Thorsby Per Medbøe Medbøe, Dahl Sandra Rinne, Smetop Tone, Lindholm Tone Hæg, Zykova Svetlana
P Thorsby, Hormone Laboratory, Department of medical Biocehmistry, Oslo University Hospital, Oslo, Norway.
S Dahl, Hormone Laboratory, Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.
Endocr Connect. 2025 Apr 1;14(5). doi: 10.1530/EC-25-0023.
Determination of metanephrines in saliva has been reported as a pain- and hazard-free alternative to plasma-based tests with a potential to reduce false-positive results during diagnostic work-up for neuroendocrine tumours. No validated method has, however, been made available in the published literature so far. The aim of this work was to develop an LC-MS/MS method for measurement of metanephrine, normetanephrine and 3-methoxytyramine in human saliva. As hyposalivation represents a real real-life challenge in situations with catecholamine excess, special effort was made to minimise specimen volume and to make the assay suitable also for paediatric and geriatric populations.
The method validation was performed according to relevant guidelines and included recovery from three different collection swabs (Salivette, SalivaBio and Salimetrics). Selectivity, interferences, matrix effects, limits of quantification, linearity of calibration, sample volume, trueness, within-run and total analytical repeatability, robustness, carry-over and stability were evaluated.
A sample volume as low as 20µl was acceptable for all analytes, but 50µl sample volume gave lower LLOQ, higher accuracy and better precision. Total analytical variation was <15% and the minimum turnaround time was 3 hours. Among the sample collection devices tested, highest recovery was achieved with SalivaBio (93 to 104%). Metanephrines were stable in saliva when stored at ambient temperature for 6 h, and tolerated at least one week of freezing at -20°C.
The non-invasiveness, ease of specimen collection, better stability of analytes compared to plasma and analytical performance make the method relevant for both research and diagnostics of states with catecholamine excess.
唾液中变肾上腺素的测定已被报道为一种无疼痛、无风险的替代血浆检测的方法,有可能减少神经内分泌肿瘤诊断检查期间的假阳性结果。然而,目前尚未在已发表的文献中找到经过验证的方法。这项工作的目的是开发一种液相色谱-串联质谱法(LC-MS/MS),用于测定人唾液中的变肾上腺素、去甲变肾上腺素和3-甲氧基酪胺。由于在儿茶酚胺过量的情况下,唾液分泌减少是一个现实生活中的挑战,因此我们特别努力地减少样本体积,并使该检测方法也适用于儿科和老年人群。
根据相关指南进行方法验证,包括从三种不同的采集拭子(Salivette、SalivaBio和Salimetrics)中回收。评估了选择性、干扰、基质效应、定量限、校准线性、样本体积、准确性、批内和总分析重复性、稳健性、残留和稳定性。
所有分析物的样本体积低至20µl是可以接受的,但50µl的样本体积给出了更低的定量下限、更高的准确性和更好的精密度。总分析变异<15%,最短周转时间为3小时。在所测试的样本采集装置中,SalivaBio的回收率最高(93%至104%)。变肾上腺素在唾液中于室温下储存6小时稳定,在-20°C下冷冻至少一周也可耐受。
该方法的非侵入性、样本采集简便、与血浆相比分析物稳定性更好以及分析性能使其在儿茶酚胺过量状态的研究和诊断中均具有相关性。