| Literature DB >> 22191676 |
Pablo Coto-Segura1, Jorge Santos-Juanes, Juan Gómez, Victoria Alvarez, Marta Díaz, Belén Alonso, Ana I Corao, Eliecer Coto.
Abstract
Mitochondrial dysfunction could contribute to the pathogenesis of psoriasis (Ps) and Ps-arthritis (PsA). Several common mtDNA polymorphisms/haplogroups have been linked to differences in the production of reactive oxygen species and mitochondrial oxidative damage. To test the hypothesis of an association between mtDNA variants and Ps/PsA, we studied the single-nucleotide polymorphisms that define the common European haplogroups in a total of 325 patients and 300 controls from Spain. No allele/haplogroup was significantly associated with the risk for Ps. However, haplogroup J was significantly less frequent among patients with PsA, suggesting a protective effect in our population (p=0.04; odds ratio=0.39). We concluded that mtDNA may have a role in Ps and PsA.Entities:
Mesh:
Substances:
Year: 2011 PMID: 22191676 DOI: 10.1089/gtmb.2011.0266
Source DB: PubMed Journal: Genet Test Mol Biomarkers ISSN: 1945-0257