Is Serum or Plasma More Appropriate for Intersubject Comparisons in Metabolomic Studies? An Assessment in Patients with Small-Cell Lung Cancer

化学 代谢组学 代谢物 色谱法 代谢组 肌酐 质谱法 内科学 药理学 生物化学 医学
作者
David C. Wedge,J. William Allwood,Warwick B. Dunn,Andrew A. Vaughan,Kathryn Simpson,Marie Brown,Lynsey Priest,Fiona Blackhall,Anthony D. Whetton,Caroline Dive,Royston Goodacre
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:83 (17): 6689-6697 被引量:126
标识
DOI:10.1021/ac2012224
摘要

In clinical analyses, the most appropriate biofluid should be analyzed for optimal assay performance. For biological fluids, the most readily accessible is blood, and metabolomic analyses can be performed either on plasma or serum. To determine the optimal agent for analysis, metabolic profiles of matched human serum and plasma were assessed by gas chromatography/time-of-flight mass spectrometry and ultrahigh-performance liquid chromatography mass spectrometry (in positive and negative electrospray ionization modes). Comparison of the two metabolomes, in terms of reproducibility, discriminative ability and coverage, indicated that they offered similar analytical opportunities. An analysis of the variation between 29 small-cell lung cancer (SCLC) patients revealed that the differences between individuals are markedly similar for the two biofluids. However, significant differences between the levels of some specific metabolites were identified, as were differences in the intersubject variability of some metabolite levels. Glycerophosphocholines, erythritol, creatinine, hexadecanoic acid, and glutamine in plasma, but not in serum, were shown to correlate with life expectancy for SCLC patients, indicating the utility of metabolomic analyses in clinical prognosis and the particular utility of plasma in relation to the clinical management of SCLC.
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