Key result
Higher baseline circulating aldosterone levels were associated with lower CO2 vasoreactivity and predicted greater improvements in executive function after 12 months of antihypertensive therapy.
Why the study?
Does antihypertensive therapy to <140/90 mm Hg improve cognitive function and cerebral hemodynamics in older adults, and is this modified by baseline aldosterone levels?
Observational (n=47)
Yes
Does antihypertensive therapy to <140/90 mm Hg improve cognitive function and cerebral hemodynamics in older adults, and is this modified by baseline aldosterone levels?
In older adults with hypertension, higher baseline aldosterone levels are associated with worse baseline cerebrovascular function but predict greater cognitive and hemodynamic improvements following blood pressure lowering.
Answers are grounded in this paper and cite their sources.
May identify patients with greater cognitive response to BP lowering; hypothesis-generating and requires randomized confirmation before guiding care.
BACKGROUND: Animal studies suggest that the renin-angiotensin-aldosterone system is involved in neurocognitive function and the response to antihypertensive therapy. We investigated the impact of circulating aldosterone and renin activity on cognition and cerebral hemodynamics at baseline and after antihypertensive therapy for 1 year. METHODS: Participants were older adults (n = 47; mean age = 71 years) enrolled in a clinical trial. Routine antihypertensive medications were replaced with the study regimen to achieve a blood pressure <140/90 mm Hg. Executive function, memory, cerebral hemodynamics (blood flow velocity), CO2 vasoreactivity (measured using transcranial Doppler ultrasonography), plasma renin activity, and aldosterone were measured at baseline and at 6 and 12 months after the initiation of treatment. RESULTS: At baseline, higher levels of circulating aldosterone were associated with lower blood flow velocity (β = -0.02; P = 0.03), lower CO2 vasoreactivity (β = -0.11; P = 0.007), and decreased autoregulation abilities (β = -0.09; P = 0.01). Those with higher levels of aldosterone at baseline demonstrated the greatest improvement in executive function (P = 0.014 for the aldosterone effect) and in CO2 vasoreactivity (P = 0.026 for the aldosterone effect) after 12 months of lowering blood pressure (<140/90 mm Hg). Plasma renin activity was not associated with any of the measures. CONCLUSIONS: Higher levels of aldosterone may be associated with decreased cerebrovascular function in hypertension. Those with higher aldosterone levels may benefit the most from lowering blood pressure. The role of aldosterone in brain health warrants further investigation in a larger trial.
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Hajjar et al. (2014) conducted an observational in Hypertension (n=47). Higher circulating aldosterone levels vs. Lower circulating aldosterone levels was evaluated on CO2 vasoreactivity at baseline (β = -0.11, p=0.007). Higher baseline circulating aldosterone levels were associated with lower CO2 vasoreactivity and predicted greater improvements in executive function after 12 months of antihypertensive therapy.
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