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Published on: December 18, 2019
Hippocampal vascular supply and its mediating role in systemic physiological influences on hippocampal volume
Tae Kim1,2, Javier Rasero3, Anna L Marsland4
1Department of Radiology, University of Pittsburgh, Pittsburgh, PA, United States.
Insights
Systemic factors like vascular inflammation and autonomic dysfunction impact hippocampal volume through blood vessel velocity. This research clarifies how these changes contribute to cognitive decline and hippocampal atrophy.
Area of Science:
- Neuroimaging
- Cardiovascular Science
- Gerontology
Background:
- Aging-related cardiovascular changes can negatively affect brain circulation, leading to hippocampal atrophy and cognitive decline.
- The precise mechanisms linking systemic health alterations to hippocampal atrophy via its vasculature are not fully understood.
Purpose of the Study:
- To investigate the mediating role of hippocampal vascular features in the relationship between systemic factors and hippocampal volume.
- To explore how metabolic, autonomic, inflammatory, and vascular parameters influence hippocampal structure.
Main Methods:
- Utilized 7T MRI to measure hippocampal volume and segment hippocampal supply vessels in 191 participants (aged 30-59).
- Assessed 23 systemic parameters including metabolic syndrome markers, autonomic function, inflammation, and vascular stiffness.
- Employed mediation analysis to determine if hippocampal vessel velocity and size mediate the link between systemic factors and hippocampal volume.
Main Results:
- Hippocampal volume strongly correlated with hippocampal supply vessel velocity, particularly on the right side.
- Vessel velocity mediated the association between hippocampal volume and markers of vascular inflammation, autonomic function (heart rate variability, spontaneous baroreflex sensitivity), and metabolic disturbances (fasting insulin).
- No mediation was observed for parameters like blood pressure, adiposity, glucose, lipids, or certain inflammatory markers.
Conclusions:
- Vascular inflammation, autonomic dysfunction, and metabolic issues contribute to hippocampal atrophy.
- Hippocampal vessel velocity is a critical mediator in this process, impacting hippocampal structural integrity.
- Findings enhance understanding of cerebrovascular mechanisms underlying cognitive health and aging.
Background:
Aging-related systemic cardiovascular changes can impair cerebrovascular circulation, contributing to hippocampal atrophy and cognitive decline. However, the mechanistic pathways by which systemic alterations may relate to hippocampal atrophy via hippocampal vascular features remain unclear.
Methods:
In this study, 191 participants (aged 30-59 years, 115 female) underwent 7T MRI to segment hippocampal supply vessels and hippocampal volume from T1-weighted images. Twenty-three systemic parameters related to the metabolic syndrome, autonomic function, inflammation, vascular stiffness, and endothelial function were measured at rest. Mediation analysis examined whether hippocampal vessel velocity and size mediated the relationship between systemic factors and hippocampal volume.
Results:
Hippocampal volume was highly associated with hippocampal supply vessel velocity, showing a pronounced right lateralized effect. Indirect associations of vessel velocity with hippocampal volume were identified for circulating vascular and intercellular adhesion molecules, heart rate variability, fasting insulin, and spontaneous baroreflex sensitivity. No significant mediated relationships were found for blood pressure, adiposity, mean heart rate, cardiac output, pre-ejection period, reactive hyperemia, pulse wave velocity, mean carotid artery intimal medial thickness, fasting glucose, lipid levels, circulating interleukin-6, hemoglobin A1C, or blood pressure variability.
Conclusion:
These findings highlight the role of vascular inflammation, autonomic dysfunction, and metabolic disturbances in hippocampal atrophy, with hippocampal vessel velocity serving as a key mediator. This insight advances our understanding of cerebrovascular contributions to hippocampal structural integrity and cognitive health.
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