Premium
Further evidence for an association of the Paraoxonase 1 (PON1) Met‐54 allele with Parkinson's disease
Author(s) -
Carmine Andrea,
Buervenich Silvia,
Sydow Olof,
Anvret Maria,
Olson Lars
Publication year - 2002
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.10172
Subject(s) - pon1 , arylesterase , paraoxonase , genotype , allele , allele frequency , genetics , medicine , parkinson's disease , polymorphism (computer science) , biology , psychology , disease , gene , oxidative stress
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 χ 2 test. Results remained significant with a two‐sided χ 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. © 2002 Movement Disorder Society