瘦素和维生素D在结直肠癌诊断和随访中的诊断价值评价

M. Fouda, Sara A Mekkawy, Mariam Ghabour, Radwa Othman, Nayera Ahmed, Nour Habbib, Salsabeel Elkholey, R. Soliman, M. Fouad, Ellen Ayad, Mayar Shaqran, Mariam Mohamed, Rokaia M Aljarwani, Khaled Aboul-Enein, M. Omran
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引用次数: 0

摘要

在全球范围内,结直肠癌(CRC)是最常诊断的实体肿瘤之一,死亡率和发病率很高。CRC的早期检测迫切需要生物标志物。传统的结直肠癌肿瘤标志物没有最好的诊断性能。评估了瘦素和维生素D的水平。本病例对照研究包括治疗前的CRC患者(n=16)、治疗后的CRC患者(n=14)和20例良性肿瘤患者。采用ELISA检测传统肿瘤标志物(CA19.9、CEA)及候选标志物(瘦素、维生素D)水平,采用区域受体工作特征分析(area receiver-operating characteristic analysis, AUC)评价单项和联合标志物的诊断效能(ROC)。三组血清CEA和ca19.9水平无显著差异。维生素D和瘦素显著降低(p= 0.03和p= 0.02;(分别)与良性患者相比。采用逐步多变量判别分析(MDA),建立了一种基于维生素D和瘦素联合诊断结直肠癌的新组合。可表示为=(4.65 -维生素D ((ng/ml)) × 0.009 +瘦素(ng/ml) × 0.441)。当瘦素作为区分CRC与良性CRC(0.78)和未治疗CRC与治疗CRC(0.67)的单一生物标志物时,报告了auc。当瘦素和维生素D联合使用时,auc分别增加到0.84和0.72。结论:瘦素和维生素D在我们的研究中被证明是有希望的CRC诊断和随访指标。
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 diagnostic performances of leptin and vitamin D for colorectal cancer diagnosis and follow-up
Globally, colorectal cancer (CRC) is one of the most often diagnosed solid tumors, with a significant death and morbidity rate. CRC biomarkers are desperately needed for early detection. Traditional CRC tumor markers do not have the best diagnostic performance. The levels of leptin and vitamin D were evaluated. CRC patients before treatment (n=16), CRC patients after treatment (n=14), and 20 patients with benign tumors were included in this case-control study. ELISA was used to determine the levels of traditional tumor markers (CA19.9 and CEA) as well as candidate markers (leptin and vitamin D). Using area receiver-operating characteristic analysis (AUC), the diagnostic performance of single and combination markers was assessed (ROC). The levels of CEA and CA 19.9 in the three groups studied were not significantly different. Vitamin D and leptin were significantly decreased (p= 0.03 and p= 0.02; respectively) in CRC patients than after benign patients. A novel combination, based on the combination of vitamin D and leptin was developed for CRC diagnosis using stepwise multivariate discriminant analysis (MDA). The combination can be represented as = (4.65 – vitamin D ((ng/ml)) × 0.009 + Leptin (ng/ml) × 0.441). AUCs were reported when leptin was used as a single biomarker for distinguishing CRC from benign (0.78) and non-treated CRC from treated CRC (0.67). When leptin and vitamin D were combined, the AUCs increased to 0.84 and0.72, respectively. Conclusion: Leptin and vitamin D were shown to be promising diagnostic and follow-up indicators for CRC in our investigation.
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