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Published on: August 22, 2012
Public Health
Xiaoying Chen1, Katie Harris2, Wang Ruirui1
1The George Institute for Global Health, Sydney, NSW, Australia.
Insights
Antihypertensive treatment appears to reduce dementia risk in individuals aged 60-80, regardless of frailty levels. However, trial data may not fully represent those with severe frailty.
Area of Science:
- Gerontology
- Neurology
- Cardiology
Background:
- High blood pressure (HBP) is a known risk factor for dementia.
- Antihypertensive treatment in individuals aged 60-80 reduces dementia risk.
- Frailty may influence the relationship between HBP and dementia.
Purpose of the Study:
- To investigate frailty as a moderator of antihypertensive treatment's effect on incident dementia.
- To analyze data from four major antihypertensive drug trials.
Main Methods:
- Individual-participant-data meta-analysis of 24,122 participants.
- Frailty Index (FI) used, modeled as continuous and binary (FI ≤ 0.21 vs. FI > 0.21).
- Multilevel multinomial regression accounting for the competing risk of death.
Main Results:
- No significant interaction between frailty and antihypertensive treatment on dementia risk (p=0.47).
- Odds ratios for antihypertensive treatment effect were similar for non-frail (0.88) and frail (0.85) groups.
- Data included participants with a median age of 68.5 years and median follow-up of 4.5 years.
Conclusions:
- Antihypertensive treatment likely benefits dementia risk reduction across frailty levels in those aged 60-80.
- Generalizability to severely frail populations is limited due to trial participant bias.
- Findings have implications for cardiovascular prevention and dementia risk management guidelines.
Background:
High blood pressure(HBP) is a risk factor for dementia. Clinical trials show antihypertensive treatment in those ∼60-80 years lowers risk of incident dementia.1 However, observational data2 show differing patterns of benefit/risk for HBP and dementia in older age which may relate to the confounding influence of frailty. Frailty is a syndromal diagnosis that reflects a loss of resilience, and exacerbates expression of dementia pathology.3,4 Since varying levels of frailty are present in clinical trial participants, we sought to examine its role as a potential moderator of the impact of antihypertensive treatment on incident dementia.
Method:
Single-stage individual-participant-data meta-analysis. Data were merged from four landmark double-blind placebo-controlled trials of antihypertensive drugs with blinded adjudicated dementia endpoints. Frailty was assessed using a robust tool, the frailty index(FI) where scores range from 0.01 to 1.00. Frailty was modelled as a continuous and binary variable FI≤0.21 for none/mild frailty and FI>0.21 moderate-severe frailty5. A multilevel multinomial regression model was used to determine the impact of baseline frailty on the impact of antihypertensive treatment on incident dementia taking account of the competing risk of death, unadjusted and adjusted for age, sex, education.
Result:
Data on dementia and frailty were available for 24122 participants (mean age 68.5(SD9.31)yr, female 44%) with a median follow up of 4.5 years. Baseline FI median score was FI 0.16 (interquartile interval 0.11-0.23). Adjusted analyses: There was no interaction between frailty (continuous) and antihypertensive treatment and incident dementia (p = 0.47). For those an F ≤.21 the odds ratio for the impact of antihypertensive treatment was of 0.88(0.72,1.07) compared to 0.85(0.65,1.10) for an FI>0.21. Unadjusted results were similar.
Conclusion:
Antihypertensive treatment is likely to reduce incident dementia in those aged∼60-80 across varying levels of frailty. However, since clinical trial populations are biassed towards less frail participants, there are limitations to the generalizability of these data to more severe frailty in the general population. Further analyses will allow the investigation of the frailty/antihypertensive/dementia relationship in more detail. These data have implications for treatment guidelines for cardiovascular prevention alongside approaches to the management of people at high-risk of dementia. 1. Eur Heart J 2022;43(48):4980-90 2. JAMA Intern Med;2022;182(2):142-52 3. Lancet Neurol;2018;18(2):17784 4. Nat Aging;2021;1:651-65 5. Lancet Health Longev;2023;2(2)e96-e104.
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