Vitamin D Deficiency Teenager

Postgrad Med J. 2007 Apr; 83(978): 230–235.

Vitamin D in childhood and adolescence

Received 2006 Aug 28; Accepted 2006 Dec 21.

Abstract

It is well‐established that prolonged and severe vitamin D deficiency leads to rickets in children and osteomalacia in adults. More marginal vitamin D deficiency is likely to be a significant contributing factor to osteoporosis risk. However, recent emerging data from studies of adults suggest that low vitamin D status (serum 25‐hydroxyvitamin D levels <50 nmol/l) may be contributing to the development of various chronic diseases, including cardiovascular disease, hypertension, diabetes mellitus, some inflammatory and autoimmune diseases, and certain cancers. Adequacy of vitamin D status in children and adolescents has been the focus of a number of recent investigations, and these studies have shown a high prevalence of low vitamin D status during the winter (especially in adolescents), with lower prevalence during the summer. Therefore, consideration of potential corrective strategies to allow children and adolescents to maintain adequate vitamin D status throughout the year, even in the absence of adequate summer sun exposure, is warranted.

Vitamin D is essential for intestinal calcium absorption and plays a central role in maintaining calcium homeostasis and skeletal integrity.1 It is well‐established that prolonged and severe vitamin D deficiency leads to rickets in children and osteomalacia in adults.2 In addition, while the aetiology of osteoporosis is multifactorial, it is believed that secondary hyperparathyroidism as a result of a more marginal vitamin D deficiency is a significant contributing factor.3 ,4 There has also been a growing body of evidence for the contribution of poor vitamin D status (ie, serum hydroxyvitamin D3 (25(OH)D3) levels below 50 nmol/l) to the development of various chronic diseases (for example, hypertension, cardiovascular diseases, diabetes mellitus, as well as some inflammatory and autoimmune diseases, and some forms of cancer) which are frequent in Western societies (for reviews, see Zitterman5 and Holick6). This may be of major concern in light of the sizeable numbers of subjects in many countries with serum 25(OH)D3 levels below 50 nmol/l, especially during winter. However, much of this evidence is from studies in adults and whether poor vitamin D status in childhood is a risk factor for these chronic diseases is less well understood. Moreover, the biochemical definition commonly used to classify an adult as marginally vitamin D deficient, or vitamin D insufficient, may not be appropriate for use in children and/or adolescents. The present review will begin with a brief recap of the physiological roles of vitamin D, and then will briefly consider the issue of defining vitamin D status. Then it will review the data on prevalence of poor vitamin D status among children and adolescents, the likely underlying causes for poor vitamin D status, and comment on possible health implications, especially those beyond rickets. Finally, some possible modes of addressing low vitamin D status in childhood and adolescence will be considered. The literature on vitamin D in childhood and adolescence in the present review was gathered from various sources, including, but not limited to, internet search engines and websites, electronic databases (in particular, Medline) and library resources.

PHYSIOLOGICAL EFFECTS OF VITAMIN D

Upon exposure of skin to solar ultraviolet B (UVB) radiation, 7‐dehydrocholesterol is converted to previtamin D3, which in turn is modified to vitamin D3 (cholecalciferol) at skin temperature. The vitamin D3 diffuses into the circulation and is transported protein‐bound to the liver where it is hydroxylated to 25(OH)D3 (calcidiol).2 Dietary‐derived vitamin D (as vitamin D3 and ergocalciferol (vitamin D2; from certain plants and fungi)) is also transported, via chylomicrons and the lymphatic system, to the liver for hydroxylation.2 Serum or plasma 25(OH)D3 is the most commonly used and appropriate biochemical marker of vitamin D status.2 ,7 In the kidney, 25(OH)D undergoes a further hydroxylation at the first carbon, catalysed by 1,α‐hydroxylase, to form 1,25(OH)2D3 (calcitriol), which is the biologically most active form of vitamin D.7 Although 1,25(OH)2D3 represents the active form of the vitamin, due to a tight regulation of its production as well as a relatively short half‐life (4–6 h), it is not a good indicator of vitamin D status.2 ,8

The biological effects of 1,25(OH)2D3 can be grouped into two categories: the "classical actions", mainly affecting calcium homeostasis; and the "non‐classical actions", which include functions unrelated to calcium metabolism, such as the regulation of cell differentiation and proliferation, cellular growth, the regulation of hormone secretion, among others.6

CLASSICAL EFFECTS OF VITAMIN D

The principal (classical) function of 1,25(OH)2D3 is to maintain serum calcium and phosphate concentration within the physiologically acceptable range. It is of utmost importance to maintain normal serum levels of calcium, as these are, in turn, needed for the normal mineralisation of bone, muscle contraction, nerve conduction and many other cellular functions.2 This tight regulation of plasma calcium concentration is achieved through a complex physiological system comprising the interaction of the calcitropic hormones, such as 1,25(OH)2D3, parathyroid hormone (PTH) and calcitonin (CT), with specific target tissues (kidney, bone and intestine) which serve to increase or to decrease the entry of calcium into the extracellular space (fig 1​ ).9 These well‐established effects of 1,25(OH)2D3 on the three target tissues have been described elsewhere in detail.2 ,6 People with prolonged vitamin D deficiency tend to have chronic elevations in serum PTH, known as secondary hyperparathyroidism, which may have consequences for the bone health (see below).1 ,10

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Figure 1 Homeostatic regulation of serum calcium. CT, calcitonin; GIT, gastrointestinal tract; PTH, parathyroid hormone.

NON‐CLASSICAL (NON‐SKELETAL) ACTIONS OF VITAMIN D

While the maintenance of calcium homeostasis and bone density are generally regarded as the main biological effects of 1,25(OH)2D3, studies have suggested other important roles of 1,25(OH)2D3 in various organs which may be independent of calcium concentration.2 In addition, the discovery that the vitamin D receptor is present in most tissues and cells of the body leads to the belief that 1,25(OH)2D3 has many biologic effects that are non‐calcaemic in nature.11 ,12 These include the regulation of cell differentiation and proliferation, cellular growth, and the regulation of hormone secretion, among others.6 It is also emerging that 1,25(OH)2D3 can be locally produced in several tissues that possess vitamin D receptors.2 Consequently, additional paracrine and autocrine roles have been proposed for 1,25(OH)2D3 apart from its calcium regulatory function.13

DEFINING VITAMIN D STATUS AND ITS ASSESSMENT

There is a general consensus that serum/plasma 25(OH)D should be used to assess vitamin D status as this reflects the amount ingested in the diet (including that from supplements and vitamin D‐fortified food products) and that produced in the skin in response to sunlight (UVB) exposure. On the other hand, there is a lack of consensus on levels of 25(OH)D that define different stages of vitamin D status. In relation to low vitamin D status, one distinction that could be drawn is that of severe clinical vitamin D deficiency, leading to overt skeletal abnormalities, versus subclinical vitamin D deficiency in which serum 25(OH)D3 levels are low but there is no or less apparent skeletal or calcium abnormalities.

It is clearly recognised that serum/plasma 25(OH)D3 levels below 12.5 nmol/l can result in bone diseases, such as rickets in infants and osteomalacia in adults.14 ,15 There is also evidence that circulating 25(OH)D3 levels below 20–25 nmol/l may result in rickets and osteomalacia in the longer term.16 ,17 In many cases, the low 25(OH)D3 levels will be accompanied by elevated serum/plasma 1,25(OH)2D3, PTH and alkaline phosphatase levels, reduced serum phosphate and normal or reduced serum calcium levels.18

Definite cut‐off levels for circulating 25(OH)D3 which reflect subclinical vitamin D deficiency have not yet been fully defined. Low vitamin D status in adults which results in elevations in serum PTH has been described as mild to moderate vitamin D deficiency,19 with variable effects on bone.18 ,19 Moderate vitamin D deficiency, characterised by serum 25(OH)D3 levels >12.5 nmol/l but <25 nmol/l, is associated with 15–30% increases in serum PTH levels and high rates of bone turnover.19 ,20 Mild vitamin D deficiency (also refereed to as vitamin D insufficiency5 ,18) is characterised by serum 25(OH)D3 levels between 25–50 nmol/l, which may be associated with serum PTH elevations up to 15% and with normal to high bone turnover.18 ,19

Beyond deficiency, there is no international consensus on how to define optimal vitamin D status. Dawson‐Hughes and colleagues have recently suggested that serum 25(OH)D3 concentration should exceed 70 nmol/l to achieve optimal status in adults.21 These authors considered a number of criteria by which to define optimal serum 25(OH)D3, including maximal suppression of PTH, greatest calcium absorption, highest bone mineral density (BMD), reduced rates of bone loss, reduced rates of falling, and reduced fracture rates.21 However, still others suggest that circulating 25(OH)D levels between 100–200 nmol/l can be regarded as adequate concentrations for optimum health, where body stores are replete, and therefore no disturbances in vitamin D‐dependent body functions occur.5 ,22

While a number of criteria can be considered, the serum 25(OH)D value at which PTH plateaus is considered by many as the most appropriate criteria for defining adequate vitamin D status in adults.4 ,20 ,23 However, it is important to stress that while it is well recognised that in elderly subjects vitamin D deficiency elevates PTH which, in turn, increases bone turnover and bone loss, contributes to mineralisation defects and increases risk of hip and other fractures,4 its effects in children and adolescents are unclear. Elevated PTH concentrations may not be driven by the same mechanism in adolescents as in adults, and may not necessarily be detrimental to bone health. For example, serum PTH concentrations are normally raised during adolescence,24 ,25 as the rate of bone remodelling and consolidation is at a peak. Therefore, the appropriateness of the various definitions used for the adult population, which are largely based on suppression of PTH, for children and adolescents might be questionable. Notwithstanding this issue, an inverse relationship between serum 25(OH)D3 and PTH during adolescence has been shown in a number of studies.26 ,27 ,28 ,29 ,30 ,31 Collectively, these studies might suggest that high serum 25(OH)D3 levels (at least >70 nmol/l) are required to suppress serum PTH levels in this age group, even though Outila et al failed to find a plateau in the relationship between serum 25(OH)D and PTH in Finnish adolescent girls.29

POSSIBLE HEALTH IMPLICATIONS OF LOW VITAMIN D STATUS DURING CHILDHOOD/ADOLESCENCE

While prolonged and severe vitamin D deficiency leads to rickets in children,2 it is possible that a more marginal deficiency of vitamin D during early life may contribute to osteoporosis risk as well as potentially to the development of various other chronic diseases which are frequent in Western societies.

Vitamin D status and skeletal health in childhood/adolescence

Although an inadequate supply of vitamin D from sunlight, diet or both is the most common cause of rickets, nutritional deficiencies of calcium and/or phosphate, genetic or acquired disorders of the gut, liver, kidney and metabolism can also lead to rickets.32 Rickets is a disorder of mineralisation of the bone matrix (osteoid) in growing bone, involving both the growth plate (epiphysis) and newly formed cortical and trabecular bone. It often develops in the early months of life with growth failure, lethargy and irritability often presenting as early symptoms.14 Clinical and laboratory manifestations include muscle weakness, tetany, bowing deformity of the long bones, indentation of lower ribs, deformities of the back, diffuse bone pain, decreased bone density and abnormal biochemistry (low serum calcium, phosphorus, vitamin D and high alkaline phosphatase, PTH). If untreated it may result in permanent dwarfing, gross bowing of the legs and a distorted pelvis which could lead to obstetric complications for females in later life.33 Rickets, although most commonly seen in infancy, can also occur during the pubertal growth spurt and adolescence. In late, or adolescent, rickets, bowing of the legs, muscle weakness and lower limb and back pain are the most common symptoms.14

While the evidence base is much weaker at present, less severe vitamin D deficiency, which although not causing rickets, may prevent children and adolescents from reaching their genetically programmed height and peak bone mass.6 As adolescence is a critical developmental period for bone health,9 the effect of vitamin D status on PTH concentrations and BMD in adolescents could be of major importance. Recent results from studies in adolescents provide evidence of a possible adverse effect of vitamin D deficiency and insufficiency for bone health in children.29 ,30 ,34 For example, in a 3‐year longitudinal study of Finnish girls, aged 9–15 years, Lehtonen‐Veromaa et al found that baseline 25(OH)D levels were positively correlated with unadjusted 3‐year change in BMD at the lumbar spine and femoral neck.34 The difference from baseline‐adjusted 3‐year BMD accumulation between those with severe hypovitaminosis D (serum 25(OH)D <20 nmol/l) and those with a normal vitamin D status (serum 25(OH)D ⩾35 nmol/l) was 4% at the lumbar spine in the girls with advanced sexual maturation.34 In another study from Finland, Outila et al showed that 13.5% and 62% of 14–16 year old girls had severe and marginal vitamin D deficiency, respectively.29 They also showed that subjects with serum 25(OH)D levels <40 nmol/l had low mean forearm BMD values at both the radial (p = 0.04) and ulnar (p = 0.08) sites.29 Of note, results from a recent 12‐month vitamin D intervention study in adolescent Finnish girls shows that vitamin D supplementation lead to bone mineral augmentation in the femur and lumbar spine.35

Vitamin D status and risk of cardiovascular disease, hypertension, diabetes, cancer and other chronic disease

While rickets and osteomalacia are the index diseases for severe vitamin D deficiency, there has been growing evidence that less severe deficiency, may also contribute to other chronic diseases, such as cardiovascular disease, hypertension, diabetes, cancer and other chronic disease. However, much of the evidence base for this comes from epidemiologic studies of adults. These have been expertly reviewed by Holick6 and Zittermann.5 There is also some evidence that supplementation with vitamin D (usually high dose (20–2500 μg/day) and in some cases in combination with calcium; (low dose vitamin D supplementation did not appear to be effective) may beneficially influence muscle function, rheumatoid arthritis, blood pressure, blood glucose and insulin levels (reviewed by Zittermann5). Unfortunately, again much of this evidence is from studies in adult or elderly populations. Far less is known of the effect of poor vitamin D status during childhood and adolescence on risk of these non‐skeletal chronic diseases. However, in his recent review of childhood vitamin D deficiency, Holick highlights evidence that living at latitudes above 35° for the first 10 years of life increases risk of multiple sclerosis by 100%, as well as increasing the risk of several other autoimmune diseases.18 Children in Finland in the 1960s who received the recommended daily 2000 IU (50 μg) of vitamin D at least during the first year of life and followed for the next 31 years demonstrated a reduced risk of developing type I diabetes by 80%.36 Furthermore, children from the same cohort who were vitamin D deficient at 1 year of age had a 2.4‐fold increased risk of type I diabetes.36

Prevalence of low vitamin D status in children and adolescence

Vitamin D deficiency rickets, once thought vanquished, has in recent years made a resurgence in neonates and young children in some countries (see review by Holick18). While the prevalence of this severe clinical vitamin D deficiency is relatively low, this is only the thin end of a much broader spectrum of low vitamin D status. As mentioned earlier, serum 25(OH)D3 levels <25 nmol/l and <50 nmol/l are regarded as subclinical vitamin D deficiency and insufficiency, respectively.

Data from national surveys in the UK, USA and New Zealand show that the prevalence of low vitamin D status is less of a concern for children than for adolescents.2 ,37 ,38 ,39 The prevalence of low vitamin D status appears to increase with age in early life, with adolescents being the life‐stage group in the UK young population with the highest prevalence of low vitamin D status (ie, deficiency and insufficiency) (​ figs 2 and 3​ ). In particular, young children of Asian decent in the UK appeared to be at particular risk of low status compared to similarly aged children of Caucasian origin. This relates to the fact that an increase in skin melanin pigmentation can notably diminish production of vitamin D3.6 ,8 Generally, the prevalence of vitamin D deficiency (serum 25(OH)D3 <25 nmol/l) in 1.5‐ to 10‐year‐old children in the UK is less than 7%, when subjects are sampled throughout the year (fig 2​ ). On the other hand, 11–16% of adolescents in the UK (aged 11–18 years) have serum 25(OH)D <25 nmol/l throughout the year (fig 2​ ). The prevalence of vitamin D deficiency could be almost twofold higher if sampling is limited to winter time only.37 Of potential concern, the prevalence of vitamin D insufficiency (serum 25(OH)D3 <50 nmol/l) in UK adolescents is in excess of 40% (fig 3​ ).

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Figure 2 The prevalence of subclinical vitamin D deficiency in children and adolescents in the UK. Raw data from the National Diet and Nutrition Surveys of children (aged 1.5–4.5 years and 4–18 years) kindly provided by Dr Anne Prentice, MRC Human Nutrition Research, Cambridge, UK. <25 F, % females with serum 25(OH)D <25 nmol/l; <25 M, % males with serum 25(OH)D <25 nmol/l; BrAsian; British Asian.

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Figure 3 The prevalence of vitamin D insufficiency in children and adolescents in the UK. Raw data from the National Diet and Nutrition Surveys of children (aged 1.5–4.5 years and 4–18 years) kindly provided by Dr Anne Prentice, MRC Human Nutrition Research, Cambridge, UK. <50 F, % females with serum 25(OH)D <50 nmol/l; <50 M, % males with serum 25(OH)D <50 nmol/l; BrAsian; British Asian.

The prevalence of low vitamin D status in adolescents in other parts of Europe,29 ,30 ,40 ,41 ,42 ,43 the USA,38 ,44 ,45 and elsewhere (New Zealand,39 the Lebanon28) is also relatively high. While these different studies used different cut‐off values of serum 25(OH)D3 to define vitamin D deficiency/insufficiency (ranging from <30 to <50 nmol/l), estimates of its prevalence among the adolescents, especially during winter, were, in general, relatively high (46–92%). Our recent work in >1000 adolescents from Northern Ireland shows that even during summer and autumn, when serum 25(OH)D3 levels should be at their highest, about 9–15% of 11‐ and 15‐year‐old boys and girls had serum 25(OH)D3 levels <50 nmol/l.43

Underlying reasons for low vitamin D status in children and adolescents

The major causes of vitamin D deficiency rickets have been discussed in detail elsewhere,18 ,33 and will not be dealt with in this review. The reasons for the high prevalence of subclinical vitamin D deficiency and insufficiency in early life, particularly in adolescents, are less clear. Dietary vitamin D (including vitamin D‐containing supplement use) and summer sunshine exposure are important contributors to vitamin D status. Several European countries are located at relatively high latitudes (above 37°N) and, consequently, during the dark winter months, when sunlight is of insufficient intensity to stimulate dermal vitamin D synthesis, status would be expected to be low. It is also likely that the children and adolescents with vitamin D insufficiency during summer time have either low exposure to sunlight and/or use a sun cream with a sun protection factor ⩾15 (which essentially reduces dermal synthesis of vitamin D by more than 98%6).

Dietary intakes of vitamin D are less than the recommended level in many children, especially in many adolescents.37 ,46 ,47 ,48 ,49 ,50 ,51 Low intakes of vitamin D in combination with low sun exposure during summer would certainly contribute to low vitamin D status in some children and adolescents. In addition, low intakes in winter would also largely determine those at risk of vitamin D deficiency.52 Data from the National Diet and Nutrition Survey show that the mean daily intake of vitamin D for adolescents (aged 11–18 years) in the UK is 2.6 μg.37 There is also some suggestion that intakes of vitamin D may be worse in females than males. For example, Moore et al reported that adolescent males in the USA were the group most likely to consume the adequate intake value for vitamin D, while adolescent females were about half as likely as males of corresponding age to meet their dietary reference intakes.50 In addition, Moore et al estimates that only 50% and 32% of girls aged 9–13 years and 14–18 years, respectively, are meeting the dietary reference intake for vitamin D.50 Suboptimal intakes of vitamin D in adolescent girls have also been confirmed in several other studies.41 ,47 ,51

A number of studies have reported a negative association between pubertal status and serum 25(OH)D,27 ,28 ,47 which may contribute to higher prevalence of low vitamin D status in adolescents compared to younger children.

Addressing poor vitamin D status in early life

Rickets can be treated effectively with vitamin D supplementation.18 In relation to addressing subclinical vitamin D deficiency and insufficiency, sun exposure and dietary vitamin D intake (including vitamin D fortified foods and supplemental vitamin D use) undoubtedly have important roles. However, the relative importance of these two routes of exposure differs from summer to winter for most people.

If sun exposure is sufficient, very little if any vitamin D is required from the diet during summer.16 It is worth remembering, however, that the production of vitamin D in the skin during summer varies with the geographical location, atmospheric conditions, time spent outdoors, clothing, and skin pigmentation53 as well as sunscreen use,6 as mentioned earlier. According to Holick,54 approximately 30 min of skin exposure (without sunscreen) of the arms and face to sunlight can provide all the daily vitamin D needs of the body. When sunlight exposure is limited, dietary intakes of vitamin D, if sufficient, can make a significant contribution to vitamin D status. In particular, at latitudes above 37°N, production of vitamin D3 in winter is virtually zero, because the zenith angle of the sunlight increases in the autumn and winter and consequently, the amount of solar ultraviolet radiation that reaches the Earth's surface is substantially reduced.6 Therefore, there is an increased reliance on dietary vitamin D for maintaining adequate vitamin D status during winter, and even in summer for those who avidly avoid sunshine exposure. While the US authorities recommend 5 μg vitamin D/day for children and adolescents (aged 1–18 years),2 respectively, in the UK children aged 1–3 years are recommended 7 μg vitamin D/day while there is no dietary recommendation for vitamin D for subjects aged 4–64 years.16 This lack of dietary recommendation is on the basis that it is assumed that skin synthesis of vitamin D will generally ensure adequacy which depends on regular exposure to summer sunlight.16 If individuals have restricted sunlight exposure, then 10 μg/day is recommended.

However, vitamin D is rather sparsely represented in the diet, which might explain the low intakes in children and adolescents during winter, as mentioned earlier. Oily fish such as salmon, mackerel and sardines contain high amounts of vitamin D. Cod liver oil is also an excellent source of vitamin D. Some meats may contain 25(OH)D3. Fortified foods can also be a major contributor to dietary vitamin D.2 Vitamin D‐fortified foods include some types of margarines, breakfast cereals, infant formulae, fruit juices, chocolates and milks, to name but a few. Use of vitamin D‐containing supplements can also make a major contribution to mean daily intake of vitamin D in both adults and children. However, the proportion of the population that take vitamin D supplements can be low. For example, in Ireland only 15% of adults (aged 18–64 years55) and 18% of children (aged 5–12 years) took a supplement containing vitamin D (E Walsh, University College Cork, personal communication, August 2006). Andersen et al recently showed that vitamin D supplement use was the only positive determinant of winter‐time vitamin D status in a cohort of young adolescent girls from four different European countries.41

CONCLUSION

While there is no doubt that severe vitamin D deficiency leads to rickets in childhood and adolescence, the impact of less severe vitamin deficiency on health, especially non‐skeletal health effects, is less clear. It has always been assumed that adolescents are not at risk of low vitamin D status; however, a number of recent studies have shown this not to be the case, especially during winter. In contrast, younger children seem to have a lower prevalence of low vitamin D status. The reasons for the high prevalence of vitamin D insufficiency during adolescence are unclear. Dietary supply of vitamin D, including vitamin D‐containing supplement use, is an important consideration in relation to improving vitamin D status during childhood and adolescence, especially during winter time. Without doubt, exposure of skin to summer sunshine is an extremely effective method of improving vitamin D status, but because of the fear of skin cancer there is still much debate among experts as to best practice.6 ,56 In the absence of sunshine exposure, dietary supply takes on a much more important role. Unfortunately, much research effort is still needed to identify what the optimal dietary recommendation for vitamin D should be. Such research should receive a high priority.

Key references

  • Zittermann A. Vitamin D in preventive medicine: are we ignoring the evidence? Brit J Nutr 2003;89:552–72.

  • Holick MF. Sunlight and vitamin D for bone health and prevention of autoimmune diseases, cancers and cardiovascular disease. Am J Clin Nutr 2004;80:1678S–88S.

  • Tylavsky FA, Cheng S, Lyytikainen A, et al. Strategies to improve vitamin D status in northern European children: exploring the merits of vitamin D fortification and supplementation. J Nutr 2006;136:1130–4.

  • Lehtonen‐Veromaa M, Mottonen T, Nuotio I, et al. Vitamin D and attainment of peak bone mass among peripubertal Finnish girls: a 3‐y prospective study. Am J Clin Nutr 2002;76:1446–53.

  • Andersen R, Molgaard C, Skovgaard LT, et al. Teenage girls and elderly women living in northern Europe have low winter vitamin D status. Eur J Clin Nutr 2005;59:533–41.

MULTIPLE CHOICE QUESTIONS (TRUE (T)/FALSE (F); ANSWERS AFTER THE REFERENCES)

1. The best biochemical indicator of vitamin D status is:

  1. serum calcium

  2. serum 25‐hydroxyvitamin D3

  3. serum 1,25‐dihydroxyvitamin D3

  4. serum alkaline phosphatase

2. What is the minimum sun protection factor (SPF) in sun creams which would essentially eliminate (ie, 98% reduction) dermal biosynthesis of vitamin D?

  1. 8

  2. 15

  3. 30

  4. 45

3. The cut‐off level of circulating 25‐hydroxyvitamin D which definitely places children at risk of rickets is:

  1. <12.5 nmol/l

  2. <25 nmol/l

  3. <50 nmol/l

  4. <80 nmol/l

4. What cut‐off level of circulating 25‐hydroxyvitamin D3 has been associated with increased risk of autoimmune diseases, cancers and cardiovascular disease?

  1. <12.5 nmol/l

  2. <25 nmol/l

  3. <50 nmol/l

  4. <80 nmol/l

5. The recommended dietary intake of vitamin D for children in the USA is:

  1. 2 μg/day

  2. 5 μg/day

  3. 10 μg/day

  4. 15 μg/day

ACKNOWLEDGEMENTS

This work was made possible by funding from the North‐South Programme for Collaborative Research, Higher Education Authority, Dublin. The author would also like to thank Dr Anne Prentice, Elsie Widdowson Laboratory, MRC Human Nutrition Research, Cambridge, UK for supplying the NDNS raw data on prevalence of serum 25(OH)D3 levels below the two cut‐off values.

Abbreviations

25(OH)D3 - hydroxyvitamin D3 (calcidiol)

BMD - bone mineral density

CT - calcitonin

PTH - parathyroid hormone

UVB - ultraviolet B

ANSWERS

  1. (A) F, (B) T, (C) F, (D) F

  2. (A) F, (B) T, (C) F, (D) F

  3. (A) T, (B) F, (C) F, (D) F

  4. (A) F, (B) F, (C) T, (D) F

  5. (A) F, (B) T, (C) F, (D) F

Footnotes

The author has no competing interests.

References

1. Parfitt A M, Gallagher J C, Heaney R P.et al Vitamin D and bone health in the elderly. Am J Clin Nutr 1982361014–1031. [PubMed] [Google Scholar]

2. Institute of Medicine Dietary reference intakes. for calcium, phosphorous, magnesium, vitamin D and fluoride. Washington, DC: National Academy Press, 1997

3. Dawson‐Hughes B, Dallal G E, Krall E A.et al Effect of vitamin D supplementation on wintertime and overall bone loss in healthy postmenopausal women. Ann Intern Med 1991115505–512. [PubMed] [Google Scholar]

4. Lips P. Vitamin D deficiency and secondary hyperparathyroidism in the elderly: consequences for bone loss and fractures and therapeutic implications. Endocr Rev 200122477–501. [PubMed] [Google Scholar]

5. Zittermann A. Vitamin D in preventive medicine: are we ignoring the evidence? Br J Nutr 200389552–572. [PubMed] [Google Scholar]

6. Holick M F. Sunlight and vitamin D for bone health and prevention of autoimmune diseases, cancers and cardiovascular disease. Am J Clin Nutr 2004801678S–88S. [PubMed] [Google Scholar]

7. Fitzpatrick S, Shead N F, Clark N G.et al Vitamin D deficienct rickets: a multifactorial disease. Nutr Rev 200058218–222. [PubMed] [Google Scholar]

8. Holick M F. Vitamin D: photobiology, metabolism, mechanism of action, and clinical applications. In: Favus M, ed. Primer on the metabolic bone diseases and disorders of mineral metabolism, 5th ed. Washington, DC: American Society for Bone and Mineral Research, 2003129–137.

9. Cashman K D. Calcium intake, calcium bioavailability and bone health. Br J Nutr 200287S169–S177. [PubMed] [Google Scholar]

10. McKenna M J, Freaney R, Meade A.et al Hypovitaminosis D and elevated serum alkaline phosphatase in elderly Irish people. Am J Clin Nutr 198541101–109. [PubMed] [Google Scholar]

11. DeLuca H F, Cantorna M T. Vitamin D: its role and uses in immunology. FASEB J 2001152579–2585. [PubMed] [Google Scholar]

12. Holick M F. Vitamin D: a millennium perspective. J Cell Biochem 200388296–307. [PubMed] [Google Scholar]

13. Bouillon R, Carmeliet G, Daci E.et al Vitamin D metabolism and action. Osteoporosis Int 19988513–519. [Google Scholar]

14. Pedersen P, Michaelsen K F, Molgaard C. Children with nutritional rickets referred to in hospitals in Copenhagen during a 10–year period. Acta Paediatrica 20039287–90. [PubMed] [Google Scholar]

15. Scharla S H. Prevalence of subclinical vitamin D deficiency in different European countries. Osteoporosis Int 19988S7–S12. [PubMed] [Google Scholar]

16. Department of Health Nutrition and bone health: with particular reference to calcium and vitamin D. Report on health and social subjects (49). London: The Stationary Office, 1998 [PubMed]

17. Basha B, Rao D S, Han Z H.et al Osteomalacia due to vitamin D depletion: a neglected consequence of intestinal malabsorption. Am J Med 2000108296–300. [PubMed] [Google Scholar]

19. Lips P. Which circulating level of 25‐hydroxyvitamin D is appropriate? J Steroid Biochem Mol Biol200489–90611–614. [PubMed] [Google Scholar]

20. McKenna M J, Freaney R. Secondary hyperparathyroidisms in the elderly: means to defining hypovitaminosis D. Osteoporos Int 19988S3–S6. [PubMed] [Google Scholar]

21. Dawson‐Hughes B, Heaney R P, Holick M F.et al Estimates of optimal vitamin D status. Osteoporos Int 200516713–716. [PubMed] [Google Scholar]

22. Peacock M. Nutritional aspects of hip fractures. Challenges of Modern Medicine 19957213–222. [Google Scholar]

23. Chapuy M C, Preziosi P, Maamer M.et al Prevalence of vitamin D insufficiency in an adult normal population. Osteoporos Int 19977439–443. [PubMed] [Google Scholar]

24. Krabbe S, Transbol I, Christiansen C. Bone mineral homeostasis, bone growth, and mineralization during years of pubertal growth spurt: a unifying concept. Arch Dis Child 198257359–363. [PMC free article] [PubMed] [Google Scholar]

25. Cadogan J, Blumsohn A, Barker M E.et al A longitudinal study of bone gain in pubertal girls: anthropometric and biochemical correlates. J Bone Miner Res 1998131602–1612. [PubMed] [Google Scholar]

26. Guillemant J, Cabrol S, Allemandou A.et al Vitamin D‐dependent seasonal variation of PTH in growing male adolescents. Bone 199517513–516. [PubMed] [Google Scholar]

27. Guillemant J, Tauoin P, Le H T.et al Vitamin D status during puberty in French healthy male adolescents. Osteoporos Int 199910222–225. [PubMed] [Google Scholar]

28. El‐Hajj Fuleihan G, Nabulsi M, Choucair M.et al Hypovitaminosis D in healthy schoolchildren. Pediatrics 2001107E53 [PubMed] [Google Scholar]

29. Outila T A, Karkkainen M U M, Lamberg‐Allardt C J E. Vitamin D status affects serum parathyroid hormone concentrations during winter in female adolescents: associations with forearm bone mineral density. Am J Clin Nutr 200174206–210. [PubMed] [Google Scholar]

30. Cheng S, Tylavsky F, Kroger H.et al Association of low 25‐hydroxyvitamin D concentrations with elevated parathyroid hormone concentrations and low cortical bone density in early pubertal and prepubertal Finnish girls. Am J Clin Nutr 200378485–492. [PubMed] [Google Scholar]

31. Harkness L, Cromer B. Low levels of 25‐hydroxy vitamin D are associated with elevated parathyroid hormone in healthy adolescent females. Osteoporos Int 200516109–113. [PubMed] [Google Scholar]

32. Wharton B, Bishop N. Rickets. Lancet 20033621389–1400. [PubMed] [Google Scholar]

33. Molgaard C, Michaelsen K. Vitamin D and bone health in early life. Proc Nutr Soc 200362823–828. [PubMed] [Google Scholar]

34. Lehtonen‐Veromaa M, Mottonen T, Nuotio I.et al Vitamin D and attainment of peak bone mass among peripubertal Finnish girls: a 3‐y prospective study. Am J Clin Nutr 2002761446–1453. [PubMed] [Google Scholar]

35. Viljakainen H T, Natri A M, Karkkainen M.et al A positive dose‐response effect of vitamin D supplementation on site‐specific bone mineral augmentation in adolescent girls: a double‐blinded randomized placebo‐controlled 1‐year intervention. J Bone Miner Res 200621836–844. [PubMed] [Google Scholar]

36. Hypponen E, Laara E, Reunanen A.et al Intake of vitamin D and risk of type 1 diabetes: a birth‐cohort study. Lancet 20013581500–1503. [PubMed] [Google Scholar]

37. Gregory J, Lowe S, Bates C J.et al National Diet and Nutrition Survey: young people aged 4 to 18 years. London: The Stationery Office, 2000

38. Looker A, Dawson‐Hughes B, Calvo M.et al Serum 25‐Hydroxyvitamin D status of adolescents and adults in two seasonal subpopulations from NHANES III. Bone 200030771–777. [PubMed] [Google Scholar]

39. Rockell J E, Green T J, Skeaff C M.et al Season and ethnicity are determinants of serum 25‐hydroxyvitamin D concentrations in New Zealand children aged 5‐14 y. J Nutr 20051352602–2608. [PubMed] [Google Scholar]

40. Guillemant J, Le H T, Maria A.et al Wintertime vitamin D deficiency in male adolescents: effect on parathyroid function and response to vitamin D3 supplements. Osteoporos Int 200112875–879. [PubMed] [Google Scholar]

41. Andersen R, Molgaard C, Skovgaard L T.et al Teenage girls and elderly women living in northern Europe have low winter vitamin D status. Eur J Clin Nutr 200559533–541. [PubMed] [Google Scholar]

42. Das G, Crocombe S, McGrath M.et al Hypovitaminosis D among healthy adolescent girls attending an inner city school. Arch Dis Child 200691569–572. [PMC free article] [PubMed] [Google Scholar]

43. Hill T R, Cotter A A, Wallace J.et al Vitamin D status of adolescents from the Northern Ireland Young Heart's Project: effects of age, gender and season. Proc Nutr Soc 20056438A [Google Scholar]

44. Gordon C, DePeter K, Feldman H.et al Prevalence of vitamin D deficiency among healthy adolescents. Arch Pediatr Adolesc Med 2004158531–537. [PubMed] [Google Scholar]

45. Sullivan S, Rosen C, Halteman W.et al Adolescent girls in Maine are at risk for vitamin D insufficiency. J Am Diet Assoc 2005105971–974. [PubMed] [Google Scholar]

46. Samuelson G, Bratteby L E, Enghardt H.et al Food habits and energy and nutrient intake in Swedish adolescents approaching the year 2000. Acta Paediatr 1996415(Suppl)1–19. [PubMed] [Google Scholar]

47. Ginty F, Cavadini C, Michaud P ‐ A.et al Effects of usual nutrient intake and vitamin D status on markers of bone turnover in Swiss adolescents. Eur J Clin Nutr 2004581257–1265. [PubMed] [Google Scholar]

48. Kiely M, Hannon E M, Walton J.et al Vitamin D intakes in Irish 5–12 year old schoolchildren. Proc Nutr Soc 20056438A [Google Scholar]

49. Salamoun M M, Kizirian A S, Tannous R I.et al Low calcium and vitamin D intake in healthy children and adolescents and their correlates. Eur J Clin Nutr 200559177–184. [PubMed] [Google Scholar]

50. Moore C, Murphy M, Keast D.et al Vitamin D intake in the United States. J Am Diet Assoc 2004104980–983. [PubMed] [Google Scholar]

51. McCarthy D, Collins A, O'Brien M.et al Vitamin D intake and status in Irish elderly women and adolescent girls. Ir J Med Sci 200617514–20. [PubMed] [Google Scholar]

52. Hill T R, Cotter A A, Wallace J.et al Determinants of 25‐hydroxyvitamin D levels in a representative sample of Northern Irish adolescents. Proc Nutr Soc 20066535A [Google Scholar]

53. Holick M F. Environmental factors that influence the cutaneous production of vitamin D. Am J Clin Nutr 199561638S–45S. [PubMed] [Google Scholar]

54. Holick M F. Vitamin D‐new horizons for the 21st century. Am J Clin Nutr 199460619–630. [PubMed] [Google Scholar]

55. Hill T R, O'Brien M M, Cashmen K D.et al Vitamin D intakes in 18‐64y‐old Irish adults. Eur J Clin Nutr 2004581509–1517. [PubMed] [Google Scholar]

Vitamin D Deficiency Teenager

Source: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600028/