Why the study?
Blood pressure variability is an emerging dementia risk factor, but its relationships with neurodegeneration markers and Alzheimer disease risk are understudied.
Does elevated blood pressure variability increase medial temporal brain volume loss in older adults, particularly apolipoprotein ϵ4 carriers?
Does elevated blood pressure variability increase medial temporal brain volume loss in older adults, particularly apolipoprotein ϵ4 carriers?
Elevated blood pressure variability is associated with accelerated medial temporal lobe atrophy in older adults, particularly in APOE ϵ4 carriers and those with Alzheimer's disease biomarker abnormalities.
No immediate practice change from BPV monitoring; leaves open whether reducing variability slows atrophy in APOE ε4 carriers.
Blood pressure variability is an emerging risk factor for dementia but relationships with markers of neurodegeneration and Alzheimer's disease risk are understudied. We investigated blood pressure variability over one year and follow-up medial temporal brain volume change in apolipoprotein ϵ4 carriers and non-carriers, and in those with and without Alzheimer's disease biomarker abnormality. 1051 Alzheimer's Disease Neuroimaging Initiative participants without history of dementia or stroke underwent 3-4 blood pressure measurements over 12 months and ≥ 1 MRI thereafter. A subset (n = 252) underwent lumbar puncture to determine Alzheimer's disease cerebral spinal fluid amyloid-beta and phosphorylated tau biomarker abnormality. Blood pressure variability over 12 months was calculated as variability independent of mean. Longitudinal hippocampal and entorhinal cortex volume data were extracted from serial brain MRI scans obtained after the final blood pressure measurement. Apolipoprotein ϵ4 carrier status was defined as at least one ϵ4 allele. Bayesian growth modelling revealed a significant interaction of blood pressure variability by ϵ4 by time on hippocampal (ß: -2.61 [95% credible interval -3.02, -2.12]) and entorhinal cortex (ß: -1.47 [95% credible interval -1.71, -1.17]) volume decline. A similar pattern emerged in subsets with Alzheimer's disease pathophysiology (i.e., abnormal levels of both amyloid-beta and phosphorylated tau). Findings suggest that elevated blood pressure variability is related to medial temporal volume loss specifically in ϵ4 carriers, and in those with Alzheimer's disease biomarker abnormality. Findings could implicate blood pressure variability in medial temporal neurodegeneration observed in older ϵ4 carriers and those with prodromal Alzheimer's disease.
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Sible et al. (2021) studied this question.
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