Increased ventricular cerebrospinal fluid lactate in depressed adolescents.

TitleIncreased ventricular cerebrospinal fluid lactate in depressed adolescents.
Publication TypeJournal Article
Year of Publication2016
AuthorsBradley KAL, Mao X, Case JAC, Kang G, Shungu DC, Gabbay V
JournalEur Psychiatry
Volume32
Pagination1-8
Date Published2016 Feb
ISSN1778-3585
KeywordsAdolescent, Aspartic Acid, Cerebral Ventricles, Cerebrospinal Fluid, Choline, Creatine, Depressive Disorder, Major, Female, Humans, Lactic Acid, Magnetic Resonance Spectroscopy, Male, Mitochondria, Statistics as Topic, Young Adult
Abstract

BACKGROUND: Mitochondrial dysfunction has been increasingly examined as a potential pathogenic event in psychiatric disorders, although its role early in the course of major depressive disorder (MDD) is unclear. Therefore, the purpose of this study was to investigate mitochondrial dysfunction in medication-free adolescents with MDD through in vivo measurements of neurometabolites using high-spatial resolution multislice/multivoxel proton magnetic resonance spectroscopy.

METHODS: Twenty-three adolescents with MDD and 29 healthy controls, ages 12-20, were scanned at 3T and concentrations of ventricular cerebrospinal fluid lactate, as well as N-acetyl-aspartate (NAA), total creatine (tCr), and total choline (tCho) in the bilateral caudate, putamen, and thalamus were reported.

RESULTS: Adolescents with MDD exhibited increased ventricular lactate compared to healthy controls [F(1,41)=6.98, P=0.01]. However, there were no group differences in the other neurometabolites. Dimensional analyses in the depressed group showed no relation between any of the neurometabolites and symptomatology, including anhedonia and fatigue.

CONCLUSIONS: Increased ventricular lactate in depressed adolescents suggests mitochondrial dysfunction may be present early in the course of MDD; however it is still not known whether the presence of mitochondrial dysfunction is a trait vulnerability of individuals predisposed to psychopathology or a state feature of the disorder. Therefore, there is a need for larger multimodal studies to clarify these chemical findings in the context of network function.

DOI10.1016/j.eurpsy.2015.08.009
Alternate JournalEur Psychiatry
PubMed ID26802978
PubMed Central IDPMC4831134
Grant ListR01 MH095807 / MH / NIMH NIH HHS / United States
R01 MH101479 / MH / NIMH NIH HHS / United States
MH 095807 / MH / NIMH NIH HHS / United States
MH101479 / MH / NIMH NIH HHS / United States
Related Institute: 
MRI Research Institute (MRIRI)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065