Evidence map›Paper›PMID 39659543›Full record

ArticleJournal of the Endocrine Society2024

Satiety Hormone LEAP2 After Low-Calorie Diet With/Without Endobarrier Insertion in Obesity and Type 2 Diabetes Mellitus.

Mimoza Emini, Raghav Bhargava, Madhawi Aldhwayan, Navpreet Chhina, Marcela Rodriguez Flores, Ghadah Aldubaikhi, Moaz Al Lababidi, Werd Al-Najim, Alexander D Miras, Aruchuna Ruban and 5 more

Abstract read
In one paragraph

Article in Journal of the Endocrine Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Trial
  2. Review
  3. LEAP2 as a therapeutic target in obesity and cardiometabolic disorders.Reviews in endocrine & metabolic disorders · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Mimoza EminiPsychoNeuroEndocrinology Research Group, Division of Psychiatry, Department of Brain Sciences, Imperial College London, Hammersmith Hospital, London W12 0NN, UK.ORCID https://orcid.org/0000-0001-5527-789X
Raghav BhargavaPsychoNeuroEndocrinology Research Group, Division of Psychiatry, Department of Brain Sciences, Imperial College London, Hammersmith Hospital, London W12 0NN, UK.ORCID https://orcid.org/0000-0002-1745-0345
Madhawi AldhwayanCollege of Applied Medical Sciences, King Saud University, Riyadh 11451, Saudi Arabia.ORCID https://orcid.org/0000-0002-9228-8712
Navpreet ChhinaPsychoNeuroEndocrinology Research Group, Division of Psychiatry, Department of Brain Sciences, Imperial College London, Hammersmith Hospital, London W12 0NN, UK.
Marcela Rodriguez FloresPsychoNeuroEndocrinology Research Group, Division of Psychiatry, Department of Brain Sciences, Imperial College London, Hammersmith Hospital, London W12 0NN, UK.ORCID https://orcid.org/0000-0002-6607-4067
Ghadah AldubaikhiPsychoNeuroEndocrinology Research Group, Division of Psychiatry, Department of Brain Sciences, Imperial College London, Hammersmith Hospital, London W12 0NN, UK.ORCID https://orcid.org/0000-0002-1186-4379
Moaz Al LababidiPsychoNeuroEndocrinology Research Group, Division of Psychiatry, Department of Brain Sciences, Imperial College London, Hammersmith Hospital, London W12 0NN, UK.
Werd Al-NajimDepartment of Metabolism, Diabetes and Reproduction, Imperial College London, Hammersmith Hospital, London W12 0NN, UK.ORCID https://orcid.org/0000-0002-0020-4391
Alexander D MirasDepartment of Metabolism, Diabetes and Reproduction, Imperial College London, Hammersmith Hospital, London W12 0NN, UK.
Aruchuna RubanDepartment of Surgery and Cancer, Imperial College London, St. Mary's Hospital, London W2 1NY, UK.ORCID https://orcid.org/0000-0002-9105-4025
Michael A GlaysherDivision of Surgery, University Hospital Southampton NHS Foundation Trust, Southampton SO16 6YD, UK.ORCID https://orcid.org/0000-0002-1746-2100
Christina G PrechtlClinical Trials Unit, Department of Public Health, Imperial College London, London W12 7TA, UK.ORCID https://orcid.org/0000-0003-4122-8899
James P ByrneDivision of Surgery, University Hospital Southampton NHS Foundation Trust, Southampton SO16 6YD, UK.ORCID https://orcid.org/0000-0003-3517-5110
Julian P TeareDepartment of Surgery and Cancer, Imperial College London, St. Mary's Hospital, London W2 1NY, UK.ORCID https://orcid.org/0000-0003-3551-9139
Anthony P GoldstonePsychoNeuroEndocrinology Research Group, Division of Psychiatry, Department of Brain Sciences, Imperial College London, Hammersmith Hospital, London W12 0NN, UK.ORCID https://orcid.org/0000-0001-8179-7071

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Context: The liver/foregut satiety hormone liver-expressed antimicrobial peptide 2 (LEAP2) is an inverse agonist at the acyl ghrelin receptor (GHSR), increasing after food intake and decreasing after bariatric surgery and short-term nonsurgical weight loss, but effects of long-term dietary weight loss are unknown. Objective: The objective of this study was to examine and compare the effects of these interventions on fasting and postprandial plasma LEAP2 and investigate potential metabolic mediators of changes in plasma LEAP2. Methods: Plasma LEAP2 was measured in a previously published 2-year trial comparing standard medical management (SMM) (including 600-kcal/day deficit) with duodenal-jejunal bypass liner (DJBL, Endobarrier) insertion (explanted after 1 year) in adults with obesity and inadequately controlled type 2 diabetes mellitus. Results: In the SMM group (n = 25-37), weight decreased by 4.3%, 8.1%, 7.8%, and 6.4% at 2, 26, 50, and 104 weeks and fasting plasma LEAP2 decreased from baseline mean ± SD 15.3 ± 0.9 ng/mL by 1.7, 3.8, 2.1, and 2.0 ng/mL, respectively. Absolute/decreases in fasting plasma LEAP2 positively correlated with absolute/decreases in body mass index, glycated hemoglobin A Conclusion: These findings add to our understanding of the regulation and potential physiological role of plasma LEAP2.

Indexed as

appetiteduodenal-jejunal bypass linerglucoseinsulinLEAP2obesityweight loss

Identifiers

PMID39659543
PMCPMC11631353

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Registered trials

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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.