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      Use of linked administrative and laboratory data to confirm that serum 25(OH)D levels in pregnant women can be predicted from satellite estimates of ultraviolet radiation

      1 , 2 , 3 , 4 , 2 , 5 , 2 , 1 , 2
      International Journal of Epidemiology
      Oxford University Press (OUP)

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          Abstract

          Background

          Serum 25 hydroxyvitamin D [25(OH)D] levels of pregnant women have been linked to various health outcomes in their offspring. Satellite-derived ultraviolet radiation (UVR) data have been used as a proxy for 25(OH)D levels, as individual-level cohort studies are time-consuming, costly and only feasible for common outcomes.

          Methods

          Data on 25(OH)D levels from a public laboratory database were linked to data from the Western Australian Midwives’ Notification System and daily erythemal UVR dose from NASA satellites. Regression analysis was used to identify the time period prior to venesection where daily UVR dose best predicted 25(OH)D levels. A predictive model was used to validate the use of daily UVR dose as a proxy for personal sun exposure during pregnancy.

          Results

          Data from 19 173 pregnancies in women aged 18–43 years in Western Australia were included. The daily UVR dose averaged over the 90 days before venesection was the strongest UVR predictor of 25(OH)D level (a 5% increase per 1000 J m–2; equal to 3.3 nmol L–1 at the median of 66 nmol L–1). Ethnicity was the strongest predictor of 25(OH)D levels (21% lower in non-Caucasian vs Caucasian: equal to 7.2 nmol L–1 difference). Other significant predictors were gestation, age, year, parity, socio-economic status, remoteness, medical conditions and season.

          Conclusion

          NASA-derived erythemal UVR dose in the 90 days prior to venesection is a significant predictor of 25(OH)D levels in pregnant women. Linked administrative data can be used to investigate associations between UVR during pregnancy and health outcomes in offspring.

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          Most cited references39

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          Vitamin D: its role and uses in immunology.

          In recent years there has been an effort to understand possible noncalcemic roles of vitamin D, including its role in the immune system and, in particular, on T cell-medicated immunity. Vitamin D receptor is found in significant concentrations in the T lymphocyte and macrophage populations. However, its highest concentration is in the immature immune cells of the thymus and the mature CD-8 T lymphocytes. The significant role of vitamin D compounds as selective immunosuppressants is illustrated by their ability to either prevent or markedly suppress animal models of autoimmune disease. Results show that 1,25-dihydroxyvitamin D3 can either prevent or markedly suppress experimental autoimmune encephalomyelitis, rheumatoid arthritis, systemic lupus erythematosus, type I diabetes, and inflammatory bowel disease. In almost every case, the action of the vitamin D hormone requires that the animals be maintained on a normal or high calcium diet. Possible mechanisms of suppression of these autoimmune disorders by the vitamin D hormone have been presented. The vitamin D hormone stimulates transforming growth factor TGFbeta-1 and interleukin 4 (IL-4) production, which in turn may suppress inflammatory T cell activity. In support of this, the vitamin D hormone is unable to suppress a murine model of the human disease multiple sclerosis in IL-4-deficient mice. The results suggest an important role for vitamin D in autoimmune disorders and provide a fertile and interesting area of research that may yield important new therapies.
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            Modulation of the immune system by UV radiation: more than just the effects of vitamin D?

            Humans obtain most of their vitamin D through the exposure of skin to sunlight. The immunoregulatory properties of vitamin D have been demonstrated in studies showing that vitamin D deficiency is associated with poor immune function and increased disease susceptibility. The benefits of moderate ultraviolet (UV) radiation exposure and the positive latitude gradients observed for some immune-mediated diseases may therefore reflect the activities of UV-induced vitamin D. Alternatively, other mediators that are induced by UV radiation may be more important for UV-mediated immunomodulation. Here, we compare and contrast the effects of UV radiation and vitamin D on immune function in immunopathological diseases, such as psoriasis, multiple sclerosis and asthma, and during infection.
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              Past exposure to sun, skin phenotype, and risk of multiple sclerosis: case-control study.

              To examine whether past high sun exposure is associated with a reduced risk of multiple sclerosis. Population based case-control study. Tasmania, latitudes 41-3 degrees S. 136 cases with multiple sclerosis and 272 controls randomly drawn from the community and matched on sex and year of birth. Multiple sclerosis defined by both clinical and magnetic resonance imaging criteria. Higher sun exposure when aged 6-15 years (average 2-3 hours or more a day in summer during weekends and holidays) was associated with a decreased risk of multiple sclerosis (adjusted odds ratio 0.31, 95% confidence interval 0.16 to 0.59). Higher exposure in winter seemed more important than higher exposure in summer. Greater actinic damage was also independently associated with a decreased risk of multiple sclerosis (0.32, 0.11 to 0.88 for grades 4-6 disease). A dose-response relation was observed between multiple sclerosis and decreasing sun exposure when aged 6-15 years and with actinic damage. Higher sun exposure during childhood and early adolescence is associated with a reduced risk of multiple sclerosis. Insufficient ultraviolet radiation may therefore influence the development of multiple sclerosis.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                International Journal of Epidemiology
                Oxford University Press (OUP)
                0300-5771
                1464-3685
                February 01 2021
                March 03 2021
                November 21 2020
                February 01 2021
                March 03 2021
                November 21 2020
                : 50
                : 1
                : 303-313
                Affiliations
                [1 ]University of Western Australia, Perth, Western Australia
                [2 ]Telethon Kids Institute, Perth, Western Australia
                [3 ]National Centre for Epidemiology and Population Health, Research School of Population Health, Australian National University, Canberra, Australia
                [4 ]Centre for Ophthalmology and Visual Sciences, University of Western Australia, Perth, Australia
                [5 ]Perth Children’s Hospital, Perth Australia
                Article
                10.1093/ije/dyaa165
                d37a0458-4833-45f4-a34f-9543762e8642
                © 2020

                https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model

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