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  • Research article
  • Open Access
  • Open Peer Review

Vitamin D in children with growth hormone deficiency due to pituitary stalk interruption syndrome

  • 1,
  • 1Email author and
  • 2
BMC PediatricsBMC series – open, inclusive and trusted201818:11

https://doi.org/10.1186/s12887-018-0992-3

  • Received: 23 May 2017
  • Accepted: 17 January 2018
  • Published:
Open Peer Review reports

Abstract

Background

Recent studies have shown a relationship between vitamin D status and growth hormone (GH) and insulin-like growth factor 1 (IGF1). The objective of this study was to assess vitamin D status in children with GH deficiency due to pituitary stalk interruption syndrome (PSIS) and to investigate the relationship between 25-hydroxyvitamin D (25OHD) and 1,25-dihydroxyvitamin D (1,25 (OH) 2D) serum levels and patient characteristics.

Methods

A retrospective single-center study of 25OHD and 1,25(OH)2D serum concentrations in 50 children with PSIS at the initial evaluation before treatment.

Results

Mean concentrations of 33.2 ± 18.0 ng/mL for 25OHD and 74.5 ± 40.7 ng/L for 1,25(OH)2D were measured. Additionally, 25OHD concentrations were significantly higher in boys than in girls (p = 0.04) and lower in the cold season than in the sunny season (p = 0.03). Significant positive correlations were observed between the GH peak and serum 1,25 (OH) 2D concentrations (Rho = 0.35; p = 0.015) and the 1,25(OH)2D/25OHD ratio (Rho = 0.29; p < 0.05). No correlation was found for other characteristics, including IGF1.

Conclusions

Vitamin D status in children with hypothalamic-pituitary deficiency due to PSIS was similar to that reported in national and European studies in healthy children. The positive significant correlations between the GH peak and the 1,25 (OH)2D concentration as well as with the 1,25 (OH)2D/25OHD ratio suggest that even in these patients who had severely impaired GH secretion and low IGF1 levels, an interplay between the GH/IGF1 axis and the vitamin D system still exists.

Keywords

  • 1,25(OH)2D
  • 1,25-dihydroxyvitamin D
  • 25OHD
  • 25-hydroxyvitamin D
  • Growth hormone
  • Growth hormone deficiency
  • Insulin-like growth factor 1
  • Pituitary stalk interruption syndrome
  • Vitamin D

Background

Growth hormone (GH) deficiency (GHD) can be congenital or acquired. Pituitary stalk interruption syndrome (PSIS), a sign of congenital and permanent GHD, is an anomaly of the pituitary gland characterized by a combination of specific findings on magnetic resonance imaging, including an interrupted pituitary stalk, an absent or ectopic posterior pituitary and anterior pituitary hypoplasia [1]. Because of the heterogeneity in clinical, biological and imaging presentations, recent efforts have focused on discriminating patients with multiple hypothalamic-pituitary (HP) deficiencies from those with isolated GHD [2]. Previous studies have shown an association between PSIS and other syndromes and/or malformations, and occurrence of familial forms have led to identification of gene mutations [37].

Humans mainly acquire vitamin D from exposure to sunlight, but it can also be obtained from food (oily fish). Vitamin D is first metabolized to 25-hydroxyvitamin D (25OHD) in the liver and then to its active form, 1,25-dihydroxyvitamin D (1,25(OH)2D), in the kidneys. Overall, the concentration of serum 25OHD reflects the vitamin D status of an individual. Although debate remains regarding the 25OHD level that defines the optimal level, vitamin D deficiency is considered to be common worldwide in both adults and children [811]. Vitamin D has a well-known role in bone development in utero and in childhood, and it maintains bone health in adults through effective calcium regulation and bone mineralization [12]. Because vitamin D receptors are present in many tissues, vitamin D may also have “non-classical” effects. Indeed, vitamin D deficiency has been associated with obesity in children [13], cardiovascular disease, type 2 diabetes, cancers (colon, prostate or breast) and auto-immune disorders [1416].

Recent studies have shown a relationship between vitamin D status and GH and insulin-like growth factor 1 (IGF1). For example, initiation of cholecalciferol treatment increases serum IGF1 levels in children and adults with vitamin D deficiency [17, 18], and Wei et al. and Saggese et al. showed that six and 12 months of GH treatment, respectively, raised 1,25(OH)2D concentrations in children with GHD [19, 20].

The first objective of the present study was to assess vitamin D status at the initial evaluation before GH treatment in a large series of children with GHD due to PSIS attended by a single endocrinologist. The second objective was to investigate the relationship between 25OHD and 1,25 (OH) 2D serum levels and patient characteristics, mainly the GH peak and serum IGF1 level.

Methods

Patients

This retrospective single-center study included 50 children (28 boys and 22 girls) of a total of 86 (58%) PSIS patients monitored for HP deficiency by a senior pediatric endocrinologist (R. Brauner) between 1982 and 2016 and for whom a serum sample preserved at the initial evaluation at − 22 °C was still available. Patients with a syndrome that can interfere with their growth rate, i.e., Fanconi or Diamond-Blackfan anemia, were excluded (Fig. 1). At the initial evaluation, the characteristics of the 50 patients were similar to those of the 36 without available samples (Table 1). The criterion for GHD was a GH peak response of less than 20 mU/L or 6.7 ng/mL after two pharmacological stimulation tests.
Fig. 1
Fig. 1

Flowchart of the inclusion in the study

Table 1

Characteristics of the included and excluded patients with PSIS

 

All PSIS

PSIS included

PSIS excluded

p

(n = 86)

(n = 50)

(n = 36)

 

Boys

54

63%

28

56%

26

72%

0.9

Girls

32

37%

22

44%

10

28%

Isolated GH deficiency

39

47%

22

44%

17

47%

0.8

Multiple HP deficiency

47

43%

28

56%

19

53%

 

Mean ± SD

Mean ± SD

Mean ± SD

 

Age at diagnosis, years

4.9 ± 4.8

5.4 ± 4.9

4.2 ± 4.2

0.1

Bone age, years

3.7 ± 3.9

3.3 ± 4.1

3.8 ± 3.5

0.8

Height, SDS

−3.1 ± 1.5

−2.8 ± 1.1

−3.2 ± 1.8

0.7

BMI, SDS

0.2 ± 2.8

0.2 ± 2.2

0.2 ± 3.4

0.2

Growth rate, SDS

− 2.7 ± 1.4

−2.8 ± 1.4

−3 ± 1.4

0.6

GH peak, mU/L

5.9 ± 6.7

6.3 ± 6.0

4.1 ± 4.6

0.3

IGF1, SDS

− 3.6 ± 1.5

−3.6 ± 1.6

−3.6 ± 1.1

0.8

Free thyroxin, pmol/L

12.3 ± 7.8

12.1 ± 7.8

12.6 ± 10.8

0.5

Methods

The following data were collected at the initial clinical evaluation: age, height, growth rate during the previous year and body mass index (BMI), all expressed in standard deviation scores (SDS) according to chronological age [21, 22]. Bone age was assessed by R. Brauner according to the Greulich and Pyle method [23]. The initial biological evaluation included the IGF1 plasma concentration (expressed in ng/mL and SDS according to age and pubertal stage) and the GH peak level after a stimulation test (ornithine, arginine-insulin and/or glucagon test) or during spontaneous hypoglycemia in a few neonates. As we used various GH assays over the study period, we expressed the GH peak concentration in mU/L using conversion factors (ng/mL mU/L) that were specific of the international standard used to calibrate the GH assay (i.e., 1 ng/mL = 2 mU/L for the assay calibrated with the old 66/217 international standard composed of poorly purified pituitary GH; 1 ng/mL = 2.6 mU/L for the assay calibrated against the 80/505 international standard composed of highly purified pituitary GH; 1 ng/mL = 3 mU/L for the assay calibrated against the 98/574 international standard composed of recombinant human (h)GH).

Multiple HP deficiency was diagnosed by GH deficiency in association with one or multiple deficiencies in the following: thyroid-stimulating hormone, adrenocorticotropic hormone, and/or luteinizing hormone and follicle-stimulating hormone [2]. Pituitary functions other than GH were evaluated by basal blood cortisol at 08.00 h, free thyroxin, prolactin, and the thyroid stimulating hormone response to thyrotropin releasing hormone; the plasma and urinary osmolalities after water deprivation for 12-h were normal in the first 29 patients evaluated, showing a normal concentration capacity. The normal limits were 12 to 28 pmol/L for plasma free thyroxin, and 0.6 to 4 mU/L for basal plasma thyroid stimulating hormone, 14 ± 7 mU/L for its peak, and < 10 mU/L for its value at 120 min after the thyrotropin releasing hormone test; and 5–25 μg/L for basal prolactin, except for neonates, who had higher concentrations. Adrenocorticotropic deficiency was diagnosed by plasma basal cortisol values below 40 μg/L in neonates, and below 80 μg/L in older children, with no increase during hypoglycemia. Gonadotropin deficiency was diagnosed as the absence of clinical signs of puberty, undetectable plasma estradiol and testosterone concentrations, and no increase in gonadotropin level after a gonadotropin-releasing hormone test. The seasonal period evaluation was defined by the month of blood sampling, and we divided the patients into two groups: the sunny season, which was from June to September, and the cold season, which was from October to May.

Serum 25OHD and 1,25(OH)2D concentrations were measured using immunochemiluminescent assays (Liaison XL, DiaSorin, Saluggia, Italy). The patients were stratified according to their serum 25OHD concentration: ≤ 12 ng/mL, 13–19 ng/mL, 20–30 ng/mL, and > 30 ng/mL. We considered that a concentration between 30 and 60 ng/mL to be an appropriate level [9, 24, 25].

Statistical analysis

Qualitative results are presented as percentages. Fisher’s exact test was performed to detect differences between qualitative variables. Quantitative results are presented as the mean ± SD. Between-group differences were assessed with the non-parametric Mann-Whitney test in cases with two groups and with the Kruskal-Wallis test in cases with 3 or more groups. Correlations were assessed with the Spearman test. A p value < 0.05 was considered significant. One boy with an abnormally high 25OHD concentration was excluded from the analysis because of probable vitamin D treatment before blood collection.

Results

The mean serum 25OHD concentration was 33.2 ± 18.0 ng/mL. Two (4%), nine (18%), 15 (30%) and 24 (48%) patients had a 25OHD level ≤ 12 ng/mL, between 13 and 19 ng/mL, between 20 and 30 ng/mL, and above 30 ng/mL, respectively (Table 2). Among these, a concentration > 60 ng/mL was found for four patients. Sex and season were the two factors that significantly influenced 25OHD concentrations, with higher levels in boys than in girls and lower levels in the “cold” than in the “sunny” season (Tables 2 and 3). Conversely, no significant difference in 25OHD level was observed according to the isolated or multiple HP character deficiency, age, bone age, height, BMI, growth rate, GH peak level or IGF1 level.
Table 2

Characteristics according to the serum 25OHD level subgroups

25OHD, ng/mL

25OHD ≤ 12

13 < 25OHD ≤ 19

20 < 25OHD ≤ 30

25OHD > 30

 
 

n = 2

n = 9

n = 15

n = 24

p

Boys

0

0%

3

33%

7

47%

18

75%

0.04

Girls

2

100%

6

67%

8

53%

6

25%

Isolated GH deficiency

1

50%

6

67%

4

27%

11

46%

0.2

Multiple HP deficiency

1

50%

3

33%

11

73%

13

54%

Sunny season

0

0%

0

0%

4

27%

11

46%

0.01

Cold season

2

100%

6

100%

11

73%

13

54%

 

Mean ± SD

Mean ± SD

Mean ± SD

Mean ± SD

 

Age at diagnosis, years

13.5 ± 4.5

4.7 ± 5.1

6.5 ± 6.7

4.4 ± 2.8

0.1

Bone age, years

12 ± 5

3.6 ± 5.6

3.2 ± 3.5

2.5 ± 1.9

0.1

Height, SDS

−2.7 ± −2.7

−2.6 ± 0.6

−3 ± 1.2

−2.8 ± 1.5

0.9

BMI, SDS

1.3 ± 0.8

0.4 ± 1.6

0.3 ± 2.3

0 ± 1.6

0.6

Growth rate, SDS

− 2.6 ± 0

− 2.4 ± 0.6

− 2.7 ± 1.2

− 3 ± 1.2

NS

IGF1, SDS

−4.7 ± 0

−2.4 ± 1.8

−3.9 ± 0.8

−3.6 ± 1

NS

Table 3

Serum 25OHD and 1,25(OH)2D levels compared with the patient characteristics

 

25OHD, ng/mL

 

1,25(OH)2D, ng/mL

 

Mean ± SD

p

Mean ± SD

p

All PSIS (n = 50)

33.2 ± 18.0

 

74.5 ± 40.7

 

Sex

 Boys (n = 28)

37.6 ± 18

0.04

70 ± 27

0.4

 Girls (n = 22)

27.6 ± 17.3

75 ± 40

Deficiency

 Isolated GH (n = 22)

32.4 ± 15

0.4

64 ± 11.9

0.1

 Multiple HP (n = 28)

33.8 ± 20

83 ± 52

Season

 Sunny (n = 15)

42 ± 18

0.03

71.5 ± 32

0.3

 Cold (n = 35)

31 ± 13

73 ± 41

Age, years

  ≤ 1.5 years (n = 8)

31.4 ± 18

0.4

92 ± 17

0.5

 1.5 < age ≤ 6 years (n = 23)

35.9 ± 19

73 ± 19

 6 < age ≤ 10 years (n = 13)

33.3 ± 17

74 ± 17

 10 < age ≤ 18 years (n = 6)

24.7 ± 9

58 ± 9

BMI, SDS

  < 0 (n = 21)

33.2 ± 13

0.9

72 ± 36

0.8

  ≥ 0 (n = 25)

33 ± 20

69 ± 16

The mean serum 1,25(OH)2D concentration was 74.5 ± 40.7 ng/L (Table 3). No significant difference in 1,25(OH)2D level was observed according to sex, isolated or multiple HP character deficiency, season, age, bone age, height, BMI and growth rate. However, we did observe a trend toward higher levels in those with multiple HP deficiency. No significant correlations were observed between serum 1,25 (OH)2D concentration and age, bone age, height, BMI, growth rate, IGF1 level or 25 OHD level. Nonetheless, significant positive correlations were observed between the GH peak level and serum 1,25 (OH)2D concentration (Rho = 0.35; p = 0.015) and the 1,25(OH)2D/25OHD ratio (Rho = 0.29; p < 0.05).

Discussion

In the present study, we evaluated vitamin D status in a large series of children with GHD due to PSIS, as observed by a single endocrinologist. We performed this study because both GHD [26] and vitamin D deficiency [27] are associated with bone fragility, impaired growth, muscle weakness, cardiac outcomes and metabolic syndrome.

In our population, the mean 25OHD concentration was 33.2 ± 18.0 ng/mL, which appears to be a satisfactory level. As we did not include a control group, we compared this level with published data for healthy French children/adolescents. Among 212 girls aged 11–16.9 years with Tanner stages of 4 and 5 and living in Normandy (northwest of France), which is at the same latitude as Paris, mean 25OHD concentrations were 20.0 ± 6.1 ng/mL at the end of summer and 15.9 ± 7.4 ng/mL between January and May [28]. Alarmingly, 41% of these otherwise healthy girls had a 25OHD < 12 ng/mL during winter, revealing a severe vitamin D deficiency. The European HELENA study evaluated the vitamin D status of 1006 adolescents with a mean age of 14.9 years living in 10 European cities [29]. The participating French city was Lille, which is located in the extreme north of France, and the mean 25OHD level was 20.4 ± 8.8 ng/mL in girls and 24.1 ± 10.8 ng/mL in boys. In a recent multicenter study of vitamin D status in 326 healthy French children aged 6–10 years, it was found that 3.1% of the participants had a 25OHD concentration below 10 ng/mL and that 34.4% had a 25OHD concentration between 10 and 19.9 ng/mL [11]. Although the mean 25OHD values were not indicated in this article, it can be concluded that the vitamin D status of these children was quite similar to what we found in our children with PSIS. In our present study, female sex and winter season (from October to May) were significantly associated with lower serum 25OHD concentrations, which is consistent with other previous published studies in adult and pediatric healthy populations [9, 30].

We then compared the 25OHD concentration measured in the present study in our patients with PSIS to the values reported in recent studies on GHD patients from various countries prior to GH treatment. Saggese et al. evaluated 26 children with GHD [20] and found normal 25OHD concentrations but low 1,25 (OH)2D levels before GH treatment and a significant increase in 1,25 (OH)2D levels after 12 months of GH treatment. Ciresi et al. evaluated 80 Sicilian children with GHD [31]. These authors reported significantly higher values in the sunny season (31.1 ± 11.1 ng/mL in June–September) than in the cold season (17.3 ± 5.3 ng/mL in November–February), with 35% having vitamin D insufficiency and 40% vitamin D deficiency. Witkowska-Sedek et al. evaluated 84 children and adolescents with GHD and found low 25OHD concentrations (22.3 ± 6.9 ng/mL) [32], and Savanelli et al. evaluated 41 adult GHD patients and found mean 25OHD concentration of 21.3 ± 12.3 ng/mL, with vitamin D deficiency present in 51% of the patients compared to 14.6% of the controls [33]. In addition, Ameri et al. evaluated 69 adult GHD patients, most with postsurgical hypopituitarism [34], and found that only 6 patients (8.7%) had a serum 25OHD concentration above 30 ng/mL. These authors reported a positive association between vitamin D status and IGF1, and they also found a trend toward higher GH doses in patients with low vitamin D status (25OHD < 15 ng/mL), suggesting that a better vitamin D status may facilitate achieving normal IGF1 values in GHD patients. In a literature review, these authors proposed that assessment of vitamin D status might be an appropriate method of determining the dose of recombinant hGH for treatment of adult patients with GHD [34].

One possible explanation for the higher vitamin D status in our study may be related to the young age of the subjects (mean 5.4 years). Indeed, in France, the French Society of Paediatrics recommends systematic vitamin D supplementation of children up to five years of age. Unfortunately, no guidelines for older children have been implemented; an exception is adolescents, in whom winter supplementation is recommended but rarely performed [35]. Surprisingly, our patients of more than 5 years old, particularly those aged 6–9 years, had a mean 25OHD level similar to that of our younger patients. This may suggest that vitamin D supplementation had been offered to some of our older patients before evaluation in our unit. In support of this is the fact that although BMI is known to influence spontaneous vitamin D status with lower 25OHD concentrations in overweight subjects, we found no difference in 25OHD levels between patients with a BMI < 0 SDS and those with a higher BMI. If the hypothesis that some of our patients received vitamin D supplementation before their assessment is correct, the finding that they have a normal vitamin D status is likely independent of their GHD. However as no information on vitamin D supplementation before our evaluation was available in the medical charts of our patients, we were unable to confirm that their rather good vitamin D status was due to vitamin D supplementation.

As GH appears to increase the level of 1,25 (OH)2D [19, 20, 36, 37], albeit likely indirectly, through the effects of IGF1, it may be hypothesized that patients with GHD due to PSIS have a low 1,25 (OH) 2D serum concentration. This was not the case in our patients who had normal levels. We, however, have no explanation for the higher 1,25(OH)2D level in those with multiple HP deficiencies. Regardless, we did find a significant positive correlation between the GH peak level obtained during a pharmacologic stimulation test and the 1,25 (OH) 2D concentration as well as with the 1,25 (OH) 2D/25OHD ratio. These findings suggest that even in these patients who had severely impaired GH secretion and low IGF1 levels, an interplay between the GH/IGF1 axis and the vitamin D system still exists.

Our study has limitations: it was retrospective and did not include a control group. However, the strength of our study pertains to the large series of GHD patients with a homogenous diagnosis (i.e., PSIS) and the same protocol of exploration for years, as they were attended by the same endocrinologist. This design allowed avoiding the considerable selection biases that affect several studies on GH deficiency. The patients who were excluded because of unavailable plasma samples might have introduced a bias, but their similarities to the included patients limit this. Another limitation is the lack of information on vitamin D supplementation before the patients were evaluated.

Conclusions

We found quite an acceptable mean vitamin D status in our series of children with GHD due to PSIS. There are currently no available data from a double-blind, placebo-controlled randomized trial of vitamin D supplementation in GH-treated GHD patients showing that vitamin D optimizes bone health, growth and possibly other outcomes. Despite this lack of high-level evidence, we believe that it is mandatory to maintain optimal vitamin D supplementation in GHD patients.

Abbreviations

1,25(OH)2D: 

1,25-dihydroxyvitamin D

25OHD: 

25-hydroxyvitamin D

BMI: 

Body mass index

GH: 

Growth hormone

GHD: 

Growth hormone deficiency

HP: 

Hypothalamic-pituitary

IGF1: 

Insulin-like growth factor 1

PSIS: 

Pituitary stalk interruption syndrome

SDS: 

Standard deviation score

Declarations

Acknowledgements

Not applicable.

Funding

The study was self-funded.

Availability of data and materials

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Authors’ contributions

CD drafted the manuscript, collected and analyzed the data; RB conceived the study and participated in its design and coordination and drafted the manuscript; JCS participated in the design of the study and drafted the manuscript. All the authors read and approved the final manuscript.

Ethics approval and consent to participate

All clinical investigations were conducted according to the principles expressed in the Declaration of Helsinki. Written informed consent for the clinical and biological evaluation was obtained from the parents of the children and included in their hospital medical records. No activity in addition to routine patient care was performed due to the study. The authors had no direct interaction with these patients, except for their medical follow-up, which was performed by R. Brauner. Each patient’s information was anonymized by the medical secretary prior to analysis.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Authors’ Affiliations

(1)
Fondation Ophtalmologique Adolphe de Rothschild and Université Paris Descartes, Paris, France
(2)
Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades, Service d’Explorations Fonctionnelles, Paris, France

References

  1. Argyropoulou M, Perignon F, Brauner R, Brunelle F. Magnetic resonance imaging in the diagnosis of growth hormone deficiency. J Pediatr. 1992;120:886–91.View ArticlePubMedGoogle Scholar
  2. Pham L-L, Lemaire P, Harroche A, Souberbielle J-C, Brauner R. Pituitary stalk interruption syndrome in 53 postpubertal patients: factors influencing the heterogeneity of its presentation. PLoS One. 2013;8:e53189.View ArticlePubMedPubMed CentralGoogle Scholar
  3. Dupuis-Girod S, Gluckman E, Souberbielle JC, Brauner R. Growth hormone deficiency caused by pituitary stalk interruption in Fanconi’s anemia. J Pediatr. 2001;138:129–33.View ArticlePubMedGoogle Scholar
  4. Leblanc T, Gluckman E, Brauner R. Growth hormone deficiency caused by pituitary stalk interruption in diamond-Blackfan anemia. J Pediatr. 2003;142:358.View ArticlePubMedGoogle Scholar
  5. Pinto G, Netchine I, Sobrier ML, Brunelle F, Souberbielle JC, Brauner R. Pituitary stalk interruption syndrome: a clinical-biological-genetic assessment of its pathogenesis. J Clin Endocrinol Metab. 1997;82:3450–4.PubMedGoogle Scholar
  6. Reynaud R, Gueydan M, Saveanu A, Vallette-Kasic S, Enjalbert A, Brue T, et al. Genetic screening of combined pituitary hormone deficiency: experience in 195 patients. J Clin Endocrinol Metab. 2006;91:3329–36.View ArticlePubMedGoogle Scholar
  7. Bashamboo A, Bignon-Topalovic J, Moussi N, McElreavey K, Brauner R. Mutations in the human ROBO1 gene in pituitary stalk interruption syndrome. J Clin Endocrinol Metab. July 2017;102(7):2401–6.View ArticlePubMedGoogle Scholar
  8. Holick MF, Binkley NC, Bischoff-Ferrari HA, Gordon CM, Hanley DA, Heaney RP, et al. Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2011;96:1911–30.View ArticlePubMedGoogle Scholar
  9. Souberbielle J-C, Massart C, Brailly-Tabard S, Cavalier E, Chanson P. Prevalence and determinants of vitamin D deficiency in healthy French adults: the VARIETE study. Endocrine. 2016;53:543–50.View ArticlePubMedGoogle Scholar
  10. Whiting SJ, Langlois KA, Vatanparast H, Greene-Finestone LS. The vitamin D status of Canadians relative to the 2011 dietary reference intakes: an examination in children and adults with and without supplement use. Am J Clin Nutr. 2011;94:128–35.View ArticlePubMedGoogle Scholar
  11. Mallet E, Gaudelus J, Reinert P, Stagnara J, Benichou J, Basuyau J-P, et al. [vitamin D status in 6- to 10-year-old children: a French multicenter study in 326 children]. Arch. Pediatr. Organe off. Soc. Francaise Pediatr. 2014;21:1106–14.Google Scholar
  12. Wacker M, Holick MF. Vitamin D - effects on skeletal and extraskeletal health and the need for supplementation. Nutrients. 2013;5:111–48.View ArticlePubMedPubMed CentralGoogle Scholar
  13. Gilbert-Diamond D, Baylin A, Mora-Plazas M, Marin C, Arsenault JE, Hughes MD, et al. Vitamin D deficiency and anthropometric indicators of adiposity in school-age children: a prospective study. Am J Clin Nutr. 2010;92:1446–51.View ArticlePubMedPubMed CentralGoogle Scholar
  14. Holick MF. Vitamin D deficiency. N Engl J Med. 2007;357:266–81.View ArticlePubMedGoogle Scholar
  15. Antico A, Tampoia M, Tozzoli R, Bizzaro N. Can supplementation with vitamin D reduce the risk or modify the course of autoimmune diseases? A systematic review of the literature. Autoimmun Rev. 2012;12:127–36.View ArticlePubMedGoogle Scholar
  16. Anderson JL, May HT, Horne BD, Bair TL, Hall NL, Carlquist JF, et al. Relation of vitamin D deficiency to cardiovascular risk factors, disease status, and incident events in a general healthcare population. Am J Cardiol. 2010;106:963–8.View ArticlePubMedGoogle Scholar
  17. Ameri P, Giusti A, Boschetti M, Murialdo G, Minuto F, Ferone D. Interactions between vitamin D and IGF-I: from physiology to clinical practice. Clin Endocrinol. 2013;79:457–63.View ArticleGoogle Scholar
  18. Soliman AT, Al Khalaf F, Alhemaidi N, Al Ali M, Al Zyoud M, Yakoot K. Linear growth in relation to the circulating concentrations of insulin-like growth factor I, parathyroid hormone, and 25-hydroxy vitamin D in children with nutritional rickets before and after treatment: endocrine adaptation to vitamin D deficiency. Metabolism. 2008;57:95–102.View ArticlePubMedGoogle Scholar
  19. Wei S, Tanaka H, Kubo T, Ono T, Kanzaki S, Seino Y. Growth hormone increases serum 1,25-dihydroxyvitamin D levels and decreases 24,25-dihydroxyvitamin D levels in children with growth hormone deficiency. Eur J Endocrinol Eur Fed Endocr Soc. 1997;136:45–51.View ArticleGoogle Scholar
  20. Saggese G, Baroncelli GI, Bertelloni S, Cinquanta L, Di Nero G. Effects of long-term treatment with growth hormone on bone and mineral metabolism in children with growth hormone deficiency. J Pediatr. 1993;122:37–45.View ArticlePubMedGoogle Scholar
  21. Sempé M, Pédron G, Roy-Pernot MP. Auxologie, méthode et séquence. Paris: Théraplix; 1979.Google Scholar
  22. Rolland-Cachera MF, Cole TJ, Sempe M, Tichet J, Rossignol C, Charraud A. Body mass index variations: centiles from birth to 87 years. Eur J Clin Nutr. 1991;45:13–21.PubMedGoogle Scholar
  23. Greulich W, Pyle S. Radiographic atlas of skeletal development of the hand and wrist. Stanford: University Press; 1959.Google Scholar
  24. Vidailhet M, Mallet E. Vitamin D in childhood. Presse Medicale Paris Fr 1983. 2013;42:1383–90.Google Scholar
  25. Saggese G, Vierucci F, Boot AM, Czech-Kowalska J, Weber G, CAJ C, et al. Vitamin D in childhood and adolescence: an expert position statement. Eur J Pediatr. 2015;174:565–76.View ArticlePubMedGoogle Scholar
  26. Molitch ME, Clemmons DR, Malozowski S, Merriam GR, Vance ML. Evaluation and treatment of adult growth hormone deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2011;96:1587–609.View ArticlePubMedGoogle Scholar
  27. Souberbielle J-C, Body J-J, Lappe JM, Plebani M, Shoenfeld Y, Wang TJ, et al. Vitamin D and musculoskeletal health, cardiovascular disease, autoimmunity and cancer: recommendations for clinical practice. Autoimmun Rev. 2010;9:709–15.View ArticlePubMedGoogle Scholar
  28. Esterle L, Nguyen M, Walrant-Debray O, Sabatier J-P, Garabedian M. Adverse interaction of low-calcium diet and low 25(OH)D levels on lumbar spine mineralization in late-pubertal girls. J Bone Miner Res Off J Am Soc Bone Miner Res. 2010;25:2392–8.View ArticleGoogle Scholar
  29. Gonzalez-Gross M, Valtuena J, Breidenassel C, Moreno LA, Ferrari M, Kersting M, et al. Vitamin D status among adolescents in Europe: the healthy lifestyle in Europe by nutrition in adolescence study. Br J Nutr. 2012;107:755–64.View ArticlePubMedGoogle Scholar
  30. Valtuena J, Gonzalez-Gross M, Huybrechts I, Breidenassel C, Ferrari M, Mouratidou T, et al. Factors associated with vitamin D deficiency in European adolescents: the HELENA study. J Nutr Sci Vitaminol (Tokyo). 2013;59:161–71.View ArticleGoogle Scholar
  31. Ciresi A, Ciccio F, Giordano C. High prevalence of hypovitaminosis D in Sicilian children affected by growth hormone deficiency and its improvement after 12 months of replacement treatment. J Endocrinol Investig. 2014;37:631–8.View ArticleGoogle Scholar
  32. Witkowska-Sedek E, Kucharska A, Ruminska M, Pyrzak B. Relationship between 25(OH)D and IGF-I in children and adolescents with growth hormone deficiency. Adv Exp Med Biol. 2016;912:43–9.View ArticlePubMedGoogle Scholar
  33. Savanelli MC, Scarano E, Muscogiuri G, Barrea L, Vuolo L, Rubino M, et al. Cardiovascular risk in adult hypopituitaric patients with growth hormone deficiency: is there a role for vitamin D? Endocrine. 2016;52:111–9.View ArticlePubMedGoogle Scholar
  34. Ameri P, Giusti A, Boschetti M, Bovio M, Teti C, Leoncini G, et al. Vitamin D increases circulating IGF1 in adults: potential implication for the treatment of GH deficiency. Eur J Endocrinol. 2013;169:767–72.View ArticlePubMedGoogle Scholar
  35. Vidailhet M, Mallet E, Bocquet A, Bresson J-L, Briend A, Chouraqui J-P, et al. Vitamin D: still a topical matter in children and adolescents. A position paper by the committee on nutrition of the French Society of Paediatrics. Arch Pediatr Organe Off Soc Francaise Pediatr. 2012;19:316–28.Google Scholar
  36. Condamine L, Menaa C, Vrtovsnik F, Friedlander G, Garabedian M. Local action of phosphate depletion and insulin-like growth factor 1 on in vitro production of 1,25-dihydroxyvitamin D by cultured mammalian kidney cells. J Clin Invest. 1994;94:1673–9.View ArticlePubMedPubMed CentralGoogle Scholar
  37. Wei S, Tanaka H, Seino Y. Local action of exogenous growth hormone and insulin-like growth factor-I on dihydroxyvitamin D production in LLC-PK1 cells. Eur J Endocrinol. 1998;139:454–60.View ArticlePubMedGoogle Scholar

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