Alessandra Santos, Mauro Geller, Spyros Mezitis, Allan E Rubenstein, Lisa Oliveira, Daniel Jm Medeiros Lima, Mendel Suchmacher Neto, Rafael Nigri, Karin Gonçalves Soares Cunha, Sanyu Takirambudde, Marcia Gonçalves Ribeiro
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引用次数: 1
Abstract
Introduction: Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant genetic disorders. Some clinical manifestations are present at birth, while some develop during childhood, and others can occur at any age. Given the early age at which patients develop clinical features, diagnosis is often made during childhood. The most prevalent features of NF1 are café au lait spots, dermal and plexiform neurofibromas, and learning disability. A variety of skeletal problems may be seen in NF1, including scoliosis, short stature, and pseudoarthrosis. Reduced skeletal bone mass has been documented to be a common phenomenon in children and adults with NF1. Decreased serum 25-hydroxyvitamin D (vitamin D) levels have been noted in adults and children with NF1 and have been reported to be inversely correlated with the number of dermal neurofibromas in adults. However, the actual correlation of vitamin D level to bone density and dermal neurofibroma number in children with NF1 remains unclear.
Objectives: The primary objective of this study was to evaluate vitamin D levels among children and adolescents with NF1. The secondary objective was to describe the levels of vitamin D among children and adolescents with NF1, to verify in which age group there is a higher frequency of vitamin D alterations, and to explore vitamin D level correlations between age, gender, sun exposure, number of neurofibromas, and number of plexiform neurofibromas.
Methods: This was an observational, cross-sectional, hospital-based study. We obtained a convenience sample of individuals with confirmed diagnosis of NF1 from patients attending the Medical Genetics Service of the IPPMG-UFRJ and Santa Casa de Misericórdia of Rio de Janeiro over a 24-month period. We evaluated vitamin D levels in blood samples of patients with NF1 by a chemiluminescent immunoassay method, and we correlated the results with gender, age, number of neurofibromas, number of plexiform neurofibromas, and satisfactory sun exposure.
Results: Of the 55 patients, 28 (50.9%) were female and 27 (49.1%) were male. Patient ages ranged from a minimum of 1.2 to a maximum of 19.6 years (mean age 10.95 years) and the median was 11.11 years. Median and mean body mass index (BMI; z score) were -0.09 (minimum value -1.63 and maximum of 4.62) and 0.16, respectively. The mean value of vitamin D was 30.82 ng/mL (±12.31) and the median was 29 ng/mL (minimum value of 10.40 ng/mL and maximum of 79.19 ng/mL).
Conclusions: The levels of vitamin D did not differ according to gender, age group, or the presence or number of cutaneous neurofibromas. Among patients with adequate sun exposure, there was a higher incidence of sufficient serum vitamin D levels. Patients with cutaneous neurofibromas in the 0 to 11 age group had a greater tendency to vitamin D sufficiency in relation to patients aged 11 to 19 years.
1型神经纤维瘤病(NF1)是最常见的常染色体显性遗传疾病之一。有些临床表现在出生时就有,而有些则在儿童时期出现,而另一些则可以在任何年龄出现。考虑到患者出现临床特征的早期年龄,诊断通常在儿童时期进行。NF1最常见的特征是咖啡渍斑点、真皮和丛状神经纤维瘤以及学习障碍。NF1可出现多种骨骼问题,包括脊柱侧凸、身材矮小和假关节。骨量减少已被证明是NF1儿童和成人的常见现象。血清25-羟基维生素D(维生素D)水平降低已在成人和儿童NF1中被注意到,并且据报道与成人真皮神经纤维瘤的数量呈负相关。然而,维生素D水平与NF1儿童骨密度和真皮神经纤维瘤数量的实际相关性尚不清楚。目的:本研究的主要目的是评估患有NF1的儿童和青少年的维生素D水平。次要目的是描述患有NF1的儿童和青少年的维生素D水平,以验证哪个年龄组维生素D改变的频率更高,并探索维生素D水平在年龄、性别、阳光照射、神经纤维瘤数量和丛状神经纤维瘤数量之间的相关性。方法:这是一项以医院为基础的观察性横断面研究。我们从参加IPPMG-UFRJ医学遗传学服务和里约热内卢Santa Casa de Misericórdia的24个月期间的患者中获得确诊为NF1的方便样本。我们用化学发光免疫分析法评估了NF1患者血液样本中的维生素D水平,并将结果与性别、年龄、神经纤维瘤数量、丛状神经纤维瘤数量和满意的日光照射程度相关联。结果:55例患者中,女性28例(50.9%),男性27例(49.1%)。患者年龄最小为1.2岁,最大为19.6岁(平均年龄10.95岁),中位数为11.11岁。中位和平均体重指数(BMI;Z评分)分别为-0.09(最小值-1.63,最大值为4.62)和0.16。维生素D的平均值为30.82 ng/mL(±12.31),中位数为29 ng/mL(最小值10.40 ng/mL,最大值79.19 ng/mL)。结论:维生素D的水平没有因性别、年龄组、皮肤神经纤维瘤的存在或数量而异。在有充足阳光照射的患者中,血清维生素D水平充足的发生率更高。与11至19岁的患者相比,0至11岁的皮肤神经纤维瘤患者更倾向于维生素D充足。