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Traceability and comparability through crosswalks with the NeuroMET Memory Metric
RISE Research Institutes of Sweden, Säkerhet och transport, Mätteknik.ORCID-id: 0000-0002-3700-3921
Modus Outcomes Ltd, UK.
Modus Outcomes Ltd, UK.
Modus Outcomes LCC, UK.
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2023 (Engelska)Ingår i: Scientific Reports, E-ISSN 2045-2322, Vol. 13, nr 1, artikel-id 5179Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Accurate assessment of memory ability for persons on the continuum of Alzheimer’s disease (AD) is vital for early diagnosis, monitoring of disease progression and evaluation of new therapies. However, currently available neuropsychological tests suffer from a lack of standardization and metrological quality assurance. Improved metrics of memory can be created by carefully combining selected items from legacy short-term memory tests, whilst at the same time retaining validity, and reducing patient burden. In psychometrics, this is known as “crosswalks” to link items empirically. The aim of this paper is to link items from different types of memory tests. Memory test data were collected from the European EMPIR NeuroMET and the SmartAge studies recruited at Charité Hospital (Healthy controls n = 92; Subjective cognitive decline n = 160; Mild cognitive impairment n = 50; and AD n = 58; age range 55–87). A bank of items (n = 57) was developed based on legacy short-term memory items (i.e., Corsi Block Test, Digit Span Test, Rey’s Auditory Verbal Learning Test, Word Learning Lists from the CERAD test battery and Mini Mental State Examination; MMSE). The NeuroMET Memory Metric (NMM) is a composite metric that comprises 57 dichotomous items (right/wrong). We previously reported on a preliminary item bank to assess memory based on immediate recall, and have now demonstrated direct comparability of measurements generated from the different legacy tests. We created crosswalks between the NMM and the legacy tests and between the NMM and the full MMSE using Rasch analysis (RUMM2030) and produced two conversion tables. Measurement uncertainties for estimates of person memory ability with the NMM across the full span were smaller than all individual legacy tests, which demonstrates the added value of the NMM. Comparisons with one (MMSE) of the legacy tests showed however higher measurement uncertainties of the NMM for people with a very low memory ability (raw score ≤ 19). The conversion tables developed through crosswalks in this paper provide clinicians and researchers with a practical tool to: (i) compensate for ordinality in raw scores, (ii) ensure traceability to make reliable and valid comparisons when measuring person ability, and (iii) enable comparability between test results from different legacy tests. © 2023, The Author(s).

Ort, förlag, år, upplaga, sidor
Nature Research , 2023. Vol. 13, nr 1, artikel-id 5179
Nyckelord [en]
aged, Alzheimer disease, cognitive defect, disease exacerbation, human, middle aged, neuropsychological assessment, verbal learning, very elderly, Aged, 80 and over, Cognitive Dysfunction, Disease Progression, Humans, Neuropsychological Tests
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URN: urn:nbn:se:ri:diva-64302DOI: 10.1038/s41598-023-32208-0Scopus ID: 2-s2.0-85151316224OAI: oai:DiVA.org:ri-64302DiVA, id: diva2:1755450
Anmärkning

Correspondence Address: Melin, J.; RISE Research Institutes of Sweden, Sweden; email: jeanette.melin@ri.se; Funding details: European Metrology Programme for Innovation and Research, EMPIR; Funding details: Horizon 2020; Funding text 1: Part of the work was done in the 15HLT04 NeuroMET and 18HLT09 NeuroMET2 projects received funding from the EMPIR programme co-financed by the Participating States (VINNOVA, the Swedish innovation agency in the present case) and from the European Union's Horizon 2020 research and innovation programme.

Tillgänglig från: 2023-05-08 Skapad: 2023-05-08 Senast uppdaterad: 2025-09-23Bibliografiskt granskad

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