除了在-80°C冷冻外,Elecsys免疫分析法对大多数分析前影响因素都是稳定的,脑脊液中的阿尔茨海默病生物标志物。

Franz Felix Konen, Hannah Benedictine Maier, Alexandra Neyazi, Stefan Bleich, Konstantin Neumann, Thomas Skripuletz
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引用次数: 0

摘要

背景:阿尔茨海默病被认为是一种神经退行性疾病,通过排除诊断,而检测特定的脑脊液(CSF)生物标志物,即淀粉样蛋白β(aβ)肽aβ1-42(aß42)、磷酸化tau(181P;P-tau)和总tau(T-tau),已被证明可以提高诊断准确性。最近,引入了新一代用于Elecsys CSF免疫测定的样品管(Sarstedt假底管),用于测定CSF中的阿尔茨海默病生物标志物,有望获得更好的可测量性。然而,分析前的影响因素尚未得到充分的研究。方法:在29名未被诊断为阿尔茨海默病的患者中,使用Elecsys免疫测定方法,在天然CSF和不同影响干预后检测CSF中Aß42、P-tau和T-tau的浓度。分析了以下影响因素:血液污染(10000和20000红细胞/µl CSF)、在4°C下储存14天、CSF的血液污染和在4°C下储存14天后、在Sarstedt管或玻璃瓶中在-80°C下冷冻14天、在玻璃瓶中在-800°C下中间储存3个月。结果:在-80°C下在Sarstedt假底管和玻璃瓶中储存14天,以及在-80°C.下在玻璃瓶中储存3个月,均导致Aß42显著降低(在Sarstedt14天后为13%,在玻璃瓶中为22%,在玻璃瓶中为42%),CSF中的P-tau(在Sarstedt中14天后为9%,在玻璃瓶中为13%,在玻璃小瓶中3个月后为12%)和T-tau(Sarstedt在14天后为12%,在玻璃瓶中为19%,在玻璃水瓶中为20%)浓度。其他预分析影响因素没有发现显著差异。结论:使用Elecsys免疫测定法测量CSF中Aß42、P-tau和T-tau的浓度,对血液污染和储存时间的预分析影响因素具有稳健性。无论储存管如何,在-80°C下冷冻都会导致生物标志物浓度显著降低,在回顾性分析中必须考虑这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Alzheimer's disease biomarkers in cerebrospinal fluid are stable with the Elecsys immunoassay to most pre-analytical influencing factors except freezing at -80 °C.

Alzheimer's disease biomarkers in cerebrospinal fluid are stable with the Elecsys immunoassay to most pre-analytical influencing factors except freezing at -80 °C.

Alzheimer's disease biomarkers in cerebrospinal fluid are stable with the Elecsys immunoassay to most pre-analytical influencing factors except freezing at -80 °C.

Alzheimer's disease biomarkers in cerebrospinal fluid are stable with the Elecsys immunoassay to most pre-analytical influencing factors except freezing at -80 °C.

Background: Alzheimer´s disease is considered a neurodegenerative disease and is diagnosed by exclusion, while the detection of specific cerebrospinal fluid (CSF) biomarkers, namely amyloid-beta (Aβ) peptides Aβ1-42 (Aß42), phospho-tau (181P; P-tau), and total-tau (T-tau), has been shown to improve diagnostic accuracy. Recently, a new generation of sample tubes (Sarstedt false-bottom tubes) for the Elecsys CSF immunoassay for the determination of Alzheimer´s disease biomarkers in CSF was introduced, promising better measurability. However, the pre-analytic influencing factors have not yet been sufficiently investigated.

Methods: In 29 patients without Alzheimer's disease diagnosis, CSF concentrations of Aß42, P-tau and T-tau were examined in native CSF and after different influencing interventions using the Elecsys immunoassay test method. The following influencing factors were analyzed: contamination with blood (10,000 and 20,000 erythrocytes/µl CSF), 14-day storage at 4 °C, blood contamination of CSF and 14-day storage at 4 °C, 14-day freezing at -80 °C in Sarstedt tubes or glass vials, 3-month intermediate storage at -80 °C in glass vials.

Results: Both storage at -80 °C for 14 days in Sarstedt false-bottom tubes and in glass vials and storage at -80 °C for 3 months in glass vials resulted in significant decreases in Aß42 (13% after 14 days in Sarstedt and 22% in glass vials, 42% after 3 months in glass vials), P-tau (9% after 14 days in Sarstedt and 13% in glass vials, 12% after 3 months in glass vials) and T-tau (12% after 14 days in Sarstedt and 19% in glass vials, 20% after 3 months in glass vials) concentrations in CSF. No significant differences were found for the other pre-analytical influencing factors.

Conclusions: Measurements of the concentrations of Aß42, P-tau, and T-tau in CSF with use of the Elecsys immunoassay are robust to the pre-analytical influencing factors of blood contamination and duration of storage. Freezing at -80 °C results in significant reduction of biomarker concentrations regardless of the storage tube and must be considered in retrospective analysis.

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