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血浆游离和总甲氧基肾上腺素及尿液中甲氧基肾上腺素片段诊断嗜铬细胞瘤的准确性。

Diagnostic accuracy of free and total metanephrines in plasma and fractionated metanephrines in urine of patients with pheochromocytoma.

机构信息

Division of Clinical Pharmacology and Toxicology, University Hospital, Lausanne, Switzerland.

出版信息

Eur J Endocrinol. 2010 May;162(5):951-60. doi: 10.1530/EJE-09-0996. Epub 2010 Feb 8.

Abstract

BACKGROUND

Plasma free and urinary metanephrines are recognized biomarkers for the assessment of pheochromocytoma. Plasma total metanephrines with a long half-life may represent another useful biomarker.

OBJECTIVE

The aim of this study is to evaluate the diagnostic performances of plasma total metanephrines alone or combined with free metanephrines and fractionated 24-h urinary metanephrines.

METHODS

A retrospective, case-control diagnostic test study was conducted between 1999 and 2007 in two university hospitals in Switzerland and two institutions in France. The patients included 46 cases with histologically proven pheochromocytoma, and 181 controls suspected of tumor with negative investigations and 3-year follow-up. None had renal dysfunction. Sensitivity and specificity were compared after expressing each measurement result as a ratio over its upper reference limit, adding the ratios of normetanephrine and metanephrine, and defining cut-off values of 1 or 2 for this sum.

RESULTS

Applying a cut-off value of 1, plasma free and total metanephrines and urinary fractionated metanephrines had similar sensitivities of 96% (95% confidence interval, 86-99%), 95% (85-99%), and 95% (84-99%) along with similar specificities of 89% (83-94%), 91% (84-95%), and 86% (80-91%). A cut-off of 2 for the sum of ratios over reference limit improves the specificity, and it can be used for a confirmation test based on another biomarker taken among the three biomarkers.

CONCLUSION

All three metanephrine-based tests perform equivalently for diagnosing pheochromocytoma in the absence of renal insufficiency, and can be conveniently associated two by two for confirming/excluding tumor.

摘要

背景

血浆游离和尿甲氧基肾上腺素已被公认为嗜铬细胞瘤评估的生物标志物。半衰期较长的血浆总甲氧基肾上腺素可能代表另一种有用的生物标志物。

目的

本研究旨在评估单独检测或联合检测血浆总甲氧基肾上腺素、游离甲氧基肾上腺素和 24 小时尿甲氧基肾上腺素片段的诊断性能。

方法

本研究是一项在瑞士的两家大学医院和法国的两家机构进行的回顾性病例对照诊断测试研究。纳入了 46 例经组织学证实的嗜铬细胞瘤患者,以及 181 例经阴性检查和 3 年随访怀疑有肿瘤的对照组。所有患者均无肾功能障碍。在将每种测量结果表示为与上限参考值的比值后,比较了敏感性和特异性,将去甲肾上腺素和甲氧基肾上腺素的比值相加,并将该总和的 1 或 2 定义为截断值。

结果

当截断值为 1 时,血浆游离和总甲氧基肾上腺素以及尿片段化甲氧基肾上腺素的敏感性分别为 96%(95%置信区间,86-99%)、95%(85-99%)和 95%(84-99%),特异性分别为 89%(83-94%)、91%(84-95%)和 86%(80-91%),具有相似的结果。截断值为 2 时,比值总和的特异性提高,可用于基于三种生物标志物中的另一种标志物进行的确认性检测。

结论

在不存在肾功能不全的情况下,所有三种基于甲氧基肾上腺素的检测方法在诊断嗜铬细胞瘤方面表现相当,可方便地两两组合,用于确认/排除肿瘤。

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