# The Relationship Between Hippocampal Cerebrovascular Reactivity and Brain Structure in Older Age

**Authors:** Congxiyu Wang, Lucy Jobbins, Graham Reid, Georgina Hobden, Raihaan Patel, Clare E. Mackay, Klaus P. Ebmeier, Joana Pinto, Daniel Bulte, Mika Kivimäki, Archana Singh‐Manoux, Sana Suri

PMC · DOI: 10.1002/hbm.70445 · Human Brain Mapping · 2026-02-18

## TL;DR

This study shows that lower blood flow reactivity in the hippocampus is linked to brain structure changes in older adults, which may be related to cognitive decline.

## Contribution

The study identifies hippocampal cerebrovascular reactivity as a potential imaging marker for structural brain changes in aging.

## Key findings

- Lower hippocampal CVR was associated with smaller left hippocampal volume and reduced white matter integrity in key brain regions.
- Reduced CVR was also linked to longitudinal decline in white matter integrity in the corpus callosum and other structures.
- No significant associations were found between hippocampal CVR and white matter hyperintensities.

## Abstract

Cerebral autoregulatory mechanisms such as cerebrovascular reactivity (CVR) are impaired in dementia. However, their associations with brain structure, especially in the hippocampus, remain unclear. We investigated associations between hippocampal CVR and hippocampal volume, white matter microstructural integrity, and white matter hyperintensities in older adults. 163 participants from the Heart and Brain Study received multimodal MRI scans, including T1‐weighted structural imaging, diffusion tensor imaging, fluid‐attenuated inversion recovery imaging at Wave 1 (2012–2014, mean age 68.2, SD 4.4 years) and Wave 2 (2019–2023, mean age 76.9, SD 4.5 years). Participants also received BOLD fMRI scans with a 5% CO2 inhalation challenge to measure CVR at Wave 2. Linear regression was used to examine the cross‐sectional associations of hippocampal CVR with brain structure at Wave 2 as well as with changes in brain structure between Waves 1 and 2. Lower hippocampal CVR was associated with lower left hippocampal volume, as well as lower fractional anisotropy, higher mean, radial, and axial diffusivity in the corpus callosum, internal capsule, and fornix at Wave 2. Lower hippocampal CVR was also associated with greater changes in white matter integrity in the corpus callosum, internal capsule, and cingulum bundle between Waves 1 and 2. There were no significant associations between hippocampal CVR and white matter hyperintensities. Our findings highlight hippocampal CVR as a potential imaging marker associated with structural brain changes relevant to cognitive decline. Further longitudinal studies are needed to clarify the directionality of this association.

Lower hippocampal cerebrovascular reactivity was associated with smaller grey matter volume and reduced white matter microstructural integrity in the corpus callosum, internal capsule, and fornix cross‐sectionally, and with longitudinal decline in the corpus callosum, internal capsule, and cingulum. No significant associations were observed with white matter hyperintensities. Our findings highlight hippocampal cerebrovascular reactivity as a potential imaging marker associated with structural brain changes relevant to cognitive decline.

## Linked entities

- **Diseases:** dementia (MONDO:0001627)

## Full-text entities

- **Diseases:** vascular insufficiency (MESH:D065666), asthma (MESH:D001249), atrophy (MESH:D001284), Alzheimer's (MESH:D000544), MCI (MESH:D060825), Diabetes (MESH:D003920), tumour (MESH:D009369), neurodegeneration (MESH:D019636), inflammation (MESH:D007249), CVR (MESH:D000085343), axonal loss (MESH:D012183), ischemia (MESH:D007511), leukoaraiosis (MESH:D049292), chronic obstructive pulmonary disease (MESH:D029424), stroke (MESH:D020521), hypercapnia (MESH:D006935), WMH (MESH:D056784), cerebrovascular dysfunction (MESH:D002561), brain structural decline (MESH:D001927), hypertension (MESH:D006973), demyelination (MESH:D003711), vascular dementia (MESH:D015140), Cognitive decline (MESH:D003072), synaptic dysfunction (MESH:C536122), MD (MESH:D008228), dementia (MESH:D003704), amyloid (MESH:C000718787), neuronal loss (MESH:D009410)
- **Chemicals:** oxygen (MESH:D010100), CVR (-), CO2 (MESH:D002245)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12916246/full.md

## References

97 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916246/full.md

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Source: https://tomesphere.com/paper/PMC12916246