Osteoporosis International

, Volume 22, Issue 3, pp 873–882 | Cite as

Sunlight exposure or vitamin D supplementation for vitamin D-deficient non-western immigrants: a randomized clinical trial

  • I. S. Wicherts
  • A. J. P. Boeke
  • I. M. van der Meer
  • N. M. van Schoor
  • D. L. Knol
  • P. Lips
Open Access
Original Article



Vitamin D deficiency is very common in non-western immigrants. In this randomized clinical trial, vitamin D 800 IU/day or 100,000 IU/3 months were compared with advised sunlight exposure. Vitamin D supplementation was more effective than advised sunlight exposure in improving vitamin D status and lowering parathyroid hormone levels.


Vitamin D deficiency (25-hydroxyvitamin D [25(OH)D] < 25 nmol/l) is common among non-western immigrants. It can be treated with vitamin D supplementation or sunlight exposure.


To determine whether the effect of vitamin D3 supplementation (daily 800 IU or 100,000 IU/3 months) or sunlight exposure advice is similar with regard to serum 25(OH)D and parathyroid hormone (PTH) concentrations. Randomized clinical trial in 11 general practices in The Netherlands. Non-western immigrants, aged 18–65 years (n = 232) and serum 25(OH)D < 25 nmol/l were randomly assigned to supplementation (daily 800 IU or 100,000 IU/3 months) or advice for sunlight exposure for 6 months (March–September). Blood samples were collected at baseline, during treatment (3 months, 6 months), and at follow-up (12 months). Statistical analysis was performed with multilevel regression modelling.


The intention-to-treat analysis included 211 persons. Baseline serum 25(OH)D was 22.5 ± 11.1 nmol/l. After 6 months, mean serum 25(OH)D increased to 53 nmol/l with 800 IU/day, to 50.5 nmol/l with 100,000 IU/3 months, and to 29.1 nmol/l with advised sunlight exposure (supplementation vs sunshine p < 0.001). Serum PTH decreased significantly in all groups after 3 months, more in the supplementation groups than in the advised sunlight group (p < 0.05). There was no significant effect on physical performance and functional limitations.


Vitamin D supplementation is more effective than advised sunlight exposure for treating vitamin D deficiency in non-western immigrants.


Non-western immigrants RCT vitamin D Secondary hyperparathyroidism Sunlight exposure Vitamin D deficiency Vitamin D supplementation 


Vitamin D deficiency is common among moderately and heavily pigmented immigrants living in Europe [1, 2, 3, 4, 5, 6] and other continents. Recent studies in the Netherlands have shown that 40% to 80% of non-western immigrants are vitamin D-deficient (serum 25-hydroxyvitamin D, 25(OH)D < 25 nmol/l) [7, 8, 9]. Approximately 1.7 million non-western immigrants are currently living in the Netherlands (, accessed 12 March 2008), suggesting that at least 680,000 of these immigrants are vitamin D-deficient.

During exposure to sunshine, UV photons (290−315 nm) penetrate the epidermis and photolyse 7-dehydrocholesterol (provitamin D3) to previtamin D3. Melanin effectively filters the UV radiation that enters the epidermis and limits the synthesis of vitamin D3 [10]. The more melanin there is in the skin, the lower the amount of previtamin D3 that is synthesized by a given dose of UVB. In heavily pigmented individuals, only a fraction of the available UVB reaches the 7-dehydrocholesterol in cells for vitamin D3 synthesis [11]. Besides skin type, low sunshine exposure, covering of the skin, use of sunscreens, aging, and low dietary vitamin D and calcium intake contribute to a deficient vitamin D status [12]. The fact that, in the Netherlands, only margarine, which is not regularly consumed by non-western immigrants, is fortified with vitamin D (3 IU per gram) also adds to the risk for developing vitamin D deficiency.

Vitamin D deficiency initially causes an increase of the serum parathyroid hormone (PTH) concentration [1], which results in bone loss, followed by a defective mineralization of the newly formed bone (the osteoid tissue), resulting in osteomalacia in the long term [5, 12, 13]. However, the degree of PTH increase may be very different, from almost none to frank secondary hyperparathyroidism. With regard to musculoskeletal health, studies have shown that poor vitamin D status (low serum 25(OH)D) is associated with poor physical performance [14, 15, 16, 17, 18, 19, 20, 21], weakness of the proximal muscles [22], and pain [23], but other studies did not find this association [24, 25]. Several clinical trials have demonstrated that vitamin D supplementation can decrease fracture risk [12, 16]

Vitamin D deficiency can be treated by sunshine exposure or vitamin D supplementation, either daily or with greater intervals such as monthly or every 3 months. However, within non-western immigrants, the efficacy of those interventions on both vitamin D status and clinical outcomes has never been compared. Social and cultural habits may hamper exposure to sunshine in some groups of immigrants. Compliance is another issue that should be addressed.

The principal aim of this study was to determine whether the effects of supplementation with vitamin D3 (daily 800 IU or 100,000 IU/3 months) or advised sunlight exposure are similar with regard to serum 25(OH)D, PTH, and alkaline phosphatase concentrations. The second aim was to investigate whether the effects of the different interventions are comparable with respect to three clinical outcomes: physical performance tests, functional limitations, and pain.


Study design and setting

The study was designed as a randomized controlled trial, comparing the effect of supplementation with vitamin D3, either a daily dose or an equivalent dose once every 3 months, with the effect of advice for sunlight exposure. The active study treatment was administered during 6 months, between March and September, as these are the months where sunlight results in vitamin D synthesis in the skin at the latitude of the Netherlands (52ºN). Data and blood samples were collected at baseline, during treatment (at 3 months and 6 months), and during the follow-up period (at 12 months). After eligibility was verified, written informed consent was obtained. The study was approved by the Medical Ethics Committee of the VU University Medical Center. The trial has been registered at the Dutch Clinical Trials Register (NRT; ISRCTN58849315,

Study participants

Participants were non-western immigrants aged 18−65 years with documented vitamin D deficiency (serum 25-OHD < 25 nmol/l, according to analysis made by local laboratory) within 3 months before the start of the study. Participants were recruited from 10 collaborating general practices (GPs) (Amsterdam, The Hague, Haarlem, Amersfoort) and one university clinic (Amsterdam) in The Netherlands. Participants were recruited between January and March 2004 and between January and March 2005 by their general practitioners. Participants were invited at their local GPs or the university clinic during the study for the assessments and blood sampling. We anticipated a high risk to lose participants during the study if they had to travel to the hospital. Potential participants were excluded if they (a) had been treated for vitamin D deficiency within the last 3 months, (b) were immobile, or (c) had diseases interfering with measurements (e.g., psychiatric disorders, rheumatoid arthritis). Research nurses and GP assistants received a central training regarding randomization, medication, and measurements.


An independent statistician, not involved in recruitment of patients, generated a random list that was stratified for general practitioner and sex by permutation of randomized blocks, with a block size of 6. A researcher opened prepared, numbered, opaque, sealed envelopes containing the treatment codes. The participants were randomized into three groups: advice for direct sunlight exposure for at least one half hour per day, vitamin D3 800 IU/day (two tablets of 400 IU), or vitamin D3 100,000 IU once in 3 months (four capsules of 25,000 IU). The participants in the sunlight group had to keep a diary on sunlight exposure.

Participants in the 800 IU group had to return the supplement bottle at the next appointment, and participants of the 100,000 IU group took the vitamin D under supervision. The vitamin D3 was provided for 6 months, as long as the sunlight is effective in the Netherlands, i.e., the end of September. The high-dose vitamin D3 group received 100,000 IU at baseline and at 3 months.


Primary outcomes: biochemistry

Blood samples were obtained at baseline (in fasting state), 3 months, 6 months (in fasting state), and 12 months. The blood was immediately centrifuged and the plasma or serum was used immediately or frozen for later measurements. Serum calcium, phosphate, albumin, creatinine, and alkaline phosphatase were measured according to routine laboratory methods in a local laboratory. For serum 25(OH)D and PTH, serum was kept frozen at −20°C until analysis at the university laboratory. All samples from one person were analyzed in the same run in order to minimize variation. Serum 25(OH)D was analyzed using radioimmunoassay (Diasorin, Stillwater, MN, USA). The intra-assay coefficient of variation was 12%, 9%, and 7% for, respectively, 8, 25, and 100 nmol/l. The inter-assay coefficient of variation was 20%, 10%, and 8% for, respectively, 8, 30, and 65 nmol/l. The lower detection limit of the assay was 5 nmol/l. Serum PTH was analyzed using immunoradiometricassay (Luminescence, Immulite 2500, DPC, Los Angeles, CA, USA). The intra-assay coefficient of variation was 3% for the 0.3−20 pmol/l range, and 4% for >20 pmol/l. The inter-assay coefficient of variation was 7% of the total range. The lower detection limit of the assay was 0.3 pmol/l.

Clinical outcomes

Both physical performance tests to measure muscle strength and questionnaires to assess functional limitations in daily activities and pain were used.

Physical performance tests

These tests were done according to the manual of the Longitudinal Aging Study Amsterdam (LASA), and the scores relate to falls and fractures [26]. Handgrip strength was used as an indicator of muscle strength (kg) and was assessed using a hand grip strength dynamometer (Takei TKK 5001, Takei Scientific Instruments, Tokyo, Japan). Subjects stood with arms and wrists stretched out at the sides of the body. They were asked to perform two maximum force trials with each hand. For the final scores, the maximum value, whether left or right hand, was used. The inter-observer coefficient of variation was 5%. Secondly, chair stands test was used as an indicator of proximal muscle strength. To test the ability to rise from a chair, persons were asked to fold their arms across their chest and to stand up and sit down five times from a standard kitchen chair. Time taken to perform the task was measured (seconds).

Functional limitations

Functional limitations were assessed with a questionnaire concerning the degree of difficulty of the following three activities of daily living: getting up from a chair, climbing the stairs, and walking several hundred meters. In these daily activities, the muscles of the upper legs are addressed in particular. The scores per activity ranged from 0 (without difficulty) to 4 (help is needed). Both summed scores (0−12) and dichotomized scores (0 = without difficulty or little difficulty, 1 = great difficulty or help needed) were analyzed. These questions were adapted from the Longitudinal Aging Study Amsterdam [27] and were used in a prior survey in the Netherlands among non-western immigrants [8].


Six questions were asked to assess pain. To assess proximal muscle pain, the following two questions were asked: “Do you have muscle pain in your upper legs, while walking a small distance?” and “Do you have muscle pain in your upper legs, while sitting on a chair?” Scores were dichotomized into 0 “no pain” and 1 “yes” (sometimes or always). Participants were asked if they had shoulder pain during the last 2 weeks and how often they experienced shoulder pain per month. Participants were also asked if they experienced headaches during the last 2 weeks and the average number of headache episodes a year.

Potential confounders

The potential confounders, gender, age (at baseline), body mass index (BMI), and time of sunshine exposure (self-reported minutes per week) were included into the statistical analyses. Age was measured at baseline. BMI was calculated as weight (kg)/height (m2). Body weight was measured without heavy clothes (e.g., jacket, coat) and shoes, using a calibrated balance beam scale. Body height was measured with a stadiometer, without shoes. BMI was categorized into three groups: underweight (BMI < 20 kg/m2), normal weight (20 kg/m2 ≤ BMI < 25 kg/m2), and overweight (BMI ≥ 25 kg/m2). Information on sunlight exposure was based on self-report. To estimate the daily sunlight exposure, the respondents were asked to indicate time of day (before 12 am, 12−15 pm, 15−18 pm, and after 18 pm) and time (minutes) spent outdoors during summer months on weekdays and weekend days, respectively. Respondents were also asked to indicate areas of uncovered skin (face, hands, forearms, upper arms, lower legs, upper legs, upper abdomen, and back) during summer months on weekdays and weekend days.

Statistical analysis

Differences in demographic and baseline variables may occur by chance in a randomized study design. The three intervention-groups were first compared on these variables. Second, data analyses were performed based on treatment assignment according to the intention-to-treat principle. Longitudinal changes were investigated using the multilevel program MLwiN 2.02 [28, 29, 30]. Linear regression was used to investigate changes in serum 25(OH)D and PTH, physical functioning, and functional limitations. The interaction between intervention and BMI was tested in the relationship between intervention and change in serum 25(OH)D by general linear models (interaction present if p value < 0.10). Logistic regression was used for investigating changes in pain in upper legs and functional limitations (dichotomized). MLwiN multilevel modelling is an extension of multiple regression, which is appropriate for analyzing hierarchically structured data. In the present longitudinal data set, a three-level hierarchy was defined, with the repeated measurements (defined as level-1 units) grouped within the individuals (who form the level-2 units), who were grouped within GPs (level 3 units). An advantage of using multilevel regression modelling compared to the traditional repeated measurement approach is that the number of measurements can vary between participants [29]. Additionally, differences between GPs can be modelled by a multilevel structure. A multilevel model describes not only underlying population trends in a response (the fixed part of the model), but also models the variation around this mean response due to the time of measurement and due to individual differences (the random part) [30]. Because some participants changed vitamin D status after screening, and were no longer vitamin D-deficient (serum 25(OH)D > 25 nmol/l) at baseline, per-protocol analyses were performed in which only participants with serum 25(OH)D < 25 nmol/l at baseline were included. All analyses were based on two-sided tests with a two-sided α value of 0.05.


Recruitment and follow-up

The study sample included 232 persons who participated at baseline. Participants who did not provide a blood sample (or whose sample was insufficient, n = 17), whose parents were both born in Europe (n = 2), or who did not answer the questionnaire at baseline (n = 1) were excluded. One person was excluded due to an exceptionally high serum 25(OH)D level 3 months after baseline (25(OH)D = 240 nmol/l). This resulted in the inclusion of data on 211 participants in the intention-to-treat analysis. The baseline serum 25(OH)D of 58 participants was above 25 nmol/l. These subjects were included in the intention-to-treat, but excluded from the per-protocol, analyses. Figure 1 shows the flow of participants by type of analysis.
Fig. 1

Flow diagram of the participants in the study

Baseline characteristics

The baseline characteristics of the 211 participants (53 men, 158 women) who were included in the intention-to-treat analysis are shown in Table 1. Their mean [SD] age was 41.3 [11.6] years and their average BMI was 28.7 [6.2] kg/m2. Almost 33% of the participants were obese (≥30 kg/m2). The baseline characteristics indicated a low social-economic status of the population studied: 63.8% had no paid job, and 53.4% had achieved an education level of primary school or less. Their mean serum 25(OH)D was 22.5 [11.1] nmol/l and 31 (14.7%) had a serum 25(OH)D of 12.5 nmol/l or less. Mean serum PTH was 9.6 [4.6] pmol/l, and 55 (26.1%) had elevated levels of PTH (>11.0 pmol/l, upper reference limit), indicating certain secondary hyperparathyroidism. Mean serum alkaline phosphatase was 93 U/l when serum 25(OH)D was lower than 12.5 nmol/l and 73.5 U/l when serum 25(OH)D was higher than 25 nmol/l. The three intervention groups were similar in demographic and prognostic variables, and baseline values of outcome measurements. However, as shown in Fig. 1, participants who did not provide a blood sample (or whose sample was insufficient) were more often randomized to the sunlight group (p = 0.003).
Table 1

Baseline characteristics of 211 participants, according to intervention, included in the intention-to-treat analysis



Capsules 800 IU

Capsules 100,000 IU



211 (100)

72 (34.1)

74 (35.1)

65 (30.8)

Gender (n = 211)


158 (74.9)

54 (34.2)

55 (34.8)

49 (31.0)

Age (years) (n = 211)

41.3 ± 11.4

40.5 ± 10.8

41.9 ± 11.6

41.5 ± 12.0

Body mass index (kg/m2) (n = 211)

28.7 ± 6.2

28.9 ± 7.1

28.5 ± 6.0

28.6 ± 5.4

 ≥30: obese

69 (32.7)

23 (33.3)

21 (30.4)

25 (36.2)

Ethnicity (n = 209)


75 (35.9)

27 (36.0)

26 (34.7)

22 (29.3)


61 (29.2)

17 (27.9)

23 (37.7)

21 (33.4)

 Suriname/Dutch Antilles/Curacao

33 (15.8)

16 (48.5)

10 (30.3)

7 (21.2)


12 (5.7)

3 (25.0)

5 (41.7)

4 (33.3)


28 (13.4)

8 (28.6)

10 (35.7)

10 (35.7)

Paid job (n = 210)


134 (63.8)

50 (37.3)

43 (32.1)

41 (30.6)

Education (n = 208)

 No or lower education

111 (53.4)

35 (31.5)

40 (36.0)

36 (32.4)

 Secondary school

44 (21.2)

14 (31.8)

13 (29.5)

17 (38.6)

 Higher education: College—University

53 (25.5)

23 (43.4)

20 (37.7)

10 (18.9)

Smoking (n = 210)


45 (21.5)

19 (42.2)

13 (28.9)

13 (28.9)

Drinking alcohol (n = 209)


33 (15.8)

13 (39.4)

13 (39.4)

7 (21.2)

25(OH)D (nmol/l) (n = 211)

22.45 ± 11.1

22.4 ± 8.9

21.8 ± 12.3

23.3 ± 12.0

PTH (pmol/l) (n = 210)

9.6 ± 4.6

9.1 ± 5.2

10.1 ± 4.4

9.5 ± 4.3

Handgrip strength in kgf (n = 210)

32.8 ± 9.9

32.7 ± 10.2

32.0 ± 9.7

33.7 ± 9.8

Chairtest in seconds (n = 208)

14.0 ± 5.2

13.8 ± 4.4

13.9 ± 5.3

14.3 ± 5.8

Functional limitations (n = 209)

4.3 ± 3.8

4.7 ± 3.8

4.1 ± 3.6

4.2 ± 4.0

Headache episode per year (n = 209)

114.6 ± 129.0

149.1 ± 141.3

74.8 ± 98.1

120.3 ± 133.6

Values are numbers (%) or means ± standard deviations (SD)

Short-term intervention effects: intention-to-treat and per-protocol analyses

Sunlight exposure

According to the questionnaire, the median time spent outside at baseline was 120 min in the three groups with no change after 3 months. Hands and face were exposed to sunlight in 98%, and about 40−50% of the subjects exposed forearms to sunlight with no difference between the groups. The sunlight diary was not completed by the subjects with only two exceptions.


Serum 25(OH)D level increased significantly in all intervention groups at 3 months after baseline compared to baseline level (Fig. 2). At both 3 and 6 months after baseline, the serum 25(OH)D concentrations were significantly higher in the supplementation groups than in the advised sunlight group. No significant differences were observed between the two supplementation groups. The proportion of participants with serum 25(OH)D < 25, 25−50 and 50−75 and >75 nmol/l at different time points is shown in Table 2. With daily supplementation, serum 25(OH)D was higher than 50 nmol/l in 73.7% of the participants. Similar values were observed in 47.5% of the 100,000 IU group and 22% of the sunlight group. At 6 months, these percentages were lower than at 3 months. At 12 months, the percentage of participants with vitamin D deficiency (serum 25(OH)D < 25 nmol/l) was still lower than at baseline, except for the sunshine group. A significant interaction was observed between BMI and the increase of serum 25(OH)D after supplementation. The increase was larger in the 100,000 IU group when BMI was lower than 25 kg/m2 (mean increase with BMI < 25, 25−30, and >30: 47, 30, and 21 nmol/l, respectively). The power was too low for a stratified analysis.
Fig. 2

a Serum 25(OH)D, nmol/1 (median, 25th–75th percentiles) in the 800 IU/day group (A), the 100,000 IU/3 months group (B), and the sunlight group (C). b Serum PTH, pmol/1 (median, 25th–75th percentiles) in groups A, B, and C

Table 2

Proportion (%) of participants with serum 25(OH)D < 25, 25−50, 50−75, or >75 nmol/l at baseline, 3, 6, and 12 months according to treatment group 800 IU/day, 100,000 IU/3 months or sunshine exposure


Serum 25(OH)D nmol/l









800 IU/day


































100,000 IU/3 months

































Advised sunlight exposure

































The treatment was provided for 6 months, from April/May till October/November

Serum PTH concentrations decreased significantly in all three intervention groups at 3 months after baseline. At 6 months after baseline, PTH concentrations of both supplementation groups were still significantly lower compared to the sunlight group (100,000 IU, p = 0.01; 800 IU, p = 0.03). Per-protocol analyses showed the same pattern of serum 25(OH)D and PTH concentrations. However, at 3 months after baseline, a significant difference in increase of serum 25(OH)D was observed between both supplementation groups, in favor of the 800-IU group.

At baseline, alkaline phosphatase was increased above the upper reference level in 12 persons (10%), which points to vitamin D-related bone disease (incipient or frank osteomalacia). After 6 months of treatment, alkaline phosphatase was increased in two persons (2%) only. Serum alkaline phosphatase significantly decreased in all treatment groups. It decreased from 80 to 71 U/l after 6 months in the 800 IU group, from 81 to 71 in the 100,000 IU group, and from 75 to 68 in the sunlight group.

Physical performance

During the active treatment period, no between-group differences were observed in chair stand test and handgrip strength. Similarly, no within-group differences were observed over time.

Functional limitations

The three intervention groups reported significantly less difficulty in daily life activities at 3 months after baseline (p < 0.05); this was only borderline significant (p = 0.07) at 6 months after baseline. No between-group differences were observed. The number of participants without any functional limitations increased at 3 and 6 months compared to baseline in all three groups.


Six months after baseline, lower odds for pain in upper legs while sitting were observed compared to baseline. However, no between-group differences were observed. Per-protocol analysis showed no differences between groups or within groups. The studied population reported a high number of days per month with shoulder pain (approximately 15 times per month) and headache episodes (approximately 118 times per year). During treatment, no differences in shoulder pain were observed over time or between groups. Remarkably, only within the group of 800 IU per day did the number of headache episodes decrease significantly over time. Per-protocol analyses showed the same pattern.

Side effects

One side effect sometimes mentioned in the sunlight group was skin itching after sunlight exposure without visible changes. Side effects of the medication were not mentioned.

Long-term intervention effects: intention-to-treat and per-protocol analyses


At 12 months after baseline, higher serum 25(OH)D concentrations were observed in the supplementation groups compared to the sunlight group (Fig. 2, Table 2). Within the sunlight group, serum 25(OH)D decreased to baseline level. Lower serum PTH concentrations were observed in supplementation groups compared to the advised sunlight intervention, which returned to baseline level. The difference was borderline significant for the 800 IU group compared to the advised sunlight group (p = 0.065).

Physical performance

No differences were observed according to intention-to-treat and per-protocol analyses in physical performance at 12 months after baseline compared to baseline, or between groups.

Functional limitations

According to intention-to-treat analyses, all groups reported less difficulty with daily life activities at 12 months after baseline, compared to baseline. However, no differences between interventions were observed.


Compared to baseline, at 12 months after baseline, no differences were observed in odds for pain in upper legs, days with shoulder pain, or number of headache episodes.


As far as we know, this is the first randomized clinical trial in which the effect of advised sunlight exposure was compared with that of vitamin D supplementation. Sunlight exposure is the natural way to increase serum 25(OH)D concentrations, although the effects depend on the season and on the area of exposed skin.

In our study, vitamin D supplementation appeared to be necessary for adequate serum 25(OH)D concentrations when treating vitamin D deficiency in non-western immigrants living in the Netherlands. In the short term, serum 25(OH)D levels increased and serum PTH levels decreased in the advised sunlight group, but significant differences were observed between the effect of oral supplementation and sunlight exposure advice on both serum 25(OH)D and PTH concentrations. In the long term, serum 25(OH)D decreased and PTH levels again increased to baseline level within the sunlight group, while the supplementation groups were still better off at 12 months than at baseline.

Although Chel and colleagues have shown that ultraviolet irradiation is as effective as vitamin D supplementation in geriatric patients [31], exposure to sunlight itself was not very effective in our study. This may be explained by the pigmented skin of the study population, by limited skin exposure due to skin-covering clothes, and by limited sunlight exposure. According to The Norwegian Institute for Air Research, it takes 2.4 times longer for persons with dark skin (skin type 5) to synthesize the same amount of vitamin D than for persons with skin type 2. For persons with skin type 6, this will take four times longer. ( The skin surface exposed to sunlight can be estimated at 5% (face and hands) to 15% (face, forearms, and lower legs) in some individuals. Non-western immigrants usually expose themselves less to sunshine than born Dutch people due to cultural and religious habits. In fact, a poor vitamin D status can be seen in pigmented persons even in regions with abundant sunshine [32].

Although the participants received supplementation during 6 months, no further increase of serum 25(OH)D levels were observed after 3 months, and PTH levels started to increase after 3 months. This could indicate a problem with compliance. However, participants took 100,000 IU under supervision, and exactly the same pattern is observed in the 800 IU group and the sunlight group. This may indicate that supplementation was inadequate. A dose-finding study in nursing home residents studied with the same 25(OH)D assays showed that serum 25(OH)D was higher than 50 nmol/l with vitamin D 600 IU/day in 90% of the participants [33]. This fact and the decrease in serum 25(OH)D between 3 and 6 months (Fig. 2, Table 2) indicate a compliance problem. Another point of concern is the interaction of the increase of serum 25(OH)D after supplementation with BMI, mainly in the 100,000 IU group. Although this analysis should be considered exploratory, it may indicate that overweight and obese persons will need higher supplementation doses. The negative relationship between body fat percentage and serum 25(OH)D has been reported in the Longitudinal Aging Study Amsterdam [34].

It is striking that PTH concentrations decreased most in the100,000 IU group, although serum 25(OH)D concentrations increased most in the 800 IU group. This might be due to a higher peak concentration of serum PTH in the 100,000 IU group. The mean serum alkaline phosphatase decreased in all groups by about 20%. The high alkaline phosphatase is a sign of high bone turnover or disturbed mineralization due to vitamin D deficiency. Besides serum 25(OH)D and PTH concentrations, several clinical outcomes were studied. An improvement in physical performance was not observed. Difficulties with daily life activities decreased significantly, but no differences were observed between the interventions. This may indicate that only a small improvement in vitamin D status is needed to improve functional limitations. Reported pain was not consistent over time or between interventions: number of days with headache episodes decreased significantly among participants in the 800-IU intervention and reported pain in upper legs improved significantly in the 100,000-IU intervention compared to the advised sunlight intervention, but no improvement was observed in shoulder pain.

The inconsistent clinical results can be explained by the methodological restrictions of this study. There was no placebo-control group as this was judged unethical in this vitamin D-deficient population. Handgrip strength is known to be positively correlated with both lower-extremity and upper-body strength, and it appears to be a reliable test [35, 36]. The chair stand test is reliable and related to vitamin D status [14], but both relationships have been established in older populations. The impact of vitamin D deficiency on muscle strength could be less in younger persons than in older persons. In addition, the tests could not be sufficiently discriminative in a younger population. The tests were conducted in 11 different centers by different observers, and this may also explain the lack of findings. A practical limitation of this study is that the diaries of sunlight exposure were poorly completed. Therefore, we only had a rough indication of sunlight exposure during the summer from questionnaires, but no measure of recent sun exposure.

Some remarkable results were found within the group of 800 IU per day: the number of headache episodes decreased significantly over time. Strangely, the same pattern was not observed in the 100,000-IU intervention. A high number of days with headache episodes per year was reported previously in vitamin D-deficient non-western immigrants in the Netherlands [8], but as far as we know, no relation between vitamin D deficiency and headache has been observed before.

Attention should be paid to the combination of obesity and vitamin D deficiency. Almost 33% of the studied population was obese (BMI > 30 kg/m2). Obesity is associated with reduced serum 25(OH)D and increased serum PTH concentrations [34, 37]. In obesity, vitamin D production in the skin is not impaired, but after sun exposure, obese individuals only show half of the increase of serum 25(OH)D compared to non-obese individuals. It is suggested that the subcutaneous fat accumulation in obese people hampers the passage of vitamin D formed in the skin into the blood circulation. In addition, obese individuals have much lower surface-to-volume ratio than normal-weight people. As a result, the vitamin D produced in the skin is distributed over a larger volume and should not be expected to produce the same increment as in thinner individuals. Advice for sunlight exposure does not appear to be an effective intervention in obese people.

Besides the fact that sunlight was not very effective in our study, and the higher dropout of participants in the sunlight group (p = 0.003), it can be questioned whether an advice about sunlight exposure will be heard at all. When promoting sunlight exposure, the strong and widespread sun safety messages in the past few years should be taken into account. Vitamin D supplementation is necessary, but compliance may be a problem. Only 73% of 800 IU group and 47% of the 100,000 IU group reached a serum 25(OH)D level over 50 nmol/l, while the level of 75 nmol/l was only reached by 21% of the 800 IU group. Therefore, the efficacy of food fortification should also be evaluated, e.g., fortification of milk and other dairy products, orange juice [38], bread [39], or vegetable oil.

Finally, the non-western immigrant population in the Netherlands is rapidly aging (the number of non-western immigrants of 65+ years increased from 28,408 in 2000 to 57,242 in 2007 (, selection population to origin and generation, accessed 15 August 2007)). They are exposed to multiple risk factors (aging, lifestyle habits, skin pigmentation). Because of the fact that vitamin D deficiency has a negative influence on health, more effort should be spent on the early detection and treatment of people with suboptimal concentrations of vitamin D.

An important limitation of the study is that it was done in many practices with many observers, increasing the variation on clinical outcome measurements. A second limitation is the poor registration of sunshine exposure and the poor compliance with it.

In conclusion, the results of this randomized controlled trial show that vitamin D supplementation is much more effective than advice for sunlight exposure when treating vitamin D deficiency in non-western immigrants. The vitamin D dose of 800 IU/day is not sufficient to increase serum 25(OH)D over 50 nmol/l in more than 90%, which probably is due to non-compliance in this group. Higher doses may be needed in persons with higher BMI.



We are grateful to all GPs for their collaboration, our colleagues from the Endocrine laboratory for their biochemical estimates, Leida van der Mark for her help in processing the data, and all interviewers for their help in collecting the data.

Author’s Contribution

ISW, AJPB, IMM, NMvS, and PL were involved in the study design; ISW, AJPB, IMM, and PL were involved in data collection; ISW, NMvS, and DLK analyzed the data; and all authors were involved in writing the manuscript.

Conflicts of interest


Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.


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Copyright information

© The Author(s) 2010

Authors and Affiliations

  • I. S. Wicherts
    • 1
    • 2
  • A. J. P. Boeke
    • 1
    • 3
  • I. M. van der Meer
    • 4
  • N. M. van Schoor
    • 1
  • D. L. Knol
    • 5
  • P. Lips
    • 1
    • 6
  1. 1.EMGO Institute for Health and Care ResearchVU University Medical CenterAmsterdamThe Netherlands
  2. 2.School of Health CareZwolleThe Netherlands
  3. 3.Department of General Practice, EMG0 Institute for Health and Care Research VU University Medical CenterAmsterdamThe Netherlands
  4. 4.Municipal Health Service of The HagueThe HagueThe Netherlands
  5. 5.Department of Clinical Epidemiology and BiostatisticsVU University Medical CenterAmsterdamThe Netherlands
  6. 6.Endocrine section, department of Internal MedicineVU University Medical CenterAmsterdamThe Netherlands

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