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The Ontario Neurodegenerative Disease Research Initiative

Sunderland, K. M.; Beaton, D.; Arnott, S. R.; Kleinstiver, P.; Kwan, D.; Lawrence-Dewar, J. M.; Ramirez, J.; Tan, B.; Bartha, R.; Black, S. E.; Borrie, M.; Brien, D.; Casaubon, L. K.; Coe, B.; Cornish, B.; Dilliott, A. A.; Dowlatshahi, D.; Finger, E.; Fischer, C.; Frank, A.; Fraser, J.; Freedman, M.; Greenberg, B.; Grimes, D. A.; Hassan, A.; Hatch, W.; Hegele, R. A.; Hudson, C.; Jog, M.; Kumar, S.; Lang, A.; Levine, B.; Lou, W.; Mandzia, J.; Marras, C.; McIlroy, W.; Montero-Odasso, M.; Munoz, D. G.; Munoz, D. P.; Orange, J. B.; Park, D. S.; Pasternak, S. H.; Pieruccini-Faria, F.; Rajji, T. K.;

2020-08-02 neurology
10.1101/2020.07.30.20165456 medRxiv
Show abstract

ObjectiveIn individuals over the age of 65, concomitant neurodegenerative pathologies contribute to cognitive and/or motor decline and can be aggravated by cerebrovascular disease, but our understanding of how these pathologies synergize to produce the decline represents an important knowledge gap. The Ontario Neurodegenerative Disease Research Initiative (ONDRI), a multi-site, longitudinal, observational cohort study, recruited participants across multiple prevalent neurodegenerative diseases and cerebrovascular disease, collecting a wide array of data and thus allowing for deep investigation into common and unique phenotypes. This paper describes baseline features of the ONDRI cohort, understanding of which is essential when conducting analyses or interpreting results. MethodsFive disease cohorts were recruited: Alzheimers disease/amnestic mild cognitive impairment (AD/MCI), amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), Parkinsons disease (PD), and cerebrovascular disease (CVD). Assessment platforms included clinical, neuropsychology, eye tracking, gait and balance, neuroimaging, retinal imaging, genomics, and pathology. We describe recruitment, data collection, and data curation protocols, and provide a summary of ONDRI baseline characteristics. Results520 participants were enrolled. Most participants were in the early stages of disease progression. Participants had a median age of 69 years, a median Montreal Cognitive Assessment score of 25, a median percent of independence of 100 for basic activities of daily living, and a median of 93 for instrumental activities. Variation between disease cohorts existed for age, level of cognition, and geographic location. ConclusionONDRI data will enable exploration into unique and shared pathological mechanisms contributing to cognitive and motor decline across the spectrum of neurodegenerative diseases.

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