Spinal Cord Injury
Conditions
Keywords
Spinal cord injury
Brief summary
The purpose of the study is to investigate inflammatory and other substances that may be elevated in the blood and blood cells following spinal cord injury (SCI). These substances will be evaluated in samples from people who have had a spinal cord injury due to trauma (e.g. car accident or a fall) within the first week (acute) or at least one year ago (chronic). Specifically, the study will evaluate the presence and levels of a protein, macrophage migration inhibitory factor (MIF). MIF is released by cells and has a specific effect on the way cells behave, communicate and work together. In several other medical conditions, MIF is known to increase inflammation in the body. By comparing blood samples from individuals with spinal cord injury and uninjured (no spinal cord injury) individuals, the investigators will try to find out if MIF levels are increased in people with SCI. Investigators will also use these samples to measure other proteins that increase inflammation in the body and to see if the biological activities of MIF can be reduced in a test tube by adding other substances to the blood samples. It is hoped that this study of MIF and other proteins related to inflammation will help improve the treatment of SCI in the future. We hope to enroll a total of 312 subjects in this study (50 with acute spinal cord injury, 125 with chronic spinal cord injury, and 137 uninjured individuals).
Detailed description
During the study visit the investigator will collect basic biographical information and health information, including some questionnaires, from the subjects and their medical record. Acute SCI subjects will also have blood drawn once daily (First blood draw will approximately be 2 tablespoons and subsequent blood draws will approximately be 1 tablespoon) . Chronic SCI subjects will have blood drawn per study visit (approximately 2 tablespoons) and will be asked to participate in two study visits, to take place 6 months apart.
Interventions
None listed
Sponsors
Northwell Health
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
SCI Subject Inclusion Criteria: To be eligible for prospective enrollment, subjects are required to meet the following inclusion criteria: * ≥18 years of age * History SCI (acute or chronic): All American Spinal Injury Association (ASIA) classifications A-D and all levels. Healthy Control Subject Inclusion Criteria: To be eligible for prospective enrollment, healthy control subjects are required to meet the following inclusion criteria: * ≥18 years of age * The absence of any current or previous medical conditions To be eligible for prospective enrollment, SCI subjects are required to not meet the following
Exclusion criteria
* \< 18 years of age * No known SCI * Concurrent infection such as UTI * Deep pressure sores * cancer, chemotherapy or neutropenia * autoimmune disease Healthy Control Subject
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| MIF | 2 | macrophage migration inhibitory factor (MIF), a pro-inflammatory cytokine |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| inflammatory mediators | 2 | circulating inflammatory mediators |
Countries
United States
Outcome results
None listed