Evidence map›Paper›PMID 30777938›Full record

ArticleJCI insight2019

Sleeve gastrectomy rapidly enhances islet function independently of body weight.

Jonathan D Douros, Jingjing Niu, Sophia Sdao, Trillian Gregg, Kelsey Fisher-Wellman, Manish Bharadwaj, Anthony Molina, Ramamani Arumugam, MacKenzie Martin, Enrico Petretto and 5 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

  1. Sleeve gastrectomy protects lean mice from future obesity.bioRxiv : the preprint server for biology · 2026
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  17. Vertical sleeve gastrectomy confers metabolic improvements by reducing intestinal bile acids and lipid absorption in mice.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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 at 4 institutions in 2 countries.

Jonathan D DourosDivision of Endocrinology, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Jingjing NiuDivision of Endocrinology, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Sophia SdaoDepartment of Medicine, Division of Endocrinology, Diabetes, and Metabolism, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Trillian GreggDepartment of Medicine, Division of Endocrinology, Diabetes, and Metabolism, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Kelsey Fisher-WellmanDivision of Endocrinology, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Manish BharadwajCenter for Diabetes Research, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Anthony MolinaCenter for Diabetes Research, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Ramamani ArumugamDivision of Endocrinology, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
MacKenzie MartinDivision of Endocrinology, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Enrico PetrettoCentre for Computational Biology, Duke-NUS Medical School, Singapore.
Matthew J MerrinsDepartment of Medicine, Division of Endocrinology, Diabetes, and Metabolism, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Mark A HermanDivision of Endocrinology, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Jenny TongDivision of Endocrinology, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Jonathan CampbellDivision of Endocrinology, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
David D'AlessioDivision of Endocrinology, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Duke University · USUniversity of Wisconsin–Madison · USWake Forest University · USDuke-NUS Medical School · SG

Funding

Endocrinology and Metabolism Training ProgramT32DK007012 · NIDDK · DUKE UNIVERSITY · PI DAVID A. D'ALESSIO · 1986 to 2026
$6.8M
Metabolic Functions of Pyruvate Kinase M2 in Pancreatic Beta CellsR01DK113103 · NIDDK · YALE UNIVERSITY · PI Matthew J. Merrins · 2017 to 2026
$3.3M
Comparative analysis of geroprotective interventions in established and novel mouse models of Alzheimer's diseaseR01AG062328 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI LAMMING, DUDLEY WILLIAM, MERRINS, MATTHEW J. · 2018 to 2022
$2.0M
Mechanisms of insulin secretion mediated by alpha cellsR01DK123075 · NIDDK · DUKE UNIVERSITY · PI CAMPBELL, JONATHAN E · 2019 to 2023
$1.9M
The Role of Ghrelin to Regulate Insulin Secretion in Health and Diabetes.R01DK097550 · NIDDK · UNIVERSITY OF CINCINNATI · PI TONG, JENNY · 2013 to 2017
$1.7M
Application for Administrative Supplement to Existing Award AG050135 to Develop Research on Alzheimer's DiseaseR21AG050135 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI LAMMING, DUDLEY WILLIAM, MERRINS, MATTHEW J. · 2016 to 2017
$568k
Assessing the Role of Glucose-Dependent Insulinotropic Polypeptide to Mediate Improved Beta-Cell Function Following Bariatric SurgeryF32DK115031 · NIDDK · DUKE UNIVERSITY · PI DOUROS, JONATHAN D. · 2017 to 2019
$137k
Medical Research Council MC_U120097112NIA NIH HHS R01 AG062328NIA NIH HHS R21 AG050135NIDDK NIH HHS F32 DK115031NIDDK NIH HHS R01 DK097550NIDDK NIH HHS R01 DK113103NIDDK NIH HHS R01 DK123075NIDDK NIH HHS T32 DK007012
6 · The paper itself

Abstract

Bariatric surgeries including vertical sleeve gastrectomy (VSG) ameliorate obesity and diabetes. Weight loss and accompanying increases to insulin sensitivity contribute to improved glycemia after surgery; however, studies in humans also suggest weight-independent actions of bariatric procedures to lower blood glucose, possibly by improving insulin secretion. To evaluate this hypothesis, we compared VSG-operated mice with pair-fed, sham-surgical controls (PF-Sham) 2 weeks after surgery. This paradigm yielded similar postoperative body weight and insulin sensitivity between VSG and calorically restricted PF-Sham animals. However, VSG improved glucose tolerance and markedly enhanced insulin secretion during oral nutrient and i.p. glucose challenges compared with controls. Islets from VSG mice displayed a unique transcriptional signature enriched for genes involved in Ca2+ signaling and insulin secretion pathways. This finding suggests that bariatric surgery leads to intrinsic changes within the islet that alter function. Indeed, islets isolated from VSG mice had increased glucose-stimulated insulin secretion and a left-shifted glucose sensitivity curve compared with islets from PF-Sham mice. Isolated islets from VSG animals showed corresponding increases in the pulse duration of glucose-stimulated Ca2+ oscillations. Together, these findings demonstrate a weight-independent improvement in glycemic control following VSG, which is, in part, driven by improved insulin secretion and associated with substantial changes in islet gene expression. These results support a model in which β cells play a key role in the adaptation to bariatric surgery and the improved glucose tolerance that is typical of these procedures.

Indexed as

Body WeightInsulin SecretionAnimalsBariatric SurgeryBlood GlucoseDiet, High-FatDisease Models, AnimalGastrectomyGlucose Tolerance TestHumansInsulinInsulin ResistanceInsulin-Secreting CellsMiceMice, Inbred C57BLObesityBlood GlucoseInsulinDiabetesEndocrinologyGlucose metabolismIslet cellsMetabolism

Identifiers

PMID30777938
PMCPMC6483064
OpenAlexW2916393499

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.