NO ASSOCIATION OF ALPHA(1)-ANTICHYMOTRYPSIN FLANKING REGION POLYMORPHISM AND ALZHEIMER-DISEASE RISK IN EARLY-ONSET AND LATE-ONSET ALZHEIMER-DISEASE PATIENTS
Mp. Bass et al., NO ASSOCIATION OF ALPHA(1)-ANTICHYMOTRYPSIN FLANKING REGION POLYMORPHISM AND ALZHEIMER-DISEASE RISK IN EARLY-ONSET AND LATE-ONSET ALZHEIMER-DISEASE PATIENTS, Neuroscience letters, 250(2), 1998, pp. 79-82
The alpha(1)-antichymotrypsin (AACT)-155 allele was found elsewhere to
have a significant effect on Alzheimer disease (AD) risk in individua
ls with at least one APOE-4 allele, We compared AACT genotypes of 284
cases of sporadic AD and 172 controls. The frequency of the AACT-155 a
llele did not differ significantly between cases and controls, either
overall or when restricted to subjects with at least one APOE-LF allel
e. Logistic regression controlling for age and sex failed to show an e
ffect due to AACT either alone or acting with APOE. There was no evide
nce of an interaction between APOE-4 and the AACT-155 allele to reduce
age at onset. Thus, our data do not support an association of AACT-15
5 with risk or age at onset in AD. (C) 1998 Elsevier Science Ireland L
td. All rights reserved.