• J Clin Neurosci · Feb 2014

    Observational Study

    Apolipoprotein E-ε4 polymorphism and cognitive dysfunction after carotid endarterectomy.

    • Eric J Heyer, Joanna L Mergeche, Yaakov Stern, Hani R Malone, Samuel S Bruce, Justin T Ward, and E Sander Connolly.
    • Department of Anesthesiology, Columbia University, 630 West 168th Street, P&S Box 46, New York, NY 10032, USA; Department of Neurology, Columbia University, New York, NY, USA. Electronic address: ejh3@columbia.edu.
    • J Clin Neurosci. 2014 Feb 1;21(2):236-40.

    AbstractApproximately 25% of patients undergoing carotid endarterectomy (CEA) exhibit cognitive dysfunction (CD) 1 day and 1 month after CEA. The apolipoprotein E (apoE)-ε4 polymorphism has been previously identified as a robust independent risk factor for CD 1 month after CEA. We aimed to determine whether the apoE-ε4 polymorphism is also an independent risk factor for CD as early as 1 day after CEA and to confirm the previous findings at 1 month. Patients undergoing elective CEA (n=411) were enrolled with written informed consent in this follow-up observational study. CD was evaluated via an extensive neuropsychometric battery. apoE-ε4 carriers exhibited significantly more CD 1 day (30.1% versus 17.9%, p=0.01) and 1 month (25.7% versus 9.8%, p=0.001) after CEA compared to non-carriers. Multivariate regression models were generated to determine independent predictors of CD. At 1 day, apoE-ε4 was significantly associated with higher risk of CD (odds ratio [OR]: 2.24 [95% confidence interval 1.29-3.84], p=0.004), while statin use was significantly associated with lower risk (OR: 0.40 [0.24-0.67], p<0.001). At 1 month, apoE-ε4 was significantly associated with higher risk of CD (OR: 3.14 [1.53-6.38], p=0.002), while symptomatic status was significantly associated with lower risk (OR: 0.45 [0.20-0.94], p=0.03). The apoE-ε4 polymorphism is an independent risk factor for CD as early as 1 day after CEA and is confirmed to be an independent risk factor for CD at 1 month as well.Copyright © 2013 Elsevier Ltd. All rights reserved.

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