Evidence map›Paper›PMID 30670070›Full record

ArticleAlzheimer's research & therapy2019

Prediction models for dementia and neuropathology in the oldest old: the Vantaa 85+ cohort study.

Anette Hall, Timo Pekkala, Tuomo Polvikoski, Mark van Gils, Miia Kivipelto, Jyrki Lötjönen, Jussi Mattila, Mia Kero, Liisa Myllykangas, Mira Mäkelä and 5 more

Open access · goldAbstract read
In one paragraph

Article in Alzheimer's research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.6field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 56 citations in OpenAlex.

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  8. Prediction of neuropathologic lesions from clinical data.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 3 countries.

Anette HallInstitute of Clinical Medicine, Neurology, University of Eastern Finland, P.O. Box 1627, 70211, Kuopio, Finland.
Timo PekkalaInstitute of Clinical Medicine, Neurology, University of Eastern Finland, P.O. Box 1627, 70211, Kuopio, Finland.
Tuomo PolvikoskiInstitute for Neuroscience, Newcastle University, Newcastle upon Tyne, UK.
Mark van GilsVTT Technical Research Centre of Finland Ltd., Tampere, Finland.
Miia KivipeltoInstitute of Clinical Medicine, Neurology, University of Eastern Finland, P.O. Box 1627, 70211, Kuopio, Finland.
Jyrki LötjönenCombinostics, Tampere, Finland.
Jussi MattilaCombinostics, Tampere, Finland.
Mia KeroDepartment of Pathology, University of Helsinki and HUSLAB, Helsinki, Finland.
Liisa MyllykangasDepartment of Pathology, University of Helsinki and HUSLAB, Helsinki, Finland.
Mira MäkeläDepartment of Pathology, University of Helsinki and HUSLAB, Helsinki, Finland.
Minna OinasDepartment of Pathology, University of Helsinki and HUSLAB, Helsinki, Finland.
Anders PaetauDepartment of Pathology, University of Helsinki and HUSLAB, Helsinki, Finland.
Hilkka SoininenInstitute of Clinical Medicine, Neurology, University of Eastern Finland, P.O. Box 1627, 70211, Kuopio, Finland.
Maarit TanskanenDepartment of Pathology, University of Helsinki and HUSLAB, Helsinki, Finland.
Alina SolomonInstitute of Clinical Medicine, Neurology, University of Eastern Finland, P.O. Box 1627, 70211, Kuopio, Finland. alina.solomon@uef.fi.
University of Helsinki · FIUniversity of Eastern Finland · FIFinnish Institute for Health and Welfare · FIKarolinska Institutet · SENewcastle University · GBVTT Technical Research Centre of Finland · FI

Funding

Academy of Finland 278457Academy of Finland 287490, 294061EU FP7 601055EU JPND - Academy of Finland (FI) 291803EU JPND - Swedish Research Council 529-2014-7503Stockholms Läns Landsting ALF 20150589, 20170304Vetenskapsrådet 2017-06105
6 · The paper itself

Abstract

backgroundWe developed multifactorial models for predicting incident dementia and brain pathology in the oldest old using the Vantaa 85+ cohort.

methodsWe included participants without dementia at baseline and at least 2 years of follow-up (N = 245) for dementia prediction or with autopsy data (N = 163) for pathology. A supervised machine learning method was used for model development, considering sociodemographic, cognitive, clinical, vascular, and lifestyle factors, as well as APOE genotype. Neuropathological assessments included β-amyloid, neurofibrillary tangles and neuritic plaques, cerebral amyloid angiopathy (CAA), macro- and microscopic infarcts, α-synuclein pathology, hippocampal sclerosis, and TDP-43.

resultsPrediction model performance was evaluated using AUC for 10 × 10-fold cross-validation. Overall AUCs were 0.73 for dementia, 0.64-0.68 for Alzheimer's disease (AD)- or amyloid-related pathologies, 0.72 for macroinfarcts, and 0.61 for microinfarcts. Predictors for dementia were different from those in previous reports of younger populations; for example, age, sex, and vascular and lifestyle factors were not predictive. Predictors for dementia versus pathology were also different, because cognition and education predicted dementia but not AD- or amyloid-related pathologies. APOE genotype was most consistently present across all models. APOE alleles had a different impact: ε4 did not predict dementia, but it did predict all AD- or amyloid-related pathologies; ε2 predicted dementia, but it was protective against amyloid and neuropathological AD; and ε3ε3 was protective against dementia, neurofibrillary tangles, and CAA. Very few other factors were predictive of pathology.

conclusionsDifferences between predictors for dementia in younger old versus oldest old populations, as well as for dementia versus pathology, should be considered more carefully in future studies.

Indexed as

Mental Status and Dementia TestsAged, 80 and overApolipoprotein E4BrainCausalityCohort StudiesDementiaFemaleFinlandFollow-Up StudiesHumansMalePredictive Value of TestsApolipoprotein E4DementiaNeuropathologyOldest oldPredictionSupervised machine learning

Identifiers

PMID30670070
PMCPMC6343349
OpenAlexW2911450760

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.