Proton spectroscopy study of the dorsolateral prefrontal cortex in youth with familial depression

Aim Structural, functional, and metabolic changes in the dorsolateral prefrontal cortex (DLPFC) are implicated in the pathogenesis of major depressive disorder (MDD). We used proton magnetic resonance spectroscopy (1 H‐MRS) to examine the metabolite choline (glycerophosphocholine plus phosphocholine...

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Published in:Psychiatry and clinical neurosciences 2016-07, Vol.70 (7), p.269-277
Main Authors: Yang, Xiao‐Ru, Langevin, Lisa Marie, Jaworska, Natalia, Kirton, Adam, Lebel, R. Marc, Harris, Ashley D., Jasaui, Yamile, Wilkes, T. Christopher, Sembo, Mariko, Swansburg, Rose, MacMaster, Frank P.
Format: Article
Language:English
Subjects:
Adolescent
Adult
choline
Choline - metabolism
creatine
depression
Depressive Disorder, Major - metabolism
Depressive Disorder, Treatment-Resistant - metabolism
Female
Humans
Male
Prefrontal Cortex - metabolism
Proton Magnetic Resonance Spectroscopy - methods
spectroscopy
Spectrum analysis
Teenagers
Young Adult
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Summary:Aim Structural, functional, and metabolic changes in the dorsolateral prefrontal cortex (DLPFC) are implicated in the pathogenesis of major depressive disorder (MDD). We used proton magnetic resonance spectroscopy (1 H‐MRS) to examine the metabolite choline (glycerophosphocholine plus phosphocholine), which is used as an index of membrane integrity in the left DLPFC, in adolescents and young adults with MDD who were treatment‐resistant and had a positive family history compared to healthy controls. Differences in the choline resonance indicate an imbalance between synthesis and degradation activity of neuronal and glia membrane phospholipids. Methods Seventeen adolescents with MDD and 11 healthy controls underwent 1 H‐MRS. A short echo point‐resolved spectroscopy (echo time = 30 ms, repetition time = 2000 ms) protocol was used with a voxel (4.5cm3, 128 averages) placed within the left DLPFC. Results There were significantly increased choline (P = 0.04) and creatine concentrations (P = 0.005) in the left DLPFC of the MDD group compared to controls. In MDD participants, choline concentration correlated with scores on the Beck Depression Inventory (r = 0.41, P = 0.03). Conclusion Increased left DLPFC choline and creatine levels in depressed adolescents may be biomarkers for the disorder. The increased choline levels may indicate abnormalities in neuronal membrane integrity, and the increased creatine could be reflective of altered energy demands and metabolism.
ISSN:1323-1316
1440-1819
DOI:10.1111/pcn.12392