Evidence map›Paper›PMID 32209584›Full record

ArticleBMJ open diabetes research & care2020

Proglucagon peptide secretion profiles in type 2 diabetes before and after bariatric surgery: 1-year prospective study.

Kleopatra Alexiadou, Joyceline Cuenco, James Howard, Nicolai Jacob Wewer Albrechtsen, Ibiyemi Ilesanmi, Anna Kamocka, George Tharakan, Preeshila Behary, Paul R Bech, Ahmed R Ahmed and 7 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMJ open diabetes research & care, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01945840 (Do Gut Hormones Mediate the Beneficial Effects of Roux-en-Y Bypass?), which is not on this map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% 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.

NCT01945840 narecruitingnot on this map

Do Gut Hormones Mediate the Beneficial Effects of Roux-en-Y Bypass?

TypeinterventionalSponsorImperial College LondonRan2013 to 2028Enrolled190ConditionsObesity, Type 2 DiabetesArmsRoux en Y Gastric Bypass Surgery, Gut hormone infusion, Placebo infusion, Very low calorie diet
3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Article
  9. The postprandial secretion of peptide YYClinical endocrinology · 2023
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Methods and Guidelines for Measurement of Glucagon in Plasma.International journal of molecular sciences · 2019
    Review
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

17 authors at 3 institutions in 2 countries.

Kleopatra Alexiadou *Department of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Joyceline Cuenco *Department of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
James Howard *Drug Development Solutions, LGC Bioscience, Fordham, Cambridgeshire, UK.
Nicolai Jacob Wewer AlbrechtsenDepartment of Clinical Biochemistry, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0003-4230-5753
Ibiyemi IlesanmiDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Anna KamockaDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
George TharakanDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Preeshila BeharyDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Paul R BechDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Ahmed R AhmedDepartment of Surgery and Cancer, Imperial College London, London, UK.
Sanjay PurkayasthaDepartment of Surgery and Cancer, Imperial College London, London, UK.
Robert WhellerDrug Development Solutions, LGC Bioscience, Fordham, Cambridgeshire, UK.
Matthieu FleuretDrug Development Solutions, LGC Bioscience, Fordham, Cambridgeshire, UK.
Jens Juul HolstDepartment of Biomedical Sciences and the NNF Center for Basic Metabolic Research, University of Copenhagen Panum Institute, Copenhagen, Denmark.
Stephen R BloomDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Bernard KhooDivision of Medicine, University College London, London, UK.ORCID 0000-0002-4223-9736
Tricia M-M TanDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK t.tan@imperial.ac.uk.ORCID 0000-0001-5873-3432
Imperial College London · GBUniversity of Copenhagen · DKUniversity College London · GB

Funding

Department of Health EME/13/121/07Department of Health NIHR130639Medical Research Council MR/K02115X/1
6 · The paper itself

Abstract

introductionHyperglucagonemia is a key pathophysiological driver of type 2 diabetes. Although Roux-en-Y gastric bypass (RYGB) is a highly effective treatment for diabetes, it is presently unclear how surgery alters glucagon physiology. The aim of this study was to characterize the behavior of proglucagon-derived peptide (glucagon, glucagon-like peptide-1 (GLP-1), oxyntomodulin, glicentin) secretion after RYGB surgery. RESEARCH DESIGN AND

methodsProspective study of 19 patients with obesity and pre-diabetes/diabetes undergoing RYGB. We assessed the glucose, insulin, GLP-1, glucose-dependent insulinotropic peptide (GIP), oxyntomodulin, glicentin and glucagon responses to a mixed-meal test (MMT) before and 1, 3 and 12 months after surgery. Glucagon was measured using a Mercodia glucagon ELISA using the 'Alternative' improved specificity protocol, which was validated against a reference liquid chromatography combined with mass spectrometry method.

resultsAfter RYGB, there were early improvements in fasting glucose and glucose tolerance and the insulin response to MMT was accelerated and amplified, in parallel to significant increases in postprandial GLP-1, oxyntomodulin and glicentin secretion. There was a significant decrease in fasting glucagon levels at the later time points of 3 and 12 months after surgery. Glucagon was secreted in response to the MMT preoperatively and postoperatively in all patients and there was no significant change in this postprandial secretion. There was no significant change in GIP secretion.

conclusionsThere is a clear difference in the dynamics of secretion of proglucagon peptides after RYGB. The reduction in fasting glucagon secretion may be one of the mechanisms driving later improvements in glycemia after RYGB. TRIAL REGISTRATION NUMBER: NCT01945840.

Indexed as

Bariatric SurgeryDiabetes Mellitus, Type 2Gastric BypassHumansProglucagonProspective StudiesProglucagonbariatric surgeryglucagonglucagon-like peptide-1 (GLP-1)obesity

Identifiers

PMID32209584
PMCPMC7103850
OpenAlexW3013228862

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.