Modifiable dementia risk score to study heterogeneity in treatment effect of a dementia prevention trial: a post hoc analysis in the preDIVA trial using the LIBRA index
Alzheimer's Research & Therapy volume 10, Article number: 62 (2018)
Selecting high-risk participants for dementia prevention trials based on a modifiable dementia risk score may be advantageous, as it increases the opportunity for intervention. We studied whether a multi-domain intervention can prevent all-cause dementia and cognitive decline in older people across three different levels of a modifiable dementia risk score.
Prevention of Dementia by Intensive Vascular Care (preDIVA) is a randomised controlled trial studying the effect of multi-domain vascular care during 6–8 years on incident all-cause dementia in community-dwelling people aged 70–78 years. For this post hoc analysis, we stratified preDIVA participants in tertiles based on their baseline LIfestyle for BRAin Health (LIBRA) index, a modifiable dementia risk score. With Cox proportional hazards regression, the intervention effect on dementia was assessed. The effect on cognition was measured every 2 years with the Mini-Mental State Examination and Visual Association Test.
Dementia developed in 220 of 3274 (6.7%) participants. In participants with a low, intermediate and high LIBRA index, the hazard ratio (HR) of the intervention on incident dementia was respectively 0.71 (95% CI 0.45–1.12), 1.06 (95% CI 0.66–1.69) and 1.02 (95% CI 0.64–1.62). Also, when adding the non-modifiable risk factors age, education and sex to the index, results were comparable (respectively HR 0.88, 95% CI 0.54–1.43; HR 0.91, 95% CI 0.57–1.47; HR 0.92, 95% CI 0.59–1.41). There was no statistically significant intervention effect on cognition during follow-up across the LIBRA groups.
In the preDIVA study population aged 70–78 years, the LIBRA modifiable dementia risk score did not identify a (high-)risk group in whom the multi-domain intervention was effective in preventing dementia or cognitive decline.
International Standard Randomised Controlled Trial Number registry, ISRCTN29711771. Registered on 14 February 2006.
The number of dementia cases worldwide is anticipated to double over the coming two decades [1, 2]. Up to a third of Alzheimer’s disease cases may be attributable to potentially modifiable risk factors, including several vascular risk factors such as diabetes mellitus, midlife hypertension and physical inactivity . This offers a window of opportunity for prevention strategies. However, selection of the optimal target population when designing a randomised controlled trial (RCT) to prevent dementia remains a challenge . Results from recent RCTs suggest that interventions may be most effective in those individuals at increased risk of dementia based on the presence of one or more dementia risk factors [5,6,7]. In such an at-risk population the potential to improve modifiable risk factors such as hypertension and physical inactivity, and thereby prevent dementia, is higher. In addition, the higher dementia incidence rates in high-risk populations increase the study power, decreasing the total number of participants required to demonstrate a treatment effect.
A dementia risk score could be a useful tool to recruit a high-risk population for prevention trials. Most risk scores that have been developed are, however, heavily dependent on non-modifiable risk factors such as age, sex and education . The LIfestyle for BRAin Health (LIBRA) index is the first, and so far only, validated dementia risk score predominantly supported by modifiable health and lifestyle factors . It consists of the following 12 risk and protective factors: depression, hypertension, obesity, smoking, hypercholesterolemia, diabetes, renal dysfunction, physical inactivity, coronary heart disease, low/moderate alcohol use, cognitive activity and adherence to the Mediterranean diet. As the index reflects an individual’s potential for dementia prevention, it may identify those most responsive to an intervention.
Prevention of Dementia by Intensive Vascular Care (preDIVA) is a cluster RCT evaluating the effect of 6–8 years of nurse-led intensive vascular care on incident dementia in community-dwelling older people aged 70–78 years . Overall, no preventive effect of the intervention was found. The intervention seemed more beneficial in a subgroup of individuals with untreated hypertension who adhered to the intervention. As the preDIVA intervention targets several vascular risk factors, our hypothesis was that a risk score capturing several modifiable risk factors may function even better at selecting those individuals responsive to the intervention.
Hence, our aim was to study whether a multi-domain intervention can prevent all-cause dementia and cognitive decline in older people across three different levels of a modifiable dementia risk score.
The current study is a post hoc analysis in the preDIVA trial, which was published previously . In short, the intervention comprised 4-monthly visits to a practice nurse who gave individually tailored lifestyle advice on smoking, diet, physical activity, weight and blood pressure (BP). If indicated, pharmacological treatment was started or optimised according to the prevailing guidelines on cardiovascular risk management . The control condition was standard care. All community-dwelling older people aged 70–78 years registered at participating Dutch general practices were invited to participate. The only exclusion criteria were a diagnosis of dementia and/or any condition likely to hinder long-term follow-up (such as terminal illness or alcoholism). The trial is registered at the International Standard Randomised Controlled Trial Number registry (ISRCTN29711771).
The LIBRA index has been designed based on a systematic review and Delphi consensus, and has been validated in several cohorts, including a cohort aged 70–79 years [9, 11, 12]. In preDIVA, 10 out of 12 LIBRA factors were measured at baseline (Table 1). Similar to one of the previously mentioned validation studies , there was no information on cognitive activity or adherence to the Mediterranean diet. Data on medical history, medication use, history of smoking and alcohol use were self-reported and cross-referenced with the electronic medical record of the general practitioner. BP, weight and height (to calculate the body mass index (BMI)) were measured using standard protocols. A blood sample was drawn to measure cholesterol and creatinine levels. The 15-item Geriatric Depression Scale was used to measure depressive symptoms and the LASA Physical Activity Questionnaire to measure physical activity [13, 14]. The measures corresponding to the 10 LIBRA items (Table 1) were aligned to the previously published validation studies [9, 11]. Each item was assigned the appropriate score (Table 1) and the sum of these items formed the LIBRA index (with a maximum potential range of − 1.0 to + 12.7). Only participants with all 10 items available to calculate the LIBRA index were included in the analysis. For a secondary analysis, the LIBRA index was extended with the non-modifiable risk factors age, sex and education (Table 1), in order to make it more comparable to other available dementia risk indices . This was also done in the previously published studies on the LIBRA index [9, 11].
Primary and secondary outcomes
The primary outcome was all-cause dementia, according to the Diagnostic and Statistical Manual of Mental Disorders IV . An independent outcome adjudication committee validated all dementia diagnoses, including a 1-year follow-up period in incident cases to assure there were no false positive diagnoses. Cognition was the secondary outcome measure, which was measured every 2 years with the Mini-Mental State Examination (MMSE) and the Visual Association Test (VAT) [17, 18]. Participants attending at least one follow-up visit were included in the analyses on cognition.
We first assessed the association between the LIBRA index in the preDIVA population and incident dementia with Cox proportional hazards regression. We then divided the study population into participants with a low, intermediate and high LIBRA index based on tertiles of the index . In each group, the crude effect of the intervention on all-cause dementia was assessed with Cox proportional hazards regression (model 1). The years from randomisation to dementia diagnosis or censoring date were used as the timescale. To assess whether the LIBRA index is more useful as a selection tool when containing both modifiable and major non-modifiable risk factors, we repeated our analysis with the LIBRA index expanded with education (model 2) and additionally with age and sex (model 3) . As history of coronary heart disease is not modifiable, we removed it from the LIBRA index in a sensitivity analysis (model 4). Our primary analysis was crude and in a secondary analysis we adjusted for baseline imbalances between the intervention and control groups. We also assessed the effect of adjusting for education, as this is an important risk factor for dementia and is associated with many of the risk/protective factors included in the LIBRA index . The proportional hazards assumption was tested using Schoenfeld residuals and was assessed graphically .
Because of the cluster-randomised design we additionally performed a multi-level analysis to account for clustering within general practices and health care centres. To account for competing risk of death, we assessed the intervention effect on mortality in the LIBRA groups, and, when appropriate, performed a competing risk analysis according to the cause-specific hazard method . We added a per-protocol analysis to assess whether the results were influenced by adherence to the intervention or control condition. In the per-protocol analysis, we excluded intervention participants who had on average less than two visits per year and inadvertent crossover control participants who had on average more than two visits per year. As the LIBRA index is more sensitive in a younger cohort , we performed a pre-defined subgroup analysis on age (dichotomised at the median). In the primary preDIVA analyses, the intervention seemed to be effective in those individuals with untreated hypertension who adhered to the intervention. However, the LIBRA definition of hypertension is rather crude (dichotomously defined as systolic BP ≥ 140 mmHg, diastolic BP ≥ 90 mmHg and/or use of antihypertensive medication). Therefore, we added subgroup analyses on World Health Organisation hypertension grades (i.e. normotension, systolic BP < 140 mmHg and/or diastolic BP < 90 mmHg; grade I hypertension, systolic BP 140–160 mmHg and/or diastolic BP 90–100 mmHg; grade II or III hypertension, systolic BP ≥ 160 mmHg and/or diastolic BP ≥ 100 mmHg) and use of antihypertensive medication . In the Netherlands, people with a history of cardiovascular disease (CVD) and diabetes visit a practice nurse as part of standard care, potentially diluting an intervention effect . We therefore added analyses in subgroups based on history of CVD and type 2 diabetes. To assess whether the intervention led to an improvement of cardiovascular risk factors, as a proxy for treatment effect, we compared decline in systolic BP, BMI and total cholesterol between baseline and the last available follow-up visit, across the three LIBRA groups.
To assess whether individual changes in cognition vary over time between treatment groups, we used a multilevel growth model stratified for participants with a low, intermediate and high LIBRA index . In this linear mixed-effect model each participant and time in years were considered random effects and a time × randomisation interaction variable was included. Since absolute values of the MMSE and VAT, or logarithmic transformation of these values, were not normally distributed, change in MMSE/VAT since baseline, which was normally distributed, was used as an outcome variable in the model. We performed our analyses in R studio version 3.2 using the survival and nlme packages .
Of the 3526 preDIVA participants at baseline, 3339 (94.7%) had all 10 LIBRA items available at baseline and could be included in the analyses (Additional file 1: Figure S1). The median LIBRA score at baseline was 3.1. Participants with the highest LIBRA index were slightly older (low 74.2 years, intermediate 74.3 years, high 74.5 years; p < 0.01) and more often had a low education level (low 19.2%, intermediate 22.1%, high 29.9%; p < 0.01; Table 2). Systolic BP was highest in the intermediate LIBRA group (low 151.5 mmHg, intermediate 157.5 mmHg, high 156.7 mmHg; p < 0.01). The baseline characteristics of the intervention and control groups within each LIBRA group were well balanced, except for small differences in total cholesterol (respectively, 5.3 vs 5.5 mmol/L; p = 0.03) in the intermediate LIBRA group and mean systolic BP (157.9 vs 155.3 mmHg; p = 0.04) and sex (37.3% vs 44.2%; p = 0.02) in the high LIBRA group (Additional file 1: Table S1).
All-cause dementia was diagnosed in 220 (6.7%) participants; 76 of 1091 participants (7.0%) participants with a low LIBRA index, 71 of 1081 (6.6%) with an intermediate LIBRA index and 73 of 1102 participants (6.6%) with a high LIBRA index. The LIBRA index (model 1) was not associated with incident dementia (crude hazard ratio (HR) 1.02 per point increase in LIBRA index, 95% confidence interval (CI) 0.96–1.09). Adding education to the LIBRA index (model 2) did not change these results (HR 1.06; 95% CI 0.90–1.24). The LIBRA index including education, age and sex (model 3) was significantly associated with incident dementia (HR 1.07, 95% CI 1.02–1.12).
The HR of the effect of intensive vascular care on incident all-cause dementia was 0.71 (95% CI 0.45–1.12) in the low, 1.06 (95% CI 0.66–1.69) in the intermediate and 1.02 (95% CI 0.64–1.62) in the high LIBRA groups (model 1; Fig. 1; Table 3). The interaction between randomisation and LIBRA index divided into tertiles was not significant. Also, when including age, sex and education in (models 2 and 3) or excluding coronary heart disease from (model 4) the LIBRA index and stratifying our study population based on this modified LIBRA index, the intervention was not effective in any of the groups (Table 3). Adjustment for baseline imbalances or education did not significantly influence the results, nor did accounting for clustering within general practices and health care centres (Additional file 1: Table S2). The results were similar in the per-protocol analysis (Additional file 1: Table S2). Mortality risk increased with increasing LIBRA index, but the intervention effect on mortality was not significantly different in the LIBRA groups (Additional file 1: Table S3). In all secondary analyses, the HR was lowest, albeit non-significant, in participants with the lowest LIBRA index (Additional file 1: Table S2). Subgroup analyses showed a significant interaction (p = 0.03) between age and randomisation in the intermediate LIBRA group with a lower HR in younger participants aged < 74.3 years (HR 0.55; 95% 0.26–1.17) compared to older participants (HR 1.65; 95% CI 0.88–3.09) (Additional file 1: Table S4). We found an interaction with diabetes in the high LIBRA group (p = 0.03), with a lower HR in participants with diabetes (HR 0.61; 95% CI 0.32–1.15) in comparison to those without (HR 1.78; 95% CI 0.87–3.64). We found no other interactions in the subgroup analyses. Participants with a higher LIBRA index had on average more decline in systolic BP (respectively in the low, intermediate and high LIBRA groups − 2.3, − 5.9 and − 5.8; p < 0.01), less decline in total cholesterol (− 0.3, − 0.3 and − 0.1; p < 0.01) and more decline in BMI (− 0.5, − 0.5 and − 0.9; p < 0.01). The intervention led to a significant decline in systolic BP in the low (intervention vs control − 3.9 vs − 0.5; p = 0.03) and intermediate (− 7.4 vs − 4.2; p = 0.04) LIBRA groups, but not in the high LIBRA group (− 7.1 vs − 4.3; p = 0.09; Additional file 1: Table S5). The intervention did not significantly reduce cholesterol or BMI in any of the LIBRA groups (Additional file 1: Table S5).
A total of 2674 participants had at least one valid MMSE score and 2671 participants at least one valid VAT score after baseline and could be included in the analyses on cognitive decline (Additional file 1: Figure S1). Participants excluded from these analyses were on average older, had a higher cardiovascular risk and had a lower baseline MMSE and VAT (Additional file 1: Table S6). After 3 years, decline in MMSE did not significantly differ between the intervention and control groups among participants with a low (mean difference (MD) − 0.08; 95% CI − 0.28 to 0.13), intermediate (MD 0.07; 95% CI − 0.14 to 0.27) or high (MD − 0.06; 95% CI − 0.30 to 0.18; Fig. 2a, Additional file 1: Table S7) LIBRA index. Decline in VAT also did not differ between treatment groups in the low (MD 0.03; 95% CI − 0.09 to 0.14), intermediate (MD − 0.04; 95% CI − 0.16 to 0.08) or high (MD 0.07; 95% CI − 0.05 to 0.19; Fig. 2b, Additional file 1: Table S7) LIBRA groups.
In the preDIVA study population, aged 70–78 years, the LIBRA index did not identify a high-risk group in whom the multi-domain intervention was effective in preventing dementia or cognitive decline. On the contrary, there was a trend for a preventive effect in the subgroup with a low LIBRA index. Results were comparable when including non-modifiable risk factors in the LIBRA index.
The concept of selecting people at increased risk of dementia for preventive interventions to magnify the intervention effect is widely supported among experts in the field and has been incorporated in the design of recent multi-domain prevention trials [6, 7]. Our results do not support this strategy, and are even in contrast with this concept, at least in later life, suggesting a more favourable effect of the intervention in those with a low LIBRA index. A potential explanation for this is that the contrast between the intervention and control conditions was too small, partly due to Hawthorne effects and improvements in the standard care for cardiovascular risk management during the trial . Although a greater reduction in systolic BP could be achieved in participants with a higher LIBRA index, this was the case in both the intervention and control groups and the difference between the treatment groups was smallest in the high LIBRA group. Another potential explanation for our results is that the LIBRA index does not successfully classify dementia risk in this older population aged 70–78 years. Indeed, our analyses did not show an association between a high LIBRA index and increased risk of dementia. Since preDIVA is an RCT, this could potentially (partly) be due to the fact that the dementia risk was influenced during the trial by the intervention and/or Hawthorne effects . For example, systolic BP decreased by approximately 8 mmHg in the intervention group and 4 mmHg in the control group, and the decline was steepest in participants with hypertension at baseline . In one of the LIBRA validation studies, a higher LIBRA index was associated (at group level) with an increased risk of dementia in people aged 70–79 years . The individual predictive accuracy in late life was poor, however, with a C statistic of 0.50, and seemed to decrease with increasing age. Investigating the utility of the LIBRA index as a selection tool for prevention trials at a younger age (55–70 years) may yield different results. A third potential explanation is that the factors in the LIBRA index and in other dementia risk scores are dichotomous and not designed to precisely quantify the magnitude of the risk/protective factor or the room for improvement. For example, the potential for improvement is different for someone with a systolic BP of 125 mmHg on antihypertensive medication compared to a person with a systolic BP of 155 mmHg without medication, although both are weighted equally in the LIBRA index with the dichotomous score for hypertension (including both high BP and/or antihypertensive medication use). In order for a risk estimation tool to be useful for selection of high-risk populations for dementia prevention trials, the potential for improvement should be taken into account (e.g. by distinguishing treated or untreated hypertension).
Regardless of the LIBRA index performance in high-age populations, the concept of selecting people at high risk of dementia may only be appropriate for younger people (i.e. age < 70 years). In older people at high risk of dementia, cerebrovascular and neurodegenerative damage may already be irreversible, while those with a low risk could still benefit from risk factor improvement in order to maintain cognitive function. Also, several observational studies have shown a diminishing or even inverting association between risk factors and incident dementia in older people, as for example the J-shaped relation with BP . Therefore, future trials should perhaps either focus on people with lowest dementia risk in old age or highest dementia risk in midlife. This would, however, imply that substantially larger sample sizes or longer follow-up will be required, as incidence rates in these groups are lower.
A strength of this analysis is that preDIVA is, up until now, the only multi-domain prevention trial with dementia as the primary outcome. The population-based approach with few exclusion criteria renders preDIVA a suitable study to test whether the LIBRA index is a promising tool to select high-risk groups from the general population. A limitation is the overall neutral result of the preDIVA trial, perhaps limiting the possibility to detect high-risk groups who benefit most. However, a significant effect of the intervention was found in the per-protocol analysis among participants with untreated hypertension at baseline (HR 0.54, 95% CI 0.32–0.92) , while the results of the present analyses do not show a trend towards improved treatment effects in higher LIBRA groups. Another limitation is that no other neuropsychological tests were performed besides the MMSE and VAT to detect more subtle cognitive changes. We did not have information on two of the 12 LIBRA items, including cognitive activity which is the strongest-weighted item in the LIBRA index . These factors were, however, already identified as risk factors that need further validation in the systematic review and Delphi consensus used to design the LIBRA index, and were also not included in the validation study among people in late life (70–79 years) [11, 12]. Furthermore, it may be argued that cognitive activity at this age is not as much a modifiable risk factor but rather an early indicator of developing cognitive decline and dementia .
Within our study population of community-dwelling people aged 70–78 years, a modifiable dementia risk score does not identify heterogeneity in the treatment effect of a multi-domain intervention to prevent dementia or cognitive decline. This suggests that in older adults a high LIBRA index may not be a suitable parameter to select participants for a dementia prevention trial. Specific characteristics of the preDIVA study, including the overall neutral effect of the intervention and relatively high age group, may have contributed to the lack of discriminating capacity of the LIBRA index.
Body mass index
International Standard Randomised Controlled Trial Number
LIfestyle for BRAin Health
Mini-Mental State Examination
Prevention of Dementia by Intensive Vascular Care
Randomised controlled trial
Visual Association Test
World Health Organisation: World report on ageing and health. World Health Organisation: Luxembourg; 2015.
Scheltens P, Blennow K, Breteler MMB, de Strooper B, Frisoni GB, Salloway S, Van der Flier WM. Alzheimer’s disease. Lancet. 2016;388:505–17.
Norton S, Matthews FE, Barnes DE, Yaffe K, Brayne C. Potential for primary prevention of Alzheimer's disease: an analysis of population-based data. Lancet Neurol. 2014;13:788–94.
Richard E, Andrieu S, Solomon A, Mangialasche F, Ahtiluoto S, Moll van Charante EP, Coley N, Fratiglioni L, Neely AS, Vellas B, et al. Methodological challenges in designing dementia prevention trials—the European Dementia Prevention Initiative (EDPI). J Neurol Sci. 2012;322:64–70.
Moll van Charante EP, Richard E, Eurelings LS, van Dalen JW, Ligthart SA, van Bussel EF, Hoevenaar-Blom MP, Vermeulen M, van Gool WA. Effectiveness of a 6-year multidomain vascular care intervention to prevent dementia (preDIVA): a cluster-randomised controlled trial. Lancet. 2016;388(10046):797–805.
Ngandu T, Lehtisalo J, Solomon A, Levalahti E, Ahtiluoto S, Antikainen R, Backman L, Hanninen T, Jula A, Laatikainen T, et al. A 2 year multidomain intervention of diet, exercise, cognitive training, and vascular risk monitoring versus control to prevent cognitive decline in at-risk elderly people (FINGER): a randomised controlled trial. Lancet. 2015;385:2255–63.
Andrieu S, Guyonnet S, Coley N, Cantet C, Bonnefoy M, Bordes S, Bories L, Cufi MN, Dantoine T, Dartigues JF, et al. Effect of long-term omega 3 polyunsaturated fatty acid supplementation with or without multidomain intervention on cognitive function in elderly adults with memory complaints (MAPT): a randomised, placebo-controlled trial. Lancet Neurol. 2017;16:377–89.
Imtiaz B, Tolppanen AM, Kivipelto M, Soininen H. Future directions in Alzheimer's disease from risk factors to prevention. Biochem Pharmacol. 2014;88:661–70.
Schiepers OJ, Kohler S, Deckers K, Irving K, O'Donnell CA, van den Akker M, Verhey FR, Vos SJ, de Vugt ME, van Boxtel MP. Lifestyle for Brain Health (LIBRA): a new model for dementia prevention. Int J Geriatr Psychiatry. 2018;33(1):167–75.
Wiersma T, Smulders YM, Stehouwer CD, Konings KT, Lanphen J. Summary of the multidisciplinary guideline on cardiovascular risk management (revision 2011). Ned Tijdschr Geneeskd. 2012;156:A5104.
Vos SJB, van Boxtel MPJ, Schiepers OJG, Deckers K, de Vugt M, Carriere I, Dartigues JF, Peres K, Artero S, Ritchie K, et al. Modifiable risk factors for prevention of dementia in midlife, late life and the oldest-old: validation of the LIBRA index. J Alzheimers Dis. 2017;58:537–47.
Deckers K, van Boxtel MP, Schiepers OJ, de Vugt M, Munoz Sanchez JL, Anstey KJ, Brayne C, Dartigues JF, Engedal K, Kivipelto M, et al. Target risk factors for dementia prevention: a systematic review and Delphi consensus study on the evidence from observational studies. Int J Geriatr Psychiatry. 2015;30:234–46.
Pocklington C, Gilbody S, Manea L, McMillan D. The diagnostic accuracy of brief versions of the Geriatric Depression Scale: a systematic review and meta-analysis. Int J Geriatr Psychiatry. 2016;31:837–57.
Stel VS, Smit JH, Pluijm SM, Visser M, Deeg DJ, Lips P. Comparison of the LASA Physical Activity Questionnaire with a 7-day diary and pedometer. J Clin Epidemiol. 2004;57:252–8.
Kivipelto M, Ngandu T, Laatikainen T, Winblad B, Soininen H, Tuomilehto J. Risk score for the prediction of dementia risk in 20 years among middle aged people: a longitudinal, population-based study. Lancet Neurol. 2006;5:735–41.
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 4th ed. Washington, DC: American Psychiatric Association; 2000.
Folstein MF, Folstein SE, McHugh PR. “Mini-mental state”. A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975;12:189–98.
Lindeboom J, Schmand B, Tulner L, Walstra G, Jonker C. Visual association test to detect early dementia of the Alzheimer type. J Neurol Neurosurg Psychiatry. 2002;73:126–33.
Bellera CA, MacGrogan G, Debled M, de Lara CT, Brouste V, Mathoulin-Pelissier S. Variables with time-varying effects and the cox model: some statistical concepts illustrated with a prognostic factor study in breast cancer. BMC Med Res Methodol. 2010;10:20.
Hinchliffe SR, Lambert PC. Flexible parametric modelling of cause-specific hazards to estimate cumulative incidence functions. BMC Med Res Methodol. 2013;13:13.
Piepoli MF, Hoes AW, Agewall S, Albus C, Brotons C, Catapano AL, Cooney MT, Corra U, Cosyns B, Deaton C, et al. European guidelines on cardiovascular disease prevention in clinical practice: the sixth joint task force of the European Society of Cardiology and Other Societies on cardiovascular disease prevention in clinical practice (constituted by representatives of 10 societies and by invited experts)developed with the special contribution of the European Association for Cardiovascular Prevention & rehabilitation (EACPR). Eur Heart J. 2016;2016(37):2315–81.
Voogdt-Pruis HR, Van Ree JW, Gorgels AP, Beusmans GH. Adherence to a guideline on cardiovascular prevention: a comparison between general practitioners and practice nurses. Int J Nurs Stud. 2011;48:798–807.
Gee KA. Multilevel growth modeling:an introductory approach to analyzing longitudinal data for evaluators. Am J Eval. 2014;35:543–61.
R Core Team. R: a language and environment for statistical computing. Vienna: R Foundation for Statistical Computing; 2017.
Ruitenberg A, Skoog I, Ott A, Aevarsson O, Witteman JC, Lernfelt B, van Harskamp F, Hofman A, Breteler MM. Blood pressure and risk of dementia: results from the Rotterdam study and the Gothenburg H-70 study. Dement Geriatr Cogn Disord. 2001;12:33–9.
Wilson RS, Barnes LL, Aggarwal NT, Boyle PA, Hebert LE, Mendes de Leon CF, Evans DA. Cognitive activity and the cognitive morbidity of Alzheimer disease. Neurology. 2010;75:990–6.
Kilbride HS, Stevens PE, Eaglestone G, Knight S, Carter JL, Delaney MP, Farmer CK, Irving J, O'Riordan SE, Dalton RN, Lamb EJ. Accuracy of the MDRD (Modification of Diet in Renal Disease) study and CKD-EPI (CKD Epidemiology Collaboration) equations for estimation of GFR in the elderly. Am J Kidney Dis. 2013;61:57–66.
The authors would like to thank all participants, general practitioners and practice nurses involved in the preDIVA study. They also would like to thank Lisa S.M. Eurelings, Suzanne A. Ligthart and Carin E. Miedema for their hard work for the preDIVA study.
The preDIVA trial was supported by the Dutch Ministry of Health, Welfare and Sports (50–50110–98-020), the Innovatiefonds Zorgverzekeraars (Innovation Fund of Collaborative Health Insurances, 05–234) and ZonMw (The Netherlands Organisation for Health Research and Development, 62000015).
The analyses presented here are based on funding from the European Union Seventh Framework Programme (FP7/2007–2013) under grant agreement n° 305374 and an EU Joint Programme—Neurodegenerative Disease Research (JPND) project. The JPND project is supported through the following funding organisations under the aegis of the JPND (www.jpnd.eu): Finland, Suomen Akatemia (Academy of Finland,291803); France, L’Agence Nationale de la Recherche (The French National Research Agency, ANR-14-JPPS-0001-02); Germany, Bundesministerium für Bildung und Forschung (BMBF) (The Federal Ministry of Education and Research, FKZ01ED1509); Sweden, Vetenskapsrådet (VR) (Swedish Research Council, 529–2014-7503); the Netherlands, ZonMw (The Netherlands Organisation for Health Research and Development, 733051041).
Availability of data and materials
The preDIVA data that support the findings of this study are available from the corresponding author upon reasonable request.
Ethics approval and consent to participate
The medical ethics committee of the Academic Medical Center approved the trial (project number 05/093) and all participants gave written informed consent.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Figure S1. Flow diagram. Table S1. Baseline characteristics per randomisation group and LIBRA group. Table S2. Secondary analyses. Table S3. Competing risk analysis. Table S4. Subgroup analyses on age, hypertension grade, antihypertensive medication, history of cardiovascular disease and diabetes. Table S5. Treatment effect on vascular risk factors in LIBRA groups. Table S6. Baseline characteristics of participants included in and excluded from cognitive analyses. Table S7. Treatment effect on cognition in LIBRA groups (DOCX 533 kb)
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van Middelaar, T., Hoevenaar-Blom, M.P., van Gool, W.A. et al. Modifiable dementia risk score to study heterogeneity in treatment effect of a dementia prevention trial: a post hoc analysis in the preDIVA trial using the LIBRA index. Alz Res Therapy 10, 62 (2018). https://doi.org/10.1186/s13195-018-0389-4
- Risk factors
- Randomised controlled trial
- Patient selection