Disease progression strikingly differs in research and real-world Parkinson’s populations

Characterization of Parkinson’s disease (PD) progression using real-world evidence could guide clinical trial design and identify subpopulations. Efforts to curate research populations, the increasing availability of real-world data, and advances in natural language processing, particularly large la...

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Veröffentlicht in:NPJ Parkinson's Disease 2024-03, Vol.10 (1), p.58-58, Article 58
Hauptverfasser: Beaulieu-Jones, Brett K., Frau, Francesca, Bozzi, Sylvie, Chandross, Karen J., Peterschmitt, M. Judith, Cohen, Caroline, Coulovrat, Catherine, Kumar, Dinesh, Kruger, Mark J., Lipnick, Scott L., Fitzsimmons, Lane, Kohane, Isaac S., Scherzer, Clemens R.
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Sprache:eng
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Zusammenfassung:Characterization of Parkinson’s disease (PD) progression using real-world evidence could guide clinical trial design and identify subpopulations. Efforts to curate research populations, the increasing availability of real-world data, and advances in natural language processing, particularly large language models, allow for a more granular comparison of populations than previously possible. This study includes two research populations and two real-world data-derived (RWD) populations. The research populations are the Harvard Biomarkers Study (HBS, N  = 935), a longitudinal biomarkers cohort study with in-person structured study visits; and Fox Insights ( N  = 36,660), an online self-survey-based research study of the Michael J. Fox Foundation. Real-world cohorts are the Optum Integrated Claims-electronic health records ( N  = 157,475), representing wide-scale linked medical and claims data and de-identified data from Mass General Brigham (MGB, N  = 22,949), an academic hospital system. Structured, de-identified electronic health records data at MGB are supplemented using a manually validated natural language processing with a large language model to extract measurements of PD progression. Motor and cognitive progression scores change more rapidly in MGB than HBS (median survival until H&Y 3: 5.6 years vs. >10, p  
ISSN:2373-8057
2373-8057
DOI:10.1038/s41531-024-00667-5