Heart failure patients demonstrated reduced, largely lateralized regional cerebral blood flow in multiple autonomic, mood, and cognitive regulatory brain sites compared with control subjects.
Observational
Heart failure
Heart failure vs Control subjects
Regional cerebral blood flow (CBF)
AIMS: Heart failure (HF) patients show significant lateralized neural injury, accompanied by autonomic, mood and cognitive deficits. Both gray and white matter damage occurs and probably develops from altered cerebral blood flow (CBF), a consequence of impaired cardiac output. However, the distribution of regional CBF changes in HF patients is unknown, but is an issue in determining mechanisms of neural injury. Our aim was to compare regional CBF changes in HF with CBF in control subjects using non-invasive pseudo-continuous arterial spin labelling (ASL) procedures. METHODS AND RESULTS: ; 18 male), using a 3.0-Tesla magnetic resonance imaging (MRI) scanner. Whole-brain CBF maps were calculated, normalized to a common space, smoothed and compared between groups using ANCOVA (covariates; age, gender and gray matter volume). Reduced CBF appeared in multiple sites in HF patients in comparison with controls, with principally lateralized lower flow in temporal, parietal and occipital regions. Areas with decreased CBF included the bilateral prefrontal, frontal, temporal and occipital cortex, thalamus, cerebellum, corona radiate, corpus callosum, hippocampus and amygdala. CONCLUSIONS: Heart failure patients showed lower, and largely lateralized, CBF in multiple autonomic, mood and cognitive regulatory sites. The reduced CBF is likely to contribute to the lateralized brain injury, leading to the autonomic and neuropsychological deficits found in the condition.
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Roy et al. (Tue,) conducted a observational in Heart failure. Heart failure vs. Control subjects was evaluated on Regional cerebral blood flow (CBF). Heart failure patients demonstrated reduced, largely lateralized regional cerebral blood flow in multiple autonomic, mood, and cognitive regulatory brain sites compared with control subjects.
synapsesocial.com/papers/6a143ba23f92ec2dd759c011 — DOI: https://doi.org/10.1002/ejhf.874
Bhaswati Roy
University of California, Los Angeles
Mary A. Woo
University of California, Los Angeles
Danny J.J. Wang
Brighton and Sussex Medical School
European Journal of Heart Failure
University of California, Los Angeles
Allen Institute for Brain Science
Olive View-UCLA Medical Center
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