Parkinson's disease (PD) is primarily an alpha -synucleinopathy, rather tha
n a tauopathy, bur there is evidence fur an indirect association of tau wit
h the pathogenetic process in PD. We therefore assessed the frequency in PD
of the tau A0 allele, a dinucleotide repeat marker that has been associate
d with a sporadic tauopathy, progressive supranuclear palsy (PSP). We found
the A0 allele to comprise 79.2% of 758 alleles from PD patients and 71.2%
of 264 control alleles (P = 0.008). We also performed a meta-analysis of th
ree previous reports, two of which failed to produce statistically signific
ant results. Taken together, they also support a PD/A0 allelic association,
even after correction for misdiagnosis of PSP as PD (P< 0.001). The A0/A0
genotype frequency in our patients (62.3%) did not differ significantly fro
m that in controls (53.0%, P = 0.062), but the mete-analysis, even after co
rrection for misdiagnosis, showed a significant result, with P = 0.002. The
frequency of A0 allele and the A0/A0 genotype were compatible with Hardy-W
einberg equilibrium. The frequency of the A0 allele and the A0/A0 genotype
in our patients with familial PD was not significantly greater than in thos
e with sporadic PD. We conclude that the tau protein map play a small role
in the pathogenesis of PD and that biochemical characterization of this rol
e may suggest opportunities for PD prophylaxis. (C) 2001 Movement Disorder
society.