Data di Pubblicazione:
2007
Citazione:
Interleukin-18 gene polymorphisms predict risk and outcome of Alzheimer's disease / P. Bossu, A. Ciaramella, M.L. Moro, L. Bellincampi, S. Bernardini, G. Federici, A. Trequattrini, F. Macciardi, I. Spoletini, F. Di Iulio, C. Caltagirone, G. Spalletta. - In: JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY. - ISSN 0022-3050. - 78:8(2007 Aug), pp. 807-811.
Abstract:
Inflammation has been extensively implicated in Alzheimer's disease (AD) pathogenesis. Although there is evidence of a key role for cytokines in neuroinflammation processes, so far the proinflammatory cytokine IL-18 has not yet been associated to AD. This study was aimed to investigate the impact of two polymorphisms of human IL-18 gene promoter at positions -607 (C/A) and -137 (G/C) on both susceptibility to and progression of AD. The results revealed that the genotype distribution of -607 (C/A) polymorphism was different between AD patients and control
subjects (χ2=7.99, df= 2, p=0.0184). In particular, carriers of CC genotype were at increased risk of developing AD (OR=2.33; 95% CI=1.29-4.22; p=0.0052). The observed genotypes were in Hardy-Weinberg equilibrium as for -607 polymorphism, whereas the -137 polymorphism appeared in Hardy-Weinberg disequilibrium only in patient group (p=0.0061). Finally, in a two year follow up
study, the -137 CC genotype was strongly and specifically associated with a faster cognitive decline (F=4.024; df=4,192; p=0.0037 for time by IL-18 -137 G/C group interaction) with no interaction effect with the ApoE ε4/non ε4 allele presence. Since IL-18 cytokine promoter gene polymorphisms have been previously described to have functional consequences on IL-18 expression, it is possible that individuals with a prevalent IL-18 gene variant have a dysregulated immune response, suggesting that IL-18 mediated immune mechanisms may play a crucial role in AD.
Tipologia IRIS:
01 - Articolo su periodico
Elenco autori:
P. Bossu, A. Ciaramella, M.L. Moro, L. Bellincampi, S. Bernardini, G. Federici, A. Trequattrini, F. Macciardi, I. Spoletini, F. Di Iulio, C. Caltagirone, G. Spalletta
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