1997
DOI: 10.1161/01.str.28.10.1961
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S-100 Protein: Serum Marker of Focal Brain Damage After Ischemic Territorial MCA Infarction

Abstract: Presence of S-100 in serum after ischemic stroke may be due to combined leakage out of necrotic glial cells and passage through an impaired brain-blood barrier, indicating severe ischemic cell injury. Therefore, S-100 in serum can be used as a peripheral marker of ischemic focal brain damage and may be helpful for therapeutic decisions in acute ischemic stroke.

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Cited by 237 publications
(187 citation statements)
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“…It is well known that S100B values increase in ischemic stroke, reaching maximum levels 2 to 4 days after onset, correlating with infarct size 4,6,13) . S100 protein level fell significantly thereafter, but still above the level seen in the control population at 3 months after stroke, suggesting partial restoration of glial cell integrity 3) .…”
Section: Discussionmentioning
confidence: 98%
“…It is well known that S100B values increase in ischemic stroke, reaching maximum levels 2 to 4 days after onset, correlating with infarct size 4,6,13) . S100 protein level fell significantly thereafter, but still above the level seen in the control population at 3 months after stroke, suggesting partial restoration of glial cell integrity 3) .…”
Section: Discussionmentioning
confidence: 98%
“…Previous studies have reported increased plasma or serum neurobiochemical markers, e.g., S-100 protein, neuron-specific enolase, and N-acetylaspartate, in the peripheral circulation of patients after stroke but failed to demonstrate that these markers offered any additional advantage over current clinical assessment scales, risk factors, or neuroradiologic techniques (5)(6)(7)(8). Correlations have been observed between marker values, infarct size, and NIHSS scores, and increased concentrations predict disability and mortality.…”
Section: Discussionmentioning
confidence: 99%
“…The blood-brain barrier is compromised in many patients with stroke, and the liberation of neurobiochemical protein markers into the circulation may allow the pathophysiology, progress, and prognosis of patients with cerebrovascular disease to be further evaluated (5)(6)(7)(8). Although increased concentrations of several neurobiochemical protein markers have been detected in the peripheral blood of patients with stroke, to date none has found a place in clinical practice.…”
mentioning
confidence: 99%
“…Several studies have demonstrated that serum S100B concentrations are increased significantly following stroke (75)(76)(77)(78)(79)(80)(81)(82), with secretion of S100B increasing up to 48 h after symptom onset and the peak concentration occurring within the first 24 h after cerebral infarction. Elting et al (78 ) reported that patients who had a TIA or normal brain CT at presentation had significantly lower S100B concentrations with minimal variation over time, in comparison with individuals who had major neurological deficits and abnormal brain imaging showing large-artery cortical infarcts.…”
Section: Matrix Metalloproteinmentioning
confidence: 99%