Principal Investigators

    SCHERZER, CLEMENS R

    Institution

    BRIGHAM AND WOMEN'S HOSPITAL

    Contact information of lead PI

    Country

    USA

    Title of project or programme

    Parkinson Disease: Predicting the Future

    Source of funding information

    NIH (NINDS)

    Total sum awarded (Euro)

    € 1,949,386.24

    Start date of award

    30/09/2016

    Total duration of award in years

    3

    The project/programme is most relevant to:

    Parkinson's disease & PD-related disorders

    Keywords

    Research Abstract

    Parkinson’s Disease: Predicting the Future It is poorly understood why some patients with Parkinson’s have an aggressive disease course. The pace of progression varies considerably, ranging from a manageable functional decline to an accelerated course that leaves patients rapidly wheelchair bound or with dementia. This is a source of anguish for patients and caregivers. In clinical trials, this variation obfuscates drug effects. Many genetic variants have been linked to susceptibility, but the genes modulating disease progression have not been well established. Our initial studies indicate multiple coding and noncoding variants predictive of a hyper-accelerated motor or memory decline. We hypothesize that genetic variants will powerfully predict the progression of Parkinson’s. We will directly address this question through high coverage, massively parallel, targeted sequencing of ten cohorts from North America and Europe that were longitudinal characterized with exceptional granularity over the course of up to twelve years. 3,939 patients with Parkinson’s disease and over thirty thousand clinical assessments will be analyzed using Cox and mixed random and fixed effect models. In Aim 1, we will identify genetic variants in susceptibility loci and familial genes that predict cognitive or motor progression. Furthermore, novel putative progression loci emerging from our exome-scale search will be evaluated. In Aim 2, we will replicate and verify forwarded genetic variants in independent populations. This study will establish the first progression genes for Parkinson’s disease, clarify prognosis, and shift the way we design clinical trials. Rare variants that disrupt protein function will inform on the underlying mechanism and reveal clues for therapies. More generally, these data will contribute towards a precision medicine poised to transform healthcare.

    Lay Summary

    The progression of Parkinson’s disease varies considerably between individuals, ranging from a manageable functional decline to an aggressive course that leaves patients rapidly wheelchair bound or with dementia. This variation is a major source of noise and inefficiency in therapeutic trials. Predictors of progression are needed to overcome this roadblock. This study will establish the first progression genes for Parkinson’s disease and shift the way we design clinical trials.

    Further information available at:

Types: Investments > €500k
Member States: United States of America
Diseases: Parkinson's disease & PD-related disorders
Years: 2016
Database Categories: N/A
Database Tags: N/A

Export as PDF