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Published on: August 18, 2023
Cerebral perfusion features linking subclinical cardiac and aortic dysfunction to vascular brain injury
Ye Zhang1, Timothy M Hughes2,3, Wenxin Zhang1
1Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Insights
Subclinical cardiovascular issues are linked to reduced cerebral blood flow and delayed transit time, increasing white matter hyperintensity burden. Impaired brain perfusion may explain how heart dysfunction leads to cerebrovascular injury.
Area of Science:
- Cardiovascular science
- Neuroimaging
- Cerebrovascular health
Background:
- Subclinical cardiovascular remodeling can affect cerebral hemodynamics.
- The specific perfusion features linking cardiovascular dysfunction to dementia risk are not well understood.
Purpose of the Study:
- To investigate the association between subclinical cardiac and aortic dysfunction and cerebral perfusion.
- To determine if impaired cerebral perfusion mediates the relationship between cardiovascular dysfunction and cerebrovascular injury.
Main Methods:
- Utilized cardiac MRI, arterial spin labeling (ASL) MRI, and structural brain MRI in 1748 UK Biobank participants.
- Analyzed six cardiac MRI biomarkers and assessed cerebral blood flow (CBF) and arterial transit time (ATT).
Main Results:
- Subclinical cardiac and aortic dysfunction correlated with lower CBF and prolonged ATT.
- Low CBF and prolonged ATT were associated with significantly increased white matter hyperintensity (WMH) burden.
- CBF and ATT jointly mediated 53% of the link between cardiovascular dysfunction and WMH.
Conclusions:
- Impaired cerebral perfusion, characterized by reduced volume and delayed timing, appears to be a key mechanism.
- This mechanism connects subclinical cardiovascular dysfunction to brain vascular injury, potentially contributing to cognitive decline.
Introduction:
Subclinical cardiovascular remodeling may impair cerebral hemodynamics and contribute to dementia, but the perfusion features linking subclinical cardiovascular dysfunction to cerebrovascular injury remain unclear.
Methods:
We studied 1748 UK Biobank participants with cardiac magnetic resonance imaging (MRI), arterial spin labeling (ASL) MRI, and structural brain MRI. Six cardiac MRI biomarkers were analyzed individually and as a composite score. Cerebral perfusion was assessed by cerebral blood flow (CBF) and arterial transit time (ATT).
Results:
Greater subclinical cardiac and aortic dysfunction was associated with lower CBF and prolonged ATT. Participants with low CBF and prolonged ATT had the greatest white matter hyperintensity (WMH) burden, equivalent to 5.5 years of age-related accumulation. CBF and ATT jointly mediated 53% of the association between subclinical cardiac and aortic dysfunction and WMH burden.
Discussion:
Impaired cerebral perfusion, captured by lower perfusion volume and delayed perfusion timing, may be a mechanism linking subclinical cardiovascular dysfunction to brain vascular injury.
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