Hostname: page-component-76fb5796d-vfjqv Total loading time: 0 Render date: 2024-04-26T10:09:58.025Z Has data issue: false hasContentIssue false

Vitamin D in public health nutrition

Published online by Cambridge University Press:  03 March 2014

Maxine P Bonham
Affiliation:
Deputy Editors
Christel Lamberg-Allardt
Affiliation:
Deputy Editors
Rights & Permissions [Opens in a new window]

Abstract

Type
Editorial
Copyright
Copyright © The Authors 2014 

The year 2013 was again a very active year in the vitamin D field. The selection of papers discussed here focus on vitamin D intake, fortification, supplements, and vitamin D status and its associations with diseases and health. Here, we discuss several of the papers in the context of methodological challenges and gaps in current knowledge.

Marker and cut-points

Serum 25-hydroxyvitamin D concentration (25(OH)D) is considered the best marker of vitamin D status, with low concentrations indicating low status. However, cut-points for vitamin D deficiency and insufficiency vary, reflecting variable views among experts. Notably, the Institute of Medicine( 1 ) concluded in 2010 that there are no systematic reviews on the cut-points, and this still stands. Papers by Chang et al.( Reference Chang, Liu and Shi 2 ) and Lee et al.( Reference Lee, Kim and Hong 3 ) used a cut-off of vitamin D < 50 nmol/l to represent deficiency, reflective of the cut-offs recommended by the Institute of Medicine( 1 ), the Endocrine Society( Reference Holick, Binkley and Bischoff-Ferrari 4 ) and the Nordic Nutrition Recommendations( Reference Lamberg-Allardt, Brustad and Meyer 5 ). The paper by Oliveira et al.( Reference Oliveira, Novaes and Azeredo 6 ) used a cut-off of ≤25 nmol/l to assess deficiency( Reference Bischoff-Ferrari, Giovannucci and Willett 7 ) whereas Wallingford et al.( Reference Wallingford, Jones and Kobayashi 8 ) and Golbahar et al.( Reference Golbahar, Al-Saffar and Altayab Diab 9 ) reported vitamin D deficiency as serum 25(OH)D < 30 nmol/l (risk for bone health) in line with the Institute of Medicine recommendations( 1 ). Other papers separated vitamin D status into quartiles( Reference Robertsen, Grimnes and Melbye 10 ) and tertiles( Reference Chung, Lee and Hong 11 ), which may be valid for their research but hinders overall assessment of vitamin D status against established cut-offs.

25-Hydroxyvitamin D assays

Also problematic is that the methods used to assess 25(OH)D differ among the papers. It is well known that there is a large variation among methods and laboratories using the same methods( Reference Barake, Daher and Salti 12 Reference Wallace, Gibson and de la Hunty 16 ), leading to different estimates of vitamin D deficiency in a population( Reference Snellman, Melhus and Gedeborg 15 ). The US National Institutes of Health recently started the Vitamin D Standardization Project (http://ods.od.nih.gov/Research/VitaminD.aspx), which aims to harmonize and standardize 25(OH)D assessment – useful, for example, for national surveys( Reference Cashman, Kiely and Kinsella 17 , Reference Sempos, Vesper and Phinney 18 ). A key factor in this process is the development of a 25(OH)D standard by the National Institute of Standards and Technology in the USA. Knowing that there is large variation in results from different assays, validating the assays used in individual studies is critical for comparing results across studies.

Estimating vitamin D intake

Estimating dietary intake of vitamin D is another challenge. In populations where natural vitamin D sources are few, food diaries are usually not enough to give a good estimation of vitamin D intake on the individual level and cannot be used in regression analyses. Moreover, many food composition databases do not cover all vitamin D sources. In an Irish study on children and teenagers( Reference Black, Walton and Flynn 19 ) food intake was recorded by either a 7 d weighed food diary (children) or a 7 d semi-weighed food diary (teens). Both food diary methods were based on the methodology used in the national North/South Ireland Food Consumption Survey( Reference Harrington, Robson and Kiely 20 ). Interestingly, they had to use British, Irish, American and Danish food composition databanks to cover all the important vitamin D sources for the study. This reflects a problem present in many countries – that food composition data may not represent real vitamin D intake.

Influence of sun exposure

Sun exposure is an important regulator of 25(OH)D concentration but also difficult to estimate. Vitamin D is produced in human skin when exposed to UVB irradiation, whether natural (sunshine) or artificial. But vitamin D production in human skin is affected by many external and individual factors. At latitudes above ∼50°N, both the qualitative and quantitative properties of the sunlight are not sufficient for vitamin D production during part of the year( Reference Engelsen 21 ). The ozone layer also effectively absorbs UVB light, and clouds can attenuate UVB radiation by as much as 99 %. Surface reflection, especially from snow, can reflect up to 95 % of UVB radiation. And at the individual level, time spent outdoors, sunscreen use and clothing affect sun-induced vitamin D production. Further, individuals with initially low 25(OH)D seem to have a lower threshold concentration for vitamin D production in skin compared with individuals with higher concentrations, and sun-induced vitamin D production can be up to six times higher in people with pale skin compared with people with dark skin( Reference Engelsen 21 ).

Despite the difficulty of estimating sun exposure, many instruments – questionnaires as well as devices for recording individual UV irradiation – have been developed to do so for research purposes. In this issue, Cook and co-workers( Reference Cook, Moon and Dong 22 ) describe a telephone-administered questionnaire used in the Ovarian Cancer in Alberta (OVAL) Study developed to assess lifetime exposure to vitamin D from sun-induced vitamin D synthesis and diet, based on assessment for every tenth year, in ninety females. The authors tested it against the questionnaire used in the Geraldton Skin Cancer Prevention Survey, considered a gold standard, in a cross-over design. The new OVAL questionnaire gave equivalent results to the Geraldton survey, with estimated average lifetime sun exposure reported in the two studies as 411 h/year and 358 h/year, respectively. The authors speculatively conclude that sun exposure may exceed the contribution of dietary intake to total vitamin D exposure during the warmer months of the year. In another study in this issue, Wallingford et al.( Reference Wallingford, Jones and Kobayashi 8 ) also addressed the contribution of UV irradiation from sun and tanning beds in their study on predictors of vitamin D status in premenopausal women (see below).

Predicting vitamin D status

Papers by Golbahar et al.( Reference Golbahar, Al-Saffar and Altayab Diab 9 ) and Wallingford et al.( Reference Wallingford, Jones and Kobayashi 8 ) in this issue discuss a range of predictors of vitamin D status. Wallingford et al.( Reference Wallingford, Jones and Kobayashi 8 ) identified vitamin D supplement use, tanning bed use and season as predictors of vitamin D status in eighty-three premenopausal, shift-working nurses in Canada. Only 4 % were deficient (<30 nmol/l) and 5 % had insufficient (<50 nmol/l) 25(OH)D concentrations after summer; the percentages after winter/spring were 6 % and 7 %, respectively. In their study in 500 Bahrainis, Golbahar and co-authors( Reference Golbahar, Al-Saffar and Altayab Diab 9 ) identified female gender and age as risk factors for vitamin D deficiency (serum 25(OH)D < 30 nmol/l) along with season and conservative clothing style. Only season predicted vitamin D insufficiency (serum 25(OHD < 50 nmol/l) in both males and females. Interestingly, summer months were associated with lower vitamin D status, possibly a result of high humidity and temperatures and reduced outside activities. The lower vitamin D status observed in women was attributed partly to women spending more time indoors and clothing style.

The high cost of screening for vitamin D insufficiency has spurred the development of questionnaires to predict the need for vitamin D assessment. Nabak et al.( Reference Nabak, Johnson and Keuler 23 ) report high sensitivity (≥89 %) but low specificity (≤35 %) of predicting low or high risk for vitamin D insufficiency (serum 25(OH)D < 50 nmol/l) based on a composite score in postmenopausal women. Predictors incorporated in the score included race, skin type, BMI, sunscreen use and use of vitamin D supplements – predictors previously reported to be associated with vitamin D status. The authors concede that revision of the questionnaire to include questions relating to exercise and fatty fish intake might improve the performance of the questionnaire. The idea of being able to accurately predict who may or may not need vitamin D status screening has important financial implications. However, as already indicated, development of a questionnaire relies on known predictors of vitamin D. Furthermore, this work needs to be extended to men and to a wider variety of age ranges.

Vitamin D status in children and adolescents

Six of the papers in this issue focus on children and adolescents( Reference Chang, Liu and Shi 2 , Reference Lee, Kim and Hong 3 , Reference Oliveira, Novaes and Azeredo 6 , Reference Chung, Lee and Hong 11 , Reference Black, Walton and Flynn 19 , Reference Lehtonen, Ormisson and Nucci 24 ). Black and co-workers( Reference Black, Walton and Flynn 19 ) studied vitamin D intakes in a group of children and a group of teens in Ireland who had participated in the Children's and Teens’ National Nutrition Surveys in 2004 and 2007. The results revealed that vitamin D intakes from food and fortified foods were very low in all age groups. Those taking supplements had a somewhat higher intake but did not reach the US Institute of Medicine dietary reference intake( 1 ). These results probably reflect the situation in many countries. Natural sources are few, and fortification may not be targeted to the right segment of the population. Fortification has to be carefully planned and researched to reach to the right individuals but also to minimize risk with excessive intake. Long-term supplementation is an option but, as seen in Black et al.'s study, may not be feasible on a population level in these age groups.

Supplements may be an important source of vitamin D in infants all over the world. Vitamin D supplements have been recommended to children aged 0–2 years in Northern Europe for decades to combat rickets( Reference Lamberg-Allardt, Brustad and Meyer 5 ). Lehtonen et al.( Reference Lehtonen, Ormisson and Nucci 24 ) conducted a survey on the use of supplements in 2159 infants aged 1–6 months in Europe, North America and Australia based on data from the TRIGR study – a longitudinal study examining the effect of infant weaning on to a hydrolysed infant formula on incidence of type I diabetes in those with increased genetic susceptibility. Their results revealed that the majority of the infants were supplemented in Europe, approximately half in Canada, yet very few in the USA and Australia. Interestingly, longer maternal education, higher gestational age and older maternal age were study-wide associated with greater use of supplements.

Three studies focus on associations between vitamin D status and health outcomes in children and/or adolescents from different parts of the world. In 160 Brazilian adolescents, of whom about 50 % were overweight, vitamin D intake was assessed by a 3 d food record. Vitamin D intake was low and no correlation between intake and 25(OH)D was apparent, which the authors suggest could be due to the food composition databank( Reference Oliveira, Novaes and Azeredo 6 ). However, seasonal variation was not taken into account, three days may be too short for assessing intake and the 25(OH)D assay was not specified. The authors also reported negative associations with weight excess, abdominal obesity, hypercholesterolaemia, higher serum parathyroid hormone concentration, insulin resistance, hyperinsulinaemia and hypertension. However, causality cannot be established and all outcomes could also be related to, for example, physical activity (related to time spent outside), although it was not associated with 25(OH)D concentration.

A study by Chung et al.( Reference Chung, Lee and Hong 11 ) reported that three-quarters of a representative adolescent population (n 1466, age 10–19 years) enrolled in the Korea National Health and Nutrition Examination Survey (KHANES, 2009–2010) were vitamin D deficient. Vitamin D status in these participants was significantly related to markers of adiposity, fat mass percentage, insulin and impaired fasting glucose after adjustment for age, sex, season and physical activity. However, UVB exposure was not assessed and there was a lack of information pertaining to sunscreen use, visceral adiposity and total vitamin D intake – all reported predictors of vitamin D status. Lee et al.( Reference Lee, Kim and Hong 3 ) also reported data on 1510 adolescents (age 12–18 years) enrolled in the 2008–2009 KHANES study. Independent predictors of low vitamin D status were winter season, higher education and a lack of supplementation with vitamin D. Both papers( Reference Lee, Kim and Hong 3 , Reference Chung, Lee and Hong 11 ) appeared to use a cut-off value of 50 nmol/l as representative of vitamin D deficiency. In another study in a paediatric population, Chang et al.( Reference Chang, Liu and Shi 2 ) reported prevalences of deficiency (<50 nmol/l) and insufficiency (<75 nmol/l ) of 21·0 % and 27.4 % respectively in 1218 children from the Chinese province of Chengdu, Sichuan, displaying a lower level of deficiency when compared with the KHANES study. In that population vitamin D insufficiency and deficiency increased with age, and the association of vitamin D deficiency with elevated serum Pb concentrations was also reported. However, dietary intakes of essential nutrients known to influence vitamin D status were not investigated and collection of samples was not controlled based on seasonality.

Vitamin D and disease risk

The association of vitamin D (insufficiency) with a variety of disease states/markers of disease in adults is well documented. In a cross-sectional study in 42 730 participants (age 40–75 years) of the Health Professionals Follow-Up Study, an association between predictors of vitamin D and lower incidence of tooth loss and periodontitis was observed( Reference Jimenez, Giovannucci and Krall Kaye 25 ). The 25(OH)D score used in that study was updated for each follow-up, conducted biannually since 1988, for most of the components in the score, e.g. physical activity, lifestyle behaviour, physical characteristics. Dietary data were collected every 4 years by FFQ. The highest quintile of the updated predicted vitamin D score was associated with a 20 % lower incidence of tooth loss compared with the lowest. Although the study cannot prove causality, the longitudinal study design with 20-year follow-up and large sample size are strengths. In a cross-sectional study in 6350 middle-aged and elderly participants in Norway( Reference Robertsen, Grimnes and Melbye 10 ), no association was observed between serum 25(OH)D and symptoms of respiratory tract infection, adding complexity to this issue. Previous studies showed mixed results, and a systematic review has called for more rigorously designed trials to clarify the relationship between ‘vitamin D and the immune response to infection’( Reference Yamshchikov, Desai and Blumberg 26 ).

Conclusion

In conclusion, the studies discussed in this editorial contribute to the consensus that vitamin D deficiency and insufficiency are prevalent and not limited to a particular age group or geographical location. Fortification of foods and supplementation with vitamin D appear to improve status but rely on the consumption of these products by those at most risk, as well as on their availability and affordability. A number of well-established predictors of status, including gender, race, sunscreen use and UVB exposure, have been incorporated into questionnaires that may be able to predict those at risk of vitamin D deficiency. But what does remain uncertain is any clearly established risk of a low vitamin D status with respect to adverse health outcomes other than those related to bone health. Associations between vitamin D status and some markers of poor health were discussed but, as with most associations, randomized controlled trials are needed to confirm these associations. Fortunately, many large trials are currently ongoing in Europe and the USA. A recent systematic review has raised the possibility that low vitamin D status is a result of ill health rather than a cause( Reference Autier, Boniol and Pizot 27 ). In probably the largest systematic review of its type on vitamin D and ill health, the authors concluded that vitamin D intervention studies ‘did not show an effect of vitamin D supplementation on disease occurrence’, again raising the question of whether low vitamin D status is the cause or result of ill health. This latest systematic review and the findings emanating from the thirteen papers in this issue, described here, further articulate the urgent need for quality randomized controlled trials to be undertaken to delineate non-bone related health effects of a low vitamin D status. Furthermore, clarity and transparency are required when describing levels of vitamin D deficiency in published research and standardization of the use of cut-offs and assessment of vitamin D status will assist public health researchers in the design and execution of future studies.

References

1. Institute of Medicine Committee to Review Dietary Reference Intakes for Vitamin D and Calcium (2011) Dietary Reference Intakes for Calcium and Vitamin D [AC Ross, CL Taylor, AL Yatkine et al., editors]. Washington, DC: National Academies Press.Google Scholar
2. Chang, L, Liu, X, Shi, H et al. (2014) Association of 25-hydroxyvitamin D with Hb and lead in children: a Chinese population-based study. Public Health Nutr 17, 827832.CrossRefGoogle ScholarPubMed
3. Lee, YA, Kim, HY, Hong, H et al. (2014) Risk factors for low vitamin D status in Korean adolescents: the Korea National Health and Nutrition Examination Survey (KNHANES) 2008–2009. Public Health Nutr 17, 764771.CrossRefGoogle ScholarPubMed
4. Holick, MF, Binkley, NC, Bischoff-Ferrari, HA et al. (2011) Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab 96, 19111930.CrossRefGoogle ScholarPubMed
5. Lamberg-Allardt, C, Brustad, M, Meyer, HE et al. (2013) Vitamin D – a systematic literature review for the 5th edition of the Nordic Nutrition Recommendations. Food Nutr Res 2013, 57.Google Scholar
6. Oliveira, RM, Novaes, JF, Azeredo, LM et al. (2014) Association of vitamin D insufficiency with adiposity and metabolic disorders in Brazilian adolescents. Public Health Nutr 17, 787794.CrossRefGoogle ScholarPubMed
7. Bischoff-Ferrari, HA, Giovannucci, E, Willett, WC et al. (2006) Estimation of optimal serum concentrations of 25-hydroxyvitamin D for multiple health outcomes. Am J Clin Nutr 84, 1828.Google Scholar
8. Wallingford, SC, Jones, G, Kobayashi, LC et al. (2014) UV and dietary predictors of serum 25-hydroxyvitamin D concentrations among young shift-working nurses and implications for bone density and skin cancer. Public Health Nutr 17, 772779.Google Scholar
9. Golbahar, J, Al-Saffar, N, Altayab Diab, D et al. (2014) Predictors of vitamin D deficiency and insufficiency in adult Bahrainis: a cross-sectional study. Public Health Nutr 17, 732738.CrossRefGoogle ScholarPubMed
10. Robertsen, S, Grimnes, G & Melbye, H (2014) Association between serum 25-hydroxyvitamin D concentration and symptoms of respiratory tract infection in a Norwegian population: the Tromsø Study. Public Health Nutr 17, 780786.CrossRefGoogle Scholar
11. Chung, SJ, Lee, YA, Hong, H et al. (2014) Inverse relationship between vitamin D status and insulin resistance and the risk of impaired fasting glucose in Korean children and adolescents: the Korean National Health and Nutrition Examination Survey (KNHANES) 2009–2010. Public Health Nutr 17, 795802.CrossRefGoogle ScholarPubMed
12. Barake, M, Daher, RT, Salti, I et al. (2012) 25-Hydroxyvitamin D assay variations and impact on clinical decision making. J Clin Endocrinol Metab 97, 835843.CrossRefGoogle ScholarPubMed
13. Bedner, M, Lippa, KA & Tai, SS (2013) An assessment of 25-hydroxyvitamin D measurements in comparability studies conducted by the Vitamin D Metabolites Quality Assurance Program. Clin Chim Acta 426, 611.Google Scholar
14. Carter, GD, Berry, JL, Gunter, E et al. (2010) Proficiency testing of 25-hydroxyvitamin D (25-OHD) assays. J Steroid Biochem Mol Biol 121, 176179.Google Scholar
15. Snellman, G, Melhus, H, Gedeborg, R et al. (2010) Determining vitamin D status: a comparison between commercially available assays. PloS ONE 5, e11555.CrossRefGoogle ScholarPubMed
16. Wallace, AM, Gibson, S, de la Hunty, A et al. (2010) Measurement of 25-hydroxyvitamin D in the clinical laboratory: current procedures, performance characteristics and limitations. Steroids 75, 477488.Google Scholar
17. Cashman, KD, Kiely, M, Kinsella, M et al. (2013) Evaluation of Vitamin D Standardization Program protocols for standardizing serum 25-hydroxyvitamin D data: a case study of the program's potential for national nutrition and health surveys. Am J Clin Nutr 97, 12351242.Google Scholar
18. Sempos, CT, Vesper, HW, Phinney, KW et al. (2012) Vitamin D status as an international issue: national surveys and the problem of standardization. Scand J Clin Lab Invest Suppl 243, 3240.Google ScholarPubMed
19. Black, LJ, Walton, J, Flynn, A et al. (2014) Adequacy of vitamin D intakes in children and teenagers from the base diet, fortified foods and supplements. Public Health Nutr 17, 721731.Google Scholar
20. Harrington, KE, Robson, PJ, Kiely, M et al. (2001) The North/South Ireland Food Consumption Survey: survey design and methodology. Public Health Nutr 4, 10371042.Google Scholar
21. Engelsen, O (2010) The relationship between ultraviolet radiation exposure and vitamin D status. Nutrients 2, 482495.CrossRefGoogle ScholarPubMed
22. Cook, LS, Moon, BL, Dong, Y et al. (2014) Reliability of self-reported sun exposure in Canadian women and estimation of lifetime exposure to vitamin D from sun and diet. Public Health Nutr 17, 747755.CrossRefGoogle Scholar
23. Nabak, AC, Johnson, RE, Keuler, NS et al. (2014) Can a questionnaire predict vitamin D status in postmenopausal women? Public Health Nutr 17, 739746.Google Scholar
24. Lehtonen, E, Ormisson, A, Nucci, A et al. (2014) Use of vitamin D supplements during infancy in an international feeding trial. Public Health Nutr 17, 810822.CrossRefGoogle Scholar
25. Jimenez, M, Giovannucci, E, Krall Kaye, E et al. (2014) Predicted vitamin D status and incidence of tooth loss and periodontitis. Public Health Nutr 17, 844852.Google Scholar
26. Yamshchikov, AV, Desai, NS, Blumberg, HM et al. (2009) Vitamin D for treatment and prevention of infectious diseases: a systematic review of randomized controlled trials. Endocr Pract 15, 438449.Google Scholar
27. Autier, P, Boniol, M, Pizot, C et al. (2014) Vitamin D status and ill health: a systematic review. Lancet Diabetes Endocrinol 2, 7689.Google Scholar