Andreas Kuehnl, Jaroslav Pelisek, Martin Bruckmeier, Wajima Safi, Hans-Henning Eckstein
{"title":"人类血液样本中CNP和NT-proCNP的比较测量:方法学评价。","authors":"Andreas Kuehnl, Jaroslav Pelisek, Martin Bruckmeier, Wajima Safi, Hans-Henning Eckstein","doi":"10.1186/1477-5751-12-7","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>C-type natriuretic peptide (CNP) has anti-inflammatory, anti-proliferative, and anti-migratory properties. During the past years, CNP has attained an increasing interest by many research groups, especially in the cardiovascular field. Nevertheless, still no reliable data exist on the difference of CNP concentration between serum and plasma samples. Also, the influence of delayed blood sample proceeding is unknown. The aim of this study was to investigate the difference of CNP and NT-proCNP concentrations between serum and plasma samples. In order to identify potential methodological bias, this study should also validate the stability of CNP and NT-proCNP in full blood samples stored at room temperature.</p><p><strong>Findings: </strong>Triplets (serum, plasma, full blood) of fasting blood samples from 12 healthy male individuals were collected. Analysis of CNP and NT-proCNP concentration was performed immediately following sampling, and after 30 minutes or 2 hours of storage at room temperature. Mean serum concentrations at baseline were 0.997 ± 0.379 ng/ml for CNP and 58.5 ± 28.3 pg/ml for NT-proCNP. Furthermore, NT-proCNP concentration did not change significantly during the allotted time and did not differ between serum, plasma, and full blood samples. At baseline, concentrations of CNP were significantly different between samples containing either sodium-citrate or EDTA as a clotting inhibitor (1.933 ± 0.699 ng/ml vs. 0.991 ± 0.489 ng/ml, p = 0.001).</p><p><strong>Conclusions: </strong>CNP and NT-proCNP are stable for at least two hours, even when sample processing is delayed or blood probes are stored at room temperature. NT-proCNP assay demonstrated more consistent and reliable data and should therefore be preferred for usage in clinical applications. Nevertheless, as recommended for ANP and BNP, immunoassays for CNP should also be standardized or harmonized in the future.</p>","PeriodicalId":73849,"journal":{"name":"Journal of negative results in biomedicine","volume":" ","pages":"7"},"PeriodicalIF":0.0000,"publicationDate":"2013-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1477-5751-12-7","citationCount":"12","resultStr":"{\"title\":\"Comparative measurement of CNP and NT-proCNP in human blood samples: a methodological evaluation.\",\"authors\":\"Andreas Kuehnl, Jaroslav Pelisek, Martin Bruckmeier, Wajima Safi, Hans-Henning Eckstein\",\"doi\":\"10.1186/1477-5751-12-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>C-type natriuretic peptide (CNP) has anti-inflammatory, anti-proliferative, and anti-migratory properties. During the past years, CNP has attained an increasing interest by many research groups, especially in the cardiovascular field. Nevertheless, still no reliable data exist on the difference of CNP concentration between serum and plasma samples. Also, the influence of delayed blood sample proceeding is unknown. The aim of this study was to investigate the difference of CNP and NT-proCNP concentrations between serum and plasma samples. In order to identify potential methodological bias, this study should also validate the stability of CNP and NT-proCNP in full blood samples stored at room temperature.</p><p><strong>Findings: </strong>Triplets (serum, plasma, full blood) of fasting blood samples from 12 healthy male individuals were collected. Analysis of CNP and NT-proCNP concentration was performed immediately following sampling, and after 30 minutes or 2 hours of storage at room temperature. Mean serum concentrations at baseline were 0.997 ± 0.379 ng/ml for CNP and 58.5 ± 28.3 pg/ml for NT-proCNP. Furthermore, NT-proCNP concentration did not change significantly during the allotted time and did not differ between serum, plasma, and full blood samples. At baseline, concentrations of CNP were significantly different between samples containing either sodium-citrate or EDTA as a clotting inhibitor (1.933 ± 0.699 ng/ml vs. 0.991 ± 0.489 ng/ml, p = 0.001).</p><p><strong>Conclusions: </strong>CNP and NT-proCNP are stable for at least two hours, even when sample processing is delayed or blood probes are stored at room temperature. NT-proCNP assay demonstrated more consistent and reliable data and should therefore be preferred for usage in clinical applications. 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引用次数: 12
摘要
背景:c型利钠肽(CNP)具有抗炎、抗增殖和抗迁移的特性。在过去的几年里,CNP已经获得了越来越多的研究小组的兴趣,特别是在心血管领域。然而,血清和血浆样品中CNP浓度的差异仍然没有可靠的数据。此外,延迟采集血样的影响尚不清楚。本研究的目的是探讨血清和血浆样品中CNP和NT-proCNP浓度的差异。为了确定潜在的方法学偏差,本研究还应验证CNP和NT-proCNP在室温下保存的全血样本中的稳定性。结果:收集了12例健康男性空腹血液样本的三胞胎(血清、血浆、全血)。取样后立即进行CNP和NT-proCNP浓度分析,室温保存30分钟或2小时。基线时CNP的平均血清浓度为0.997±0.379 ng/ml, NT-proCNP为58.5±28.3 pg/ml。此外,NT-proCNP浓度在指定的时间内没有显著变化,在血清、血浆和全血样本之间没有差异。在基线时,含有柠檬酸钠或EDTA作为凝血抑制剂的样品中CNP的浓度显著不同(1.933±0.699 ng/ml vs 0.991±0.489 ng/ml, p = 0.001)。结论:即使样品处理延迟或血液探针在室温下保存,CNP和NT-proCNP至少在两小时内是稳定的。NT-proCNP分析显示了更一致和可靠的数据,因此应优先用于临床应用。然而,正如推荐的ANP和BNP一样,未来CNP的免疫测定也应该标准化或统一。
Comparative measurement of CNP and NT-proCNP in human blood samples: a methodological evaluation.
Background: C-type natriuretic peptide (CNP) has anti-inflammatory, anti-proliferative, and anti-migratory properties. During the past years, CNP has attained an increasing interest by many research groups, especially in the cardiovascular field. Nevertheless, still no reliable data exist on the difference of CNP concentration between serum and plasma samples. Also, the influence of delayed blood sample proceeding is unknown. The aim of this study was to investigate the difference of CNP and NT-proCNP concentrations between serum and plasma samples. In order to identify potential methodological bias, this study should also validate the stability of CNP and NT-proCNP in full blood samples stored at room temperature.
Findings: Triplets (serum, plasma, full blood) of fasting blood samples from 12 healthy male individuals were collected. Analysis of CNP and NT-proCNP concentration was performed immediately following sampling, and after 30 minutes or 2 hours of storage at room temperature. Mean serum concentrations at baseline were 0.997 ± 0.379 ng/ml for CNP and 58.5 ± 28.3 pg/ml for NT-proCNP. Furthermore, NT-proCNP concentration did not change significantly during the allotted time and did not differ between serum, plasma, and full blood samples. At baseline, concentrations of CNP were significantly different between samples containing either sodium-citrate or EDTA as a clotting inhibitor (1.933 ± 0.699 ng/ml vs. 0.991 ± 0.489 ng/ml, p = 0.001).
Conclusions: CNP and NT-proCNP are stable for at least two hours, even when sample processing is delayed or blood probes are stored at room temperature. NT-proCNP assay demonstrated more consistent and reliable data and should therefore be preferred for usage in clinical applications. Nevertheless, as recommended for ANP and BNP, immunoassays for CNP should also be standardized or harmonized in the future.