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首页> 外文期刊>BMC Bioinformatics >A minimally invasive multiple marker approach allows highly efficient detection of meningioma tumors
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A minimally invasive multiple marker approach allows highly efficient detection of meningioma tumors

机译:微创多标记方法可高效检测脑膜瘤肿瘤

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Background The development of effective frameworks that permit an accurate diagnosis of tumors, especially in their early stages, remains a grand challenge in the field of bioinformatics. Our approach uses statistical learning techniques applied to multiple antigen tumor antigen markers utilizing the immune system as a very sensitive marker of molecular pathological processes. For validation purposes we choose the intracranial meningioma tumors as model system since they occur very frequently, are mostly benign, and are genetically stable. Results A total of 183 blood samples from 93 meningioma patients (WHO stages I-III) and 90 healthy controls were screened for seroreactivity with a set of 57 meningioma-associated antigens. We tested several established statistical learning methods on the resulting reactivity patterns using 10-fold cross validation. The best performance was achieved by Na?ve Bayes Classifiers. With this classification method, our framework, called Minimally Invasive Multiple Marker (MIMM) approach, yielded a specificity of 96.2%, a sensitivity of 84.5%, and an accuracy of 90.3%, the respective area under the ROC curve was 0.957. Detailed analysis revealed that prediction performs particularly well on low-grade (WHO I) tumors, consistent with our goal of early stage tumor detection. For these tumors the best classification result with a specificity of 97.5%, a sensitivity of 91.3%, an accuracy of 95.6%, and an area under the ROC curve of 0.971 was achieved using a set of 12 antigen markers only. This antigen set was detected by a subset selection method based on Mutual Information. Remarkably, our study proves that the inclusion of non-specific antigens, detected not only in tumor but also in normal sera, increases the performance significantly, since non-specific antigens contribute additional diagnostic information. Conclusion Our approach offers the possibility to screen members of risk groups as a matter of routine such that tumors hopefully can be diagnosed immediately after their genesis. The early detection will finally result in a higher cure- and lower morbidity-rate.
机译:背景技术开发有效的框架以准确诊断肿瘤,尤其是在早期阶段,仍然是生物信息学领域的巨大挑战。我们的方法使用统计学习技术,将免疫系统用作分子病理过程的非常敏感的标志物,将其应用于多种抗原肿瘤抗原标志物。为了验证的目的,我们选择颅内脑膜瘤肿瘤作为模型系统,因为它们发生的频率很高,大多是良性的,并且遗传稳定。结果筛选了93例脑膜瘤患者(WHO I-III期)和90例健康对照者的183份血样的血清反应性,其中包括一组57例脑膜瘤相关抗原。我们使用10倍交叉验证对所得反应性模式测试了几种已建立的统计学习方法。朴素贝叶斯分类器达到了最佳性能。使用这种分类方法,我们的框架被称为微创多标记(MIMM)方法,特异性为96.2%,灵敏度为84.5%,准确度为90.3%,ROC曲线下的各个面积为0.957。详细分析显示,预测对低度(WHO I)肿瘤的效果特别好,这与我们早期肿瘤检测的目标一致。对于这些肿瘤,仅使用一组12种抗原标记即可获得最佳分类结果,特异性为97.5%,灵敏度为91.3%,准确度为95.6%,ROC曲线下面积为0.971。通过基于互信息的子集选择方法检测该抗原集。值得注意的是,我们的研究证明,不仅在肿瘤中而且在正常血清中检测到的非特异性抗原的加入均显着提高了性能,因为非特异性抗原会提供其他诊断信息。结论我们的方法为常规筛查高危人群提供了可能性,从而有望在肿瘤发生后立即对其进行诊断。尽早发现将最终导致更高的治愈率和更低的发病率。

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