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使用液相色谱-串联质谱法定量测定尿8-异前列腺素F2α及其与肌钙蛋白水平升高的关系。

Quantification of urinary 8-iso-PGF2alpha using liquid chromatography-tandem mass spectrometry and association with elevated troponin levels.

作者信息

Saenger Amy K, Laha Thomas J, Edenfield Michael J, Sadrzadeh Sayed M H

机构信息

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Clin Biochem. 2007 Nov;40(16-17):1297-304. doi: 10.1016/j.clinbiochem.2007.07.023. Epub 2007 Aug 17.

Abstract

OBJECTIVES

Increased lipid peroxidation (i.e. "oxidative stress") has been identified as a central mechanism in the development of atherosclerosis and inflammatory vascular damage. Measurement of 8-iso-PGF(2alpha) has demonstrated to be a reliable indicator of in vivo oxidative stress levels. The purpose of this study was to develop a rapid, sensitive, and specific LC-MS/MS method for detection of urinary 8-iso-PGF(2alpha), establish reference intervals, and correlate isoprostane levels with cardiac troponin I.

DESIGN AND METHODS

Urinary 8-iso-PGF(2alpha) was detected after direct injection onto a C18 silica column and monitored in the MRM mode using m/z transitions of 353.2>193.25 (8-iso-PGF(2alpha)) and 357.2>197.25 (8-iso-PGF(2alpha)-d(4)). The LC-MS/MS method was also compared to an ELISA kit. Reference interval studies were evaluated against a separate population of patients presenting with chest pain that had positive cTnI values.

RESULTS

Elution of 8-iso-PGF(2alpha) was achieved after 7 min, with a total run time of 10 min. Inter-assay CVs were 13.8-20.0% and intra-assay CVs were 10.9-17.0%. Linearity ranged from 100 pg/mL to 100 ng/mL. Deming regression of ELISA and LC-MS/MS methods for 8-iso-PGF(2alpha) levels yielded poor correlation, with a slope of 0.0265, y-intercept of 0.255 ng/mL, and R(2) value of 0.0434. Urine 8-iso-PGF(2alpha) concentrations in samples obtained from healthy individuals (n=34) ranged from 57 to 390 ng/g creatinine with a mean of 221 ng/g creatinine. 8-iso-PGF(2alpha) levels were statistically significant in troponin-positive (n=35) versus troponin-negative (n=36) patients (p<0.0049).

CONCLUSIONS

This LC-MS/MS method provides a rapid, accurate, sensitive, and cost-effective alternative to other methods for detection of 8-iso-PGF(2alpha) in urine. 8-iso-PGF(2alpha) has potential to be a great prognostic risk indicator in individuals with a high probability for future coronary events.

摘要

目的

脂质过氧化增加(即“氧化应激”)已被确认为动脉粥样硬化和炎症性血管损伤发展的核心机制。8-异前列腺素F2α(8-iso-PGF(2α))的测量已被证明是体内氧化应激水平的可靠指标。本研究的目的是开发一种快速、灵敏且特异的液相色谱-串联质谱(LC-MS/MS)方法来检测尿中的8-iso-PGF(2α),建立参考区间,并将异前列腺素水平与心肌肌钙蛋白I相关联。

设计与方法

将尿液直接进样到C18硅胶柱后检测8-iso-PGF(2α),并在多反应监测(MRM)模式下使用m/z跃迁353.2>193.25(8-iso-PGF(2α))和357.2>197.25(8-iso-PGF(2α)-d(4))进行监测。还将该LC-MS/MS方法与酶联免疫吸附测定(ELISA)试剂盒进行了比较。参考区间研究是针对另一组肌钙蛋白I值为阳性的胸痛患者进行评估的。

结果

8-iso-PGF(2α)在7分钟后洗脱,总运行时间为10分钟。批间变异系数(CV)为13.8 - 20.0%,批内CV为10.9 - 17.0%。线性范围为100 pg/mL至100 ng/mL。8-iso-PGF(2α)水平的ELISA法和LC-MS/MS法的戴明回归相关性较差,斜率为0.0265,截距为0.255 ng/mL,决定系数(R(2))值为0.0434。从健康个体(n = 34)获得的样本中尿8-iso-PGF(2α)浓度范围为57至390 ng/g肌酐,平均值为221 ng/g肌酐。肌钙蛋白阳性(n = 35)与肌钙蛋白阴性(n = 36)患者的8-iso-PGF(2α)水平具有统计学显著性差异(p < 0.0049)。

结论

这种LC-MS/MS方法为检测尿液中8-iso-PGF(2α)提供了一种快速、准确、灵敏且经济高效的替代其他方法。8-iso-PGF(2α)有可能成为未来发生冠状动脉事件可能性高的个体的一个重要预后风险指标。

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