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Antral atrophy intestinal metaplasia and pre-neoplastic markers in Mexican children with Helicobacter pylori-positive and negative gastritis

机译:墨西哥儿童幽门螺杆菌阳性和阴性胃炎患儿的肛门萎缩肠上皮化生和肿瘤前标记

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摘要

Chronic inflammation and infection are major risk factors for gastric carcinogenesis in adults. As chronic gastritis is common in Mexican children, diagnosis of Helicobacter pylori and other causes of gastritis are critical for the identification of children who would benefit from closer surveillance. Antral biopsies from 82 Mexican children (mean age 8.3±4.8y) with chronic gastritis (36 H. pylori +, 46 H. pylori -) were examined for gastritis activity, atrophy, intestinal metaplasia, and immunohistochemical expression of gastric carcinogenesis biomarkers CDX2, ephrin type-B receptor 4, matrix metalloproteinase 3 (MMP3), macrophage migration inhibitory factor (MIF), p53, β-catenin, and E-cadherin. Atrophy was diagnosed in 7/82 (9%) and intestinal metaplasia in 5/82 (6%) by routine histology, while 6 (7%) additional children (3 H. pylori +) exhibited aberrant CDX2 expression without intestinal metaplasia. Significant positive correlations were seen between EphB4, MMP3, and MIF (p<0.0001). Atrophy and follicular pathology were more frequent in H. pylori + biopsies (p<0.0001), while intestinal metaplasia and CDX2 expression showed no significant correlation with H. pylori status. Antral biopsies demonstrating atrophy, intestinal metaplasia, and/or aberrant CDX2 expression were seen in 21.95 % (18/82) of the children, potentially identifying those who would benefit from closer surveillance and preventive dietary strategies. Biomarkers CDX2, EphB4, MMP3, and MIF may be useful in the work-up of pediatric gastritis.
机译:慢性炎症和感染是成年人胃癌发生的主要危险因素。由于慢性胃炎在墨西哥儿童中很常见,因此对幽门螺杆菌和其他胃炎原因的诊断对于识别将受益于密切监视的儿童至关重要。检查了82例患有慢性胃炎(36 H. pylori +,46 H. pylori-)的墨西哥儿童(平均年龄8.3±4.8y)的胃窦活检的胃癌活性,萎缩,肠化生以及胃癌发生生物标志物CDX2的免疫组织化学表达, ephrin B型受体4,基质金属蛋白酶3(MMP3),巨噬细胞迁移抑制因子(MIF),p53,β-catenin和E-cadherin。常规组织学诊断为萎缩7/82(9%),肠上皮化生为5/82(6%),另有6(7%)儿童(3 H. pylori +)表现出CDX2异常表达而无肠上皮化生。 EphB4,MMP3和MIF之间存在显着的正相关(p <0.0001)。幽门螺杆菌+活检组织中萎缩和滤泡病理更为常见(p <0.0001),而肠上皮化生和CDX2表达与幽门螺杆菌状态无显着相关性。在21.95%(18/82)的儿童中,可见表现出萎缩,肠上皮化生和/或CDX2表达异常的肛门活检,可能识别出那些将从更严格的监测和预防性饮食策略中受益的孩子。生物标志物CDX2,EphB4,MMP3和MIF在儿科胃炎的检查中可能有用。

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