Department of Pediatrics, Division of Pulmonary Medicine, Seattle Children's Hospital, University of Washington, Seattle, WA, USA.
J Breath Res. 2010 Dec;4(4):046002. doi: 10.1088/1752-7155/4/4/046002. Epub 2010 Nov 15.
Cysteinyl leukotrienes (CysLTs) can be measured in exhaled breath condensate (EBC); however, there is considerable variation in reported EBC CysLT concentrations from asthmatic and healthy subjects between published studies, which may be partially explained by CysLT degradation during processing and storage. We assessed CysLT stability over 6 months in EBC from healthy subjects stored at -80 °C, layered with argon and then stored at -80 °C or stored in 0.2% formic acid in methanol at -80 °C following solid-phase extraction (SPE). We found significant CysLT degradation over time in both spiked and unspiked EBC samples stored at -80 °C or layered with argon. CysLT recovery was significantly greater after storage for 6 months in 0.2% formic acid in methanol following SPE; however, there was substantial variability in endogenous CysLT recovery over time, possibly attributable to inter- and intra-assay variability at the low end of the CysLT assay range. Despite the greater recovery of CysLTs in EBC stored in methanol following SPE, the degree of variability introduced by this method appears unacceptably high. We believe that the development of more sensitive and less variable methods for quantifying CysLTs in EBC are required before CysLTs can reliably be utilized as biomarkers in exhaled breath. Sample processing and storage, as well as inter- and intra-assay variability, should be carefully considered in the design of clinical studies that include assessments of EBC constituents as biomarkers.
半胱氨酰白三烯 (CysLTs) 可在呼出气冷凝物 (EBC) 中测量;然而,在已发表的研究中,哮喘患者和健康受试者的 EBC CysLT 浓度存在相当大的差异,这可能部分解释为 CysLT 在处理和储存过程中降解。我们评估了健康受试者 EBC 在 -80°C 下储存 6 个月的 CysLT 稳定性,EBC 用氩气分层后再储存在 -80°C 下,或在经过固相萃取 (SPE) 后用 0.2%甲酸甲醇储存于 -80°C。我们发现,在 -80°C 或氩气分层储存的有或无添加物的 EBC 样本中,CysLT 随时间明显降解。SPE 后在 0.2%甲酸甲醇中储存 6 个月后,CysLT 回收率显著增加;然而,内源性 CysLT 回收率随时间的变化存在很大的差异,这可能归因于 CysLT 测定范围低值的试验内和试验间变异性。尽管 SPE 后在甲醇中储存的 EBC 中 CysLT 回收率更高,但该方法引入的变异性程度似乎高得无法接受。我们认为,在 CysLT 能够可靠地作为呼出气中的生物标志物之前,需要开发更灵敏、变异性更小的定量 EBC 中 CysLT 的方法。在设计包括评估 EBC 成分作为生物标志物的临床研究时,应仔细考虑样本处理和储存以及试验内和试验间的变异性。