Department of Pathology, UT Southwestern Medical Center, Dallas, TX, United States.
Department of Pathology, UT Southwestern Medical Center, Dallas, TX, United States.
Adv Clin Chem. 2019;92:59-103. doi: 10.1016/bs.acc.2019.04.001. Epub 2019 Jun 8.
Inborn errors of metabolism (IEMs) are a large class of genetic disorders that result from defects in enzymes involved in energy production and metabolism of nutrients. For every metabolic pathway, there are defects that can occur and potentially result in an IEM. While some defects can go undetected in one's lifetime, some have moderate to severe clinical consequences. In the latter case, the biochemical defect leads to accumulation of metabolites and byproducts that are toxic or interfere with normal biological function. Disorders of amino acid metabolism, organic acid metabolism and the urea cycle comprise a large portion of IEMs. Two essential tools required for the diagnosis of these categories of disorders are amino acid and organic acid profiling. Most all clinical laboratories offering metabolic testing perform amino acid analysis, while organic acid profiling is restricted to more specialized pediatric hospitals and reference laboratories. In this chapter, we will provide an overview of various methodologies employed for amino acid and organic acid profiling as well as specific examples to demonstrate how these techniques are applied in clinical laboratories for the diagnosis of IEMs.
先天性代谢缺陷(IEM)是一大类遗传疾病,由参与能量产生和营养物质代谢的酶的缺陷引起。对于每一种代谢途径,都有可能发生缺陷,并可能导致 IEM。虽然有些缺陷在人的一生中可能不会被发现,但有些缺陷具有中度至严重的临床后果。在后一种情况下,生化缺陷会导致代谢物和副产物的积累,这些代谢物和副产物有毒或干扰正常的生物功能。氨基酸代谢、有机酸代谢和尿素循环紊乱构成了 IEM 的很大一部分。诊断这些类别的疾病需要两种必不可少的工具,即氨基酸和有机酸分析。大多数提供代谢测试的临床实验室都进行氨基酸分析,而有机酸分析则限于更专业的儿科医院和参考实验室。在这一章中,我们将概述用于氨基酸和有机酸分析的各种方法,并提供具体示例,说明这些技术如何在临床实验室中用于 IEM 的诊断。