The Australian National University Alzheimer's Disease Risk Index (ANU‐ADRI) score as a predictor for cognitive decline and potential surrogate outcome in the FINGER lifestyle randomized controlled trial

Author:

Hall Anette12,Barbera Mariagnese13ORCID,Lehtisalo Jenni4,Antikainen Riitta56,Huque Hamidul78,Laatikainen Tiina49,Ngandu Tiia24,Soininen Hilkka110,Stephen Ruth124,Strandberg Timo1112,Kivipelto Miia23913,Anstey Kaarin J.78,Solomon Alina123

Affiliation:

1. Department of Neurology, Institute of Clinical Medicine University of Eastern Finland Kuopio Finland

2. Division of Clinical Geriatrics, Center for Alzheimer Research, Department of Neurobiology, Care Sciences and Society Karolinska Institutet Stockholm Sweden

3. Ageing Epidemiology Research Unit, School of Public Health Imperial College London London UK

4. Population Health Unit, Department of Public Health and Welfare Finnish Institute for Health and Welfare Helsinki Finland

5. Center for Life Course Health Research/Geriatrics University of Oulu Oulu Finland

6. Medical Research Center Oulu University Hospital Oulu Finland

7. School of Psychology University of New South Wales, Sydney Sydney New South Wales Australia

8. Neuroscience Research Australia Randwick New South Wales Australia

9. Institute of Public Health and Clinical Nutrition University of Eastern Finland Kuopio Finland

10. Neurocenter Finland, Department of Neurology Kuopio University Hospital Kuopio Finland

11. University of Helsinki and Helsinki University Hospital Helsinki Finland

12. Center for Life Course Health Research University of Oulu Oulu Finland

13. Theme Inflammation and Aging Karolinska university hospital Stockholm Sweden

Abstract

AbstractBackground and purposeThe complex aetiology of Alzheimer's disease suggests prevention potential. Risk scores have potential as risk stratification tools and surrogate outcomes in multimodal interventions targeting specific at‐risk populations. The Australian National University Alzheimer's Disease Risk Index (ANU‐ADRI) was tested in relation to cognition and its suitability as a surrogate outcome in a multidomain lifestyle randomized controlled trial, in older adults at risk of dementia.MethodsIn this post hoc analysis of the Finnish Intervention Study to Prevent Cognitive Impairment and Disability (FINGER), ANU‐ADRI was calculated at baseline, 12, and 24 months (n = 1174). The association between ANU‐ADRI and cognition (at baseline and over time), the intervention effect on changes in ANU‐ADRI, and the potential impact of baseline ANU‐ADRI on the intervention effect on changes in cognition were assessed using linear mixed models with maximum likelihood estimation.ResultsA higher ANU‐ADRI was significantly related to worse cognition, at baseline (e.g., estimate for global cognition [95% confidence interval] was −0.028 [−0.032 to −0.025]) and over the 2‐year study (e.g., estimate for 2‐year changes in ANU‐ADRI and per‐year changes in global cognition [95% confidence interval] was −0.068 [−0.026 to −0.108]). No significant beneficial intervention effect was reported for ANU‐ADRI, and baseline ANU‐ADRI did not significantly affect the response to the intervention on changes in cognition.ConclusionsThe ANU‐ADRI was effective for the risk prediction of cognitive decline. Risk scores may be crucial for the success of novel dementia prevention strategies, but their algorithm, the target population, and the intervention design should be carefully considered when choosing the appropriate tool for each context.

Funder

Alzheimerfonden

EU Joint Programme – Neurodegenerative Disease Research

European Research Council

Vetenskapsrådet

NordForsk

Suomen Kulttuurirahasto

Ella ja Georg Ehrnroothin Säätiö

Center for Innovative Medicine

Publisher

Wiley

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