Genomic Translation for Amyotrophic Lateral Sclerosis Care
- Conditions
- ALS
- Registration Number
- NCT02795897
- Lead Sponsor
- Columbia University
- Brief Summary
The purpose of this study is to look for abnormal genes and gene expression profiles that help determine why a person develops amyotrophic lateral sclerosis (ALS) and related motor neuron diseases (MND) and why their symptoms present and progress with a particular pattern.
- Detailed Description
In all patients, ALS/MND is caused by the progressive death of motor neurons. However, every patient is affected differently. Some develop symptoms in their 80's while others get sick in adolescence. Swallowing/speech are affected first in some patients, but most have weakness in their hands or feet at onset. Some individuals show very rapid progression, even as others live for decades. Finally, some patients have loss of mainly motor neurons in the brain (as in primary lateral sclerosis), while others lose mainly lower motor neurons in the spinal cord and brain stem (as in progressive muscular atrophy). Research has uncovered a few genetic factors that contribute to the variability of ALS/MND. For example, mutations in the superoxide dismutase 1 (SOD1) gene makes onset in the legs more likely and decreases the chance of developing dementia. Conversely, having a mutated C9ORF72 gene makes dementia much more likely. Uncovering additional factors causing ALS variability is an important research priority and is likely to provide clues about how to better diagnose and treat the disease.
This study is called "Genomic Translation for ALS Care" (GTAC). The investigators will analyze the genome and gene expression patterns of people with ALS/MND and carry out research on that data, finding insights that the investigators hope will translate into better care for ALS/MND patients.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 254
Study participants meeting all of the following criteria will be eligible for enrollment in GTAC:
- Men or women of any race or ethnicity aged 18 or older
- Diagnosis of familial or sporadic ALS (definite, probable, or possible according to El Escorial Criteria, Appendix 1), or those with primary lateral sclerosis or progressive bulbar/muscular atrophy forms of motor neuron disease. All-comers with ALS/MND should be enrolled without regard to familial vs sporadic or gene mutation status (i.e. participants with known gene mutations should still be enrolled), or phenotype.
- Capable of providing informed consent and following study procedures (in the case that a subject lacks the ability to provide informed consent, informed consent will be sought from the subject's surrogate representative).
- Willing to return to clinic site (or another participating center) for follow-up care.
Study participants meeting any of the following criteria during screening evaluation will be excluded from enrolling in GTAC:
- Invasive ventilation (i.e. tracheostomy) in place.
- Non-invasive ventilation dependent (defined as >22 hours per day)
- Pregnancy.
- Known Human Immunodeficiency Virus (HIV) , chronic Hepatitis B, or Hepatitis C (because cells will be frozen down for future cell line generation).
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Correlation of DNA genotype with ALS phenotypes 36 months Because subjects are followed over their entire disease course and undergo whole genome sequencing of their DNA, this project will study the distinct features (progression and particular symptoms) of subjects with and without mutations in already known ALS genes.
Correlation of gene expression in blood with ALS phenotypes 36 months Because subjects are followed over their entire disease course and undergo gene expression profiling on their blood sample, this project will study the distinct features (progression and particular symptoms) of subjects with different types of gene expression profiles.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (14)
University of Minnesota
๐บ๐ธMinneapolis, Minnesota, United States
Houston Methodist Neurological Institute
๐บ๐ธHouston, Texas, United States
University of Washington
๐บ๐ธSeattle, Washington, United States
University of Utah
๐บ๐ธSalt Lake City, Utah, United States
Oregon Health & Sciences University
๐บ๐ธPortland, Oregon, United States
Univeristy of Michigan
๐บ๐ธAnn Arbor, Michigan, United States
Columbia University
๐บ๐ธNew York, New York, United States
Washington University
๐บ๐ธSaint Louis, Missouri, United States
The University of Edinburgh
๐ฌ๐งEdinburgh, United Kingdom
Cedar Sinai Medical Center
๐บ๐ธLos Angeles, California, United States
Duke University
๐บ๐ธDurham, North Carolina, United States
University of Pittsburgh Medical Center
๐บ๐ธPittsburgh, Pennsylvania, United States
Penn State College of Medicine
๐บ๐ธHershey, Pennsylvania, United States
University of Colorado School of Medicine
๐บ๐ธAurora, Colorado, United States