National Centre for Inherited Metabolic Disorders, Children's University Hospital, Dublin, Ireland.
Ann Nutr Metab. 2013;63(1-2):168-73. doi: 10.1159/000354869. Epub 2013 Sep 10.
Phenylketonuria (PKU) is caused by a severe phenylalanine hydroxylase deficiency; the mainstay of treatment is a low-phenylalanine diet. A diet which is so restrictive is associated with a risk of nutritional deficiencies. We investigated plasma concentrations for 46 elements, including minerals and trace elements.
We enrolled 20 children and adolescents with PKU and 20 matched controls. Multi-elementary quantification was carried out by solution-based inductively coupled plasma atomic emission spectroscopy (ICP-AES) and ICP mass spectrometry (ICP-MS).
With the exception of manganese and aluminium, no significant differences were found for element levels between PKU patients and controls. As a trend, manganese levels were lower in PKU patients than in control subjects (p < 0.05) but were within the reference range. There was a positive linear relationship between manganese and tyrosine levels in subjects with PKU (r(2) = 0.2295, p < 0.05). If detectable, potentially toxic elements were only identified in ultra-trace quantities in plasma samples of either group; aluminium levels were found to be slightly higher in PKU subjects than in controls (p < 0.01).
The combination of ICP-AES and ICP-MS data is a useful diagnostic tool for element quantification at a high analytical rate and for monitoring bio-element status, e.g. in patients on a restrictive diet.
苯丙酮尿症(PKU)是由严重的苯丙氨酸羟化酶缺乏引起的;治疗的主要方法是低苯丙氨酸饮食。这种严格限制的饮食与营养缺乏的风险有关。我们研究了 46 种元素的血浆浓度,包括矿物质和微量元素。
我们纳入了 20 名 PKU 患儿和 20 名匹配的对照。采用基于溶液的电感耦合等离子体原子发射光谱法(ICP-AES)和电感耦合等离子体质谱法(ICP-MS)进行多元素定量分析。
除了锰和铝,PKU 患者和对照组之间的元素水平没有显著差异。作为一个趋势,PKU 患者的锰水平低于对照组(p<0.05),但仍在参考范围内。PKU 患者的锰水平与酪氨酸水平呈正线性关系(r²=0.2295,p<0.05)。如果可检测到,两种组别的血浆样本中仅以超痕量的形式存在潜在毒性元素;PKU 患者的铝水平略高于对照组(p<0.01)。
ICP-AES 和 ICP-MS 数据的组合是一种有用的诊断工具,可用于以高分析速率定量元素,并监测生物元素状态,例如在限制饮食的患者中。