Department of Child and Adolescent Psychiatry, NYU Child Study Center, NYU School of Medicine, New York University Langone Medical Center, 577 First Avenue, New York, NY 10016, USA.
J Neural Transm (Vienna). 2012 Feb;119(2):253-60. doi: 10.1007/s00702-011-0685-7. Epub 2011 Jul 24.
To address the heterogeneous nature of adolescent major depression (MDD), we investigated anhedonia, a core symptom of MDD. We recently reported activation of the kynurenine pathway (KP), a central neuroimmunological pathway which metabolizes tryptophan (TRP) into kynurenine (KYN) en route to several neurotoxins, in a group of highly anhedonic MDD adolescents. In this study, we aimed to extend our prior work and examine the relationship between KP activity and anhedonia, measured quantitatively, in a group of MDD adolescents and in a combined group of MDD and healthy control adolescents. Thirty-six adolescents with MDD (22 medication-free) and 20 controls were included in the analysis. Anhedonia scores were generated based on clinician- and subject-rated assessments and a semi-structured clinician interview. Blood KP metabolites, collected in the AM after an overnight fast, were measured using high-performance liquid chromatography. The rate-limiting enzyme of the KP, indoleamine 2,3-dioxygenase (IDO), was estimated by the ratio of KYN/TRP. Pearson correlation tests were used to assess correlations between anhedonia scores and KP measures while controlling for MDD severity. IDO activity and anhedonia scores were positively correlated in the group psychotropic medication-free adolescents with MDD (r = 0.42, P = 0.05) and in a combined group of MDD subjects and healthy controls (including medicated patients: r = 0.30, P = 0.02; excluding medicated patients: r = 0.44, P = 0.004). In conclusions, our findings provide further support for the role for the KP, particularly IDO, in anhedonia in adolescent MDD. These results emphasize the importance of dimensional approaches in the investigation of psychiatric disorders.
为了研究青少年重度抑郁症(MDD)的异质性,我们调查了快感缺失这一 MDD 的核心症状。我们最近报告了犬尿氨酸途径(KP)的激活,这是一条中枢神经免疫途径,在一组重度快感缺失的 MDD 青少年中,它会将色氨酸(TRP)代谢为犬尿氨酸(KYN),进而产生几种神经毒素。在这项研究中,我们旨在扩展之前的工作,在 MDD 青少年和 MDD 与健康对照组青少年的混合组中,检查 KP 活性与快感缺失的关系,并用定量方法进行测量。共纳入 36 名 MDD 青少年(22 名未用药)和 20 名对照组。快感缺失评分基于临床医生和患者的评估以及半结构化临床访谈得出。在夜间禁食后采集的 AM 血液 KP 代谢物,用高效液相色谱法测量。KP 的限速酶,色氨酸 2,3-双加氧酶(IDO),通过 KYN/TRP 的比值来估算。Pearson 相关检验用于评估快感缺失评分与 KP 指标之间的相关性,同时控制 MDD 严重程度。在未服用精神药物的 MDD 青少年组(r = 0.42,P = 0.05)和 MDD 患者和健康对照组的混合组(包括服用药物的患者:r = 0.30,P = 0.02;不包括服用药物的患者:r = 0.44,P = 0.004)中,IDO 活性与快感缺失评分呈正相关。总之,我们的研究结果为 KP,特别是 IDO,在青少年 MDD 快感缺失中的作用提供了进一步的支持。这些结果强调了在研究精神疾病时采用维度方法的重要性。