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Vitamin D status in a representative sample of Irish adults aged ≥18 years

Published online by Cambridge University Press:  09 September 2010

S. Muldowney
Affiliation:
School of Food and Nutritional Sciences, University College Cork, Cork, Republic of Ireland
E. Walsh
Affiliation:
School of Food and Nutritional Sciences, University College Cork, Cork, Republic of Ireland
J. Walton
Affiliation:
School of Food and Nutritional Sciences, University College Cork, Cork, Republic of Ireland
B. McNulty
Affiliation:
Department of Medicine, University College Cork, Cork, Republic of Ireland
A. Nugent
Affiliation:
Department of Medicine, University College Cork, Cork, Republic of Ireland
M. J. Gibney
Affiliation:
Department of Medicine, University College Cork, Cork, Republic of Ireland
A. Flynn
Affiliation:
School of Food and Nutritional Sciences, University College Cork, Cork, Republic of Ireland
K. D. Cashman
Affiliation:
School of Food and Nutritional Sciences, University College Cork, Cork, Republic of Ireland Institute for Food and Health, University College Dublin, Dublin, Republic of Ireland
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Abstract

Type
Abstract
Copyright
Copyright © The Authors 2010

Recent data on vitamin D status in Ireland is limited to convenience samples(Reference Cashman, Hill and Lucey1Reference Hill, Flynn and Kiely3). The objective of this study was to evaluate vitamin D status in a more representative sample of Irish adults aged ≥18 years. Analysis was based on a sub-sample (n 519) of the National Adult Nutrition Survey of adults aged ≥18 years, which is still ongoing. Serum 25-hydroxyvitamin D (25(OH)D) concentration was measured in 249 men and 270 women using an ELISA method. Given that Ireland is at 51–55°N, ultraviolet blue radiation from the sun is insufficient to stimulate dermal synthesis of vitamin D between November and March(Reference Webb, Kline and Holick4), and so we nominated November–March as winter and April–October as summer.

Gender (female, 52%) and season (winter, 49%) were evenly distributed in this sub-sample, whereas most subjects donated a fasting blood sample (76%) and were from Munster (74%). Median (Interquartile range) serum 25(OH)D concentration was 55.8 (41.6–72.2) nmol/l for the sub-sample, with significant differences (P<0.0001) between winter (48.9 [37.5–65.2] nmol/l) and summer (61.7 [48.9–76.1] nmol/l), after adjustment for age, gender, region and fasting/non-fasting blood samples. Furthermore, serum 25(OH)D concentration was higher (P=0.041) in those who were fasting for blood donation (56.8 [42.6–72.0]) compared to those who were non-fasting at the time of donation (53.5 [38.3–73.3] nmol/l); however, 76% were fasting at time of blood donation. There was no differences in serum 25(OH)D concentration according to gender, age, or region (P>0.2). 2%, 40% and 84% of this sub-sample had serum 25(OH)D levels throughout the year<25 nmol/l <50 nmol/l and <80 nmol/l, respectively, which are internationally recognised thresholds of vitamin D deficiency and insufficiency. The figure shows the difference in prevalence rates of serum 25(OH)D<25, 50 and 80 nmol/l, stratified by season.

In conclusion, these data show a high prevalence of serum 25(OH)D concentrations <50 and <80 nmol/l which, while still under debate, are commonly used as thresholds for vitamin D insufficiency. Severe vitamin D deficiency (serum 25(OH)D<25 nmol/l) was not common. As expected, serum 25(OH)D concentration differed significantly according to season. It would be interesting to see if similar trends are present when the complete representative sample is analysed and then the data can be used to develop effective nutrition policies and health promotion campaigns to improve vitamin D status.

We wish to acknowledge the Irish Department of Agriculture, Fisheries and Food under the Food for Health Research Initiative (2007–2012) for their support.

References

1.Cashman, KD, Hill, TR, Lucey, AJ et al. (2008) Am J Clin Nutr 88, 15351542.CrossRefGoogle Scholar
2.Cashman, KD, Wallace, JM, Horigan, G et al. (2009) Am J Clin Nutr 89, 13661374.CrossRefGoogle Scholar
3.Hill, TR, Flynn, A, Kiely, M et al. (2006) Ir Med J 99, 4849.Google Scholar
4.Webb, AR, Kline, L & Holick, MF (1988) J Clin Endocrinol Metab 67, 373378.CrossRefGoogle Scholar