The aspartyl protease Cathepsin D has previously been suggested to play a r
ole in the Alzheimer's disease (AD) process because of its ability to cleav
e the P-amyloid precursor protein and the possibility that it may be one of
the 'secretase' enzymes. A functional C double right arrow T polymorphism
in the Cathepsin D gene (CATD) has been reported to be associated with incr
eased risk for AD in Caucasian case-control studies; specifically, the T-ca
rrying genotypes confer increased risk. We have examined this association i
n our own Caucasian dataset of 210 AD cases and 120 controls, and in an add
itional Hispanic dataset comprising 79 AD cases a nd 112 controls. In Hispa
nics we fi nd a modest interaction between CATD genotype and age of onset o
n risk for AD, such that the non-T-carrying genotype confers increased risk
. In our Caucasian dataset we find no evidence for association between the
CATD polymorphism and AD, although we do observe a small tendency towards a
n increase in the T-carrying genotypes in the case group, consistent with p
revious studies. We conducted an aggregate analysis of the published Caucas
ian datasets and found evidence that this CATD polymorphism (or another loc
us in linkage disequilibrium) does contribute significant, but small (<2%)
risk for AD. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.