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Pieter Jelle Visser

Publications and source records attributed to Pieter Jelle Visser.

2 recordsLinked to original sources

MRI-based and metabolomics-based age scores act synergetically for mortality prediction shown by multi-cohort federated learning

Biological age scores are an emerging tool to characterize aging by estimating chronological age based on physiological biomarkers. Various scores have shown associations with aging-related outcomes. This study assessed the relation between an age score based on brain MRI images (BrainAge) and an age score based on metabolomic biomarkers (MetaboAge). We trained a federated deep learning model to estimate BrainAge in three cohorts. The federated BrainAge model yielded significantly lower error for age prediction across the cohorts than locally trained models. Harmonizing the age interval between cohorts further improved BrainAge accuracy. Subsequently, we compared BrainAge with MetaboAge using federated association and survival analyses. The results showed a small association between BrainAge and MetaboAge as well as a higher predictive value for the time to mortality of both scores combined than for the individual scores. Hence, our study suggests that both aging scores capture different aspects of the aging process.

q-bio.QM↗

Detecting functional decline from normal ageing to dementia: development and validation of a short version of the Amsterdam IADL Questionnaire

INTRODUCTION: Detecting functional decline from normal ageing to dementia is relevant for diagnostic and prognostic purposes. Therefore, the Amsterdam IADL Questionnaire (A-IADL-Q) was developed: a 70-item proxy-based tool with good psychometric properties. We aimed to design a short version whilst preserving its psychometric quality. METHODS: Study partners of subjects (n=1355), ranging from cognitively normal to dementia subjects, completed the original A-IADL-Q. We selected the short version items using a stepwise procedure combining missing data, Item Response Theory and input from respondents and experts. We investigated internal consistency of the short version as well as concordance with the original version. To assess its construct validity, we additionally investigated concordance between the short version and the Mini-Mental State Examination (MMSE) and Disability Assessment for Dementia (DAD). Lastly, we investigated differences in IADL scores between diagnostic groups across the dementia spectrum. RESULTS: We selected 30 items covering the entire spectrum of IADL functioning. Internal consistency (.98) and concordance with the original version (.97) were very high. Concordance with the MMSE (.72) and DAD (.87) scores was high. IADL impairment scores increased across the spectrum from normal cognition to dementia. DISCUSSION: The A-IADL-Q Short Version (A-IADL-Q-SV) consists of 30 items. The A-IADL-Q-SV has maintained the psychometric quality of the original A-IADL-Q. As such, it is a concise measure of functional decline.

q-bio.NC↗