2007
DOI: 10.1111/j.1365-2990.2006.00794.x
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Traumatic axonal damage in the brain can be detected using β‐APP immunohistochemistry within 35 min after head injury to human adults

Abstract: Immunohistochemistry staining for beta-amyloid precursor protein (beta-APP) is a sensitive method to detect early axonal damage in traumatic brain injury, which was previously estimated to be of minimum 60-90 min after head injury. We present seven cases of well-documented posttraumatic survival of 35-60 min where beta-APP detects early axonal damage. Cases were selected from routine work where documentation about survival is judged to be accurate. These are divided into three groups: group 1: severe head inju… Show more

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Cited by 122 publications
(86 citation statements)
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“…Presently, beta amyloid precursor protein (b-APP) staining for swollen axons is a useful technique for commenting on the likely survival time following injury to the CNS, as the earliest signs of diffuse axonal injury occur at least a half hour post-injury. 34,35 Nestin reactivity may prove valuable as a further modality to determine time between injury and death.…”
Section: Discussionmentioning
confidence: 99%
“…Presently, beta amyloid precursor protein (b-APP) staining for swollen axons is a useful technique for commenting on the likely survival time following injury to the CNS, as the earliest signs of diffuse axonal injury occur at least a half hour post-injury. 34,35 Nestin reactivity may prove valuable as a further modality to determine time between injury and death.…”
Section: Discussionmentioning
confidence: 99%
“…Brains were immersed in 10% buffered formalin for 3 weeks according to standard procedures [17] to allow good fixation. We measured the formalin-fixed whole brain and brainstem & cerebellum weight, respectively, to have the weight ratio of the supra-and infratentorial part as an index of atrophy or weight gain (e.g.…”
Section: Neuropathological Analysismentioning
confidence: 99%
“…29,31,34,61 A recent study using APP knockout mice demonstrates that endogenous APP is beneficial after mTBI and that this neuroprotective activity is related to the soluble a form of APP (sAPPa). 13 Under normal conditions, most of the APP is processed along the nonamyloidogenic pathway leading to the formation of sAPPa, which promotes neuroprotection, synaptic plasticity, neurite outgrowth, and synaptogenesis.…”
Section: Discussionmentioning
confidence: 99%