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Effects of postgastric 13 C‐acetate processing on measurement of gastric emptying: a systematic investigation in health
Author(s) -
Goetze O.,
Fox M.,
Kwiatek M. A.,
Treier R.,
Schwizer W.,
Thumshirn M.,
Fried M.,
Fruehauf H.
Publication year - 2009
Publication title -
neurogastroenterology and motility
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.489
H-Index - 105
eISSN - 1365-2982
pISSN - 1350-1925
DOI - 10.1111/j.1365-2982.2009.01337.x
Subject(s) - bolus (digestion) , gastric emptying , excretion , chemistry , tracer , meal , zoology , nuclear medicine , stomach , medicine , biochemistry , physics , nuclear physics , biology
  Uniform postgastric processing of the gastric emptying (GE) marker 13 C‐acetate (Ac) is an unverified assumption behind its widespread application to measure GE. This study assessed the postgastric processing of Ac administered by intraduodenal (i.d.) infusion simulating different physiological conditions. 13 CO 2 in breath was assessed in three groups of six volunteers after i.d. administration of A: Different caloric densities (0.75/1.5/3 kcal min −1 ) in a 200 mL meal at constant 1 mg Ac min −1 simulating a physiological range of nutrient delivery rates; B: different tracer delivery rates (0.5/1.0/2.5 mg Ac min −1 ) simulating delayed, normal and increased GE; C1: a 500 mL meal resulting in same marker and caloric delivery compared to protocol A; C2: 50 mL water bolus injections of 12.5/25/50/100 mg Ac and C3 bolus injections of 50 mg Ac in 50/100/200 mL water in randomized order. A: 13 CO 2 excretion was independent of caloric load ( P  = 0.59). B: The dynamic of 13 CO 2 excretion was modulated by tracer elimination which was in turn dependent on the speed of tracer delivery, i.e. with faster deliveries resulting in lower 13 CO 2 recovery during infusion ( P  < 0.001). C: Increasing Ac doses resulted in decreased 13 CO 2 recovery ( P  < 0.001) over the first hour. 13 CO 2 recovery kinetics was independent of the volume delivered. This study shows 13 C‐acetate absorption and metabolism is independent of the volume and caloric delivery of test meals. The ‘lag’ in estimates of GE derived from 13 CO 2 breath tests is due to a postgastric, dose‐dependent delay to 13 CO 2 elimination. This can be corrected for in analytical derivations of GE parameters based on 13 C‐acetate breath test measurements.

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