Matches in SemOpenAlex for { <https://semopenalex.org/work/W2890107658> ?p ?o ?g. }
Showing items 1 to 52 of
52
with 100 items per page.
- W2890107658 abstract "Abstract Background Reduced appetite and weight loss after esophagectomy (ES) occur in the context of an exaggerated postprandial satiety gut hormone response. Satiety gut hormones modulate central processing of food reward, resulting in reduced energy intake. The aim of this study was to investigate the effect of satiety gut hormone attenuation using the somatostatin analogue octreotide on appetitive behavior among patients after curative ES. Methods In this randomized, double-blind, placebo-controlled crossover study, disease-free patients at least one year after ES with gastric conduit reconstruction and matched controls received either 1mL 0.9% saline or 1mL (100μg) octreotide subcutaneously, before completing a progressive ratio task (PRT). A measure of appetitive behavior, the PRT requires subjects to undertake progressively increasing amounts of work to obtain a reinforcer—the final completed increment (breakpoint) representing reinforcer reward value in different states. Separate cohorts were studied in the fasted or 1-hour postprandial states. The institutional Research Ethics Committee approved the study (REC 2015/21/02), which was registered on ClinicalTrials.gov prior to recruitment of the first participant (NCT02381249). Results 36 subjects (ES, n = 18, matched controls, n = 18) were studied. 2.5 ± 0.3 years postoperatively, ES patients demonstrated 14.6 ± 2.6% weight loss and an elevated postprandial GLP-1 (49.2 ± 13.4 versus controls with 20.2 ± 2.3 pM, P = 0.038). Octreotide did not alter appetite among ES or control subjects when tested fasting (breakpoint, ES: 980 ± 371 versus 1700 ± 583, P = 0.16; control: 1056 ± 274 versus 1124 ± 273, P = 0.80). When tested one hour postprandially, octreotide was associated with increased appetitive behavior versus placebo among ES subjects (breakpoint, 322 ± 143 versus 246 ± 149, P = 0.037), but not controls (248 ± 119 versus 247 ± 120, P = 0.98). Conclusion Attenuation of the exaggerated postprandial satiety gut hormone response is associated with increased appetitive behavior towards a sweet-fat stimulus among patients post ES. Suppression of satiety gut hormones may represent a novel target to increase appetite, food intake and body weight in patients after esophagectomy. Disclosure All authors have declared no conflicts of interest." @default.
- W2890107658 created "2018-09-27" @default.
- W2890107658 creator A5000574895 @default.
- W2890107658 creator A5000861567 @default.
- W2890107658 creator A5026768097 @default.
- W2890107658 creator A5037122959 @default.
- W2890107658 creator A5043990013 @default.
- W2890107658 creator A5079991869 @default.
- W2890107658 creator A5086799331 @default.
- W2890107658 date "2018-09-01" @default.
- W2890107658 modified "2023-09-27" @default.
- W2890107658 title "PS02.220: ATTENUATION OF SATIETY GUT HORMONES INCREASES APPETITE AFTER CURATIVE ESOPHAGECTOMY FOR ESOPHAGEAL CANCER" @default.
- W2890107658 doi "https://doi.org/10.1093/dote/doy089.ps02.220" @default.
- W2890107658 hasPublicationYear "2018" @default.
- W2890107658 type Work @default.
- W2890107658 sameAs 2890107658 @default.
- W2890107658 citedByCount "0" @default.
- W2890107658 crossrefType "journal-article" @default.
- W2890107658 hasAuthorship W2890107658A5000574895 @default.
- W2890107658 hasAuthorship W2890107658A5000861567 @default.
- W2890107658 hasAuthorship W2890107658A5026768097 @default.
- W2890107658 hasAuthorship W2890107658A5037122959 @default.
- W2890107658 hasAuthorship W2890107658A5043990013 @default.
- W2890107658 hasAuthorship W2890107658A5079991869 @default.
- W2890107658 hasAuthorship W2890107658A5086799331 @default.
- W2890107658 hasConcept C121608353 @default.
- W2890107658 hasConcept C126322002 @default.
- W2890107658 hasConcept C2777297899 @default.
- W2890107658 hasConcept C2779742542 @default.
- W2890107658 hasConcept C71315377 @default.
- W2890107658 hasConcept C71924100 @default.
- W2890107658 hasConcept C75908981 @default.
- W2890107658 hasConcept C90924648 @default.
- W2890107658 hasConceptScore W2890107658C121608353 @default.
- W2890107658 hasConceptScore W2890107658C126322002 @default.
- W2890107658 hasConceptScore W2890107658C2777297899 @default.
- W2890107658 hasConceptScore W2890107658C2779742542 @default.
- W2890107658 hasConceptScore W2890107658C71315377 @default.
- W2890107658 hasConceptScore W2890107658C71924100 @default.
- W2890107658 hasConceptScore W2890107658C75908981 @default.
- W2890107658 hasConceptScore W2890107658C90924648 @default.
- W2890107658 hasLocation W28901076581 @default.
- W2890107658 hasOpenAccess W2890107658 @default.
- W2890107658 hasPrimaryLocation W28901076581 @default.
- W2890107658 hasRelatedWork W1992110729 @default.
- W2890107658 hasRelatedWork W2081873224 @default.
- W2890107658 hasRelatedWork W2408198533 @default.
- W2890107658 hasRelatedWork W2505636559 @default.
- W2890107658 isParatext "false" @default.
- W2890107658 isRetracted "false" @default.
- W2890107658 magId "2890107658" @default.
- W2890107658 workType "article" @default.