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首页> 外文期刊>Digestive Diseases and Sciences >Effect of addition of short course of prednisolone to gluten-free diet on mucosal epithelial cell regeneration and apoptosis in celiac disease: A pilot randomized controlled trial
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Effect of addition of short course of prednisolone to gluten-free diet on mucosal epithelial cell regeneration and apoptosis in celiac disease: A pilot randomized controlled trial

机译:无麸质饮食中添加短时泼尼松龙对乳糜泻粘膜上皮细胞再生和凋亡的影响:一项随机对照试验

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Background: Identification of adjuvant treatment is necessary for rapid and effective treatment in patients with celiac disease. In a pilot randomized controlled trial, the effect of prednisolone on enterocyte apoptosis and regeneration in celiac disease was investigated. Patients and Methods: Thirty-three treatment-na?ve patients with celiac disease were randomized to either gluten-free diet (GFD, n = 17) or GFD + prednisolone (1 mg/kg for 4 weeks, n = 16). Duodenal biopsies were taken at baseline and at 4 and 8 weeks posttreatment. Six patients with functional dyspepsia were recruited as controls. All these biopsies were stained for markers of intrinsic apoptotic pathway (AIF, H2AX, p53), common apoptotic pathway (CC3, M30), apoptotic inhibitors (XIAP, Bcl2), and epithelial proliferation (Ki-67). Apoptotic (AI) and proliferation indices (PI) were compared. Results: At baseline duodenal biopsies, the end apoptotic products H2AX and M30 were significantly increased. In comparison with those treated with GFD alone, after 4 weeks of GFD + prednisolone treatment, some markers of both intrinsic and common apoptotic pathways showed rapid decline. After prednisolone withdrawal, there was overexpression of H2AX, CC3, and p53 in the latter group. In comparison with those treated with only GFD, patients treated with prednisolone showed suppression of mucosal PI, which started rising again after withdrawal of prednisolone. Conclusions: Apoptosis takes place in mucosal epithelium in celiac disease. Addition of short course of prednisolone suppresses apoptosis rapidly. However, it also suppresses epithelial regeneration; hence, if used, it should be withdrawn after an initial short course. (Registered at clinicaltrials.gov; NCT01045837)
机译:背景:为快速有效地治疗乳糜泻,必须确定辅助治疗方法。在一项随机对照试验中,研究了泼尼松龙对腹腔疾病肠细胞凋亡和再生的影响。患者和方法:将33例初治的乳糜泻患者随机分为无麸质饮食(GFD,n = 17)或GFD +泼尼松龙(1 mg / kg,持续4周,n = 16)。在基线以及治疗后4周和8周进行十二指肠活检。招募了6例功能性消化不良患者作为对照。对所有这些活检标本进行染色,分析其固有凋亡途径(AIF,H2AX,p53),常见凋亡途径(CC3,M30),凋亡抑制剂(XIAP,Bcl2)和上皮增殖(Ki-67)的标记。比较细胞凋亡(AI)和增殖指数(PI)。结果:在十二指肠基线活检时,凋亡末产物H2AX和M30显着增加。与单独使用GFD进行治疗的患者相比,经过GFD +泼尼松龙治疗4周后,固有和常见凋亡途径的某些标志物均呈快速下降趋势。泼尼松龙停药后,后者中H2AX,CC3和p53的过度表达。与仅用GFD治疗的患者相比,用泼尼松龙治疗的患者表现出对粘膜PI的抑制作用,在停用泼尼松龙后又开始升高。结论:乳糜泻在粘膜上皮中发生凋亡。添加短途泼尼松龙可迅速抑制细胞凋亡。但是,它也抑制上皮再生。因此,如果使用,应在最初的短期课程后将其撤回。 (注册在Clinicaltrials.gov; NCT01045837)

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