Abstract
Background Renal dysfunction is a serious complication of cardiac surgery that is highly associated with short- and long-term adverse outcome. While the apolipoprotein E (APOE) ε4 allele has been linked to the occurrence of both postcardiac surgery acute renal injury (ε4 favorable) and ascending aortic arteriosclerosis (ε4 unfavorable), the role of ε4 in the relationship between these two conditions is unknown. We hypothesized that patients with and without the ε4 allele (E4/non-E4) would have different associations between atheroma burden and postoperative renal dysfunction. Methods Ascending, arch, and descending aorta atheromatous burden and APOE status were evaluated for 130 coronary bypass patients. Multivariable analyses were performed for aortic regions to assess the relationship of atheroma burden and APOE ε4 status with peak in-hospital postoperative serum creatinine. All p < 0.05 were considered significant. Results We found an interaction between E4 status (E4/non-E4; 24/106) and atheroma burden, with a much greater predicted peak in-hospital postoperative serum creatinine for increases in ascending aorta atheroma load for non-E4 patients versus E4 patients (beta coefficient -0.13; p = 0.002). We also confirmed the association between ascending aorta atheroma and peak creatinine (beta coefficient 0.11; p = 0.0008), after controlling for E4 status, preoperative creatinine, and the E4-atheroma interaction. Conclusions Equivalent ascending aortic atheroma burden is associated with a greater susceptibility to postoperative renal injury among patients undergoing cardiac operation who lack the APOE ε4 allele. Findings may be attributable to APOE-related differences in inflammation, susceptibility to atheroma detachment (eg, during operative aortic manipulation), or renal vulnerability to embolic injury.
Original language | English |
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Pages (from-to) | 520-526 |
Number of pages | 7 |
Journal | Annals of Thoracic Surgery |
Volume | 78 |
Issue number | 2 |
DOIs | |
State | Published - Aug 2004 |
Bibliographical note
Funding Information:Supported in part by National Institutes of Health Grant 1R01HL54316, Clinical Research Centers Program National Institutes of Health Grant MO1-RR-30, and American Heart Association Grant-In-Aid 95010970. The authors thank Cheryl J. Stetson for editorial assistance with the manuscript.
Keywords
- 23
ASJC Scopus subject areas
- Surgery
- Pulmonary and Respiratory Medicine
- Cardiology and Cardiovascular Medicine