Effect of apolipoprotein E genotype on cerebral autoregulation during cardiopulmonary bypass

Stroke. 2001 Jul;32(7):1514-9. doi: 10.1161/01.str.32.7.1514.

Abstract

Background and purpose: The presence of the apolipoprotein E epsilon4 (apoE4) allele has been associated with cognitive decline after cardiac surgery. We compared autoregulation of cerebral blood flow (CBF), cerebral metabolic rate for oxygen (CMRO(2)), and arterial-venous oxygen content difference [C(A-V)O(2)], during cardiopulmonary bypass (CPB) in patients with and without the apoE4 allele to help define the mechanism of association with cognitive decline.

Methods: One hundred fifty-four patients underwent coronary artery bypass grafting with CPB, nonpulsatile flow, and alpha-stat management. CBF was measured by using (133)Xe washout methods. C(A-V)O(2), CMRO(2), and oxygen delivery were calculated. Pressure-flow autoregulation was tested by using 2 CBF measurements at stable hypothermia: the first at stable mean arterial pressure (MAP) and the second 15 minutes later, when MAP had increased or decreased >/=20%. Metabolism-flow autoregulation was tested by varying the temperature and measuring the coupling of CBF and CMRO(2).

Results: In patients with (n=41) or without (n=113) the apoE4 allele, there were no differences in CBF, CMRO(2), C(A-V)O(2), pressure-flow and metabolism-flow autoregulation corrected for age, gender, non-insulin-dependent diabetes, hemoglobin, CPB time, and temperature.

Conclusions: We conclude that apoE genotype does not affect global CBF and oxygen delivery/extraction during CPB, which suggests that other mechanisms are responsible for the apoE isoform-related neurocognitive dysfunction seen in patients undergoing CPB.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Apolipoproteins E / genetics*
  • Blood Pressure
  • Cardiopulmonary Bypass*
  • Cerebral Cortex / blood supply*
  • Cerebral Cortex / metabolism
  • Cerebrovascular Circulation*
  • Female
  • Genotype
  • Homeostasis
  • Humans
  • Male
  • Middle Aged
  • Oxygen / blood
  • Oxygen Consumption
  • Rewarming

Substances

  • Apolipoproteins E
  • Oxygen