Correlation between neurochemical metabolism and memory function in adolescent patients with depression: A multi‐voxel 1 H magnetic resonance spectroscopy study

• Published in: Psychiatry and clinical neurosciences Vol. 70; no. 4; pp. 167 - 174
• Main Authors: Mao, Ning, Fang, Junfang, Xie, Haizhu, Liu, Xinjiang, Jiang, Xingyue, Wang, Guangbin, Cui, Minghu, Wang, Bin, Liu, Qiang
• Format: Journal Article
• Language: English
• Published: 01.04.2016
• ISSN: 1323-1316; 1440-1819
• DOI: 10.1111/pcn.12372

Aims We utilized multi‐voxel proton magnetic resonance spectroscopy ( 1 H ‐ MRS ) to detect biochemical abnormalities in dorsolateral prefrontal white matter and anterior cingulate gray matter and to determine the correlation of biochemical changes with memory function in depressed adolescents. Methods A total of 24 depressed patients and 23 healthy controls were enrolled in this study. MRS was performed to assess the N ‐acetylaspartate ( NAA )/creatine C r and choline ( C ho)/ C r ratios in dorsolateral prefrontal white matter and anterior cingulate gray matter of participants. Memory function was measured on the basis of Wechsler Memory Scale scores, and depression was diagnosed on the basis of clinical observation, interview, and Hamilton Depression Rating Scale scores. Results Compared with controls, depressed patients had significantly lower NAA / C r and C ho/ C r ratios in left dorsolateral prefrontal white matter and lower NAA / C r ratios in right dorsolateral prefrontal white matter ( P  < 0.05). No biochemical differences were identified in the bilateral anterior cingulate gray matter between the two groups. Nevertheless, the depressed patients showed significantly lower memory quotient than controls ( P  < 0.05). The NAA / C r ratio in dorsolateral prefrontal white matter positively correlated with memory quotient (left: P  < 0.01; right: P  < 0.05). Conclusions These findings suggest that biochemical abnormalities in prefrontal white matter are involved in the pathophysiology of adolescent depression. In particular, such abnormalities are already present at the early stage of the disorder, and low NAA / C r in bilateral anterior frontal white matter may be associated with memory impairment and related neuropathology.