评价骨代谢参数与骨显像筛查骨转移的临床价值。

Johann Schoenberger, Silke Rozeboom, Eva Wirthgen-Beyer, Christoph Eilles
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引用次数: 15

摘要

背景:骨转移在许多类型的癌症中都很常见。作为筛查方法,不同的成像模式是可用的。一种新的方法筛选骨转移代表骨代谢标志物的测量。因此,本研究的目的是评估测定骨代谢标志物I型前胶原的氨基末端前肽(PINP,成骨细胞活性)和I型胶原的羧基末端吡啶啉交联末端肽(ICTP,破骨细胞活性)对检测其他恶性肿瘤相关骨转移的有用性。方法:对88例21 ~ 82岁恶性肿瘤患者进行前瞻性研究。测定血清PINP、ICTP浓度,并与骨显像、骨片、CT、MRI及临床随访结果进行比较。结果:21例患者出现骨转移。其中19例经骨显像正确鉴别(灵敏度90%)。骨代谢标志物的检测结果如下:ICTP敏感性71%,特异性42%;PINP敏感性:24%,特异性:96%。结论:作为骨代谢标志物,PINP和ICTP在检测骨转移方面的敏感性和/或特异性较低。所提出的标记物似乎不足以识别骨转移患者或取代现有的筛查方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of the clinical value of bone metabolic parameters for the screening of osseous metastases compared to bone scintigraphy.

Evaluation of the clinical value of bone metabolic parameters for the screening of osseous metastases compared to bone scintigraphy.

Evaluation of the clinical value of bone metabolic parameters for the screening of osseous metastases compared to bone scintigraphy.

Evaluation of the clinical value of bone metabolic parameters for the screening of osseous metastases compared to bone scintigraphy.

BACKGROUND: Bone metastases are common in many types of cancer. As screening methods different imaging modalities are available. A new approach for the screening of osseous metastases represents the measurement of bone metabolic markers. Therefore aim of this study was to evaluate the usefulness of the determination of bone metabolic markers aminoterminal propeptide of type I procollagen (PINP, osteoblastic activity) and the carboxyterminal pyridinoline cross-linked telopeptide of type I collagen (ICTP, osteoclastic activity) for the detection of bone metastases associated with other malignancies. METHODS: 88 patients aged 21 - 82 years with malignant tumors were prospectively studied. The serum concentrations of PINP and ICTP were measured and compared to the results of bone scintigraphy, radiological bone series, CT, MRI and clinical follow-up. RESULTS: Osseous metastases were found in 21 patients. 19 of them were correctly identified by bone scintigraphy (sensitivity: 90%). For bone metabolic markers results were as follows: ICTP sensitivity: 71%, specificity: 42%; PINP sensitivity: 24%, specificity: 96%. CONCLUSIONS: As markers of bone metabolism PINP and ICTP showed low sensitivity and/or specificity for the detection of osseous metastases. The presented markers did not seem to be sufficient enough to identify patients with bone metastases or to replace established screening methods.

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