Abstract
Objective
The APOE epsilon‐4 allele has consistently emerged as a susceptibility factor for Alzheimer's disease (AD). Pro‐inflammatory cytokines are detectable at abnormal levels in AD, and are thought to play a pathophysiological role. Animal studies have shown dose‐dependent correlations between the number of APOE epsilon‐4 alleles and the levels of pro‐inflammatory cytokines. The aims of this study were to investigate the influence of APOE genotypes on TNF‐α, IL‐6, and IL‐1__β__ secreted by peripheral blood mononuclear cells (PBMC) from human patients with AD and to analyze the correlation between cytokine production and AD clinical features.
Methods
Outpatients with AD (n = 40) were clinically evaluated for cognitive decline (MMSE) and psychiatric symptoms (Cornell Scale for Depression in Dementia; Neuropsychiatric Inventory) and genotyped for APOE variants. PBMCs were isolated from the donors and used to assess spontaneous and PMA‐stimulated secretion of TNF‐α, IL‐6, and IL‐1__β__. Cytokine production was determined by immuno‐enzymatic assays (ELISA).
Results
In comparison with their counterparts without APOE4, patients with at least one copy of the APOE epsilon‐4 allele showed higher spontaneous (p = 0.037) and PMA‐induced (p = 0.039) production of IL‐1__β__ after controlling for clinical variables. Significant correlations were reported between NPI scores (psychotic symptoms) and IL‐6 production.
Conclusion
These preliminary findings suggest the involvement of inflammatory response in the pathogenic effect of the APOE epsilon‐4 allele in AD, although their replication in larger samples is mandatory. The modest correlations between pro‐inflammatory cytokines released at peripheral level and AD features emphasizes the need for further research to elucidate the role of neuroinflammation in pathophysiology of AD. Copyright © 2009 John Wiley & Sons, Ltd.