1. Chronic traumatic encephalopathy in American Football: The State of the Science
John F. Crary, MD-PhD
Associate Professor
Lillian and Henry M. Stratton-Hans Popper Department of Pathology
Fishberg Department of Neuroscience
Friedman Brain Institute
Ronald M. Loeb Center for Alzheimer’s Disease
Icahn School of Medicine at Mount Sinai
Wednesday, April 18th, 2018

2. “The scientific evidence linking youth casual sports play to brain injury, brain injury to CTE, and CTE to dementia is not strong.

3. In a sample of 202 deceased players of American football from a brain donation program, CTE was neuropathologically diagnosed in 177 players across all levels of play (87%)
Level of play
CTE positive
(Percent)
Professional
110 of 111
99%
College football
48 of 53
91%
High school football
3 of 14
21%

4. >1,700 brains, CTE in 21/66 contact sport athletes (32%)
0/165 with CTE in controls without brain trauma or contact sports
0/33 brains with CTE with a single TBI
Strong evidence linking contact sports to CTE
Exposure
CTE Present
CTE Absent
Total
Contact Sports 21 45 66
No Contact Sports
198
243
264
p = 1.44 x 10-14

5. “CTE pathology in the brain has been shown by British pathologists to be present in approximately 12 percent of normal healthy aged people who died at an average age of 81 years (Ling et al. Acta Neuropathologica). The presence of CTE pathology in the brain on autopsy has not been shown to correlate with neurologic symptoms before death. To be clear, CTE pathology could be present in a normal person.”

6. 13% of normal individuals have CTE pathology?
Ling, H., J. L. Holton, K. Shaw, K. Davey, T. Lashley and T. Revesz (2015). "Histological evidence of chronic traumatic encephalopathy in a large series of neurodegenerative diseases." Acta Neuropathol 130(6):

7. FAKE NEWS! 13% of normal individuals have CTE pathology?
Ling, H., J. L. Holton, K. Shaw, K. Davey, T. Lashley and T. Revesz (2015). "Histological evidence of chronic traumatic encephalopathy in a large series of neurodegenerative diseases." Acta Neuropathol 130(6):

8. Chronic traumatic encephalopathy: diagnosis at autopsy
Brain atrophy in CTE
Microscopic – neurofibrillary tangles
Diagnostic CTE injury
Age-related changes
PART
ARTAG

9. “The pathology and link between head impacts and long-term neurological conditions such as CTE is still unclear, with questions of causation yet to be settled.”

10. Bradford Hill criteria for causation
Strength. The larger the association, the more likely it is causal
Consistency: Reproducibility in different persons/places/samples strengthens the likelihood of an effect
Specificity: Causation is likely if there is a very specific population and disease with no other likely explanation. The more specific, the more likely a causal relationship
Temporality: The cause must occur before the effect
Biological gradient: Greater exposure should lead to greater incidence of the effect
Plausibility: A plausible mechanism between cause and effect is helpful
Coherence: Coherence between epidemiological and laboratory findings increases the likelihood of an effect
Experiment: Occasionally it is possible to appeal to experimental evidence
Analogy: The effect of similar factors may be considered
Hill AB. The Environment and Disease: Association or Causation? Proc R Soc Med. 1965;58:

11. Have we achieved a consensus among experts?

12. Walter J. Koroshetz, M.D.
National Institutes of Health
Director, National Institute of Neurological Disorders and Stroke
“I don't think there's any wiggle room. It's pretty clear this is due to head injury. Whether there are other things involved, and when it starts, that's hard to know, but I don't think there's any question that it's related to head injury.” March 6, ESPN

13. Daniel Perl, M.D.
Professor
Director of CTE Research
Department of Defense
Uniformed Services University
“CTE is only seen in the setting of repeated head trauma. At the end of the day, this is produced by head trauma. I'm sorry, that's what all the research says.” March 6, ESPN

14. “CTE is a neurodegenerative disease that is associated with changes and deficits in cognition, behavior, mood, and motor skills. It is believed to be caused in part by exposure to repetitive head impacts, including concussions as well as subconcussive trauma (i.e., head impacts that do not cause symptoms of concussion).”