Vreken P, van Lint A E, Bootsma A H, Overmars H, Wanders R J, van Gennip A H
Academic Medical Center, University of Amsterdam, Emma Children's Hospital and Dept. of Clinical Chemistry, The Netherlands.
J Chromatogr B Biomed Sci Appl. 1998 Aug 25;713(2):281-7. doi: 10.1016/s0378-4347(98)00186-8.
A common feature of most peroxisomal disorders is the accumulation of very-long-chain fatty acids (VLCFAs) and/or pristanic and phytanic acid in plasma. Previously described methods utilizing either gas chromatography alone or gas chromatography-mass spectrometry are, in general, time-consuming and unable to analyze VLCFAs, pristanic and phytanic acid within a single analysis. We describe a simple, reproducible and rapid method using gas chromatography/mass spectrometry with deuterated internal standards. The method was evaluated by analysing 30 control samples and samples from 35 patients with defined peroxisomal disorders and showed good discrimination between controls and patients. This method is suitable for routine screening for peroxisomal disorders.
大多数过氧化物酶体疾病的一个共同特征是血浆中极长链脂肪酸(VLCFA)和/或降植烷酸及植烷酸的蓄积。先前描述的仅使用气相色谱法或气相色谱-质谱联用的方法通常耗时较长,且无法在单次分析中同时分析VLCFA、降植烷酸及植烷酸。我们描述了一种使用带有氘代内标的气相色谱/质谱联用的简单、可重复且快速的方法。通过分析30份对照样品和35例明确诊断为过氧化物酶体疾病患者的样品对该方法进行了评估,结果显示该方法在对照和患者之间具有良好的区分度。此方法适用于过氧化物酶体疾病的常规筛查。