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血浆和血斑中酰基肉碱谱的差异。

Differences between acylcarnitine profiles in plasma and bloodspots.

机构信息

Department of Medical Genetics, UMC Utrecht, The Netherlands Wilhelmina Children's Hospital, University Medical Centre (UMC) Utrecht, Utrecht, The Netherlands.

出版信息

Mol Genet Metab. 2013 Sep-Oct;110(1-2):116-21. doi: 10.1016/j.ymgme.2013.04.008. Epub 2013 Apr 13.

Abstract

UNLABELLED

Quantification of acylcarnitines is used for screening and diagnosis of inborn error of metabolism (IEM). While newborn screening is performed in dried blood spots (DBSs), general metabolic investigation is often performed in plasma. Information on the correlation between plasma and DBS acylcarnitine profiles is scarce. In this study, we directly compared acylcarnitine concentrations measured in DBS with those in the corresponding plasma sample. Additionally, we tested whether ratios of acylcarnitines in both matrices are helpful for diagnostic purpose when primary markers fail.

STUDY DESIGN

DBS and plasma were obtained from controls and patients with a known IEM. (Acyl)carnitines were converted to their corresponding butyl esters and analyzed using HPLC/MS/MS.

RESULTS

Free carnitine concentrations were 36% higher in plasma compared to DBS. In contrast, in patients with carnitine palmitoyltransferase 1 (CPT-1) deficiency free carnitine concentration in DBS was 4 times the concentration measured in plasma. In carnitine palmitoyltransferase 2 (CPT-2) deficiency, primary diagnostic markers were abnormal in plasma but could also be normal in DBS. The calculated ratios for CPT-1 (C0/(C16+C18)) and CPT-2 ((C16+C18:1)/C2) revealed abnormal values in plasma. However, normal ratios were found in DBS of two (out of five) samples obtained from patients diagnosed with CPT-2.

CONCLUSIONS

Relying on primary acylcarnitine markers, CPT-1 deficiency can be missed when analysis is performed in plasma, whereas CPT-2 deficiency can be missed when analysis is performed in DBS. Ratios of the primary markers to other acylcarnitines restore diagnostic recognition completely for CPT-1 and CPT-2 in plasma, while CPT-2 can still be missed in DBS.

摘要

未加说明

酰基肉碱的定量分析用于筛查和诊断先天性代谢错误(IEM)。虽然新生儿筛查是在干血斑(DBS)中进行的,但一般代谢研究通常是在血浆中进行的。关于血浆和 DBS 酰基肉碱谱之间相关性的信息很少。在这项研究中,我们直接比较了 DBS 中测量的酰基肉碱浓度与相应血浆样本中的浓度。此外,我们还测试了当主要标志物失败时,两种基质中酰基肉碱的比值是否有助于诊断。

研究设计

从已知 IEM 的对照和患者中获得 DBS 和血浆。(酰基)肉碱被转化为相应的丁酯,并使用 HPLC/MS/MS 进行分析。

结果

与 DBS 相比,血浆中的游离肉碱浓度高 36%。相比之下,在肉碱棕榈酰转移酶 1(CPT-1)缺陷患者中,DBS 中的游离肉碱浓度是血浆中浓度的 4 倍。在肉碱棕榈酰转移酶 2(CPT-2)缺陷中,主要诊断标志物在血浆中异常,但也可能在 DBS 中正常。计算的 CPT-1(C0/(C16+C18))和 CPT-2((C16+C18:1)/C2)比值在血浆中显示异常值。然而,在从诊断为 CPT-2 的五名患者中获得的两个(共五个)DBS 样本中发现了正常比值。

结论

当在血浆中进行分析时,依赖于主要酰基肉碱标志物,CPT-1 缺陷可能会被遗漏,而当在 DBS 中进行分析时,CPT-2 缺陷可能会被遗漏。对于 CPT-1 和 CPT-2,主要标志物与其他酰基肉碱的比值在血浆中完全恢复了诊断识别,而在 DBS 中仍可能遗漏 CPT-2。

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