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首页> 外文期刊>Physiological Research >Chromogranin A, a Member of Neuroendocrine Secretory Proteins as a Selective Marker for Laboratory Diagnosis of Pheochromocytoma
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Chromogranin A, a Member of Neuroendocrine Secretory Proteins as a Selective Marker for Laboratory Diagnosis of Pheochromocytoma

机译:嗜铬粒蛋白A,神经内分泌蛋白的成员,作为嗜铬细胞瘤实验室诊断的选择性标记

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摘要

The function of chromogranin A (CGA) is reviewed, and the radioimmunometric determination of plasma CGA was evaluated as a marker of pheochromocytoma using a comparison of pheochromocytoma patients immediately before surgery (group P, n=25, 635±451 ng/ml) with other groups of patients, i.e. pheochromocytoma patients approximately 1 year after removal of tumor (group PP, n=13, 69±33 ng/ml), medullary thyroid carcinoma patients (group M, n= 22, 106±59 ng/ml), congenital adrenal hyperplasy patients (n=33, 65±40 ng/ml), and controls (n=31, 66±29 ng/ml). A CGA level above cut off value 130 ng/ml was found in 24 of 25 patients in group P, 1 (relapse) of 13 patients in group PP, and 4 of 22 patients in group M. In the group P we found a significant association between the size of the tumors removed and plasma CGA concentrations (p=0.0016), and also a significant (p=0.0016) relationship between plasma CGA concentrations and PASS score rating the malignity of pheochromocytoma. We can conclude that plasma CGA concentration as determined by radioimmunometric assay (which is simple without the necessity of special laboratory equipment) is an effective marker of pheochromocytoma with association to malignity and tumor mass.
机译:回顾了嗜铬粒蛋白A(CGA)的功能,并通过比较术前即刻嗜铬细胞瘤患者(P组,n = 25,635±451 ng / ml)对嗜铬细胞瘤患者的比较,评估了血浆CGA的放射免疫测定作为嗜铬细胞瘤的标志物。其他类型的患者,即肿瘤切除后大约一年的嗜铬细胞瘤患者(PP组,n = 13,69±33 ng / ml),甲状腺髓样癌患者(M组,n = 22,106±59 ng / ml) ,先天性肾上腺增生患者(n = 33,65±40 ng / ml)和对照组(n = 31,66±29 ng / ml)。 P组的25名患者中有24名患者,C组的13名患者中有1名(复发),M组的22名患者中有4名发现CGA水平高于临界值130 ng /ml。P组中我们发现切除的肿瘤大小与血浆CGA浓度之间的相关性(p = 0.0016),以及血浆CGA浓度与PASS评分之间的显着(p = 0.0016)关系评估了嗜铬细胞瘤的恶性。我们可以得出结论,通过放射免疫法测定的血浆CGA浓度(这很简单,无需特殊的实验室设备)是嗜铬细胞瘤的有效标志物,与恶性肿瘤和肿块有关。

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