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      Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease.

      Movement Disorders
      Adult, Aged, Alleles, Amino Acid Substitution, genetics, Aryldialkylphosphatase, Esterases, Female, Gene Frequency, Genotype, Humans, Leucine, Lipid Peroxidation, Male, Methionine, Middle Aged, Parkinson Disease, diagnosis, Polymorphism, Genetic, Reference Values, Sweden

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          Abstract

          Paraoxonase1 (PON1) is an arylesterase mainly expressed in the liver that hydrolyzes organophosphates such as pesticides, reported risk factors for Parkinson's disease (PD), and other neurotoxins. A Leu-Met 54 polymorphism in the gene for PON1-affecting enzyme activity was recently shown, employing a new restriction enzyme technique, to be associated with Parkinson's disease. We examined the same polymorphism by automated capillary sequencing in a sample of Caucasian subjects from the Stockholm area in Sweden (127 healthy individuals and 114 patients with PD) and found similar distributions and a similar difference in our sample. The genotype distribution in our PD material was LL 36.0%, LM 45.6%, and MM 18.4%; in our control material, it was LL 45.7%, LM 44.1%, and MM 10.2%. Based on the previously established increase in allele frequencies of the lower-activity Met-variant of PON1, we could confirm a significant association using a one-sided chi(2) test. Results remained significant with a two-sided chi(2) test, allowing for both increases and decreases in frequencies. Our data confirm an association between the PON1 Leu-Met 54 polymorphism and PD by demonstrating a similar association. The distribution between familial and nonfamilial PD patients was equal. No other synonymous or nonsynonymous polymorphisms were found in the sequenced coding region of PON1. Copyright 2002 Movement Disorder Society

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