Cardiovascular risks impact human brain N-acetylaspartate in regionally specific patterns.
Joshua ChiappelliLaura M RowlandS Andrea WijtenburgHongji ChenAndrew A MaudsleySulaiman SheriffShuo ChenAnya SavranskyWyatt MarshallMeghann C RyanHeather A BruceAlan R ShuldinerBraxton D MitchellPeter KochunovL Elliot HongPublished in: Proceedings of the National Academy of Sciences of the United States of America (2019)
Cardiovascular risk factors such as dyslipidemia and hypertension increase the risk for white matter pathology and cognitive decline. We hypothesize that white matter levels of N-acetylaspartate (NAA), a chemical involved in the metabolic pathway for myelin lipid synthesis, could serve as a biomarker that tracks the influence of cardiovascular risk factors on white matter prior to emergence of clinical changes. To test this, we measured levels of NAA across white matter and gray matter in the brain using echo planar spectroscopic imaging (EPSI) in 163 individuals and examined the relationship of regional NAA levels and cardiovascular risk factors as indexed by the Framingham Cardiovascular Risk Score (FCVRS). NAA was strongly and negatively correlated with FCVRS across the brain, but, after accounting for age and sex, the association was found primarily in white matter regions, with additional effects found in the thalamus, hippocampus, and cingulate gyrus. FCVRS was also negatively correlated with creatine levels, again primarily in white matter. The results suggest that cardiovascular risks are related to neurochemistry with a predominantly white matter pattern and some subcortical and cortical gray matter involvement. NAA mapping of the brain may provide early surveillance for the potential subclinical impact of cardiovascular and metabolic risk factors on the brain.
Keyphrases
- white matter
- cardiovascular risk factors
- multiple sclerosis
- cognitive decline
- cardiovascular disease
- metabolic syndrome
- risk factors
- high resolution
- blood pressure
- public health
- type diabetes
- mild cognitive impairment
- molecular docking
- magnetic resonance
- functional connectivity
- resting state
- mass spectrometry
- cerebral ischemia
- blood brain barrier