Related Experiment Video
Updated: May 14, 2026

08:17
A Mouse Model of Orthopedic Surgery to Study Postoperative Cognitive Dysfunction and Tissue Regeneration
Published on: February 27, 2018
Genetic variation and cognitive dysfunction one year after cardiac surgery
A Stewart1, R Katznelson, N Kraeva
1University of Toronto, Toronto, Canada.
Anaesthesia
|February 7, 2013
Summary
Genetic variants in platelet glycoprotein-IIIa (Pl(A2) allele) are associated with long-term postoperative cognitive dysfunction after cardiac surgery. Apolipoprotein E-ε4 showed no significant association. Further validation is needed.
Area of Science:
- Cardiovascular Surgery
- Neuroscience
- Genetics
Background:
- Postoperative cognitive dysfunction (POCD) is a concern after cardiac surgery.
- Candidate gene polymorphisms are potential risk factors for POCD, but evidence is limited.
- Platelet glycoprotein-IIIa and apolipoprotein-E are implicated in cognitive function.
Purpose of the Study:
- To investigate the association between specific gene variants and POCD one year after cardiac surgery.
- To examine the role of platelet glycoprotein-IIIa (Pl(A2) allele) and apolipoprotein E-ε4 (APOE ε4) in long-term POCD.
- To determine if combined alleles influence POCD risk.
Main Methods:
- A cohort of 155 patients undergoing cardiac surgery was studied.
- Neuropsychological testing was performed at one-year follow-up to assess cognitive function.
- Genotyping for Pl(A2) allele and APOE ε4 was conducted.
Main Results:
- Cognitive dysfunction was observed in 20% of patients at one year.
- The Pl(A2) allele was significantly more prevalent in patients with POCD (42% vs. 20%, p=0.012).
- The combined presence of Pl(A2) and APOE ε4 alleles was also significantly associated with POCD (19% vs. 4%, p=0.003).
Conclusions:
- The Pl(A2) allele of the platelet glycoprotein-IIIa gene may be a risk factor for developing long-term POCD after cardiac surgery.
- APOE ε4 alone did not show a significant association, but its combination with Pl(A2) increased risk.
- Further research, including age-adjusted non-surgical controls, is necessary to validate these genetic associations.
