# Cerebrovascular burden and neurodegeneration linked to 15-year odor identification decline in older adults

**Authors:** Javier Oltra, Grégoria Kalpouzos, Ingrid Ekström, Maria Larsson, Yuanjing Li, Chengxuan Qiu, Erika J. Laukka

PMC · DOI: 10.3389/fnagi.2025.1539508 · Frontiers in Aging Neuroscience · 2025-03-24

## TL;DR

This study finds that brain changes like vascular issues and brain shrinkage are linked to a decline in the ability to identify odors over 15 years in older adults.

## Contribution

The study reveals a novel longitudinal link between cerebrovascular and neurodegenerative markers and odor identification decline in aging.

## Key findings

- Higher baseline perivascular spaces and lower hippocampal and gray matter volumes are associated with faster odor identification decline.
- Longitudinal increases in cerebrovascular lesions and brain atrophy are linked to accelerated odor identification decline.
- Both cerebrovascular burden and brain atrophy contribute to olfactory decline in older adults.

## Abstract

The mechanisms underlying olfactory decline in aging need further investigation. Noticeably, the longitudinal relationship of biological markers with olfaction remains underexplored. We investigated whether baseline levels and progression of microvascular lesions and brain atrophy are associated with odor identification (OID) decline.

The association between structural MRI markers and OID decline was examined in participants from the SNAC-K MRI study who were free from dementia at baseline (n = 401, mean age = 70.2 years, 60% females). OID was repeatedly assessed over 15 years. Presence of lacunes, white matter hyperintensities (WMH), perivascular spaces (PVS), and lateral ventricular, hippocampal, amygdalar, and total gray matter (GM) volumes were assessed up to 6 years, concurrent with the first 6 years of olfactory assessments.

Higher PVS count and lower hippocampal and GM volumes at baseline were associated with accelerated OID decline (pFWE < 0.05). Longitudinally (n = 225), presence of lacunes at follow-up, faster WMH volume and PVS count increases, faster lateral ventricular enlargement, and faster hippocampal, amygdalar, and GM atrophy were associated with accelerated OID decline (pFWE < 0.05).

Olfactory decline is related to both increased cerebrovascular burden and accelerated brain atrophy over time.

## Full-text entities

- **Diseases:** ventricular enlargement (MESH:D006332), atrophy (MESH:D001284), neurodegeneration (MESH:D019636), dementia (MESH:D003704), Olfactory decline (MESH:D000857), microvascular lesions (MESH:D017566), brain atrophy (MESH:C566985), WMH (MESH:D056784)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11973317/full.md

## References

106 references — full list in the complete paper: https://tomesphere.com/paper/PMC11973317/full.md

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Source: https://tomesphere.com/paper/PMC11973317