Stroke-Related Acceleration of Brain Atrophy Beyond Aging in the Framingham Study: Paired Pre and Post MRI Evidence and Cognitive Associations
INTRODUCTION: Stroke induces structural brain disruption, accelerating cognitive decline. Using data from the Framingham Heart Study (FHS), we sought to separate aging-only versus aging plus stroke atrophy rates and its cognitive correlates. METHODS: We included cognitively intact FHS participants with first incident stroke. We include pre- and post-index MRIs in both stroke cases and matched controls (2:1), allowing us to estimate aging-only versus aging plus stroke atrophy rates. We computed annualized rates of change in brain volume metrics and cognitive decline, adjusting for relevant factors. RESULTS: We included 45 stroke cases (67.8±10.3 years, 17(38%) female). Compared to controls, accelerated ipsilesional brain atrophy (adjusted Δ=-2.39 mm3/year, p<0.001) and white matter hyperintensity progression (adjusted Δ=0.71 mm3/year, p=0.003) were observed. Voxel-based analysis revealed maximal atrophy subcortically. Accelerated atrophy correlated with global cognition and executive function decline among stroke survivors but not controls. DISCUSSION: This paired-MRI study provides preliminary evidence that stroke modestly accelerates ipsilesional atrophy, predominantly in subcortical regions plausibly linked to processing-speed decline. These findings are hypothesis-generating and require validation in larger prospective studies before firm conclusions can be drawn.
Authors
- Jose Rafael Romero (ORCID: https://orcid.org/0000-0002-1101-2950)
- Hugo J. Aparicio (ORCID: https://orcid.org/0000-0001-8584-1455)
- Vasileios‐Arsenios Lioutas (ORCID: https://orcid.org/0000-0002-8521-0036)
- Charles DeCarli
- Hyacinth I. Hyacinth
- Evan Fletcher
- Alexa Beiser
- Sudha Seshadri
Publication Details
- Journal
- Cerebrovascular Diseases
- Published
- 2026-07-24
- DOI
- https://doi.org/10.1159/000553203
- Primary Topic
- Acute Ischemic Stroke Management
- Type
- article
- Field-Weighted Citation Impact
- 0.00