D-xylose kinetics and hydrogen breath tests in functionally anephric patients using the 15-gram dose

Citation
Rm. Craig et al., D-xylose kinetics and hydrogen breath tests in functionally anephric patients using the 15-gram dose, J CLIN GAST, 31(1), 2000, pp. 55-59
Citations number
13
Categorie Soggetti
Gastroenerology and Hepatology
Journal title
JOURNAL OF CLINICAL GASTROENTEROLOGY
ISSN journal
01920790 → ACNP
Volume
31
Issue
1
Year of publication
2000
Pages
55 - 59
Database
ISI
SICI code
0192-0790(200007)31:1<55:DKAHBT>2.0.ZU;2-P
Abstract
Malabsorptive evaluation in renal failure is difficult because most absorpt ive testing requires urinary collections. Kinetic analysis of d-xylose abso rption and d-xylose breath testing were performed in an effort to establish an effective absorption test in functionally anephric patients. We studied 13 fasting renal failure patients with no diarrhea or symptoms suggesting malabsorption on two separate nondialysis days after they received 15 g ora l d-xylose on day 1 and 10 g IV on day. Serum collections were used to calc ulate the kinetic rate constants and extent of d-xylose absorption. After t he oral d-xylose, end expiratory breaths were collected every 15 minutes fo r 3 hours and were analyzed for H-2 with gas chromatography. Five subjects also allowed upper endoscopy and duodenal biopsy. The mean absorption rate constant (Ka) and bioavailability (F) were similar to published values for normal subjects using the 15-g dose (0.936 min(-1) range, 0.227-1.96; and 7 4%, range 46-99, respectively). Of the patients, 12 had normal 1-hour serum d-xylose concentrations (>20 mg/dL). There was no clear in verse correlati on between the rate constant for absorption or bioavailability and peak bre ath hydrogen or the area under the curve for breath H-2 versus time. Using 15 g oral d-xylose, mean bioavailability and absorption rate constants are normal in functionally anephric patients with no clinical evidence of malab sorption. Three patients had elevated breath peak H-2 concentrations, but t here was no clear inverse correlation between bioavailability and the breat h H-2 values. A 1-hour serum d-xylose concentration >20 mg/dL may be consid ered normal in this patient group, similar to patients with normal renal fu nction.