Key result
Donepezil treatment over 6 months did not significantly change overall plasma BNP levels in dementia patients (P=0.262), but significantly decreased BNP in a subgroup with elevated baseline levels.
Why the study?
The cardiovascular influences and potential therapeutic benefits of donepezil in patients with dementia and subclinical heart failure were not well understood.
Cohort (n=49)
Supports donepezil safety without overall BNP rise; hypothesis-generating for reduction in elevated-baseline subgroup.
To study prospectively influences of donepezil, an acetylcholinesterase inhibitor against Alzheimer disease, on cardiovascular system, we evaluated cardiovascular changes occurring during new initialized treatment with donepezil in 49 dementia patients over 6 months. No patient suffered from cardiovascular events. In clinical changes between baseline and the first evaluation after donepezil treatment, heart rate and plasma brain natriuretic peptide (BNP) levels as a marker for heart failure did not change (BNP: 59.62 ± 62.71 pg/mL at baseline to 53.18 ± 42.34 pg/mL at first evaluation; P = 0.262). We further examined plasma BNP levels in 2 groups into which the patients were divided at baseline according to the cut-off plasma BNP level of 60 pg/mL. In patients with high level of BNP, the BNP levels decreased after administration of donepezil (116.39 ± 76.58 pg/mL at baseline to 82.24 ± 46.64 pg/mL at first evaluation; P = 0.011) with the tendency to be reduced in the follow-up period. BNP did not change in patients with low level of BNP. Donepezil seemed to be safe in patients with dementia without symptomatic heart disease and significantly decreased plasma BNP levels in patients with subclinical chronic heart failure.
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Kubo et al. (2012) conducted a cohort in Dementia (n=49). Donepezil vs. Baseline (pre-treatment) was evaluated on Change in plasma brain natriuretic peptide (BNP) levels (p=0.262). Donepezil treatment over 6 months did not significantly change overall plasma BNP levels in dementia patients (P=0.262), but significantly decreased BNP in a subgroup with elevated baseline levels.
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