Preliminary report of a genetic basis for cognitive decline after cardiac operations

  • Barbara E. Tardiff
  • , Mark F. Newman
  • , Ann M. Saunders
  • , Warren J. Strittmatter
  • , James A. Blumenthal
  • , William D. White
  • , Narda D. Croughwell
  • , R. Duane Davis
  • , Allen D. Roses
  • , Joseph G. Reves

Research output: Contribution to journalArticlepeer-review

257 Scopus citations

Abstract

Background. Changes in memory and cognition frequently follow cardiac operations. We hypothesized that patients with the apolipoprotein E-ε4 allele are genetically predisposed to cognitive dysfunction after cardiac operations. : Methods. The apolipoprotein E-ε4 allele was evaluated as a predictor variable for postoperative cognitive dysfunction in 65 patients undergoing cardiac bypass grafting at Duke University Medical Center. The primary outcome measure was performance on a cognitive battery administered preoperatively and at 6 weeks postoperatively. Results. In a multivariable logistic regression analysis including apolipoprotein E-ε4, preoperative score, age, and years of education, a significant association was found between apolipoprotein E-ε4 and change in cognitive test score in measures of short-term memory at 6 weeks postoperatively. Patients with lower educational levels were more likely to show a decline in cognitive function associated with the apolipoprotein E-ε4 allele. Conclusions. This study suggests that apolipoprotein E genotype is related to cognitive dysfunction after cardiopulmonary bypass. Cardiac surgical patients may be susceptible to deterioration after physiologic stress as a result of impaired genetically determined neuronal mechanisms of maintenance and repair.

Original languageEnglish
Pages (from-to)715-720
Number of pages6
JournalAnnals of Thoracic Surgery
Volume64
Issue number3
DOIs
StatePublished - Sep 1997

Bibliographical note

Funding Information:
This work was supported by The National Institutes of Health, National Institute on Aging, Claude D. Pepper Older Americans Independence Center, #5 P60AG-11268; National Institutes of Health grant ROI-AG-09663; National Institutes of Health Leadership and Excellence Award #5 R35AG-07922; National Institutes of Health Alzheimer’s Disease Research Center #5 P50AG-05128; American Heart Association grant-in-aid #95010970, and a grant from the Anesthesia Patient Safety Foundation.

Funding

This work was supported by The National Institutes of Health, National Institute on Aging, Claude D. Pepper Older Americans Independence Center, #5 P60AG-11268; National Institutes of Health grant ROI-AG-09663; National Institutes of Health Leadership and Excellence Award #5 R35AG-07922; National Institutes of Health Alzheimer’s Disease Research Center #5 P50AG-05128; American Heart Association grant-in-aid #95010970, and a grant from the Anesthesia Patient Safety Foundation.

FundersFunder number
National Institutes of Health Alzheimer’s Disease Research Center5 P50AG-05128
National Institutes of Health (NIH)
National Institute on AgingR01AG009663
Anesthesia Patient Safety Foundation
American Heart Association95010970
Claude D. Pepper Older Americans Independence Center, University of California San Francisco5 P60AG-11268, 5 R35AG-07922, ROI-AG-09663

    ASJC Scopus subject areas

    • Surgery
    • Pulmonary and Respiratory Medicine
    • Cardiology and Cardiovascular Medicine

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