Key result
Both APOE ɛ4 status and elevated pulse pressure predicted greater functional difficulty over 4 years, with elevated pulse pressure driving greater functional decline in ɛ4 non-carriers.
Why the study?
Does elevated pulse pressure and APOE ɛ4 status predict functional decline in cognitively normal older adults?
Cohort (n=738)
Does elevated pulse pressure and APOE ɛ4 status predict functional decline in cognitively normal older adults?
Elevated pulse pressure is a modifiable risk factor that predicts functional decline in cognitively normal older adults, particularly in those without the APOE ɛ4 allele.
Answers are grounded in this paper and cite their sources.
Elevated pulse pressure may predict functional decline in APOE ɛ4 non-carriers; hypothesis-generating and requires prospective confirmation before practice change.
BACKGROUND/OBJECTIVE: The APOE ɛ4 allele and increased vascular risk have both been independently linked to cognitive impairment and dementia. Since few studies have characterized how these risk factors affect everyday functioning, we investigated the relationship between APOE ɛ4 genotype and elevated pulse pressure (PP) on functional change in cognitively normal participants from the Alzheimer's Disease Neuroimaging Initiative (ADNI). METHODS: 738 normally aging participants underwent APOE genotyping, and baseline PP was calculated from blood pressure indices. The Functional Activities Questionnaire (FAQ) was completed by participants' informant at baseline and 6, 12, 24, 36, and 48-month follow-up visits. Multiple linear regression and multilevel modeling were used to examine the effects of PP and APOE ɛ4 genotype on cross-sectional and longitudinal FAQ scores, respectively. RESULTS: Adjusting for demographic and clinical covariates, results showed that both APOE ɛ4 status and elevated PP predicted greater functional difficulty trajectories across four years of follow-up. Interestingly, however, elevated PP was associated with greater functional decline over time in ɛ4 non-carriers versus carriers. CONCLUSION: Results show that, although APOE ɛ4 status is the prominent predictor of functional difficulty for ɛ4 carriers, an effect of arterial stiffening on functional difficulty was observed in non-carriers. Future studies are needed in order to clarify the etiology of the association between PP and different brain aging processes, and further explore its utility as a marker of dementia risk. The present study underscores the importance of targeting modifiable risk factors such as elevated PP to prevent or slow functional decline and pathological brain aging.
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Werhane et al. (2018) conducted a cohort in Cognitively normal older adults (n=738). APOE ɛ4 status and elevated pulse pressure vs. APOE ɛ4 non-carriers and lower pulse pressure was evaluated on Functional Activities Questionnaire (FAQ) scores. Both APOE ɛ4 status and elevated pulse pressure predicted greater functional difficulty over 4 years, with elevated pulse pressure driving greater functional decline in ɛ4 non-carriers.
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