LOWER EXTREMITY MOTOR FUNCTION IN CHRONIC SPINAL CORD INJURY AFTER EXPOSURE TO IBUPROFEN & INTERMITTENT HYPOXIA A RANDOMIZED TRIAL Meaghan Lynch, MD; Sudarshan Srivatsan, BS; Kelly Deatsch, DPT; Lynsey Duffell, PhD; Allison Kessler, MD; Arun Jayaraman, PhD, PT; William Zev Rymer, MD, PhD AAP&MR November 2014
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LOWER EXTREMITY MOTOR FUNCTION IN CHRONIC SPINAL CORD INJURY AFTER EXPOSURE TO IBUPROFEN & INTERMITTENT HYPOXIA A RANDOMIZED TRIAL Meaghan Lynch, MD; Sudarshan.
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LOWER EXTREMITY MOTOR FUNCTION IN CHRONIC SPINAL CORD INJURY AFTER EXPOSURE TO IBUPROFEN & INTERMITTENT HYPOXIAA RANDOMIZED TRIAL
Replicates ability of AIH to enhance motor output in chronic incomplete SCI
No differential effect with pre-treatment of single dose of ibuprofen 800mg
Length of study limited, perhaps difference seen if outcome measures repeated later
DISCUSSION continued
Change in inflammatory cytokine level unknown
Future directions: • Alternative ibuprofen dosing or corticosteroids to better
reduce inflammatory inhibitory pathway• SSRIs to target neuroexcitatory pathway
Long term consequences/safety of AIH
CONCLUSION
AIH holds promise in promoting plasticity and motor output in spared neural pathways.
AIH enhances lower extremity strength in individuals with chronic SCI, but is not affected by single dose of ibuprofen 800mg.
REFERENCES 1 Devivo MJ. Epidemiology of traumatic spinal cord injury: trends and implications. Spine Cord 2012;50:365-372. 2 Shin JC, et al. Epidemiology change of patients with spinal cord injury. Ann Rehabil Med 2013;37:50-56. 3 Golder FJ, Mitchell GS. Spinal synaptic enhancement with acute intermittent hypoxia improves respiratory function after
chronic cervical spinal cord injury. J Neurosci 2005;25:2925-2932. 4 Fuller DD et al. Synaptic pathways to phrenic motoneurons are enhanced by chronic intermittent hypoxia after cervical
spinal cord injury. J Neurosci 2003;23:2993-3000. 5 LovetteBarr MR, et al. Repetitive intermittent hypoxia induces respiratory and somatic motor recovery after chronic
cervical spinal cord injury. J Neurosci 2012;32:3591-3600. 6 Trumbower RD, et al. Exposure to acute intermittent hpyoxia augments somatic motor function in humans with
incomplete spinal cord injury. Neurorehabil Neural Repair 2012;26:163-172. 7 Hayes HB, et al. Daily intermittent hpyoxia enhances walking after chronic spinal cord injury: a randomized trial.
Neurology 2014;82:1-10. 8 Baker-Herman TL, Mitchell GS. Phrenic long-term facilitation requires spinal serotonin receptor activation and protein
synthesis. J Neurosci 2002;22:6239-6246.. 9 Kinkead R, et al. Plasticity in respiratory motor control: intermittent hypoxia and hypercapnia activate opposing
serotonergiv and noradreniergic modulatory systems. Comp Biochem Physiol A Mol Integr Physiol 2001;130:207-218. 10 Huxtable AG, et al. Systemic LPS induces spinal inflammatory gene expression and impairs phrenic long-term
facilitation following acute intermittent hypoxia. J Appl Physiol 2013;114:879-887. 11 Wang TD, et al. Circulating levels of markers of inflammation and endothelial activation are increased in men with
chronic spinal cord injury. J Formos Med Assoc 2007;106:919-928. 12 Silva Alves E, et al. Low grade inflammation and spinal cord injury: exercise as therapy? Mediators Inflamm.
2013;2013:971841. 13 Morse LR, at al. Association between mobility mode and C-reactive protein levels in men with chronic spinal cord injury.
Arch Phys Med Rehabil 2008;89:726-31. 414 14 Powell, F. Mini review: Physiological effects of intermittent hypoxia. High Altitude Medicine & Biology. 2000; 1(2): 125-
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132.
QUESTIONS
RESULTS: HEMODYNAMICS
WHAT IS ACUTE INTERMITTENT HYPOXIA (AIH)?
AIH restores breathing capacity in rats with high cervical spinal hemisection3
Strengthening of phrenic nerve synapses via long-term potentiation4
Similar findings seen in non-respiratory somatic motor nuclei5
In humans with chronic incomplete SCI, when compared to sham normoxia breathing treatment, AIH: Promotes lower extremity motor output as assessed by
ankle plantar flexion torque6
Improves walking speed and endurance when combined with PT7
WHY IBUPROFEN?
In rats: CNS inflammation & cytokine release impairs AIH-
induced phrenic nerve long-term potentiation10
Pre-treatment with the NSAID ketoprofen restores this long-term potentiation10
Systemic administration of ibuprofen enhances neuroplasticity and locomotor recovery following spinal contusion via RhoA inhibitory pathways16
Effects of non-ibuprofen NSAIDs not as robust16
In humans with chronic SCI: Low-grade inflammation exists in the absence of active
infection or wounds11-13
ADDITIONAL DISCUSSION POINTS
Individuals with incomplete SCI likely recruit muscles in different patterns in order to produce resultant torque
No sham breathing treatment
Study intended to be a pilot to investigate the effects of ibuprofen, not a proof-of-concept study for AIH
Imperative that AIH protocols be chosen above the threshold to elicit neuroplasticity, but below threshold for serious morbidity