Gill Kiren, Horsley Harry, Kupelian Anthony S, Baio Gianluca, De Iorio Maria, Sathiananamoorthy Sanchutha, Khasriya Rajvinder, Rohn Jennifer L, Wildman Scott S, Malone-Lee James
Division of Medicine, University College London, Archway Campus, London, UK.
Research Department of Clinical Medicine, Division of Medicine, University College London, Wolfson House, 2 - 10 Stephenson Way, NW1 2HE, London, UK.
BMC Urol. 2015 Feb 21;15(1):7. doi: 10.1186/s12894-015-0001-1.
Adenosine-5'-triphosphate (ATP) is a neurotransmitter and inflammatory cytokine implicated in the pathophysiology of lower urinary tract disease. ATP additionally reflects microbial biomass thus has potential as a surrogate marker of urinary tract infection (UTI). The optimum clinical sampling method for ATP urinalysis has not been established. We tested the potential of urinary ATP in the assessment of lower urinary tract symptoms, infection and inflammation, and validated sampling methods for clinical practice.
A prospective, blinded, cross-sectional observational study of adult patients presenting with lower urinary tract symptoms (LUTS) and asymptomatic controls, was conducted between October 2009 and October 2012. Urinary ATP was assayed by a luciferin-luciferase method, pyuria counted by microscopy of fresh unspun urine and symptoms assessed using validated questionnaires. The sample collection, storage and processing methods were also validated.
75 controls and 340 patients with LUTS were grouped as without pyuria (n = 100), pyuria 1-9 wbc μl(-1) (n = 120) and pyuria ≥10 wbc μl(-1) (n = 120). Urinary ATP was higher in association with female gender, voiding symptoms, pyuria greater than 10 wbc μl(-1) and negative MSU culture. ROC curve analysis showed no evidence of diagnostic test potential. The urinary ATP signal decayed with storage at 23°C but was prevented by immediate freezing at ≤ -20°C, without boric acid preservative and without the need to centrifuge urine prior to freezing.
Urinary ATP may have a role as a research tool but is unconvincing as a surrogate, clinical diagnostic marker.
三磷酸腺苷(ATP)是一种神经递质和炎症细胞因子,与下尿路疾病的病理生理学有关。此外,ATP还反映微生物生物量,因此有潜力作为尿路感染(UTI)的替代标志物。目前尚未确定用于ATP尿液分析的最佳临床采样方法。我们测试了尿液ATP在评估下尿路症状、感染和炎症方面的潜力,并验证了临床实践中的采样方法。
在2009年10月至2012年10月期间,对出现下尿路症状(LUTS)的成年患者和无症状对照进行了一项前瞻性、盲法、横断面观察研究。采用荧光素-荧光素酶法检测尿液ATP,通过新鲜未离心尿液显微镜检查计数脓尿,并使用经过验证的问卷评估症状。还对样本收集、储存和处理方法进行了验证。
75名对照和340名LUTS患者分为无脓尿组(n = 100)、脓尿1 - 9个白细胞/微升组(n = 120)和脓尿≥10个白细胞/微升组(n = 120)。尿液ATP水平较高与女性性别、排尿症状、脓尿大于10个白细胞/微升以及中段尿培养阴性有关。ROC曲线分析显示没有诊断测试潜力的证据。尿液ATP信号在23°C储存时会衰减,但通过立即冷冻至≤ -20°C可防止衰减,无需硼酸防腐剂,且冷冻前无需离心尿液。
尿液ATP可能作为一种研究工具,但作为替代的临床诊断标志物并不令人信服。