Holleran Grainne, Hall Barry, O'Regan Myra, Smith Sinead, McNamara Deirdre
Departments of *Gastroenterology and Clinical Medicine, Tallaght Hospital †Biostatistics, Trinity College Dublin, Dublin, Ireland.
J Clin Gastroenterol. 2015 Nov-Dec;49(10):831-6. doi: 10.1097/MCG.0000000000000260.
To identify putative angiogenic factors associated with sporadic small bowel angiodysplasia (SBA).
SBAs account for 50% of obscure gastrointestinal bleeding and due to delays in diagnosis and ineffective treatments, are associated with high levels of morbidity and mortality. Treatment development is impeded by a limited knowledge of the pathophysiology behind SBA formation.
We identified patients with definite sporadic SBA, and fecal immunochemical-negative controls were recruited from our institution's colorectal cancer screening program. Serum levels of VEGF, endoglin, Angiopoietin-2 (Ang-2), PDGF, Angiopoietin-1 (Ang-1), and TNF-α were measured using commercially available enzyme-linked immunosorbent assay kits. On the basis of serum results, we measured gene expression of target angiogenic factors in small bowel biopsy samples from angiodysplasias and unaffected tissue by quantitative PCR assessment.
Serum samples were analyzed from 40 SBA patients and 40 controls. Median serum levels of Ang-2 were significantly higher in patients than controls with levels of Ang-1 and TNF-α significantly lower. There were no differences in serum levels of VEGF, endoglin, or PDGF. Gene expression levels of Ang-1, Ang-2, and their receptor Tie2 were all significantly higher in biopsies from areas of angiodysplasia compared with normal small bowel.
This study, the first to explore the role of angiogenic factors in SBA, has identified a positive association between SBA and the Angiopoietin pathway, with increased serum and mucosal expression of Ang-2, which could potentially be used as a serum biomarker and future therapeutic target to improve outcome in affected patients.
确定与散发性小肠血管发育异常(SBA)相关的潜在血管生成因子。
SBA占不明原因胃肠道出血的50%,由于诊断延误和治疗无效,其发病率和死亡率较高。SBA形成背后的病理生理学知识有限,阻碍了治疗方法的发展。
我们确定了患有明确散发性SBA的患者,并从我们机构的结直肠癌筛查项目中招募了粪便免疫化学检测呈阴性的对照者。使用市售的酶联免疫吸附测定试剂盒测量血清中血管内皮生长因子(VEGF)、内皮糖蛋白、血管生成素-2(Ang-2)、血小板衍生生长因子(PDGF)、血管生成素-1(Ang-1)和肿瘤坏死因子-α(TNF-α)的水平。根据血清检测结果,我们通过定量PCR评估测量血管发育异常和未受影响组织的小肠活检样本中目标血管生成因子的基因表达。
分析了40例SBA患者和40例对照者的血清样本。患者血清Ang-2的中位数水平显著高于对照组,而Ang-1和TNF-α的水平显著低于对照组。VEGF、内皮糖蛋白或PDGF的血清水平没有差异。与正常小肠相比,血管发育异常区域活检样本中Ang-1、Ang-2及其受体Tie2的基因表达水平均显著升高。
本研究首次探讨了血管生成因子在SBA中的作用,确定了SBA与血管生成素途径之间存在正相关,Ang-2的血清和黏膜表达增加,这可能潜在地用作血清生物标志物和未来的治疗靶点,以改善受影响患者的预后。