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嗜铬粒蛋白A免疫放射分析在嗜铬细胞瘤诊断中的应用:与血浆甲氧基肾上腺素及123I-间碘苄胍扫描的比较

Chromogranin A immunoradiometric assay in diagnosis of pheochromocytoma: comparison with plasma metanephrines and 123I-MIBG scan.

作者信息

Giovanella L, Squin N, Ghelfo A, Ceriani L

机构信息

Division of Nuclear Medicine and Molecular Imaging, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

出版信息

Q J Nucl Med Mol Imaging. 2006 Dec;50(4):344-7.

Abstract

AIM

The aim of this study is to investigate the diagnostic performance of serum chromogranin A (CgA) and plasma metanephrines (MN) assays in the diagnosis of pheochromocytoma.

METHODS

We enrolled 44 patients affected by histologically proved adrenal pheochromocytoma. All patients underwent abdominal computed tomography and whole body 123I-MIBG scan to stage the disease. One hundred healthy blood donors and 148 patients affected by essential hypertension were enrolled as controls. Serum CgA and plasma MN were assayed by immunoradiometric assay (IRMA) and high-performance liquid chromatography. Cut-off levels were selected to obtain 99% specificity in healthy control subjects.

RESULTS

Both MN and CgA showed 95% sensitivity with comparable high specificity and diagnostic accuracy (96% and 96% for CgA, 94% and 95% for MN, respectively). By employing both markers and considering CgA or MN positivity, a 100% sensitivity was obtained with 95% accuracy. MN and CgA concentration clearly increased from controls to patients with pheochromocytomas (P<0.0001). A relationship between serum CgA (but not MN) and tumor mass was found (P<0.0001).

CONCLUSIONS

Both markers are sensitive and specific in chromaffin-tumors detection: CgA IRMA assay employed a simple and feasible technology and showed to be as sensitive and slightly more accurate than MN.

摘要

目的

本研究旨在探讨血清嗜铬粒蛋白A(CgA)和血浆甲氧基肾上腺素(MN)检测在嗜铬细胞瘤诊断中的性能。

方法

我们纳入了44例经组织学证实患有肾上腺嗜铬细胞瘤的患者。所有患者均接受腹部计算机断层扫描和全身123I-间碘苄胍(MIBG)扫描以对疾病进行分期。纳入100名健康献血者和148例原发性高血压患者作为对照。采用免疫放射分析法(IRMA)和高效液相色谱法检测血清CgA和血浆MN。选择临界值以在健康对照受试者中获得99%的特异性。

结果

MN和CgA均显示出95%的敏感性,具有相当高的特异性和诊断准确性(CgA分别为96%和96%,MN分别为94%和95%)。通过同时使用这两种标志物并考虑CgA或MN阳性,获得了100%的敏感性和95%的准确性。从对照组到嗜铬细胞瘤患者,MN和CgA浓度明显升高(P<0.0001)。发现血清CgA(而非MN)与肿瘤大小之间存在相关性(P<0.0001)。

结论

两种标志物在嗜铬细胞瘤检测中均敏感且特异:CgA的IRMA检测采用简单可行的技术,并且显示出与MN一样敏感且准确性略高。

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