Neurofibromatosis 1 (NF1) is a tumour suppressor gene syndrome characterized by multiple cutaneous and plexiform neurofibromas. Focal osseous abnormalities, short stature, and decreased bone mineral density are also frequent in people with NF1. We measured serum 25-hydroxyvitamin D concentrations in 55 patients with NF1 and 58 healthy controls, and correlated the findings in the patients with NF1 with their estimated number of dermal neurofibromas. Geometric mean (SD) serum 25-hydroxyvitamin D concentration was 14.0 (1.6) ng/mL among the patients with NF1 compared with 31.4 (1.7) ng/mL among healthy controls (p<<0.0001). The serum vitamin D concentration and number of dermal neurofibromas reported by patients with NF1 were inversely correlated (Spearman’s ρ = −0.572, p<0.00001). The occurrence of low serum vitamin D concentrations in people with NF1, especially those with many dermal neurofibromas, may provide new pathogenic insights and have important therapeutic implications.
- MPNSTs, malignant peripheral nerve sheath tumours
- NF1, neurofibromatosis 1
- neurofibromatosis 1
- vitamin D
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Neurofibromatosis 1 (NF1) is an autosomal dominant disease caused by mutations of the NF1 gene on chromosome 17.1–3 Multiple café au lait spots and cutaneous neurofibromas occur in almost all affected individuals. Less frequent but more serious manifestations include plexiform neurofibromas, central nervous system gliomas, malignant peripheral nerve sheath tumours (MPNSTs), and NF1 vasculopathy.4,5 At least 10% of people with NF1 have characteristic focal bony abnormalities such as sphenoid wing lesions, dystrophic scoliosis, or tibial pseudarthrosis. In addition, people with NF1 frequently have a generalized skeletal abnormality, evidenced by mild short stature6 and decreased bone mineral density.7,8,9,10
Vitamin D regulates calcium homeostasis and plays a key role in bone metabolism.11 Patients with NF1 with severe osteomalacia respond favourably to vitamin D therapy,12 and topical vitamin D treatment has been reported to reduce the pigmentation in café au lait spots, one of the cardinal features of NF1.13 We measured serum 25-hydroxyvitamin D concentrations in a series of patients with NF1 and assessed the relationship of these concentrations to the number of dermal neurofibromas reported by the patients.
This study was approved by the ethics committee of Hamburg University. We measured serum 25-hydroxyvitamin D concentrations in 69 unselected adults with NF1 diagnosed by standard clinical criteria.14 For comparison, we also measured serum 25-hydroxyvitamin D levels in 58 apparently healthy employees of the testing laboratory. After assessment by the laboratory medical officer, fasting blood samples were taken and stored at −80°C until analysis. Individuals with diseases of the gastrointestinal tract, liver, kidneys, parathyroid glands, or skin which can affect vitamin D metabolism were excluded from both groups, as were individuals known to be taking supplemental vitamin D or to have unusually high ultraviolet light exposure. Serum concentrations of 25-hydroxyvitamin D were measured by an automated chemiluminescence protein binding assay (Nichols Institute Diagnostics, San Clemente, CA, USA). Data on the crossreactivity of the vitamin D binding protein, based on spike and recovery studies, revealed an equimolar 100% recovery of 25-hydroxyvitamin D3 and 25-hydroxyvitamin D2. Although some patient samples containing 25-hydroxyvitamin D2 may exhibit reduced recovery with this assay, vitamin D2 originates entirely from dietary sources, and none of the tested control subjects or patients with NF1 was receiving vitamin D2 supplementation.
All 58 control subjects and 55 of the 69 patients with NF1 were tested in the autumn or winter. The serum 25-hydroxyvitamin D concentrations in the other 14 patients with NF1 were measured in the summer. Because serum vitamin D concentrations are known to be substantially higher in summer than in winter,15 these 14 patients with NF1 were excluded from the analyses. However, the results were very similar if the14 patients tested in the summer were included and the analysis was adjusted for the season of the year in which the serum was obtained.
Of the 55 patients with NF1 included in the present study, 45 (61 of the total 69 patients with NF1 tested) completed a questionnaire regarding the approximate number of skin tumours present, and this estimate agreed well with the number counted by one of us (ML) on physical examination of 19 of the patients.
Geometric mean serum vitamin D concentrations in patients with NF1 and controls were compared using Student’s t test. Discrete comparisons were assessed with χ2 test. Correlations between number of dermal neurofibromas (categorized as 10–99, 100–999, or ⩾1000) and the log serum hydroxyvitamin D concentration were tested with Spearman’s ρ. The geometric mean vitamin D concentration in patients with NF1 with different numbers of neurofibromas were compared using analysis of variance. Again, inclusion of the patients with NF1 whose sera were collected in the summer for vitamin D measurement produced very similar results if the analysis was adjusted for seasonality.
Table 1 compares the findings in 55 patients with NF1 and 58 controls whose serum 25-hydroxyvitamin D concentrations were measured in autumn or winter. The groups were similar for sex ratio, but the patients with NF1 were, on average, about 4 years older than the controls. The distribution of serum 25-hydroxyvitamin D concentrations was log normal (fig 1), and age was not related to the serum vitamin D concentration in either the patients or controls (data not shown). The geometric mean (SD) in patients with NF1 (14.0 (1.6) ng/mL) was much lower than that in controls (31.4 (1.7) ng/mL) (table 1). Nearly three quarters (72%) of the patients with NF1 but only 21% of the healthy comparison group had serum 25-hydroxyvitamin D concentrations <20 ng/mL, which is considered to be the minimum requirement for normal physiological function.11,16 These differences are very highly statistically significant (table 1).
The estimated number of dermal neurofibromas in the 47 patients with NF1 who reported this information ranged from 14 to “more than a thousand”. For analysis, these estimates were converted into orders of magnitude: 10–99, 100–999, and ⩾1000. The number of dermal neurofibromas was associated with age, as expected (table 2). We also observed a very strong and highly significant inverse correlation between the serum vitamin D concentration and the number of dermal neurofibromas reported by the patients with NF1 (fig 2) (Spearman’s ρ = −0.572, p<0.00001). The geometric mean serum vitamin D concentrations of the three groups (10–99, 100–999, and ⩾1000 external neurofibromas) were very significantly different after adjustment for age (p = 0.0003, table 2).
Our observation of much lower serum vitamin D concentrations in patients with NF1 than controls is consistent with, and may be pathogenically related to, the decreased bone mineral density that we and others have observed among people with NF1.7,8,9,10 Osteomalacia and associated low serum vitamin D concentrations have previously been described in people with NF1 in case reports and small clinical series,12 but the frequency with which this occurs has not been determined. The fact that patients with NF1 and osteomalacia respond well to treatment with pharmacological doses of vitamin D raises the possibility that similar treatment may help to prevent the development of osteomalacia and osteoporosis in people with NF1. Other interventions such as increased weight bearing exercise may also be beneficial.
We measured vitamin D as the serum 25-hydroxyvitamin D concentration. Although 1,25-dihydroxyvitamin D is the active form, its measurement is not useful in determining vitamin D status.16 The major circulating form, 25-hydroxyvitamin D, is converted to active 1,25-dihydroxyvitamin D by the kidney. When vitamin D deficiency occurs, parathyroid hormone secretion increases, which in turn increases renal 1-α-hydroxylase activity, converting more 25-hydroxyvitamin D to 1,25-dihydroxyvitamin D. Sunlight induced cutaneous vitamin D synthesis can produce all of the vitamin D needed to maintain normal physiological functions.11 We do not know why the serum vitamin D concentrations in people with NF1 are low. We are not aware of any studies of vitamin D intake, absorption, synthesis, transport, or catabolism in people with NF1. Thus this issue needs to be investigated.
The strong correlation we observed between the number of skin neurofibromas and serum vitamin D concentrations was unexpected. It is possible that patients with NF1 with multiple dermal neurofibromas are more likely to cover their skin and thus receive less sunlight than patients with NF1 who have fewer dermal tumours. None of the subjects we studied was reclusive, and none habitually wore a scarf over the head or face. We do not have information on the amount of cutaneous hyperpigmentation in the patients studied, but this is not usually severe in people with NF1.
Our analysis was limited to patients tested in the autumn or winter, so a major difference in sun exposure seems unlikely to account for the very large effect we observed. It seems more likely that the presence of large numbers of neurofibromas causes vitamin D deficiency in patients with NF1 in some other manner, that adequate serum concentrations of vitamin D inhibit the development of neurofibromas, that low serum vitamin D concentrations promote the development of neurofibromas, or that both low serum vitamin D concentration and large numbers of neurofibromas are related to NF1 haploinsufficiency in some other way.
Although cutaneous neurofibromas may occur in very large numbers in people with NF1, these benign tumours very rarely, if ever, undergo transformation to MPNSTs. In contrast, plexiform neurofibromas may give rise to MPNSTs, which occur in about 10% of patients with NF117 and are a frequent cause of premature death.18,19 Plexiform neurofibromas occur in at least 40% of adults with NF120,21 but often are not apparent without imaging studies. We do not know whether the development of plexiform neurofibromas or MPNSTs is associated with low serum vitamin D concentrations in people with NF1.
Several molecular mechanisms might be responsible for the association of low serum vitamin D levels and the occurrence of neurofibromas in people with NF1. Neurofibromin, the protein product of the NF1 gene, is a negative regulator of the Ras signal transduction pathway,22,23 which is involved in normal development and maintenance of bone.24,25 Vitamin D treatment inhibits the growth of some cell lines in vitro, but this effect can be blocked through activation of the Ras signalling pathway,26 which occurs as a result of NF1 haploinsufficiency. Alternatively, vitamin D and neurofibromin could interact at the level of cellular proliferation; reduction in the normal antiproliferative and proapoptotic effects of vitamin D27 in patients with NF1 and vitamin deficiency might foster the tendency to tumour development associated with neurofibromin haploinsufficiency.
In any case, our findings provide a new perspective on the pathogenesis of NF1. Systematic studies of vitamin D metabolism and its relationship to bone mineral density, osteoporosis, focal osseous lesions, and tumour development in people with NF1 are clearly needed. There are also obvious clinical implications; we need to explore the possibility that treatment with vitamin D may inhibit tumour development as well as improving bone mineralization in patients with NF1.
Published Online First 29 March 2006
Competing interests: there are no competing interests.
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