“…The results have not been consistent (Lehmann et al, 2001), although several have found that the low activity alleles seem to be associated with lower susceptibility to AD and/or later age of onset (Alvarez-Arcaya et al, 2000;Lane et al, 2006Lane et al, , 2008Mateo et al, 2008), or a significantly reduced rate of progression of cognitive decline in individuals with severe AD (Holmes et al, 2005). The presence of the K variant has also been associated with lower benefits from rivastigmine treatment (Bullock et al, 2005). Thus, some studies do suggest a role for BuChE in a disease process (Alzheimer's disease), especially in association with other genetic risk factors such as ApoE4 (Lane et al, 2008), although, as noted earlier, the putative direction of the effect is that the presence of BuChE activity is detrimental rather than protective, and some authors have called for studies to identify cholinesterase inhibitors that are selective for BuChE as potentially advantageous in treatment of AD (Lane et al, 2006).…”