Abstract
The association between the K-variant of the butyrylcholinesterase gene (BCHE-K) and Alzheimer disease (AD) or AD-related neuropathology has been reported to date with conflicting results. Here, we determined in a sample of 521 cases the severity of AD-related neuropathology and the polymorphisms of both BCHE-K and apolipoprotein E (ApoE). Histopathologically, all brains were classified according to procedures permitting differentiation of the evolutionary stages of neurofibrillary tangles (NFTs) and amyloid-β-protein deposition (Aβ-deposits). The results show that the association between BCHE-K and AD-related neuropathology only was limited to homozygotes for the K allele ( P=0.036 for NFTs, and P=0.045 for Aβ-deposits) at ages ≥70 years but not 50–69 years. Furthermore, no interaction was apparent between BCHE-K and ApoE.
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