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. 2010 Apr;112(4):852-9.
doi: 10.1097/ALN.0b013e3181d31fd7.

Cognitive function after major noncardiac surgery, apolipoprotein E4 genotype, and biomarkers of brain injury

Collaborators, Affiliations

Cognitive function after major noncardiac surgery, apolipoprotein E4 genotype, and biomarkers of brain injury

David L McDonagh et al. Anesthesiology. 2010 Apr.

Abstract

Background: Postoperative cognitive dysfunction (POCD) is a significant cause of morbidity after noncardiac surgery. Identified risk factors are largely limited to demographic characteristics. We hypothesized that POCD was associated with apolipoprotein E4 (APOE4) genotype and plasma biomarkers of brain injury and inflammation.

Methods: Three hundred ninety-four patients older than 55 yr undergoing major elective noncardiac surgery were enrolled in this prospective observational study. Apolipoprotein E genotyping was performed at baseline. Plasma was collected at baseline and end of surgery and at 4.5, 24, and 48-h postoperatively. Six protein biomarkers were assayed (B-type natriuretic peptide, C-reactive protein, D-dimer, matrix metalloproteinase-9, neuron-specific enolase, and S-100B). Neurocognitive testing was conducted at baseline and at 6 weeks and 1 yr after surgery; scores were subjected to factor analysis. The association of APOE4 and biomarkers with POCD was tested using multivariable regression modeling.

Results: Three hundred fifty patients (89%) completed 6-week neurocognitive testing. POCD occurred in 54.3% of participants at 6 weeks and 46.1% at 1 yr. There was no difference in POCD between patients with or without the APOE4 allele (56.6 vs. 52.6%; P = 0.58). The continuous cognitive change score (mean +/- SD) was similar between groups (APOE4: 0.05 +/- 0.27 vs. non-APOE4: 0.07 +/- 0.28; P = 0.53). Two hundred ninety-one subjects (74%) completed testing at 1 yr. POCD occurred in 45.9% of APOE4 subjects versus 46.3% of non-APOE4 subjects (P = 0.95). The cognitive score was again similar (APOE4: 0.08 +/- 0.27 vs. non-APOE4: 0.05 +/- 0.25; P = 0.39). Biomarker levels were not associated with APOE4 genotype or cognition at 6 weeks or 1 yr.

Conclusion: Cognitive decline after major noncardiac surgery is not associated with APOE4 genotype or plasma biomarker levels.

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Figures

Figure 1
Figure 1
A: Boxplots of biomarker levels in non-APOE4 (white) and APOE4 (shaded) subjects for perioperative time points. Boxes enclose 25th to 75th percentiles; vertical whiskers extend to 10th and 90th percentiles. Median (50th percentile) is marked by the line inside of the box. (Where all five percentile lines are not visible in a plot, the percentiles coincide). BNP B: CRP C: D-Dimer D: MMP-9 E: NSE F: S100b (100 mcg/ml is the lower limit of the assay)
Figure 1
Figure 1
A: Boxplots of biomarker levels in non-APOE4 (white) and APOE4 (shaded) subjects for perioperative time points. Boxes enclose 25th to 75th percentiles; vertical whiskers extend to 10th and 90th percentiles. Median (50th percentile) is marked by the line inside of the box. (Where all five percentile lines are not visible in a plot, the percentiles coincide). BNP B: CRP C: D-Dimer D: MMP-9 E: NSE F: S100b (100 mcg/ml is the lower limit of the assay)
Figure 1
Figure 1
A: Boxplots of biomarker levels in non-APOE4 (white) and APOE4 (shaded) subjects for perioperative time points. Boxes enclose 25th to 75th percentiles; vertical whiskers extend to 10th and 90th percentiles. Median (50th percentile) is marked by the line inside of the box. (Where all five percentile lines are not visible in a plot, the percentiles coincide). BNP B: CRP C: D-Dimer D: MMP-9 E: NSE F: S100b (100 mcg/ml is the lower limit of the assay)
Figure 1
Figure 1
A: Boxplots of biomarker levels in non-APOE4 (white) and APOE4 (shaded) subjects for perioperative time points. Boxes enclose 25th to 75th percentiles; vertical whiskers extend to 10th and 90th percentiles. Median (50th percentile) is marked by the line inside of the box. (Where all five percentile lines are not visible in a plot, the percentiles coincide). BNP B: CRP C: D-Dimer D: MMP-9 E: NSE F: S100b (100 mcg/ml is the lower limit of the assay)
Figure 1
Figure 1
A: Boxplots of biomarker levels in non-APOE4 (white) and APOE4 (shaded) subjects for perioperative time points. Boxes enclose 25th to 75th percentiles; vertical whiskers extend to 10th and 90th percentiles. Median (50th percentile) is marked by the line inside of the box. (Where all five percentile lines are not visible in a plot, the percentiles coincide). BNP B: CRP C: D-Dimer D: MMP-9 E: NSE F: S100b (100 mcg/ml is the lower limit of the assay)
Figure 1
Figure 1
A: Boxplots of biomarker levels in non-APOE4 (white) and APOE4 (shaded) subjects for perioperative time points. Boxes enclose 25th to 75th percentiles; vertical whiskers extend to 10th and 90th percentiles. Median (50th percentile) is marked by the line inside of the box. (Where all five percentile lines are not visible in a plot, the percentiles coincide). BNP B: CRP C: D-Dimer D: MMP-9 E: NSE F: S100b (100 mcg/ml is the lower limit of the assay)

Comment in

References

    1. Moller JT, Cluitmans P, Rasmussen LS, Houx P, Rasmussen H, Canet J, Rabbitt P, Jolles J, Larsen K, Hanning CD, Langeron O, Johnson T, Lauven PM, Kristensen PA, Biedler A, van Beem H, Fraidakis O, Silverstein JH, Beneken JEW, Gravenstein JS for the International Study of Postoperative Cognitive Dysfunction investigators. Long-term postoperative cognitive dysfunction in the elderly: International Study of Postoperative Cognitive Dysfunction 1 study. Lancet. 1998;351:857–61. - PubMed
    1. Rasmussen LS, Johnson T, Kuipers HM, Kristensen D, Siersma VD, Vila P, Jolles J, Papaioannou A, Abildstrom H, Silverstein JH, Bonal JA, Raeder J, Nielsen IK, Korttila K, Munoz L, Dodds C, Hanning CD, Moller JT. International Study of Postoperative Cognitive Dysfunction 2 Investigators: Does anaesthesia cause postoperative cognitive dysfunction? A randomised study of regional versus general anaesthesia in 438 elderly patients. Acta Anaesthesiol Scand. 2003;47:260–6. - PubMed
    1. Monk TG, Weldon BC, Garvan CW, Dede DE, van der Aa MT, Heilman KM, Gravenstein JS. Predictors of cognitive dysfunction after major noncardiac surgery. Anesthesiology. 2008;108:18–30. - PubMed
    1. Steinmetz J, Christensen KB, Lund T, Lohse N, Rasmussen LS for the International Study of Postoperative Cognitive Dysfunction Group. Long-term consequences of postoperative cognitive dysfunction. Anesthesiology. 2009;110:548–55. - PubMed
    1. Abildstrom H, Rasmussen LS, Rentowl P, Hanning CD, Rasmussen H, Kristensen PA, Moller JT. Cognitive dysfunction 1-2 years after non-cardiac surgery in the elderly. International Study of Postoperative Cognitive Dysfunction group. International Study of Post-Operative Cognitive Dysfunction. Acta Anaesthesiol Scand. 2000;44:1246–51. - PubMed

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