Ongay Sara, Sikma Marijke, Horvatovich Peter, Hermans Jos, Miller Bruce E, Ten Hacken Nick H T, Bischoff Rainer
University of Groningen, Department of Pharmacy, Analytical Biochemistry, Groningen, The Netherlands.
Van Hall Larenstein Hogeschool, Leeuwarden, Agora, The Netherlands.
Chronic Obstr Pulm Dis. 2016 Mar 1;3(2):560-569. doi: 10.15326/jcopdf.3.2.2015.0159.
Desmosine (DES) and isodesmosine (IDES) have been widely discussed as potential biomarkers of COPD. However, their clinical utility and validity remains unproven. This study aims to progress DES/IDES evaluation as a chronic obstructive pulmonary disease (COPD) biomarker by investigating its urinary excretion in a large sample cohort with respect to a) which factors influence DES/IDES levels in a population of healthy control individuals and COPD individuals; b) whether DES/IDES levels enable the differentiation between COPD individuals and healthy control individuals; c) whether DES/IDES can be used to differentiate between fast and slow decliners in lung function. Urinary DES and IDES were quantified in 365 individuals (147 healthy control individuals and 218 COPD individuals) from the Evaluation of COPD Longitudinally to Indentify Predictive Surrogate Endpoints (ECLIPSE) study (NCT00292552) by employing a validated liquid chromatography tandem mass spectrometry (LC-MS/MS) method. Age, gender, body mass index (BMI) and smoking have a significant (<0.05) influence on DES/IDES urinary excretion and need to be corrected for when investigating DES/IDES as a disease biomarker. Urinary DES/IDES allowed a statistically relevant differentiation (<0.05) between stable COPD individuals and healthy control individuals, however, assay sensitivity and specificity were low (62% and 73%, respectively). Furthermore, urinary DES/IDES does not allow the differentiation of fast and slow decliners in lung function. The present results suggest that while urinary DES/IDES excretion is related to COPD, it is not a sensitive or specific biomarker for COPD diagnosis or prognosis.
去甲双氢锁链素(DES)和异去甲双氢锁链素(IDES)作为慢性阻塞性肺疾病(COPD)的潜在生物标志物已被广泛讨论。然而,它们的临床效用和有效性仍未得到证实。本研究旨在通过在一个大样本队列中调查其尿排泄情况,推进将DES/IDES评估作为慢性阻塞性肺疾病(COPD)生物标志物的研究,具体涉及以下方面:a)哪些因素影响健康对照个体和COPD个体群体中的DES/IDES水平;b)DES/IDES水平是否能够区分COPD个体和健康对照个体;c)DES/IDES是否可用于区分肺功能快速下降者和缓慢下降者。采用经过验证的液相色谱串联质谱(LC-MS/MS)方法,对慢性阻塞性肺疾病纵向评估以识别预测替代终点(ECLIPSE)研究(NCT00292552)中的365名个体(147名健康对照个体和218名COPD个体)的尿DES和IDES进行了定量分析。年龄、性别、体重指数(BMI)和吸烟对DES/IDES尿排泄有显著(<0.05)影响,在将DES/IDES作为疾病生物标志物进行研究时需要进行校正。尿DES/IDES在稳定的COPD个体和健康对照个体之间实现了具有统计学意义的区分(<0.05),然而,检测灵敏度和特异性较低(分别为62%和73%)。此外,尿DES/IDES无法区分肺功能快速下降者和缓慢下降者。目前的结果表明,虽然尿DES/IDES排泄与COPD有关,但它不是用于COPD诊断或预后的敏感或特异性生物标志物。