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首页> 外文期刊>Scandinavian journal of gastroenterology. >A novel one-hour ~13C-sorbitol breath test versus the H2-sorbitol breath test for assessment of coeliac disease
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A novel one-hour ~13C-sorbitol breath test versus the H2-sorbitol breath test for assessment of coeliac disease

机译:一种新的一小时〜13C-山梨糖醇呼吸试验与H2-山梨糖醇呼吸试验评估腹腔病

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摘要

Objective. The H2-sorbitol breath test (H2-SBT) has previously been suggested as a screening tool for coeliac disease. We developed an alternative 13C-sorbitol breath test (13C-SBT). The aim of the study was to compare the diagnostic properties of the H2-SBT and the 13C-SBT in a clinical setting. Material and methods. Thirty-nine coeliac patients, 40 patient controls (mainly patients with irritable bowel syndrome) and 26 healthy volunteers underwent the breath tests. The patients were given an oral load of 5 g sorbitol and 100 mg 13C-sorbitol dissolved in 250 ml tap-water. H2, CH4 and 13CO2 concentrations were measured in end-expiratory breath samples every 30 min for 4 h. Increased H2 concentration ]20 ppm from basal values was used as the cut-off for the H2-SBT. Results. The H2-SBT had a sensitivity of 71%, a specificity of 46% versus healthy controls, and a specificity of 25% versus patient controls. Individuals with methane-producing intestinal flora had significantly lower peak H2 concentrations than non-methane producers. The 13C-SBT reached maximal combined sensitivity/specificity (74%/85%) for both control groups after 1 h. A diagnostic algorithm which stratified patients into high-, moderate- and low risk for coeliac disease was proposed. Following the algorithm, 62% of coeliac patients were detected with 100% specificity. The 13C-SBT, but not the H2-SBT, correlated with age and serum IgA tissuetransglutaminase antibody levels in coeliac patients. Conclusions. The novel 13C-SBT has superior diagnostic properties compared to the H2-SBT, which has unsatisfactory specificity in clinical practice. The 1-h 13C-SBT may be a useful supplemental test when investigating for coeliac disease.
机译:客观的。先前已提出H2-山梨糖醇呼气试验(H2-SBT)作为乳糜泻的筛选工具。我们开发了替代的13C-山梨糖醇呼吸试验(13C-SBT)。该研究的目的是将H2-SBT和13C-SBT的诊断性能进行比较临床环境中。材料与方法。三十九十九个乳糜烃患者,40例患者对照(主要是肠综合征患者)和26例健康志愿者经历了呼吸测试。患者给予口服载量为5g山梨糖醇,100mg 13C-山梨糖醇溶解在250ml滴水中。每隔30分钟以4小时以每30分钟测量H 2,CH 4和13CO2浓度。 H 2浓度的增加]从基础值20 ppm用作H2-SBT的截止值。结果。 H2-SBT的灵敏度为71%,特异性为46%,与健康对照组,特异性为25%,而患者对照。产生甲烷的肠道菌群的个体显着降低了比非甲烷生产商的峰值H2浓度显着降低。 1小时后,13C-SBT达到了对照组的最大组合敏感性/特异性(74%/ 85%)。提出了一种诊断算法,将患者分解为腹腔疾病的高,中等,低,低风险。在算法之后,用100%特异性检测62%的乳糜泻患者。 13C-SBT,但不是H2-SBT,与腹腔患者的年龄和血清IgA Tissuetransgutamina酶抗体水平相关。结论。与H2-SBT相比,新型13C-SBT具有优异的诊断性能,其在临床实践中具有不令人满意的特异性。在研究乳糜泻时,1-H 13C-SBT可能是一种有用的补充测试。

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