Anesthesia & Analgesia · 2004 · 28 citations · 21 references
Life SciencesCardiologyNeuroscienceAnesthesiaNeurochemistryPathophysiologyBiomarkers Of NeurodegenerationBiomarkers Of NeurotoxicityNeurologic PathophysiologyApoe GeneticsApolipoprotein E Genotype RiskApolipoprotein E VariantsBiochemical Stress MarkersNeurochemical BiomarkersNeuron-specific EnolaseNeuronal Injury Biomarkers
In Brief We tested the hypothesis that two biochemical markers of brain injury would be increased after cardiac surgery in patients with the apolipoprotein (Apo) ε4 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-100β, 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-100β (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-100β (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 Apoε4 allele. Patients with the Apoε4 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 ε4 gene, a gene linked to Alzheimer’s disease. There may be genetic differences in susceptibility to neurologic problems after surgery.
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Long-term postoperative cognitive dysfunction in the elderly: ISPOCD1 study
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