Key result
Serum S-100 levels rise following neurosurgery and strongly correlate with tumor-brain contact surface.
Why the study?
Intraoperative biochemical monitoring is needed to detect and prevent brain damage caused by surgical trauma or postoperative complications in neurosurgery.
Are serum S-100 protein levels a reliable marker for the extent of acute cerebral damage caused by surgical trauma or postoperative complications in patients undergoing intracranial tumor surgery?
Observational (n=20)
Are serum S-100 protein levels a reliable marker for the extent of acute cerebral damage caused by surgical trauma or postoperative complications in patients undergoing intracranial tumor surgery?
Effect estimate: R = 0.71
p-value: p=0.0009
Serum S-100 levels correlate with the extent of surgical trauma (tumor-brain contact surface) and clinical worsening, suggesting its utility as a biomarker for acute CNS damage during neurosurgery.
S-100 may flag perioperative brain injury; leaves open intraoperative monitoring utility pending prospective validation.
Although minimally invasive neurosurgical techniques are highly sophisticated nowadays, almost any operative procedure causes an inevitable surgical trauma to the brain. As a consequence unfavorable functional outcomes are not rare. Intraoperative biochemical monitoring can be helpful first to detect but also to prevent brain damage. We investigated if serum S-100 protein (S-100) levels are a reliable marker for the extent of acute cerebral damage caused by surgical trauma or postoperative complication. S-100 is present in the cytosol of glial cells. This protein leaks into the extracellular space after cell damage and can be detected both in the cerebrospinal fluid (CSF) and serum. To determine S-100 protein levels, serum samples from 20 patients with various intracranial tumors were collected before surgery, and at one day, as well as at seven days after surgery. It was hypothesised that the size of the tumor-brain contact surface (TBCS) was closely related to the dimension of the surgical trauma. TBCS was measured from radiological imaging. The pre- and postoperative (day 1 and day 7) clinical condition of each patient was assessed. The S-100 levels were correlated with the TBCS and the clinical condition. Levels of S-100 on day 1 and day 7 were significantly higher as compared with levels on day 0 ( p = 0.02, respectively p = 0.01). There was a significant relationship between rise of S-100 level and worsening of clinical condition between day 0 and day 1 ( p = 0.001). Also a significant positive relationship between TBCS and the level of S-100 could be found on day 1 and on day 7 ( R = 0.71, p = 0.0009, respectively R = 0.73, p = 0.004). Furthermore, a significant relationship between the rise of S-100 level between day 0 and day 1, as well as between day 0 and day 7, and TBCS could be documented ( R = 0.61, p = 0.01, respectively R = 0.64, p = 0.005). In conclusion, serum S-100 levels are a reliable marker for acute or recent CNS damage caused by neurosurgical manipulation or as a result of secondary postoperative complications. Therefore, intraoperative monitoring of serum S-100 levels seems very promising. In such a setting the negative effects of surgical manipulation can be measured instantaneously, which should bring the neurosurgeon to change his strategy. As a consequence the surgical trauma can be minimized and functional outcome can be optimized.
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Vries et al. (2003) conducted an observational in Intracranial tumors (n=20). Neurosurgical manipulation (tumor-brain contact surface) vs. Preoperative baseline was evaluated on Correlation between serum S-100 protein levels and tumor-brain contact surface (TBCS) (R = 0.71, p=0.0009). Serum S-100 levels significantly increased following neurosurgical manipulation (p=0.02 at day 1) and positively correlated with the tumor-brain contact surface (R=0.71, p=0.0009).
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