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采用亲水相互作用液相色谱-串联质谱法测定尿、血浆和干血斑中乳清酸的参考区间。

Reference intervals for orotic acid in urine, plasma and dried blood spot using hydrophilic interaction liquid chromatography-tandem mass spectrometry.

机构信息

Department of Biomedical Sciences, University of Foggia, Foggia, Italy.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2012 Feb 1;883-884:155-60. doi: 10.1016/j.jchromb.2011.09.054. Epub 2011 Oct 6.

Abstract

Orotic acid (OA), a marker of hereditary orotic aciduria, is usually used for the differential diagnosis of some hyperammonemic inherited defects of urea cycle and of basic amino acid transporters. This study was aimed to establish age related reference intervals of OA in urine, and for the first time in plasma, and dried blood spot (DBS) from 229 apparently healthy subjects aged from three days to 40 years. The quantification of OA was performed by a previously implemented method, using a stable isotope dilution with 1,3-[(15)N(2)]-orotic acid and hydrophilic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS/MS). The method has proved to be sensitive and accurate for a quantitative analysis of OA also in DBS and plasma. According to previous studies, urinary OA levels (mmol/mol of creatinine) decrease significantly with age. The upper limits (as 99th %ile) were of 3.44 and 1.30 in groups aged from three days to 1 year (group 1) and from 1 year to 12 years (group 2), respectively; in teenagers (from 13 to 19 years; group 3) and adults (from 20 to 40 years; group 4) urinary levels became more stable and the upper limits were of 0.64 and 1.21, respectively. Furthermore, OA levels in DBS (μM) also resulted significantly higher in subjects of group 1 (upper limit of 0.89) than in subjects of groups 2, 3 and 4 (upper limits of 0.24, 0.21, and 0.29, respectively). OA levels in plasma (μM) were significantly lower in subjects of group 3 (upper limit of 0.30) than in subjects of groups 1, 2, and 4 (upper limits of 0.59, 0.48, and 0.77, respectively). This method was also employed for OA quantification in plasma and DBS of 17 newborns affected by urea cycle defects, resulting sensitive and specific enough to screen these disorders.

摘要

乳清酸(OA)是遗传性乳清酸尿症的标志物,通常用于鉴别一些氨血症遗传性尿素循环缺陷和碱性氨基酸转运体的疾病。本研究旨在建立尿中 OA 的年龄相关参考区间,这也是首次在血浆和干血斑(DBS)中建立参考区间,研究对象为 229 名年龄从 3 天至 40 岁的健康个体。OA 的定量分析采用先前建立的方法,使用 1,3-[(15)N(2)]-乳清酸稳定同位素稀释法和亲水作用液相色谱-串联质谱法(HILIC-MS/MS)。该方法已被证明对 DBS 和血浆中 OA 的定量分析具有较高的灵敏度和准确性。根据之前的研究,尿中 OA 水平(mmol/mol 肌酐)随年龄显著降低。第 1 组(3 天至 1 岁)和第 2 组(1 岁至 12 岁)的尿中 OA 水平的上限(第 99 个百分位)分别为 3.44 和 1.30;青少年组(13 岁至 19 岁;第 3 组)和成年组(20 岁至 40 岁;第 4 组)的尿中 OA 水平变得更加稳定,上限分别为 0.64 和 1.21。此外,第 1 组 DBS 中 OA 水平(μM)的上限(0.89)也明显高于第 2、3 和 4 组(上限分别为 0.24、0.21 和 0.29)。第 3 组(上限 0.30)的血浆中 OA 水平明显低于第 1、2 和 4 组(上限分别为 0.59、0.48 和 0.77)。该方法还用于 17 例患有尿素循环缺陷的新生儿血浆和 DBS 中 OA 的定量分析,结果表明该方法具有较高的灵敏度和特异性,可用于筛查这些疾病。

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