Evidence map›Paper›PMID 30796570›Full record

ArticleEuropean radiology2019

Automatically computed rating scales from MRI for patients with cognitive disorders.

Juha R Koikkalainen, Hanneke F M Rhodius-Meester, Kristian S Frederiksen, Marie Bruun, Steen G Hasselbalch, Marta Baroni, Patrizia Mecocci, Ritva Vanninen, Anne Remes, Hilkka Soininen and 7 more

Open access · greenAbstract read
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In one paragraph

Article in European radiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Development and validation of MethylCog, a blood DNA methylation proxy for cognition.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
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  10. APOE ε4 carrier status moderates the effect of lifestyle factors on cognitive reserve.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
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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

17 authors at 8 institutions in 6 countries.

Juha R KoikkalainenCombinostics Ltd., Hatanpään valtatie 24, 33100, Tampere, Finland.
Hanneke F M Rhodius-MeesterAlzheimer Center, Department of Neurology, VU University Medical Centre, Amsterdam Neuroscience, Amsterdam, the Netherlands.
Kristian S FrederiksenDanish Dementia Research Centre, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Marie BruunDanish Dementia Research Centre, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Steen G HasselbalchDanish Dementia Research Centre, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Marta BaroniInstitute of Gerontology and Geriatrics, University of Perugia, Perugia, Italy.
Patrizia MecocciInstitute of Gerontology and Geriatrics, University of Perugia, Perugia, Italy.
Ritva VanninenInstitute of Clinical Medicine, Radiology, University of Eastern Finland, Kuopio, Finland.
Anne RemesDepartment of Clinical Radiology, Kuopio University Hospital, Kuopio, Finland.
Hilkka SoininenDepartment of Clinical Radiology, Kuopio University Hospital, Kuopio, Finland.
Mark van GilsVTT Technical Research Center of Finland Ltd, Tampere, Finland.
Wiesje M van der FlierAlzheimer Center, Department of Neurology, VU University Medical Centre, Amsterdam Neuroscience, Amsterdam, the Netherlands.
Philip ScheltensAlzheimer Center, Department of Neurology, VU University Medical Centre, Amsterdam Neuroscience, Amsterdam, the Netherlands.
Frederik BarkhofAlzheimer Center, Department of Neurology, VU University Medical Centre, Amsterdam Neuroscience, Amsterdam, the Netherlands.
Timo ErkinjunttiClinical Neurosciences, Neurology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Jyrki M P LötjönenCombinostics Ltd., Hatanpään valtatie 24, 33100, Tampere, Finland. jyrki.lotjonen@combinostics.com.ORCID http://orcid.org/0000-0002-8698-4340
Alzheimer’s Disease Neuroimaging Initiative
University of Copenhagen · DKAmsterdam Neuroscience · NLKuopio University Hospital · FIUniversity of Eastern Finland · FIUniversity of Helsinki · FITheranostics (New Zealand) · NZUniversity of Perugia · ITVTT Technical Research Centre of Finland · FI

Funding

European Union's Seventh Framework Programme for research, technological development and demonstration 601055European Union's Seventh Framework Programme for research, technological development and demonstration 611005
6 · The paper itself

Abstract

objectivesThe aims of this study were to examine whether visual MRI rating scales used in diagnostics of cognitive disorders can be estimated computationally and to compare the visual rating scales with their computed counterparts in differential diagnostics.

methodsA set of volumetry and voxel-based morphometry imaging biomarkers was extracted from T1-weighted and FLAIR images. A regression model was developed for estimating visual rating scale values from a combination of imaging biomarkers. We studied three visual rating scales: medial temporal lobe atrophy (MTA), global cortical atrophy (GCA), and white matter hyperintensities (WMHs) measured by the Fazekas scale. Images and visual ratings from the Amsterdam Dementia Cohort (ADC) (N = 513) were used to develop the models and cross-validate them. The PredictND (N = 672) and ADNI (N = 752) cohorts were used for independent validation to test generalizability.

resultsThe correlation coefficients between visual and computed rating scale values were 0.83/0.78 (MTA-left), 0.83/0.79 (MTA-right), 0.64/0.64 (GCA), and 0.76/0.75 (Fazekas) in ADC/PredictND cohorts. When performance in differential diagnostics was studied for the main types of dementia, the highest balanced accuracy, 0.75-0.86, was observed for separating different dementias from cognitively normal subjects using computed GCA. The lowest accuracy of about 0.5 for all the visual and computed scales was observed for the differentiation between Alzheimer's disease and frontotemporal lobar degeneration. Computed scales produced higher balanced accuracies than visual scales for MTA and GCA (statistically significant).

conclusionsMTA, GCA, and WMHs can be reliably estimated automatically helping to provide consistent imaging biomarkers for diagnosing cognitive disorders, even among less experienced readers. KEY POINTS: • Visual rating scales used in diagnostics of cognitive disorders can be estimated computationally from MRI images with intraclass correlations ranging from 0.64 (GCA) to 0.84 (MTA). • Computed scales provided high diagnostic accuracy with single-subject data (area under the receiver operating curve range, 0.84-0.94).

Indexed as

AgedAlzheimer DiseaseAtrophyBiomarkersCerebral CortexCognition DisordersDiagnosis, DifferentialFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedTemporal LobeWhite MatterBiomarkersAtrophyCognition disordersMagnetic resonance imaging

Identifiers

PMID30796570
OpenAlexW2917767332

What OpenQuestion holds

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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.