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唾液样本中脑利钠肽前体 N 端的测定及其稳定性与心力衰竭监测。

Determination and stability of N-terminal pro-brain natriuretic peptide in saliva samples for monitoring heart failure.

机构信息

Department of Chemistry and Industrial Chemistry, University of Pisa, 56124, Pisa, Italy.

Institute of Analytical Sciences (ISA) - UMR 5280, University Claude Bernard Lyon 1, 69100, Lyon, France.

出版信息

Sci Rep. 2021 Jun 22;11(1):13088. doi: 10.1038/s41598-021-92488-2.

Abstract

Heart failure (HF) is the main cause of mortality worldwide, particularly in the elderly. N-terminal pro-brain natriuretic peptide (NT-proBNP) is the gold standard biomarker for HF diagnosis and therapy monitoring. It is determined in blood samples by the immunochemical methods generally adopted by most laboratories. Saliva analysis is a powerful tool for clinical applications, mainly due to its non-invasive and less risky sampling. This study describes a validated analytical procedure for NT-proBNP determination in saliva samples using a commercial Enzyme-Linked Immuno-Sorbent Assay. Linearity, matrix effect, sensitivity, recovery and assay-precision were evaluated. The analytical approach showed a linear behaviour of the signal throughout the concentrations tested, with a minimum detectable dose of 1 pg/mL, a satisfactory NT-proBNP recovery (95-110%), and acceptable precision (coefficient of variation ≤ 10%). Short-term (3 weeks) and long-term (5 months) stability of NT-proBNP in saliva samples under the storage conditions most frequently used in clinical laboratories (4, - 20, and - 80 °C) was also investigated and showed that the optimal storage conditions were at - 20 °C for up to 2.5 months. Finally, the method was tested for the determination of NT-proBNP in saliva samples collected from ten hospitalized acute HF patients. Preliminary results indicate a decrease in NT-proBNP in saliva from admission to discharge, thus suggesting that this procedure is an effective saliva-based point-of-care device for HF monitoring.

摘要

心力衰竭(HF)是全球主要的死亡原因,尤其是在老年人中。N 末端脑利钠肽前体(NT-proBNP)是 HF 诊断和治疗监测的金标准生物标志物。它通过大多数实验室普遍采用的免疫化学方法在血液样本中确定。唾液分析是一种用于临床应用的强大工具,主要是因为它具有非侵入性和较小的风险采样。本研究描述了一种使用商业酶联免疫吸附测定法(ELISA)测定唾液样本中 NT-proBNP 的经过验证的分析程序。评估了线性、基质效应、灵敏度、回收率和分析精度。分析方法显示信号在整个测试浓度范围内具有线性行为,最小检测剂量为 1 pg/mL,NT-proBNP 回收率令人满意(95-110%),且精密度可接受(变异系数≤10%)。在临床实验室最常使用的储存条件下(4、-20 和-80°C)研究了 NT-proBNP 在唾液样本中的短期(3 周)和长期(5 个月)稳定性,结果表明最佳储存条件是在-20°C 下储存长达 2.5 个月。最后,该方法用于测定来自 10 名住院急性 HF 患者的唾液样本中的 NT-proBNP。初步结果表明,从入院到出院时唾液中的 NT-proBNP 减少,因此表明该程序是一种有效的基于唾液的 HF 监测即时检测设备。

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