Differences of 25-hydroxyvitamin D3 concentrations in children and adults with neurofibromatosis type 1

被引:13
作者
Schnabel, Claudia [1 ]
Dahm, Stefan [2 ]
Streichert, Thomas [1 ]
Thierfelder, Wulf [2 ]
Kluwe, Lan [3 ]
Mautner, Victor F. [3 ]
机构
[1] Univ Hosp Hamburg Eppendorf, Inst Clin Chem, D-20246 Hamburg, Germany
[2] Robert Koch Inst, Berlin, Germany
[3] Univ Hosp Hamburg Eppendorf, Dept Neurol, D-20246 Hamburg, Germany
关键词
Neurofibromatosis type 1; Vitamin D3 deficiency; VITAMIN-D STATUS; BONE-MINERAL-DENSITY; D DEFICIENCY; PARATHYROID-HORMONE; METABOLISM; EXPOSURE; MARKERS; INACTIVATION; ADOLESCENTS; PREVALENCE;
D O I
10.1016/j.clinbiochem.2014.02.020
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder, frequently associated with reduced bone mineral density. Serum25-hydroxyvitamin D3 concentrations in NF1 adults are lower than in healthy controls in autumn respectively winter and are inversely correlated with the number of dermal neurofibromas. We investigated 25-hydroxyvitamin D3 levels in children and adults with neurofibromatosis type 1 in winter and summer and compared them to healthy controls to get more pathogenic insights in vitamin D3 metabolism in NF1 patients. Design and methods: NF1 patients were clinically examined and serum 25-hydroxyvitamin D3 concentrations were measured in 58 NF1 adults and 46 children in winter as well as in summer and compared to sex-, age-and month-matched controls. Results: 52 adults suffered from 10 to 5000 dermal neurofibromas, whereas none of the children presented neurofibromas. 25-Hydroxyvitamin D3 increased from winter to summer (mean: 21.0 to 46.5 nmol/l) in NF1 adults. This increase was even larger (p= 0.0001) than in healthy controls (mean: 50.5 to 60.5 nmol/l). However, there were no differences of 25-hydroxyvitamin D3 concentrations in NF1 children and healthy controls both in winter and in summer. Conclusions: Only adults with NF1 showed lower 25-hydroxyvitamin D3 levels in winter and summer, which are unlikely due to impaired UV-dependent dermal synthesis, but rather might be caused by an accelerated catabolism. (C) 2014 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:560 / 563
页数:4
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