Department of Gastroenterology and Human Nutrition, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India.
Dig Dis Sci. 2012 Dec;57(12):3116-25. doi: 10.1007/s10620-012-2294-1. Epub 2012 Jun 30.
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.
Thirty-three treatment-naïve 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.
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.
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 However, it also suppresses epithelial regeneration; hence, if used, it should be withdrawn after an initial short course.
识别辅助治疗对于乳糜泻患者的快速有效治疗是必要的。在一项初步的随机对照试验中,研究了泼尼松龙对乳糜泻中肠细胞凋亡和再生的影响。
33 名未经治疗的乳糜泻患者被随机分为无麸质饮食(GFD,n = 17)或 GFD +泼尼松龙(1mg/kg 持续 4 周,n = 16)组。在基线和治疗后 4 周和 8 周时采集十二指肠活检。招募了 6 名功能性消化不良患者作为对照。所有这些活检均用于标记固有凋亡途径(AIF、H2AX、p53)、共同凋亡途径(CC3、M30)、凋亡抑制剂(XIAP、Bcl2)和上皮增殖(Ki-67)。比较了凋亡(AI)和增殖指数(PI)。
在基线十二指肠活检中,终末凋亡产物 H2AX 和 M30 明显增加。与单独接受 GFD 治疗的患者相比,在接受 GFD +泼尼松龙治疗 4 周后,固有和共同凋亡途径的一些标志物迅速下降。泼尼松龙停药后,后者组 H2AX、CC3 和 p53 过度表达。与仅接受 GFD 治疗的患者相比,接受泼尼松龙治疗的患者黏膜 PI 受到抑制,在泼尼松龙停药后再次升高。
乳糜泻中黏膜上皮发生凋亡。短期使用泼尼松龙可迅速抑制凋亡。然而,它也抑制上皮细胞再生;因此,如果使用,应在初始短期疗程后停药。