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| Name | Class |
|---|---|
| New York University | OTHER |
| Massachusetts General Hospital | OTHER |
| State University of New York at Buffalo | OTHER |
| University of Alabama at Birmingham |
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The purpose of this study is to better understand multiple sclerosis (MS) in children and adolescents, to learn if it differs from adult MS and to investigate if genes or environmental exposures or a combination of both put children and adolescents at risk for getting MS.
The overall goal of this project is to determine whether well-established environmental and genetic risk factors for adult onset MS play an important role in susceptibility to pediatric-onset MS. Our study design is based on the hypothesis that genetic influences, specifically variation at HLA-DRB1 and other confirmed non-MHC MS loci, as well as environmental exposures including EBV infection and tobacco smoke, contribute to disease risk. In addition, we will also examine the relationship between serum levels of 25(OH) vitamin D3 and prior vitamin D status, and risk for pediatric onset MS. Finally, we will investigate whether specific G x E, and other multivariable relationships influencing risk exist for pediatric-onset MS. There are 16 collaborating sites other than UCSF that will enroll cases and controls for this study.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Pediatric MS Case | Demographic and Medical History Questionnaire, Environmental Exposure Questionnaire, Food Frequency Questionnaire, Blood Sample Collection | ||
| Pediatric Control | Demographic and Medical History Questionnaire, Environmental Exposure Questionnaire, Food Frequency Questionnaire, Blood Sample Collection |
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| Measure | Description | Time Frame |
|---|---|---|
| Identify risk factors and their respective contribution to developing pediatric multiple sclerosis | The primary objective of this study is to determine if risk factors identified for adult MS such as HLA-DRB1*1501/1503, EBV, 25(OH) vitamin D3 insufficiency, and exposure to cigarette smoking are also risk factors for pediatric MS, and if there are interactions between them analyzing data collected from questionnaires for environmental exposure, demographic and food frequency as well as sample blood specimens. | 4 year data collection, 1 year analysis |
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Children are eligible for this study as cases if:
They have MS or clinically isolated syndrome (CIS):
They are three years of age or older; AND
Disease onset occurred before 18 years of age.
Patients are not eligible for study participation if:
Children are not eligible to participate as pediatric controls if:
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Case patients seen at the 16 participating Pediatric MS Center Clinics. Control patients seen at the Pediatric Clinics of the same institution as MS cases.
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| Name | Affiliation | Role |
|---|---|---|
| Emmanuelle L Waubant, MD, PhD | University of California, San Francisco | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Center for pediatric-onset demyelinating diseases at the Children's Hospital of Alabama, Birmingham | Birmingham | Alabama | 35294 | United States |
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| OTHER |
| Mayo Clinic | OTHER |
| Children's Hospital of Philadelphia | OTHER |
| Boston Children's Hospital | OTHER |
| Baylor College of Medicine | OTHER |
| Loma Linda University | OTHER |
| Children's Hospital Colorado | OTHER |
| University of Texas | OTHER |
| Ann & Robert H Lurie Children's Hospital of Chicago | OTHER |
| Washington University School of Medicine | OTHER |
| Children's National Research Institute | OTHER |
| Primary Children's Hospital | OTHER |
| The Cleveland Clinic | OTHER |
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Total 41ml sample: 17ml plasma/DNA, 10ml serum, 9ml lymphocytes and 5ml RNA frozen.
| Pediatric MS Clinic, Children's Hospital, Loma Linda University | San Bernardino | California | 92408 | United States |
| UCSF Pediatric MS Center | San Francisco | California | 94143 | United States |
| Children's Hospital Colorado, University of Colorado School of Medicine | Aurora | Colorado | 80045 | United States |
| Pediatric MS Clinic, Children's National Medical Center | Washington D.C. | District of Columbia | 20010 | United States |
| Pediatric MS Clinic, Ann & Robert H. Lurie Children's Hospital of Chicago | Chicago | Illinois | 60611 | United States |
| Partners Pediatric MS Center at the Massachusetts General Hospital for Children | Boston | Massachusetts | 02114 | United States |
| Pediatric MS Clinic, Children's Hospital Boston | Boston | Massachusetts | 02115 | United States |
| Regional Pediatric MS Center at Mayo Clinic | Rochester | Minnesota | 55905 | United States |
| Pediatric MS Clinic, Washington University School of Medicine | St Louis | Missouri | 63110 | United States |
| Pediatric MS Center of the Jacobs Neurological Institute, University of Buffalo | Buffalo | New York | 14203 | United States |
| New York University Langone Medical Center | New York | New York | 10016 | United States |
| The Cleveland Clinic | Cleveland | Ohio | 44195 | United States |
| Pediatric MS Clinic, Children's Hospital of Philadelphia | Philadelphia | Pennsylvania | 19104 | United States |
| Pediatric MS Center, University of Texas, Southwestern Medical Center | Dallas | Texas | 75390 | United States |
| The Blue Bird Circle Clinic for MS at Texas Children's Hospital | Houston | Texas | 77030 | United States |
| Pediatric Neurology Clinic, Primary Children's Hospital | Salt Lake City | Utah | 84113 | United States |
| ID | Term |
|---|---|
| D020529 | Multiple Sclerosis, Relapsing-Remitting |
| D003711 | Demyelinating Diseases |
| ID | Term |
|---|---|
| D009103 | Multiple Sclerosis |
| D020278 | Demyelinating Autoimmune Diseases, CNS |
| D020274 | Autoimmune Diseases of the Nervous System |
| D009422 | Nervous System Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |
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