ArticleFrontiers in aging neuroscience2026
Atrial fibrillation/atrial flutter and reduced volumes of the hippocampus, amygdala, and thalamus: evidence from a community-based MRI study.
Article in Frontiers in aging neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Introduction: Atrial fibrillation (AF) is associated with cognitive decline and dementia even in the absence of clinical stroke, potentially through mechanisms such as silent infarction, small-vessel disease, hypoperfusion, and systemic inflammation. However, most previous studies have focused on global brain measures, and little is known about region-specific structural alterations, particularly within deep gray-matter structures and hippocampal subfields. Evidence regarding atrial flutter (AFL) remains limited. This study aimed to investigate the association between AF/AFL and regional brain and hippocampal subfield volumes in cognitively normal older adults. Materials and methods: This cross-sectional analysis included 7,074 community-dwelling participants aged ≥65 years from the Japan Prospective Studies Collaboration for Aging and Dementia (JPSC-AD). Structural magnetic resonance imaging with 3D T1-weighted images was processed using FreeSurfer 7.0. Volumes of the cortex, cortical white matter, subcortical gray matter, eight regional brain areas, and hippocampal subfields were evaluated. AF/AFL was identified using electrocardiography. Adjusted mean regional brain volumes and 95% confidence intervals (CIs) were estimated using analysis of covariance. The false discovery rate was controlled using the Benjamini-Hochberg method. Additional exploratory analyses based on self-reported AF history were also performed. Stratified analyses were performed by age (<75 vs. ≥75 years) and sex. Results: After multivariable adjustment, AF/AFL (171 participants, 2.4%) was associated with smaller volumes of the cortex, cortical white matter, and subcortical gray matter. Among regional structures, AF/AFL was significantly associated with smaller hippocampal and amygdala volumes. At the hippocampal subfield level, reduced fimbria, dentate gyrus, CA1, and subiculum volumes were observed. Analyses based on self-reported history of AF did not demonstrate significant associations with any brain regions. In stratified analyses, participants aged <75 years showed a trend toward smaller hippocampal-tail volume with a significant interaction effect, whereas women exhibited smaller hippocampal volume without a significant sex interaction. Discussion: In this large community-based sample of cognitively normal older adults, AF/AFL was associated with widespread structural brain alterations and selective vulnerability in memory-related regions, including the hippocampus and amygdala, as well as specific hippocampal subfields. These findings suggest that AF/AFL may be associated with region-specific brain vulnerability before the onset of clinically apparent cognitive impairment.
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