Key result
POCD affects ~17% of high-risk CABG patients and is linked to specific differentially expressed genes.
Why the study?
Gene-level changes were hypothesized to be involved in the pathogenesis of postoperative cognitive dysfunction, but the incidence and associated differentially expressed genes in high-risk CABG patients required evaluation.
Cohort (n=46)
Answers are grounded in this paper and cite their sources.
Gene expression profiling identified five differentially expressed genes associated with postoperative cognitive dysfunction in high-risk CABG patients, highlighting potential targets for diagnostic and predictive biomarkers.
Postoperative cognitive dysfunction (POCD) is cognitive decline after surgery. The authors hypothesized that gene-level changes could be involved in the pathogenesis of POCD. The present study evaluated the incidence of POCD and its associated differentially expressed genes. This was a prospective cohort study conducted on high-risk coronary artery bypass graft patients aged 40 to 75 years. POCD classification was based on a one standard deviation decline in the postoperative scores compared to the preoperative scores. The differentially expressed genes were identified using microarray analysis and validated using quantitative RT-PCR. Forty-six patients were recruited and completed the study. The incidence of POCD was identified using a set of neurocognitive assessments and found to be at 17% in these high-risk CABG patients. Six samples were selected for the gene expression analyses (3 non-POCD and 3 POCD samples). The findings showed five differentially expressed genes in the POCD group compared to the non-POCD group. The upregulated gene was ERFE, whereas the downregulated genes were KIR2DS2, KIR2DS3, KIR3DL2, and LIM2. According to the results, the gene expression profiles of POCD can be used to find potential proteins for POCD diagnostic and predictive biomarkers. Understanding the molecular mechanism of POCD development will further lead to early detection and intervention to reduce the severity of POCD, and hence, reduce the mortality and morbidity rate due to the condition.
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Yazit et al. (2023) conducted a cohort in Postoperative cognitive dysfunction (n=46). Postoperative cognitive dysfunction (POCD) vs. non-POCD was evaluated on Incidence of POCD and differentially expressed genes. Postoperative cognitive dysfunction occurred in 17% of high-risk CABG patients and was associated with five differentially expressed genes compared to non-POCD patients.
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