埃及溃疡性结肠炎患者血清中作为疾病活动性预测因子的三叶草因子 3 及其在结直肠癌中的作用。

Walaa M Hashem, Amir H Samy, Sarah A Ali, Christina A Anwar, Mina W N Abd El Malak, Mohamed N B Al-Ashram
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引用次数: 0

摘要

溃疡性结肠炎(UC)是一种慢性特发性炎症疾病,由肠道微生物菌群的异常免疫反应引起。结直肠癌(CRC)是导致癌症相关死亡的主要原因之一。确定诊断和评估疾病活动性的金标准仍然是内窥镜检查和组织病理学检查。由于大多数患者不接受内窥镜评估,因此需要无创生物标志物来及时诊断 CRC 和评估疾病活动性。胃肠道损伤后,三叶因子 3(TFF3)表达增强。在本研究中,我们研究了血清 TFF3 作为天真 UC 患者疾病活动性潜在诊断生物标志物的意义及其在 CRC 患者中的诊断准确性。我们收集了 20 例活动性 UC 患者、20 例 CRC 患者和 20 例正常对照者的血清和粪便样本。活动性 UC 患者的 TFF3 水平高于对照组(P < 0.001)。TFF3的临界值为7.9纳克/毫升,可预测疾病活动,灵敏度和特异度分别为90%和100%。然而,TFF3、C反应蛋白(CRP)和粪便钙粘蛋白(FC)的组合比单独使用每种生物标志物更能预测疾病的活动性,其敏感性和特异性都提高到了100%。TFF3、FC与溃疡性结肠炎内镜下严重程度指数(UCEIS)评估的UC内镜下活动性之间没有相关性。在 CRC 患者组中,TFF3 的血清水平明显高于对照组(P=0.012)。TFF3 与发育不良程度明显相关(r=0.496,p=0.026)。以 5.9 纳克/毫升为临界值,血清 TFF3 对 CRC 的诊断敏感性和特异性分别为 82% 和 90%。总之,血清 TFF3 可作为一种非侵入性生物标志物,单独或与 CRP 和 FC 联用来预测 UC 的疾病活动性,并可在诊断 CRC 中发挥潜在作用。
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Trefoil Factor 3 in human serum as a predictor of disease activity in Egyptian ulcerative colitis patients and its role in colorectal cancer.

Ulcerative colitis (UC), a chronic idiopathic inflammatory disease, is caused by abnormal immune response to intestinal microflora. Colorectal cancer (CRC) is one of the leading causes of cancer-related mortality. The gold standard to establish diagnosis and assess disease activity remains endoscopy and histopathology. Non-invasive biomarkers are required for timely diagnosis of CRC and to assess disease activity as endoscopic assessment is not accepted by most patients. Enhanced trefoil factor 3 (TFF3) expression is seen following gastrointestinal tract injury. In the current study, the significance of serum TFF3 as a potential diagnostic biomarker of disease activity in naїve UC patients, and its diagnostic accuracy in CRC patients were investigated. We collected serum and fecal samples from 20 cases with active UC, 20 CRC patients, and 20 normal controls. TFF3 levels were higher in patients with active UC than in controls (p < 0.001). TFF3 cut-off value of 7.9 ng/ml could predict disease activity with sensitivity and specificity of 90% and 100%, respectively. However, the combination of TFF3, C-reactive protein (CRP), and fecal calprotectin (FC) was able to predict disease activity better than each biomarker alone by raising the sensitivity and specificity to 100%. There was no correlation between TFF3, FC, and endoscopic activity in UC assessed by ulcerative colitis endoscopic index of severity (UCEIS). In the CRC patient group, the serum level of TFF3 was significantly higher when compared to controls (p=0.012). TFF3 and the degree of dysplasia were significantly correlated (r=0.496, p=0.026). At a cut-off value of 5.9 ng/ml, serum TFF3 had a diagnostic sensitivity and specificity for CRC of 82% and 90%, respectively. In conclusion, serum TFF3 may be used as a non-invasive biomarker to predict disease activity in UC both alone and in combination with CRP and FC and it could have a potential role in diagnosis of CRC.

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