Is there a relationship between serum S-100 beta protein and neuropsychologic dysfunction after cardiopulmonary bypass?

Citation
S. Westaby et al., Is there a relationship between serum S-100 beta protein and neuropsychologic dysfunction after cardiopulmonary bypass?, J THOR SURG, 119(1), 2000, pp. 132-137
Citations number
29
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY
ISSN journal
00225223 → ACNP
Volume
119
Issue
1
Year of publication
2000
Pages
132 - 137
Database
ISI
SICI code
0022-5223(200001)119:1<132:ITARBS>2.0.ZU;2-9
Abstract
Objectives: Over the past decade, the glial protein S-100 beta has been use d to detect cerebral injury in a number of clinical settings including card iac surgery. Previous investigations suggest that S-100 beta is capable of identifying patients with cerebral dysfunction after cardiopulmonary bypass . Whether detection of elevated levels S-100 beta reflects long-term cognit ive impairment remains to be shown. The present study evaluated whether per ioperative release of S-100 beta after coronary artery operations with card iopulmonary bypass could predict early or late neuropsychologic impairment. Methods: A total of 100 patients undergoing elective coronary bypass witho ut a previous history of neurologic events were prospectively studied. To e xclude noncerebral sources of S-100 beta, we did not use cardiotomy suction or retransfusion of shed mediastinal blood. Serial perioperative measureme nts of S-100 beta were performed with the use of a new sensitive immunolumi nometric assay up to 8 hours after the operation. Patients underwent cognit ive testing on a battery of 11 tests before the operation, before discharge from the hospital, and 3 months later. Results: No significant correlation was found between S-100 beta release and neuropsychologic measures either 5 days or 3 months after the operation, Conclusion: Despite using a sensiti ve immunoluminometric assay of S-100 beta, we found no evidence to support the suggestion that early release of S-100 beta may reflect long-term neuro logic injury capable of producing cognitive impairment.