ABSTRACT
As a member of the Population Health Research Network Australia, being an Australian collaboration established to support the use of linked data for research and other purposes, the Tasmanian Data Linkage Unit [TDLU) provides linked-data services in Australia's smallest state, and as part of the Menzies Institute for Medical Research at the state's only University, the University of Tasmania. The TDLU works in close collaboration with the Tasmanian Government Department of Health and other key stakeholders both in Tasmania and Australia representing government, education, research, and the community sector. The TDLU is one of the newest data linkage services in Australia, and the smallest node of the PHRN having operated for almost nine years by less than three full time equivalent staff. However, despite its size and relative maturity as a provider of linked-data services, the TDLU continues to grow the number of datasets linked on a routine and ad-hoc basis, the number of projects completed, the size of its Master Linkage Map and number of 'keys' stored in this Map. The TDLU places high-emphasis on security, privacy preservation, innovation, quality assurance, stakeholder engagement and providing responsive and exemplary services to users of linked-data.
ABSTRACT
UNLABELLED: We studied the association between osteoporotic fractures and prior non-melanoma skin cancer (NMSC, a biomarker for cumulative sun exposure). The risk of prior NMSC in our fracture cohort was significantly reduced (standardised incidence ratio 0.69, 95% CI 0.61, 0.78). Adequate lifetime sun exposure may be necessary to protect against osteoporotic fractures in later life. INTRODUCTION: The relationship between cumulative sun exposure and osteoporotic fractures is uncertain. We aimed to study the association between non-melanoma skin cancer (NMSC), a marker of cumulative sun exposure, and osteoporotic fractures in an older cohort. METHODS: A retrospective cohort study in southern Tasmania in people aged at least 50 years with incident radiographic fracture (n = 2,283) was carried out. By record linkage to the Tasmanian Cancer Registry the cohort was followed backwards through time until the occurrence of NMSC or end-of follow-up. Relative risk was estimated by the standardised incidence ratio (SIR) using sex-, age- and calendar year-specific cancer incidence rates in southern Tasmania as reference. RESULTS: The incidence of prior NMSC in the fracture cohort was 31% lower than for the general population (SIR 0.69, 95% CI 0.61, 0.78). This effect was significant for most fracture subtypes except pelvic and wrist fractures and observed for both NMSC subtypes, squamous cell carcinoma and basal cell carcinoma. CONCLUSIONS: Older people with osteoporotic fractures may have had lifestyles linked to lower cumulative sunlight exposure. Achieving a balance between adequate lifetime sun exposure and protection against its adverse effects (such as fractures and skin cancer) may require assessment of individual risks.
