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Cerebrovascular reactivity at rest and its association with cognitive function in people with genetic frontotemporal dementia

Year: 2025
Type: article
Abstract: Background and Objectives: Cerebrovascular reactivity is an indicator of cerebrovascular health and its signature in familial frontotemporal dementia (FTD) remains unknown. The primary aim was to investigate cerebrovascular reactivity in genetic FTD using an fMRI index of vascular contractility termed resting-state fluctuation amplitudes (RSFA) and to assess whether RSFA differences are moderated by age. A secondary aim was to study the relationship between RSFA and cognition. Methods: Participants included pre-symptomatic and symptomatic C9orf72, GRN, and MAPT pathogenic variant carriers, along with non-carriers from the prospective Genetic FTD Initiative (GENFI) cohort study. Cross-sectional differences in cerebrovascular reactivity were assessed using both component-based and voxel-level RSFA maps. To study disease progression-related effects, the moderating effect of age on differences between genetic status groups was analyzed using generalized linear models. The influence of RSFA, and its interaction with genetic status, on participants’ cognitive function was also examined. All models were adjusted for sex, handedness, and scanning site, and false discovery rate-corrected at p < 0.05. Results: A total of 284 pre-symptomatic and 124 symptomatic pathogenic variant carriers, and 265 non-carriers, were included in the analysis (mean age = 48.17, 55% females). Across the sample, symptomatic carriers exhibited lower RSFA and a greater age-related RSFA decline predominantly in medial frontal (-0.07 standard units, p=.046, 95 % CI:-0.13,-0.01) and posterior parietal cortex (-0.06 standard units, p=.048, 95 % CI:-0.12,0.01), compared to pre-symptomatic and non-carriers. RSFA was inversely correlated with age (-0.43 standard units, p<.001, 95 % CI:-0.48,-0.37) and positively associated with cognitive function (0.09 standard units, p=.008, 95 % CI:0.04,0.15), particularly in prefrontal cortex, in pathogenic variant carriers across the sample, independent of disease stage. Discussion: CVR impairment in genetic FTD has a predilection for the middle frontal and posterior cortex, and its preservation may yield a cognitive benefit for at-risk individuals. Although findings do not provide causality and warrant replication, they support the notion that vascular dysfunction in familial FTD may be a target for biomarker identification and disease-modifying efforts.
DOI: 10.17863/cam.116883
Language: English
Field: Medicine
Open Access status: green
OpenAlex ID: W6887985028
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