Wassell J, Reed P, Kane J, Weinkove C
Department of Biochemistry, Wythenshawe Hospital, Southmoor Rd., Manchester M23 9LT, UK.
Clin Chem. 1999 Dec;45(12):2216-23.
Determination of urinary free catecholamine and total (i. e., free plus conjugated) metanephrine excretion is considered the most clinically sensitive biochemical test for pheochromocytoma. In this study, we evaluated new immunoassay methods for the measurement of these analytes for potential drug-based interference.
Urine samples collected from patients on a variety of medications were grouped by specific drug type. The significance of any difference in the free catecholamine or total metanephrine concentrations in the different groups was assessed by one-way ANOVA. A group of patients receiving no medication was included as a control (no analytical interference). Additionally, analytical accuracy, detection limit, and precision were determined.
No significant differences were found in the concentrations of free catecholamines or total metanephrines in urine from patients taking the medications investigated and the control group: P = 0.649 (fE), 0.221 (fNE), 0.149 (tM), and 0.170 (tNM). For free catecholamines, intraassay CVs were 4.6-18%; interassay CVs were 10-25%. For total metanephrines, intraassay CVs were 9.6-27%; interassay CVs were 5. 8-22%. Detection limits were 0.009 and 0.027 micromol/L for fE and fNE and 0.119 and 0.346 micromol/L for tM and tNM, respectively.
None of the drugs examined in this study interfered in the measurement of free catecholamines or total metanephrines by these immunoassays. The technique is easier to use, requires less equipment, and is more accessible than HPLC. In combination, these assays are suitable as initial screening tests for pheochromocytoma.
尿游离儿茶酚胺及总(即游离加结合型)甲氧基肾上腺素排泄量的测定被认为是嗜铬细胞瘤临床上最敏感的生化检测方法。在本研究中,我们评估了用于测量这些分析物的新型免疫测定方法是否存在基于药物的潜在干扰。
收集服用各种药物患者的尿液样本,并按特定药物类型进行分组。通过单因素方差分析评估不同组中游离儿茶酚胺或总甲氧基肾上腺素浓度的任何差异的显著性。纳入一组未服用药物的患者作为对照(无分析干扰)。此外,还测定了分析准确性、检测限和精密度。
服用所研究药物的患者尿液中游离儿茶酚胺或总甲氧基肾上腺素的浓度与对照组相比无显著差异:P = 0.649(游离肾上腺素),0.221(游离去甲肾上腺素),0.149(总甲氧基肾上腺素)和0.170(总去甲氧基肾上腺素)。对于游离儿茶酚胺,批内变异系数为4.6 - 18%;批间变异系数为10 - 25%。对于总甲氧基肾上腺素,批内变异系数为9.6 - 27%;批间变异系数为5.8 - 22%。游离肾上腺素和游离去甲肾上腺素的检测限分别为0.009和0.027 μmol/L,总甲氧基肾上腺素和总去甲氧基肾上腺素的检测限分别为0.119和0.346 μmol/L。
本研究中检测的药物均未干扰这些免疫测定法对游离儿茶酚胺或总甲氧基肾上腺素的测量。该技术比高效液相色谱法更易于使用,所需设备更少,且更易获得。综合来看,这些检测方法适合作为嗜铬细胞瘤的初步筛查试验。