Kim K W, Jhoo J H, Lee J H, Lee K U, Lee D Y, Youn J C, Youn J Y, Woo J I
Department of Neuropsychiatry, Kyunggi Provincial Hospital for the Elderly, Yongin, Korea.
J Neural Transm (Vienna). 2001;108(10):1159-66. doi: 10.1007/s007020170005.
To investigate the possible involvement of the butyrylcholinesterase (BCHE) K variant and transferrin (TF) C2 variant in the manifestation of Alzheimer's disease (AD), we analyzed the BCHE, TF and apolipoprotein E (APOE) genotypes of 164 sporadic AD patients and 239 normal elderly controls. The frequencies of the BCHE K and TF C2 did not differ between the AD patients and controls (P > 0.1). The occurrence of the APOE epsilon4 did not influence the distribution of the BCHE K and TF C2 variants (P > 0.1). No linkage disequilibrium between the BCHE K and TF C2 was observed either in both the AD patients and controls (P > 0.1). In conclusion, neither the BCHE K nor the TF C2 confers a risk for AD.