Recently, inflammatory pathways have been recognized as possible pathophysi
ological mechanisms of aging-associated neurodegenerations, and slowing of
the progression of Alzheimer's disease can be achieved with anti-inflammato
ry drugs. The formation of endogenous inflammatory lipid mediators, leukotr
ienes, is initiated by 5-lipoxygenase (5-LOX), which is also expressed in n
eurons. We recently reported that aging is associated with a significant in
crease in neuronal 5-LOX gene expression and with increased, 5-LOX inhibito
r-sensitive, vulnerability of neurons to degeneration. On the basis of thes
e findings we have proposed that the 5-LOX pathway may influence the progre
ssion of aging-associated diseases, such as Alzheimer's. In humans, mutatio
ns of the promoter of the 5-LOX gene occur in a normal population with a fr
equency of about 25%. These mutations result in a decreased expression of t
he 5-LOX gene. Thus, it is hypothesized here that the onset of Alzheimer's
disease will be delayed in subjects who display a mutation in the 5-LOX gen
e promoter, and that consequently the frequency of occurrence of the three
known 5-LOX mutated alleles will be greater in subjects with onset of Alzhe
imer's at a very old age than in subjects with an earlier onset. (C) 2000 H
arcourt Publishers Ltd.