Ann Rheum Dis. Published Online First: 17 August 2007. doi:10.1136/ard.2007.074666
Extended Report |
-463 G/A myeloperoxidase promoter polymorphism in giant cell arteritis
1 Arcispedale S Maria Nuova, Italy
* To whom correspondence should be addressed. E-mail: salvarani.carlo{at}asmn.re.it.
Accepted 27 July 2007
Abstract
Objective: To investigate potential associations between -463 G/A myeloperoxidase (MPO) promoter polymorphism and susceptibility to, and clinical features of giant cell arteritis (GCA).
Methods: A total of 156 patients with biopsy-proven GCA who were residents of Reggio Emilia, Italy, and 235 population-based controls from the same geographic area were genotyped for -463 G/A promoter polymorphism of the MPO gene by molecular methods. The patients were subgrouped according to the presence or absence of polymyalgia rheumatica and severe ischemic complications (visual loss and/or cerebrovascular accidents).
Results: The distribution of the MPO-G/A genotype differed significantly between GCA patients and the controls (Pcorr = 0.003). Allele G was significantly more frequent in GCA patients than in the controls (P corr = 0.0002, OR 2.0, 95% CI 1.4-2.9). Homozygosity for the G allele was significantly more frequent in GCA patients than in controls (P corr = 0.0002, OR 2.2, 95% CI 1.4-3.4). No significant associations were found when GCA patients with and without polymyalgia rheumatica or with and without severe ischemic complications were compared.
Conclusion: Our findings show that the -463 G/A promoter polymorphism of the MPO gene is associated with GCA susceptibility and support a role for MPO in the pathophysiology of GCA.
Keywords: giant cell arteritis, ischemic complication, myeloperoxidase polymorphism, myeloperoxise
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