Prolonged large bowel transit increases serum deoxycholic acid: a risk factor for octreotide induced gallstones

Citation
Mj. Veysey et al., Prolonged large bowel transit increases serum deoxycholic acid: a risk factor for octreotide induced gallstones, GUT, 44(5), 1999, pp. 675-681
Citations number
44
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
GUT
ISSN journal
00175749 → ACNP
Volume
44
Issue
5
Year of publication
1999
Pages
675 - 681
Database
ISI
SICI code
0017-5749(199905)44:5<675:PLBTIS>2.0.ZU;2-O
Abstract
Background-Treatment of acromegaly with octreotide increases the proportion of deoxycholic acid in, and the cholesterol saturation of, bile and induce s the formation of gallstones. Prolongation of intestinal transit has been proposed as the mechanism for the increase in the proportion of deoxycholic acid in bile. Aims-To study the effects of octreotide on intestinal transit in acromegali c patients during octreotide treatment, and to examine the relation between intestinal transit and bile acid composition in fasting serum. Methods-Mouth to caecum and large bowel transit times, and the proportion o f deoxycholic acid in fasting serum were measured in non-acromegalic contro ls, acromegalic patients untreated with octreotide, acromegalics on long te rm octreotide, and patients with simple constipation. Intestinal transit an d the proportion of deoxycholic acid were compared in acromegalic patients before and during octreotide. Results-Acromegalics untreated with octreotide had longer mouth to caecum a nd large bowel transit times than controls. Intestinal transit was further prolonged by chronic octreotide treatment. There were significant linear re lations between large bowel transit time and the proportion of deoxycholic acid in the total, conjugated, and unconjugated fractions of fasting serum. Conclusions-These data support the hypothesis that, by prolonging large bow el transit, octreotide increases the proportion of deoxycholic acid in fast ing serum (and, by implication, in bile) and thereby the risk of gallstone formation.