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Department of Anesthesia, University of Pennsylvania, Philadelphia, Pennsylvania
Address correspondence to W. Andrew Kofke, MD, MBA, FCCM, Department of Anesthesia, University of Pennsylvania, 7 Dulles, 3400 Spruce St, Philadelphia, PA 191044283. Address email to kofkea{at}uphs.upenn.edu
We tested the hypothesis that two biochemical markers of brain injury would be increased after cardiac surgery in patients with the apolipoprotein (Apo)
4 allele. Arterial blood samples were drawn before and 8 and 24 h after induction of anesthesia and later assayed for neuron specific enolase (NSE), S-100ß, and apoE genotype. There was a highly significant temporal effect with increases in NSE (2.2 ± 1.6 ng/L to 11.8 ± 8.9 ng/L; P < 0.0001) (mean ± SD) and S-100ß (0.15 ± 0.1 µg/L to 0.45 ± 0.42 µg/L, P < 0.0001). At 8 and 24 h after induction of anesthesia S-100ß (0.28 ± 0.18 µg/L versus 0.91 ± 0.54 µg/L; P =0.004) and NSE (8.6 ± 5.6 ng/L versus 19.0 ± 19.7 ng/L; P = 0.02) levels, respectively, were higher in patients with the Apo
4 allele. Patients with the Apo
4 allele may be more susceptible to perioperative neural insults.
IMPLICATIONS: Two blood tests thought to be biomarkers for brain injury were found to be increased after cardiac surgery with larger increases in patients with the apolipoprotein
4 gene, a gene linked to Alzheimers disease. There may be genetic differences in susceptibility to neurologic problems after surgery.
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