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[血清嗜铬粒蛋白A水平在高血压患者嗜铬细胞瘤诊断中的临床意义]

[Clinical significant of serum chromogranin A levels for diagnosing pheochromocytoma in hypertensive patients].

作者信息

Biausque F, Jaboureck O, Devos P, D'Herbomez M, Hainaut Ph, Carré A, Mounier-Vehier Cl

机构信息

Service de médecine interne et HTA, CHRU-Lille.

出版信息

Arch Mal Coeur Vaiss. 2003 Jul-Aug;96(7-8):780-3.

Abstract

OBJECTIVE

CMA is a widespread glycoprotein located in the secretory vesicles of neuroendocrine cells and is co-released with peptides and biogenic amines into the circulation. The present study set out to investigate the clinical utility of assessing serum CGA levels in comparison with the urinary KTCO and their urinary metabolites concentrations, which are to date the gold standard validated diagnostic test.

METHODS

From January 2000 to June 2001, 202 consecutive patients, aged 53 +/- 12.7, 102 males, were admitted to our department for a hypertension evaluation. Blood samples for measurements of plasma concentrations of chromogranin A were collected and serum CGA levels were quantified by RIA technique (RIACT). This radioimmunometric technique consisted in using 2 monoclonal antibodies directed to 2 specific antigenic domains of the middle portion of the CGA. The fixed threshold value for identifying positive results was, set at 100 ng/ml according to previous studies.

RESULTS

No pheochomocytoma was diagnosed by conventional urinary KTCO essay. Of the 202 CGA blood samples, 32 turned out to be positive, due to commonly encountered false positive causes (inhibitor of the pump with protons, corticotherapy, hypergastrinemia, chronic renal insufficiency, respectively, in 11, 2, 1, 18 cases). The CGA plasma concentration averaged 77 +/- 77 mg/ml and 203 +/- 125 ng/ml in the CGA subgroup over the threshold value.

CONCLUSION

The reliability of immunoradiometric serum CGA concentrations appeared according to this work to be comparable to that of the urinary KTCO levels and their urinary metabolites in hypertensives. Moreover, it solely requires a simple, easily done blood taking, less expensive than urinary KTCO collection. Besides, no antihypertensive drugs interfered with the analysis of CGA levels. However, some false positive results have to be mentioned in the presence of renal impairment, hypergastrinemia, corticotherapy, inhibitor of the pump with protons.

摘要

目的

嗜铬粒蛋白A(CGA)是一种广泛存在的糖蛋白,位于神经内分泌细胞的分泌囊泡中,并与肽类和生物胺类一起共同释放到循环系统中。本研究旨在探讨与尿甲氧基肾上腺素(KTCO)及其尿代谢物浓度相比,评估血清CGA水平的临床效用,尿甲氧基肾上腺素及其尿代谢物浓度是迄今为止经过验证的金标准诊断检测方法。

方法

2000年1月至2001年6月,202例连续患者(年龄53±12.7岁,男性102例)因高血压评估入住我科。采集血样以测量血浆嗜铬粒蛋白A浓度,并通过放射免疫分析技术(RIACT)对血清CGA水平进行定量。这种放射免疫分析技术包括使用针对CGA中部两个特定抗原结构域的2种单克隆抗体。根据先前的研究,将识别阳性结果的固定阈值设定为100 ng/ml。

结果

通过传统的尿KTCO检测未诊断出嗜铬细胞瘤。在202份CGA血样中,32份结果为阳性,原因是常见的假阳性因素(分别在11、2、1、18例中为质子泵抑制剂、皮质激素治疗、高胃泌素血症、慢性肾功能不全)。CGA亚组中超过阈值的CGA血浆浓度平均为77±77 mg/ml和203±125 ng/ml。

结论

根据本研究,免疫放射法测定血清CGA浓度的可靠性在高血压患者中似乎与尿KTCO水平及其尿代谢物的可靠性相当。此外,它仅需要简单、易于操作的采血,比收集尿KTCO成本更低。此外,没有降压药物干扰CGA水平的分析。然而,在存在肾功能损害、高胃泌素血症、皮质激素治疗、质子泵抑制剂的情况下,必须提及一些假阳性结果。

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