PT - JOURNAL ARTICLE AU - De Smit, Elisabeth AU - Clarke, Linda AU - Sanfilippo, Paul G AU - Merriman, Tony R AU - Brown, Matthew A AU - Hill, Catherine L AU - Hewitt, Alex W ED - , TI - Geo-epidemiology of temporal artery biopsy-positive giant cell arteritis in Australia and New Zealand: is there a seasonal influence? AID - 10.1136/rmdopen-2017-000531 DP - 2017 Aug 01 TA - RMD Open PG - e000531 VI - 3 IP - 2 4099 - http://rmdopen.bmj.com/content/3/2/e000531.short 4100 - http://rmdopen.bmj.com/content/3/2/e000531.full SO - RMD Open2017 Aug 01; 3 AB - Objective Previous studies, although inconclusive, have suggested possible associations of environmental risk factors with the development of giant cell arteritis (GCA). We aim to investigate seasonal influence on the incidence of GCA across Australia and New Zealand.Methods In establishing an international study to investigate the molecular aetiology of GCA, archived temporal artery biopsy (TAB) specimens primarily from Australia and New Zealand were obtained. Demographic details including age, sex and date of TAB were collected from collaborating pathology departments. The season in which GCA was diagnosed was determined and compared with previous reports investigating the association between environmental risk factors and GCA.Results Our study comprises data from 2224 TAB-positive patients with GCA; 2099 of which were from patients in Australia and New Zealand. The mean age at time of diagnosis was 76.4 years of age. The female-to-male ratio was 2.2:1. We noted equal distribution of the incidence rate across all four seasons (530–580 cases diagnosed every quarter). Statistical analysis of seasonal variation by Poisson regression and cosinor methods showed no incidence preponderance across seasons. Our results do not support a seasonal component contributing to the onset of disease. Our literature search identifies no consistent environmental risk factor in association with GCA.Conclusion This is the largest GCA data set reported outside of Europe. Our results demonstrate equal distribution of the incidence rate across all four seasons. In contrast to some earlier reports, we did not identify evidence of a seasonal component contributing to the onset of disease.