Validation of Biomarkers in Amyotrophic Lateral Sclerosis (ALS)



Status:Completed
Conditions:Neurology
Therapuetic Areas:Neurology
Healthy:No
Age Range:30 - 80
Updated:6/4/2016
Start Date:April 2008
End Date:November 2015

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A Multicenter Study for the Validation of ALS Biomarkers

The purpose of this study is to collect 650 blood and 300 cerebrospinal fluid (CSF) samples
from people with amyotrophic lateral sclerosis (ALS), pure lower or upper motor neuron
diseases, as well as other neurodegenerative diseases and from people with no neurological
disorder. Through comparison of these samples, the researchers hope to learn more about the
underlying cause of ALS, as well as find unique biological markers, which could be used to
diagnose ALS and monitor disease progression.

Additionally, up to 600 blood samples will be collected for a sub-study for DNA analysis.
Studying components of the blood, such as DNA, may help us understand what happens when
genes function abnormally and how it might be related to disease.

Researchers tested what changes happen in volunteers with ALS that can be seen in the blood
and what changes are unique to ALS and are different from those found in healthy volunteers
and volunteers with neurological diseases other than ALS. These changes are called
biomarkers. Biomarkers for ALS have been found in blood collected in earlier phases of this
study. Biomarkers are non-genetic elements in your blood that may help to make diagnosing
ALS easier. In the next phase, comparison of these changes in the blood of volunteers with
ALS and without ALS will be used to confirm these biomarkers and to develop a tool to
diagnose and monitor progression of ALS.

1. ALS Volunteers

Inclusion Criteria:

- Diagnosis of possible (excluding volunteers with UMN signs ONLY), probable,
probable-laboratory supported, or definite ALS, either sporadic or familial
according to revised El Escorial criteria

- Disease duration of less than or equal to two years from symptom onset

- Age 30-80 years at the time of disease onset

- Ability to provide informed consent

- Ability to comply with study procedures

- Medically safe to have lumbar puncture (lumbar puncture volunteers only)

Exclusion Criteria:

- Clinical evidence of chronic liver or renal failure

- Presence of a bleeding disorder, problems with CSF pressure, allergy to local
anesthetics, or a topical or other skin infection at the LP site (lumbar
puncture volunteers only)

- Use of any anti-platelet or anticoagulant drugs, such as plavix, aggrenox,
ticlid, warfarin or coumadin (lumbar puncture volunteers only)

2. Suspected ALS (PMND) Volunteers

Inclusion Criteria:

- Diagnosis of suspected ALS defined as presence of UMN or LMN signs alone and the
diagnosis of Clinically Probably Laboratory-Supported ALS CANNOT be proven by
evidence in clinical grounds in conjunction with electrodiagnostic,
neurophysiologic, neuroimaging or clinically laboratory studies

- Disease duration of less than or equal to four years from symptom onset

- Age 30-80 years at time of disease onset

- Ability to provide informed consent

- Ability to comply with study procedures

- Medically safe to have lumbar puncture (lumbar puncture volunteers only)

Exclusion Criteria:

- Clinical evidence of chronic liver or renal failure

- Genetically confirmed diagnosis of hereditary spastic paraparesis or spinal
motor atrophy (SMA) disease

- Presence of a bleeding disorder, problems with CSF pressure, allergy to local
anesthetics, or a topical or other skin infection at the LP site (lumbar
puncture volunteers only)

- Use of any anti-platelet or anticoagulant drugs, such as plavix, aggrenox,
ticlid, warfarin or coumadin (lumbar puncture volunteers only)

3. Neurological Disease Mimic Volunteers

Inclusion Criteria:

Diagnosis of one of the following:

Pure Lower Motor Neuron Disease (LMND) mimics:

- Multi-focal motor neuropathy

- Autoimmune motor neuropathy

- Cervical or lumbosacral radiculopathies

Peripheral mononeuropathies:

- Ulnar neuropathy

- Carpal tunnel syndrome/median neuropathy

- Peroneal neuropathy

- Sciatic neuropathy

- Spinal muscular atrophy

- Spinobulbar muscular atrophy (Kennedy's disease)

- Charcot Marie-Tooth Disease (CMT)

Pure Upper Motor Neuron Disease (UMND) mimics:

- Cervical myelopathy

- Multiple sclerosis

- Hereditary spastic paraparesis

- Age 30-80 years

- Ability to provide informed consent

- Ability to comply with study procedures

- Medically safe to have lumbar puncture (lumbar puncture volunteers only)

Exclusion Criteria:

- Diagnosis of suspected, possible, probable or definite ALS either sporadic or
familial

- Presence of positive family history of ALS

- Clinical evidence of chronic renal or liver failure

- Presence of a bleeding disorder, problems with CSF pressure, allergy to local
anesthetics, or a topical or other skin infection at the LP site (lumbar
puncture volunteers only)

- Use of any anti-platelet or anticoagulant drugs, such as plavix, aggrenox,
ticlid, warfarin or coumadin (lumbar puncture volunteers only)

4. Healthy Control Volunteers Inclusion Criteria

- Absence of a known neurological disorder.

- Age 30 - 80 years.

- Ability to provide informed consent.

- Ability to comply with study procedures.

- Medically safe to have lumbar puncture.

Exclusion Criteria:

- History of ALS, myopathy, neuropathy, ALS mimic disorder or other neurodegenerative
disease.

- Presence of positive family history of ALS.

- Clinical evidence of chronic liver or renal failure.

- Presence of bleeding disorder, problems with CSF pressure, allergy to local
anesthetics, or a topical or other skin infection at the LP site (LP research
volunteers only).

- Research participant must not be taking anti-platelet or anticoagulant drugs, such as
plavix, aggrenox, ticlid, warfarin or coumadin (LP research volunteers only).
We found this trial at
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Hershey, Pennsylvania 17033
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201 Dowman Dr
Atlanta, Georgia 30303
(404) 727-6123
Emory University Emory University, recognized internationally for its outstanding liberal artscolleges, graduate and professional schools,...
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3400 N Charles St
Baltimore, Maryland 21205
410-516-8000
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185 Cambridge Street
Boston, Massachusetts 02114
617-724-5200
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5801 South Ellis Avenue
Chicago, Illinois 60637
 773.702.1234
University of Chicago One of the world's premier academic and research institutions, the University of...
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Jacksonville, Florida 32224
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Miami, Florida 33124
(305) 284-2211
University of Miami A private research university with more than 15,000 students from around the...
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5090 N 40th St # 250
Phoenix, Arizona 85018
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4200 Fifth Ave
Pittsburgh, Pennsylvania 15260
(412) 624-4141
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3181 Southwest Sam Jackson Park Road
Portland, Oregon 97239
503 494-8311
Oregon Health and Science University In 1887, the inaugural class of the University of Oregon...
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201 Presidents Circle
Salt Lake City, Utah 84108
801) 581-7200
University of Utah Research is a major component in the life of the U benefiting...
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Albany, New York 12205
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41 Mall Road
Burlington, Massachusetts 1805
781-744-5100
Lahey Clinic When Frank Lahey, MD, founded a group practice in 1923, his vision was...
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Charlotte, North Carolina 28207
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Columbus, Ohio 43210
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2301 Erwin Rd
Durham, North Carolina 27710
919-684-8111
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Grand Rapids, Michigan 49503
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Houston, Texas 77030
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1 Medical Center Dr
Lebanon, New Hampshire 03756
 (603) 650-5000
Dartmouth Hitchcock Medical Center Dartmouth-Hitchcock is a national leader in patient-centered health care and building...
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Minneapolis, Minnesota 55414
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New Brunswick, New Jersey 08901
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New York, New York 10003
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Orange, California 92868
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2900 W Queen Ln
Philadelphia, Pennsylvania 19129
(215) 991-8100
Drexel University College of Medicine Drexel University College of Medicine represents the consolidation of two...
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Portland, Oregon 97213
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Saint Louis, Missouri 63110
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Saint Louis, Missouri 63110
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750 East Adams Street
Syracuse, New York 13210
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Winston-Salem, North Carolina 27157
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