相关。
研究对象为 24 名 MDD 患者和 25 名年龄、性别和种族(日本人)相匹配的健康对照者。我们通过市售的免疫测定试剂盒测量 CSF CART 水平,并分析水平与抗抑郁药剂量和 21 项汉密尔顿抑郁评定量表 (HAMD-21) 评估的症状之间的关系。
CSF CART 水平在患者中明显低于对照组(p < 0.05)。在 MDD 患者组中,CART 水平与抗抑郁药剂量(丙咪嗪等效剂量)呈负相关(ρ=-0.55,p < 0.01),且与对照组相比,在接受抗抑郁治疗的患者中明显降低(AD 治疗组)(p < 0.05)。CSF CART 水平与精神运动迟滞、躯体焦虑和全身躯体症状呈显著负相关(均 p < 0.05),与强迫和强迫症状呈正相关(p < 0.05)。
在我们的分析中,所有类别的抗抑郁药都合并在一起,并且药物使用的影响没有在纵向方式上得到确认。
我们首次报道,与健康对照组相比,MDD 患者的 CSF CART 肽水平降低。CART 水平与抗抑郁药剂量和某些症状呈负相关,支持 CART 肽参与抑郁症状发展的可能性。