Li Kefeng, Naviaux Jane C, Bright A Taylor, Wang Lin, Naviaux Robert K
The Mitochondrial and Metabolic Disease Center, University of California, San Diego, School of Medicine, 214 Dickinson St., Bldg CTF, Rm C102, San Diego, CA 92103-8467 USA.
Department of Medicine, University of California, San Diego, School of Medicine, 214 Dickinson St., Bldg CTF, Rm C102, San Diego, CA 92103-8467 USA.
Metabolomics. 2017;13(10):122. doi: 10.1007/s11306-017-1264-1. Epub 2017 Sep 4.
Metabolomics is a powerful emerging technology for studying the systems biology and chemistry of health and disease. Current targeted methods are often limited by the number of analytes that can be measured, and/or require multiple injections.
We developed a single-injection, targeted broad-spectrum plasma metabolomic method on a SCIEX Qtrap 5500 LC-ESI-MS/MS platform. Analytical validation was conducted for the reproducibility, linearity, carryover and blood collection tube effects. The method was also clinically validated for its potential utility in the diagnosis of chronic fatigue syndrome (CFS) using a cohort of 22 males CFS and 18 age- and sex-matched controls.
Optimization of LC conditions and MS/MS parameters enabled the measurement of 610 key metabolites from 63 biochemical pathways and 95 stable isotope standards in a 45-minute HILIC method using a single injection without sacrificing sensitivity. The total imprecision (CV) of peak area was 12% for both the control and CFS pools. The 8 metabolites selected in our previous study (PMID: 27573827) performed well in a clinical validation analysis even when the case and control samples were analyzed 1.5 years later on a different instrument by a different investigator, yielding a diagnostic accuracy of 95% (95% CI 85-100%) measured by the area under the ROC curve.
A reliable and reproducible, broad-spectrum, targeted metabolomic method was developed, capable of measuring over 600 metabolites in plasma in a single injection. The method might be a useful tool in helping the diagnosis of CFS or other complex diseases.
代谢组学是一种用于研究健康与疾病的系统生物学及化学的新兴强大技术。当前的靶向方法常常受到可测量分析物数量的限制,和/或需要多次进样。
我们在SCIEX Qtrap 5500液相色谱 - 电喷雾串联质谱平台上开发了一种单次进样的靶向广谱血浆代谢组学方法。对该方法的重现性、线性、残留和采血管效应进行了分析验证。还使用22名男性慢性疲劳综合征(CFS)患者和18名年龄及性别匹配的对照组成的队列,对该方法在CFS诊断中的潜在效用进行了临床验证。
液相色谱条件和串联质谱参数的优化使得在45分钟的亲水作用色谱法中,通过单次进样能够测量来自63条生化途径的610种关键代谢物和95种稳定同位素标准品,且不牺牲灵敏度。对照样本组和CFS样本组的峰面积总不精密度(CV)均为12%。我们之前研究中选择的8种代谢物(PMID:27573827)在临床验证分析中表现良好,即使病例和对照样本在1.5年后由不同的研究者在不同仪器上进行分析,通过ROC曲线下面积测得的诊断准确率仍为95%(95%CI 85 - 100%)。
开发了一种可靠且可重现的广谱靶向代谢组学方法,能够单次进样测量血浆中600多种代谢物。该方法可能是辅助CFS或其他复杂疾病诊断的有用工具。