2009 Articles

Inducible Nitric Oxide Synthase Promoter Polymorphism Affords Protection Against Cognitive Dysfunction After Carotid Endarterectomy

Yocum, Gene T.; Gaudet, John G.; Lee, Susie S.; Stern, Yaakov; Teverbaugh, Lauren A.; Sciacca, Robert R.; Emala, Charles W.; Quest, Donald O.; McCormick, Paul C.; McKinsey, James F.; Morrissey, Nicholas J.; Solomon, Robert A.; Connolly, E. Sander; Heyer, Eric J.

Background and Purpose—Cognitive dysfunction occurs in 9% to 23% of patients during the first month after carotid endarterectomy (CEA). A 4-basepair (AAAT) tandem repeat polymorphism (either 3 or 4 repeats) has been described in the promoter region of inducible nitric oxide synthase (iNOS), a gene with complex roles in ischemic injury and preconditioning against ischemic injury. We investigated whether the 4-repeat variant (iNOSϩ) affects the incidence of cognitive dysfunction after CEA. Methods—One-hundred eighty-five CEA and 60 spine surgery (control) subjects were included in this nested cohort analysis. Subjects underwent a battery of 7 neuropsychometric tests before and 1 day and 1 month after surgery. Multivariate logistic regression analyses were performed to determine if the iNOS promoter variant was independently associated with the incidence of cognitive dysfunction at 1 day and 1 month. Further, all right-hand-dominant CEA subjects were grouped by operative side and performance on each test was compared between iNOSϩ and iNOSϪ groups. Results—Forty-four of 185 CEA subjects had at least 1 iNOS promoter allele containing 4 copies of the tandem repeat (iNOSϩ). iNOSϩ status was significantly protective against moderate/severe cognitive dysfunction 1 month after CEA. Right-hand-dominant iNOSϩ CEA subjects undergoing left-side CEA performed significantly better than iNOSϪ subjects on a verbal learning test and those undergoing right-side CEA performed significantly better on a test of visuospatial function. Conclusion—We demonstrate an iNOS promoter polymorphism variant provides protection against moderate/severe cognitive dysfunction 1 month after CEA. Further, this protection appears to involve cognitive domains localized ipsilateral to the operative carotid artery. (Stroke. 2009;40:1597-1603.)