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Association between Parkinson's disease and polymorphisms in the nNOS and iNOS genes in a community-based case-control study.

Abstract : Excess of nitric oxide (NO) has been shown to exert neurotoxic impacts in the brain. Moreover, inhibition of two NO-synthesizing enzymes, neuronal NOS (nNOS) and inducible NOS (iNOS), displays neuroprotective effects in the MPTP model of Parkinson's disease (PD). These data suggest a possible involvement of NOS as factors controlling the resistance of the nigral dopaminergic neurons to environmental insults. Therefore, we investigated whether polymorphisms present in these genes could contribute to the risk of developing PD. We carried out a community-based case-control study among subjects enrolled in the Mutualit?ociale Agricole, the French health insurance organization for workers connected to agriculture. Two-hundred and nine PD patients and 488 controls of European (mostly French) ancestry and matched for age, sex and region of residency were included in this study. Associations were observed with polymorphisms present in exon 22 of iNOS (OR for AA carriers=0.50, 95% CI=0.29-0.86, P=0.01) and in exon 29 of nNOS (OR for carriers of the T allele=1.53, 95% CI=1.08-2.16, P=0.02); no association was observed with a polymorphism in exon 18 of nNOS (OR for carriers of the T allele=1.20, 95% CI=0.85-1.69, P=0.30). Moreover, a significant interaction of the nNOS polymorphisms with current and ever cigarette smoking was found (nNOS 18, P=0.05; nNOS 29, P=0.04). All together, these data favour an involvement of these two genes as new modifier genes in PD.
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https://www.hal.inserm.fr/inserm-00266834
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Submitted on : Tuesday, March 25, 2008 - 3:51:28 PM
Last modification on : Wednesday, August 19, 2020 - 11:58:38 AM

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Clotilde Levecque, Alexis Elbaz, Jacqueline Clavel, Florence Richard, Jean-Sébastien Vidal, et al.. Association between Parkinson's disease and polymorphisms in the nNOS and iNOS genes in a community-based case-control study.. Human Molecular Genetics, Oxford University Press (OUP), 2003, 12 (1), pp.79-86. ⟨10.1093/hmg/ddg009⟩. ⟨inserm-00266834⟩

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