Advanced brain ageing in Parkinson’s disease is related to disease duration and individual impairment

Author:

Eickhoff Claudia R12,Hoffstaedter Felix13,Caspers Julian4,Reetz Kathrin15ORCID,Mathys Christian6,Dogan Imis15,Amunts Katrin12,Schnitzler Alfons2,Eickhoff Simon B13ORCID

Affiliation:

1. Institute of Neuroscience and Medicine (INM-1, INM-7, INM-11), Jülich, Germany

2. Institute of Clinical Neuroscience and Medical Psychology, Medical Faculty, Heinrich-Heine University Düsseldorf, Düsseldorf, Germany

3. Institute of Systems Neuroscience, Medical Faculty, Heinrich-Heine University Düsseldorf, Düsseldorf, Germany

4. Institute of Diagnostic and Interventional Radiology, Medical Faculty, Heinrich-Heine University Düsseldorf, Düsseldorf, Germany

5. Department of Neurology, University Hospital RWTH Aachen, Aachen, Germany

6. Evangelisches Krankenhaus Oldenburg, Oldenburg, Germany

Abstract

Abstract Machine learning can reliably predict individual age from MRI data, revealing that patients with neurodegenerative disorders show an elevated biological age. A surprising gap in the literature, however, pertains to Parkinson’s disease. Here, we evaluate brain age in two cohorts of Parkinson’s patients and investigated the relationship between individual brain age and clinical characteristics. We assessed 372 patients with idiopathic Parkinson’s disease, newly diagnosed cases from the Parkinson’s Progression Marker Initiative database and a more chronic local sample, as well as age- and sex-matched healthy controls. Following morphometric preprocessing and atlas-based compression, individual brain age was predicted using a multivariate machine learning model trained on an independent, multi-site reference sample. Across cohorts, healthy controls were well predicted with a mean error of 4.4 years. In turn, Parkinson’s patients showed a significant (controlling for age, gender and site) increase in brain age of ∼3 years. While this effect was already present in the newly diagnosed sample, advanced biological age was significantly related to disease duration as well as worse cognitive and motor impairment. While biological age is increased in patients with Parkinson’s disease, the effect is at the lower end of what is found for other neurological and psychiatric disorders. We argue that this may reflect a heterochronicity between forebrain atrophy and small but behaviourally salient midbrain pathology. Finally, we point to the need to disentangle physiological ageing trajectories, lifestyle effects and core pathological changes.

Funder

Deutsche Forschungsgemeinschaft

Helmholtz Portfolio Theme ‘Supercomputing and Modeling for the Human Brain’

European Union’s Horizon 2020 Research and Innovation Programme

Publisher

Oxford University Press (OUP)

Subject

General Earth and Planetary Sciences,General Environmental Science

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