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Effect of chronic octreotide treatment on intestinal absorption in patients with acromegaly

dc.contributor.authorGreenstein, Ellenen_US
dc.contributor.authorHo, J. Jeanen_US
dc.contributor.authorBoyajy, Louis D.en_US
dc.contributor.authorBarkan, Ariel L.en_US
dc.date.accessioned2006-09-11T14:46:13Z
dc.date.available2006-09-11T14:46:13Z
dc.date.issued1993-02en_US
dc.identifier.citationHo, J. Jean; Boyajy, Louis D.; Greenstein, Ellen; Barkan, Ariel L.; (1993). "Effect of chronic octreotide treatment on intestinal absorption in patients with acromegaly." Digestive Diseases and Sciences 38(2): 309-315. <http://hdl.handle.net/2027.42/44417>en_US
dc.identifier.issn0163-2116en_US
dc.identifier.issn1573-2568en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44417
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8425442&dopt=citationen_US
dc.description.abstractThe adverse gastrointestinal effects of octreotide, a synthetic analog of somatostatin, have not been fully elucidated. Low-dose octreotide frequently causes adverse gastrointestinal symptoms in normal individuals. We investigated the adverse gastrointestinal effects of high-dose octreotide, which is required for the normalization of growth hormone hypersecretion in some patients with acromegaly. Patients with acromegaly ( N =8) were treated with octreotide, 450 μg/day, then 1500 μg/day for two months at each dosage. Carbohydrate absorption was assessed using the d -xylose test, and fat absorption using fecal fat excretion and serum carotene concentrations, at baseline, at each dosage of octreotide, and after one month of washout. Ultrasonography was used to monitor for cholelithiasis. Growth hormone and insulin-like growth factor-I concentrations were significantly suppressed at both dosages. Adverse gastrointestinal symptoms were mild and transient. d -Xylose absorption remained normal at each dosage and after one month of washout. Fecal fat excretion increased from 7±2 to 12±2 g/24 hr ( P <0.05) after the higher dosage and resumed baseline levels after the washout. Mean fasting serum carotene levels remained normal, and carotene loading test (15,000 units three times a day for three days) was unreliable in identifying patients with high fecal fat. No new cholelithiasis was detected by ultrasonography. One of two patients with preexisting cholelithiasis developed biliary colic several days after the treatment period. Although steatorrhea was common, small intestinal absorptive capacity was otherwise unchanged by four months of high-dose octreotide treatment, which significantly suppressed growth hormone secretion in acromegalic patients.en_US
dc.format.extent791651 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Mediaen_US
dc.subject.otherGastroenterologyen_US
dc.subject.otherXyloseen_US
dc.subject.otherAdverse Effectsen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherHepatologyen_US
dc.subject.otherOncologyen_US
dc.subject.otherTransplant Surgeryen_US
dc.subject.otherBiochemistry, Generalen_US
dc.subject.otherIntestinal Absorptionen_US
dc.subject.otherOctreotideen_US
dc.subject.otherAcromegalyen_US
dc.subject.otherFaten_US
dc.subject.otherCaroteneen_US
dc.subject.otherCholelithiasisen_US
dc.titleEffect of chronic octreotide treatment on intestinal absorption in patients with acromegalyen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Endocrinology and Metabolism, Department of Internal Medicine, Department of Veterans Affairs Medical Center and University of Michigan Medical Center, 48109, Ann Arbor, Michigan; Sandoz Pharmaceuticals Corporation, 07936, East Hanover, New Jerseyen_US
dc.contributor.affiliationumDivision of Endocrinology and Metabolism, Department of Internal Medicine, Department of Veterans Affairs Medical Center and University of Michigan Medical Center, 48109, Ann Arbor, Michigan; Sandoz Pharmaceuticals Corporation, 07936, East Hanover, New Jerseyen_US
dc.contributor.affiliationumDivision of Endocrinology and Metabolism, Department of Internal Medicine, Department of Veterans Affairs Medical Center and University of Michigan Medical Center, 48109, Ann Arbor, Michigan; Sandoz Pharmaceuticals Corporation, 07936, East Hanover, New Jerseyen_US
dc.contributor.affiliationumDivision of Endocrinology and Metabolism, Department of Internal Medicine, Department of Veterans Affairs Medical Center and University of Michigan Medical Center, 48109, Ann Arbor, Michigan; Sandoz Pharmaceuticals Corporation, 07936, East Hanover, New Jersey; Division of Endocrinology and Metabolism, University of Michigan Medical Center, 3920 Taubman Center, Box 0354, 48109-0354, Ann Arbor, Michiganen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid8425442en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44417/1/10620_2005_Article_BF01307549.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01307549en_US
dc.identifier.sourceDigestive Diseases and Sciencesen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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