解开作为偏头痛生物标志物的 CGRP 水平之谜:深入的文献综述和我们的实验经验分析

Gabriel Gárate, Julio Pascual, Marta Pascual-Mato, Jorge Madera, María Muñoz-San Martín, Vicente González-Quintanilla
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引用次数: 0

摘要

降钙素基因相关肽(CGRP)是最有希望成为首个偏头痛生物标志物的候选物质。然而,文献显示了相互冲突的结果,并提出了造成这种差异的方法学来源。我们旨在研究其中的一些方法因素,以评估 CGRP 作为生物标志物的实际作用。在实验部分之前,我们对偏头痛患者 CGRP 测量的文献进行了回顾。利用我们的 399 份生物库血清样本,我们进行了一系列实验,以测试所使用的不同 ELISA 试剂盒、样本处理时间、长期储存、休息时或适度运动后采样的有效性。我们对内部数据进行了分析,以分析肽的平均水平以及性别和年龄的影响。文献综述显示,偏头痛患者 CGRP 测定等研究在研究设计、测定方法、结果和结论方面存在很大差异。CGRP 的测定取决于所采用的方法和特定试剂盒,也取决于所检测的同工酶,显示出完全不同的浓度范围。α-CGRP和β-CGRP的中位数和IQR水平分别为37.5(28.2-54.4)和4.6(2.4-6.4)pg/mL。当样本凝结并立即离心后储存于 4°C 时,血清中的 CGRP 含量会在 24 小时内保持不变。在零下 80 摄氏度储存 6 个月以上会导致 CGRP 水平下降。抽血前进行适度运动不会影响肽的浓度。年龄与β-CGRP含量呈正相关,男性的α-CGRP水平高于女性。我们为血清中 CGRP 的测量提供了有价值的信息。实验前应测试 ELISA 试剂盒的适用性。α-CGRP和β-CGRP水平应分开分析,因为即使在同一条件下,它们也会表现出不同的行为。如果样本保存在 4°C 温度下,可在 24 小时内处理完毕,但在化验前不应在 -80°C 温度下保存超过 6 个月。除非患者进行了高端耐力运动,否则抽血前无需休息。在进行比较研究时,应考虑性别和年龄因素,因为这些参数会影响 CGRP 的浓度。
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Untangling the mess of CGRP levels as a migraine biomarker: an in-depth literature review and analysis of our experimental experience
Calcitonin gene-related peptide (CGRP) is the most promising candidate to become the first migraine biomarker. However, literature shows clashing results and suggests a methodological source for such discrepancies. We aimed to investigate some of these methodological factors to evaluate the actual role of CGRP as biomarker. Previous to the experimental part, we performed a literature review of articles measuring CGRP in migraine patients. Using our 399 bio-bank sera samples, we performed a series of experiments to test the validity of different ELISA kits employed, time of sample processing, long-term storage, sampling in rest or after moderate exercise. Analysis of in-house data was performed to analyse average levels of the peptide and the effect of sex and age. Literature review shows the high variability in terms of study design, determination methods, results and conclusions obtained by studies including CGRP determinations in migraine patients. CGRP measurements depends on the method and specific kit employed, also on the isoform detected, showing completely different ranges of concentrations. Alpha-CGRP and beta-CGRP had median with IQR levels of 37.5 (28.2–54.4) and 4.6 (2.4–6.4)pg/mL, respectively. CGRP content is preserved in serum within the 24 first hours when samples are stored at 4°C after clotting and immediate centrifugation. Storages at -80°C of more than 6 months result in a decrease in CGRP levels. Moderate exercise prior to blood extraction does not modulate the concentration of the peptide. Age positively correlates with beta-CGRP content and men have higher alpha-CGRP levels than women. We present valuable information for CGRP measurements in serum. ELISA kit suitability should be tested prior to the experiments. Alpha and beta-CGRP levels should be analysed separately as they can show different behaviours even within the same condition. Samples can be processed in a 24-h window if they have been kept in 4°C and should not be stored for more than 6 months at -80°C before assayed. Patients do not need to rest before the blood extraction unless they have performed a high-endurance exercise. For comparative studies, sex and age should be accounted for as these parameters can impact CGRP concentrations.
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