Phenotype, Genotype & Biomarkers in ALS and Related Disorders
- Conditions
- Multisystem ProteinopathyAmyotrophic Lateral SclerosisFrontotemporal DementiaProgressive Muscular AtrophyPrimary Lateral SclerosisHereditary Spastic Paraplegia
- Registration Number
- NCT02327845
- Lead Sponsor
- University of Miami
- Brief Summary
The goals of this study are: (1) to better understand the relationship between the phenotype and genotype of amyotrophic lateral sclerosis (ALS) and related diseases, including primary lateral sclerosis (PLS), hereditary spastic paraplegia (HSP), progressive muscular atrophy (PMA), and frontotemporal dementia (FTD); and (2) to develop biomarkers that might be useful in aiding therapy development for this group of disorders.
- Detailed Description
This study will recruit patients with ALS, ALS-FTD, PLS, HSP, and PMA, with a focus on incident cases. Patients with both familial and sporadic forms of these diseases will be enrolled and followed longitudinally using a standardized set of evaluations. Biological samples (blood, urine, CSF) will be collected from all study participants, and will be used for biomarker discovery and validation. Family members of affected individuals may also be enrolled and asked to contribute DNA and biological samples to aid genetic and biomarker discovery.
Recruitment & Eligibility
- Status
- ENROLLING_BY_INVITATION
- Sex
- All
- Target Recruitment
- 700
-
Member of at least one of the following categories:
- Individuals with a clinical diagnosis of ALS or a related disorder, including FTD, HSP, PLS, PMA and MSP (sporadic or familial).
- Family member of an enrolled affected individual.
-
Able and willing to comply with relevant procedures.
- Affected with end or late stage disease.
- A condition or situation which, in the PI's opinion, could confound the study finding or may interfere significantly with the individual's participation and compliance with the study protocol. This includes (but is not limited to) neurological, psychological and/or medical conditions.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Genetic determinants of phenotype 24 months By combining longitudinally collected deep phenotypic data with deep genetic data (e.g. whole exome or whole genome sequencing), this project aims to define genetic variants that are associated with identifiable phenotypic features in patients with ALS and related disorders.
Phenotypic correlates of genotype 24 months Using longitudinally collected deep phenotypic data, this project aims to define the natural history (i.e. temporal rate of disease progression) of the motor and frontotemporal system (behavior, cognition and language) phenotypes of ALS and related disorders in patients with identifiable genetic mutations.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (15)
Twin Cities ALS Research Consortium
๐บ๐ธMinneapolis, Minnesota, United States
Cleveland Clinic
๐บ๐ธCleveland, Ohio, United States
University of Texas Southwestern (UTSW)
๐บ๐ธDallas, Texas, United States
University of Texas Health Science Center San Antonio (UTHSCSA)
๐บ๐ธSan Antonio, Texas, United States
University of California San Diego (UCSD)
๐บ๐ธSan Diego, California, United States
California Pacific Medical Center (CPMC)
๐บ๐ธSan Francisco, California, United States
University of Virginia (UVA)
๐บ๐ธCharlottesville, Virginia, United States
University of Miami
๐บ๐ธMiami, Florida, United States
University of Iowa
๐บ๐ธIowa City, Iowa, United States
University of Pennsylvania
๐บ๐ธPhiladelphia, Pennsylvania, United States
Kansas University Medical Center (KUMC)
๐บ๐ธKansas City, Kansas, United States
Stanford University
๐บ๐ธPalo Alto, California, United States
University of Cape Town
๐ฟ๐ฆCape Town, South Africa
Wake Forest University
๐บ๐ธWinston-Salem, North Carolina, United States
Eberhard Karls University of Tรผbingen
๐ฉ๐ชTรผbingen, Germany