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Ventricular cerebrospinal fluid lactate is increased in chronic fatigue syndrome compared with generalized anxiety disorder: an in vivo 3.0 T 1 H MRS imaging study
Author(s) -
Mathew Sanjay J.,
Mao Xiangling,
Keegan Kathryn A.,
Levine Susan M.,
Smith Eric L. P.,
Heier Linda A.,
Otcheretko Viktor,
Coplan Jeremy D.,
Shungu Dikoma C.
Publication year - 2009
Publication title -
nmr in biomedicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.278
H-Index - 114
eISSN - 1099-1492
pISSN - 0952-3480
DOI - 10.1002/nbm.1315
Subject(s) - cerebrospinal fluid , medicine , generalized anxiety disorder , chronic fatigue syndrome , cardiology , analysis of variance , anxiety , magnetic resonance imaging , pathology , psychiatry , radiology
Abstract Chronic fatigue syndrome (CFS) is a controversial diagnosis because of the lack of biomarkers for the illness and its symptom overlap with neuropsychiatric, infectious, and rheumatological disorders. We compared lateral ventricular volumes derived from tissue‐segmented T 1 ‐weighted volumetric MRI data and cerebrospinal fluid (CSF) lactate concentrations measured by proton MRS imaging ( 1 H MRSI) in 16 subjects with CFS (modified US Centers for Disease Control and Prevention criteria) with those in 14 patients with generalized anxiety disorder (GAD) and in 15 healthy volunteers, matched group‐wise for age, sex, body mass index, handedness, and IQ. Mean lateral ventricular lactate concentrations measured by 1 H MRSI in CFS were increased by 297% compared with those in GAD ( P < 0.001) and by 348% compared with those in healthy volunteers ( P < 0.001), even after controlling for ventricular volume, which did not differ significantly between the groups. Regression analysis revealed that diagnosis accounted for 43% of the variance in ventricular lactate. CFS is associated with significantly raised concentrations of ventricular lactate, potentially consistent with recent evidence of decreased cortical blood flow, secondary mitochondrial dysfunction, and/or oxidative stress abnormalities in the disorder. Copyright © 2008 John Wiley & Sons, Ltd.