When controlling for sex and age at death in logistic regression, the association between TDP‐43 pathologies and HS‐Aging remained highly significant (hippocampal neurites: OR:85.68, 95%CI: 11.53–636.61; entorhinal cortex inclusions: OR:93.13, 95%CI: 12.53–692.34; entorhinal cortex neurites: OR: 109.86, 95%CI: 14.81–815.05).
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Hippocampal sclerosis, hippocampal neuron loss patterns and TDP-43 in the aged population.
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