4.5 Article

Poor Corticospinal Motor Neuron Health Is Associated with Increased Symptom Severity in the Acute Phase Following Repetitive Mild TBI and Predicts Early ALS Onset in Genetically Predisposed Rodents

Journal

BRAIN SCIENCES
Volume 11, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/brainsci11020160

Keywords

amyotrophic lateral sclerosis; traumatic brain injury; concussion; corticospinal motor neurons; chronic traumatic encephalopathy

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Funding

  1. ALS Finding a Cure(R), a program of The Leandro P. Rizzuto Foundation

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Traumatic brain injury (TBI) has been linked to earlier disease onset and shortened survival in a genetically predisposed ALS population, with poor health of corticospinal motor neurons playing a key role in predicting disease outcome.
Traumatic brain injury (TBI) is a well-established risk factor for several neurodegenerative disorders including Alzheimer's disease and Parkinson's disease, however, a link between TBI and amyotrophic lateral sclerosis (ALS) has not been clearly elucidated. Using the SOD1(G93A) rat model known to recapitulate the human ALS condition, we found that exposure to mild, repetitive TBI lead ALS rats to experience earlier disease onset and shortened survival relative to their sham counterparts. Importantly, increased severity of early injury symptoms prior to the onset of ALS disease symptoms was linked to poor health of corticospinal motor neurons and predicted worsened outcome later in life. Whereas ALS rats with only mild behavioral injury deficits exhibited no observable changes in corticospinal motor neuron health and did not present with early onset or shortened survival, those with more severe injury-related deficits exhibited alterations in corticospinal motor neuron health and presented with significantly earlier onset and shortened lifespan. While these studies do not imply that TBI causes ALS, we provide experimental evidence that head injury is a risk factor for earlier disease onset in a genetically predisposed ALS population and is associated with poor health of corticospinal motor neurons.

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