Evidence map›Paper›PMID 27811952›Full record

Trial reportInternational journal of obesity (2005)2017

Lipid stimulation of fatty acid sensors in the human duodenum: relationship with gastrointestinal hormones, BMI and diet.

N Cvijanovic, N J Isaacs, C K Rayner, C Feinle-Bisset, R L Young, T J Little

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in International journal of obesity (2005), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Saponins fromNutrients · 2022
    Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Obesity: Obesity alters fatty acid sensing.Nature reviews. Endocrinology · 2017
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

N CvijanovicDiscipline of Medicine, University of Adelaide, Adelaide, SA, Australia.
N J IsaacsDiscipline of Medicine, University of Adelaide, Adelaide, SA, Australia.
C K RaynerDiscipline of Medicine, University of Adelaide, Adelaide, SA, Australia.
C Feinle-BissetDiscipline of Medicine, University of Adelaide, Adelaide, SA, Australia.
R L YoungDiscipline of Medicine, University of Adelaide, Adelaide, SA, Australia.
T J LittleDiscipline of Medicine, University of Adelaide, Adelaide, SA, Australia.
University of Adelaide · AUNational Health and Medical Research Council · AUSouth Australian Health and Medical Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsThe small intestinal free fatty acid (FFA) sensors, FFA receptor 1 (FFAR1), FFAR4, G-protein receptor 119 (GPR119) and cluster of differentiation-36 (CD36), mediate the fat-induced release of gastrointestinal (GI) hormones. We investigated whether expression of duodenal FFA sensors in humans was (i) altered by intraduodenal (ID) lipid infusion, (ii) disordered in overweight or obese individuals, (iii) related to lipid-induced GI hormone secretion or (iv) affected by habitual dietary patterns.

methodsEndoscopic duodenal biopsies were collected from 20 lean (body mass index (BMI): 22±1 kg m

resultsBaseline FFAR1 and FFAR4 expression were lower, and CD36 was higher, in obese participants compared with lean participants. ID lipid increased GPR119 and FFAR1 expression equally across study groups, but did not alter FFAR4 or CD36 expression. Increased FFAR1 expression correlated positively with glucose-dependent insulinotropic polypeptide (GIP) secretion (r=0.3, P<0.05), whereas there was no relationship between habitual diet with the expression of FFA sensors.

conclusionsObesity is associated with altered duodenal expression of FFAR1, FFAR4 and CD36, suggesting altered capacity for the sensing, absorption and metabolism, of dietary lipids. GPR119 and FFAR1 are early transcriptional responders to the presence of ID lipid, whereas FFAR1 may be an important trigger for lipid-induced GIP release in humans.

Indexed as

Body Mass IndexDietEnteral NutritionAdultAppetite RegulationCD36 AntigensDuodenumEnergy IntakeFemaleHormonesHumansLipidsMaleObesityOverweightReceptors, G-Protein-CoupledCD36 AntigensFFAR1 protein, humanFFAR4 protein, humanGPR119 protein, humanHormonesLipidsReceptors, G-Protein-CoupledRNA, Messenger

Identifiers

PMID27811952
OpenAlexW2547875969

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.