Acute Spinal Cord Injury, Spinal Cord Injuries
Conditions
Keywords
Spasticity, Recovery, Bio-markers
Brief summary
Spasticity is one of the most common symptoms manifested in humans with spinal cord injury (SCI). However, the neural mechanisms underlying the development of spasticity over time after an acute SCI are not yet understood. Using electrophysiological and imaging techniques along with traditional measurements of neurological recovery in the acute rehabilitation setting including physical exam and functional assessments; the investigators aim to examine the relationship between development of spasticity, residual descending motor pathways and functional and neurological recovery in humans with SCI from acute to subacute phase
Detailed description
The purpose of this study is to measure changes to motor-evoked potentials (MEPs) and to evaluate if the development of spasticity is related to residual descending motor pathways and to a better neurological recovery and functional improvement in individuals with SCI from the acute to the subacute phase. The investigators will also test for the presence of biological markers in the blood that may correlate with levels of spasticity or neurological recovery and functional improvement, including the presence or absence of neuroplastic genetic polymorphisms (e.g. BDNF Val66Met polymorphism), as well as circulating levels of neuroplastic (e.g. BDNF) or inflammatory factors (e.g. interleukins, TNF) that may affect neuronal growth and functional restoration.
Interventions
OTHERMeasures of spasticity, connectivity and analysis of single nucleotide polymorphisms and biomarkers of inflammation
We will test for presence of biological markers in blood that may correlate with levels of spasticity or neurological recovery and functional improvement, including the presence or absence of neuroplastic genetic polymorphisms (e.g. BDNF Val66Met polymorphism), as well as circulating levels of neuroplastic(e.g. BDNF) or inflammatory factors (e.g. interleukins, TNF) that may affect neuronal growth and functional restoration.
OTHERAnalysis of biomarkers
We will test for the presence of biological markers in the blood to compare the distribution of polymorphisms and biomarkers with the spinal cord injury patient population.
Sponsors
Shirley Ryan AbilityLab
Study design
Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
Individuals with SCI: Inclusion criteria: * Male and females 18 years of age or greater * Basic proficiency in English language communication * Are admitted to the Shirley Ryan AbilityLab as a spinal cord injury patient * International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI) level above L2 * American Spinal Cord Injury Association Impairment Scale (AIS) grades A, B, C, or D * Patients with SCI within the first week of inpatient admission to the Shirley Ryan AbilityLab after sustaining a SC
Exclusion criteria
* Under 18 years of age * Severe cognitive impairment that precludes the ability to participate in a comprehensive physical exam or give verbal consent * ISNCSCI level below L2 * People who have sustained SCI \>30 days * Uncontrolled medical problems including pulmonary, cardiovascular or orthopedic disease * Any debilitating disease prior to the SCI that caused exercise intolerance * Premorbid, ongoing major depression or psychosis, altered cognitive status * History of head injury or stroke * Vascular, traumatic, tumoral, infectious, or metabolic lesion of the brain, even without history of seizure, and without anticonvulsant medication * History of seizures or epilepsy * Ongoing cord compression or a syrinx in the spinal cord or people who suffer from a spinal cord disease such as spinal stenosis, spina bifida, MS, or herniated disk 13. Metal plate in skull * Individuals with scalp shrapnel, cochlear implants, or aneurysm clips * Skull fractures, skull deficits or concussion within the last 6 months * Presence of orthoses and presence of spinal precautions or healing incisions that make the area inaccessible to the testing procedures. This criterion will be applied as needed for the specific study procedures that may need to access the areas under restriction. * Formal diagnosis of Post-Traumatic Stress Disorder (PTSD) Individuals in the control group: Inclusion criteria: 1. Male and females 18 years of age or greater 2. Basic proficiency in English language communication
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| First swing test (FST) | From the time of admission to the hospital and enrolled in the study till the time of the discharge (up to 12 weeks) | We will use the pendulum test to measure muscle tone at the knee by using gravity to provoke muscle stretch reflexes during passive swinging of the lower limb. |
| Modified Ashworth scale (MAS) | From the time of admission to the hospital and enrolled in the study till the time of discharge (up to 12 weeks) | This clinical scale will be used by measuring resistance encountered during manual passive muscle stretching using a six-point ordinal scale (0=no increase in tone, 1/+1=slight increase in tone with a catch and release or minimal resistance at the end or less than half of the range of movement, respectively, 2=more marked increased tone through most of the range of movement but affected parts easily moved, 3=considerable increase in tone and passive movement difficultly, and 4=affected parts rigid) |
| Motor evoked potential (MEP) | From the time of admission to the hospital and enrolled in the study till the time of discharge (up to 12 weeks) | Transcranial magnetic stimulation will be delivered and the coil will be positioned over the vertex and moved around this point to determine the optimal position for eliciting a motor evoked potentials (MEPs) in legs muscles. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI) | From the time of admission to the hospital and enrolled in the study till the time of discharge (up to 12 weeks) | At the time of the admission, after obtaining consent, and at the time of discharge, the chart will be reviewed to obtain the ISNCSCI score |
| Circulating biomarkers of inflammation and neuroplasticity | From the time of admission to the hospital and enrolled in the study till the time of discharge (up to 12 weeks) | In this study, we will focus on tracking expression of key inflammatory cytokines that have been shown to play a pivotal role in activating the major nuclear factor kappa-B (NF-κB) inflammatory pathway. Specifically, we will characterize serum levels of pro-inflammatory cytokines interleukin-1 beta (IL-1β), interleukin-6 (IL-6), tumor necrosis factor (TNF-α) and anti-inflammatory marker interleukin-10 (IL-10). We will also measure levels of circulating neuroplasticity marker Brain-derived neurotrophic factor (BDNF) |
Countries
United States
Outcome results
None listed