Tveito Kari, Brunborg Cathrine, Sandvik Leiv, Løberg Else Marit, Skar Viggo
Department of Medicine, Lovisenberg Diakonale Hospital, Oslo, Norway.
Scand J Gastroenterol. 2008;43(2):166-73. doi: 10.1080/00365520701659118.
Xylose absorption testing has traditionally involved measurement of serum xylose and/or measurement of excreted xylose in urine. However, by enriching xylose with a 13C- or 14C-isotope, absorption of an oral xylose load will be reflected in the time-dependent pattern of 13CO2 or 14CO2 exhaled in breath. Our objectives were to evaluate the diagnostic properties of 13C-xylose and 14C-xylose breath tests in coeliac disease, and to develop a diagnostic breath test index.
We reviewed data from 41 coeliac patients who underwent the 14C-xylose breath test before and after commencement of a gluten-free diet, and 60 coeliac patients who underwent the 13C-xylose breath test, 37 of whom repeated the test after starting a gluten-free diet. Coeliac patients were compared with healthy control subjects.
Coeliac patients exhaled significantly less 13CO2 or 14CO2 than healthy controls during the first hour of the test and more isotope-labelled CO2 than control subjects after 3 h. Diagnostic accuracy was optimal with test duration of 210 min combining gas measurements at 30 min and 210 min in a simple fraction. This gas fraction index (30 min/210 min) distinguished between coeliac patients and healthy control subjects with 84-95% sensitivity and 87-94% specificity. After commencement of a gluten-free diet, the gas fraction index increased in most coeliac patients, but remained lower than that in healthy control subjects.
13C-xylose- and 14C-xylose breath tests discriminate between coeliac patients and healthy control subjects with high sensitivity and specificity. The stable isotope 13C-xylose breath test has comparable diagnostic accuracy to the radioactive isotope 14C-xylose breath test and should be the preferred alternative to traditional xylose absorption tests.
传统的木糖吸收试验涉及测定血清木糖和/或尿中排泄的木糖。然而,通过用13C或14C同位素富集木糖,口服木糖负荷的吸收情况将反映在呼出气体中13CO2或14CO2随时间变化的模式中。我们的目的是评估13C - 木糖和14C - 木糖呼气试验在乳糜泻中的诊断特性,并制定一个诊断呼气试验指标。
我们回顾了41例乳糜泻患者在开始无麸质饮食前后进行14C - 木糖呼气试验的数据,以及60例进行13C - 木糖呼气试验的乳糜泻患者的数据,其中37例在开始无麸质饮食后重复了该试验。将乳糜泻患者与健康对照者进行比较。
在试验的第一个小时内,乳糜泻患者呼出的13CO2或14CO2明显少于健康对照者,而在3小时后呼出的同位素标记的CO2比对照者多。在210分钟的试验持续时间内,结合30分钟和210分钟时的气体测量,以简单分数形式得出的诊断准确性最佳。这个气体分数指数(30分钟/210分钟)区分乳糜泻患者和健康对照者的敏感性为84 - 95%,特异性为87 - 94%。开始无麸质饮食后,大多数乳糜泻患者的气体分数指数增加,但仍低于健康对照者。
13C - 木糖和14C - 木糖呼气试验能以高敏感性和特异性区分乳糜泻患者和健康对照者。稳定同位素13C - 木糖呼气试验与放射性同位素14C - 木糖呼气试验具有相当的诊断准确性,应成为传统木糖吸收试验的首选替代方法。