Haeney M R, Culank L S, Montgomery R D, Sammons H G
Gastroenterology. 1978 Sep;75(3):393-400.
The assessment of D-xylose absorption by measurement of urinary excretion is subject to several sources of error. An investigation has been made into the use of the blood levels obtained after a 5-g dose as an assessment of malabsorption. We have shown that optimal discrimination between normal and impaired xylose absorption is achieved by measuring blood xylose levels 1 hr after oral administration and then correcting the results to a constant body surface area. The reference range was 0.65 to 1.33 mmoles per liter for values corrected to 1.73m2. In a prospective study of the value of this modification in investigating malabsorption, the incidence of false-negatives and false-positives was found to be 4.8 and 2.2%, respectively. The test is of particular value in the elderly because surface area corrected 1-hr blood xylose levels are independent of age, eliminating the expected and observed declines in renal function and urinary xylose excretion in this age group.
通过测量尿排泄量来评估D-木糖吸收情况存在多种误差来源。已对口服5克剂量后所测得的血药浓度作为吸收不良评估指标的应用进行了研究。我们发现,通过在口服给药后1小时测量血木糖水平,然后将结果校正至恒定体表面积,可实现对正常和受损木糖吸收的最佳区分。校正至1.73平方米时,参考范围为每升0.65至1.33毫摩尔。在一项关于此改良方法在吸收不良研究中价值的前瞻性研究中,发现假阴性和假阳性的发生率分别为4.8%和2.2%。该检测方法对老年人具有特殊价值,因为校正体表面积后的1小时血木糖水平与年龄无关,消除了该年龄组中预期和观察到的肾功能及尿木糖排泄量下降的影响。