Abstract
Simple SummaryWe herein describe the relevance of Vitamin D for human health, with a special focus on its role in Neurofibromatosis type 1 (NF1) disease. Indeed, epidemiological studies revealed that low circulating vitamin D levels inversely correlate with cutaneous manifestations and bone abnormalities, clinical hallmarks of NF1. NF1 is an autosomal dominant syndrome with a severe predisposition in developing tumors and for which limited treatment options are thus far available. In this context, vitamin D or its analogues has been used to treat both skin and bone lesions in NF1 patients, alone or in association with other therapeutic agents. We provide an exhaustive and detailed analysis of the most relevant preclinical and clinical studies aimed at analyzing the correlation between vitamin D deficiency and NF1 lesion progression. This review can add a valuable contribution to the current knowledge of NF1 disease investigating possible therapeutic strategies to ameliorate NF1 conditions.Vitamin D is a fat-soluble steroid hormone playing a pivotal role in calcium and phosphate homeostasis as well as in bone health. Vitamin D levels are not exclusively dependent on food intake. Indeed, the endogenous production—occurring in the skin and dependent on sun exposure—contributes to the majority amount of vitamin D present in the body. Since vitamin D receptors (VDRs) are ubiquitous and drive the expression of hundreds of genes, the interest in vitamin D has tremendously grown and its role in different diseases has been extensively studied. Several investigations indicated that vitamin D action extends far beyond bone health and calcium metabolism, showing broad effects on a variety of critical illnesses, including cancer, infections, cardiovascular and autoimmune diseases. Epidemiological studies indicated that low circulating vitamin D levels inversely correlate with cutaneous manifestations and bone abnormalities, clinical hallmarks of neurofibromatosis type 1 (NF1). NF1 is an autosomal dominant tumour predisposition syndrome causing significant pain and morbidity, for which limited treatment options are available. In this context, vitamin D or its analogues have been used to treat both skin and bone lesions in NF1 patients, alone or combined with other therapeutic agents. Here we provide an overview of vitamin D, its characteristic nutritional properties relevant for health benefits and its role in NF1 disorder. We focus on preclinical and clinical studies that demonstrated the clinical correlation between vitamin D status and NF1 disease, thus providing important insights into disease pathogenesis and new opportunities for targeted therapy.
Highlights
Esposito et al demonstrated that a Mediterranean diet and curcumin, a turmeric-derived polyphenol, induced a significant reduction in the number and size of neurofibromas, suggesting that an integrated and healthy nutritional supply can be effective in the management of neurofibromatosis type 1 (NF1) subjects [384,385]
This study demonstrated that the number of dermal neurofibromas inversely correlated with both vitamin D receptors (VDRs) mRNA and serum vitamin D levels in NF1 subjects, further corroborating the previous findings [417] and suggesting that low vitamin D content may contribute to the onset/development of the disease
Differing from Stevenson et al [419], this study revealed no significant variation in vitamin D status between NF1 children and healthy controls, observing in all cases low mean 25(OH)D concentrations
Summary
The serum concentration of 25(OH)D is a well-established marker to assess the clinical vitamin. Environmental factors, for example, pollution or poor UVB exposure, as well as lifestyle, such as decreased outdoor activities and/or poor intake of vitamin D-rich foods, influence the aetiology of vitamin D deficiency [90,129,130]. Another common cause of vitamin D deficiency is medication use, for example, anticonvulsants or glucocorticoids, which can increase the catabolism of vitamin D [18,121]. Vitamin D intake shows remarkable effects on the pharmacodynamics and pharmacokinetics of frequently used drugs, influencing their efficacy or promoting adverse reactions [131,132,133]
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