Evidence map›Paper›PMID 28359093›Full record

ArticleThe Journal of clinical endocrinology and metabolism2017

Diabetes-Specific Regulation of Adipocyte Metabolism by the Adipose Tissue Extracellular Matrix.

Nicki A Baker, Lindsey A Muir, Alexandra R Washabaugh, Christopher K Neeley, Sophie Yu-Pu Chen, Carmen G Flesher, John Vorwald, Jonathan F Finks, Amir A Ghaferi, Michael W Mulholland and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
4.7field-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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. A Hydrogel Culture System Regulates Human Adipocyte Function.International journal of molecular sciences · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Adipose Tissue Hypoxia in Obesity: Clinical Reappraisal of Hypoxia Hypothesis.Advances in experimental medicine and biology · 2024
    Review
  9. Article
  10. Receptor for the Advanced Glycation End Products (International journal of molecular sciences · 2023
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Impact of Bariatric Surgery on Adipose Tissue Biology.Journal of clinical medicine · 2021
    Review
  20. Age and Sex: Impact on adipose tissue metabolism and inflammation.Mechanisms of ageing and development · 2021
    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

13 authors at 3 institutions in 1 country.

Nicki A BakerDepartment of Surgery.
Lindsey A MuirDepartment of Pediatrics and Communicable Diseases.
Alexandra R WashabaughDepartment of Surgery.
Christopher K NeeleyDepartment of Surgery.
Sophie Yu-Pu ChenCenter for Statistical Consultation & Research and.
Carmen G FlesherUndergraduate Research Opportunity Program, University of Michigan, Ann Arbor, Michigan 48109; and.
John VorwaldUndergraduate Research Opportunity Program, University of Michigan, Ann Arbor, Michigan 48109; and.
Jonathan F FinksDepartment of Surgery.
Amir A GhaferiDepartment of Surgery.
Michael W MulhollandDepartment of Surgery.
Oliver A VarbanDepartment of Surgery.
Carey N LumengDepartment of Pediatrics and Communicable Diseases.
Robert W O'RourkeDepartment of Surgery.
Ann Arbor Center for Independent Living · USStatistical Research (United States) · USUniversity of Michigan–Ann Arbor · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Kanakadurga Singer · 2010 to 2026
$20.3M
Regulation of Adipose Tissue Inflammation By Antigen Presenting CellsR01DK090262 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, CAREY N · 2011 to 2024
$5.3M
Multidisciplinary Training Program in Basic Diabetes ResearchT32DK101357 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PETER ARVAN, Ormond A MacDougald · 2014 to 2026
$4.1M
Targeting hypoxia-inducible mediators to manipulate human adipocyte phenotypeR01DK097449 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI O'ROURKE, ROBERT W · 2013 to 2017
$1.7M
Regulation of lipid laden adipose tissue macrophages in metabolic dysfunctionF32DK105676 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MUIR, LINDSEY ALLISON · 2015 to 2016
$112k
NIDDK NIH HHS R01 DK090262NIDDK NIH HHS R01 DK097449NIDDK NIH HHS T32 DK101357
6 · The paper itself

Abstract

Context: The role of the extracellular matrix (ECM) in regulating adipocyte metabolism in the context of metabolic disease is poorly defined. Objective: The objective of this study was to define the metabolic phenotype of adipocytes associated with human diabetes (DM) and the role of the ECM in regulating adipocyte metabolism. Design: Adipose tissues from obese patients were studied in standard 2-dimensional (2D) cell culture and an in vitro model of decellularized adipose tissue ECM repopulated with human adipocytes, and results were correlated with DM status. Setting: This study was conducted at the Academic University Medical Center and Veteran's Administration Hospital. Patients: Seventy patients with morbid obesity undergoing bariatric surgery were included in the study. Interventions: Visceral and subcutaneous adipose tissues were collected at the time of bariatric surgery. Outcome measures: This study used metabolic assays for glucose uptake, lipolysis, and lipogenesis in adipocytes in 2D cell culture and 3-dimensional ECM culture. Results: Adipocytes from subjects with DM manifest decreased glucose uptake and decreased lipolysis in 2D culture. ECM supports differentiation of mature adipocytes and recapitulates DM-specific differences in adipocyte metabolism observed in 2D culture. ECM from subjects without DM partially rescues glucose uptake and lipolytic defects in adipocytes from subjects with DM, whereas ECM from subjects with DM impairs glucose uptake in adipocytes from subjects without DM. Conclusions: DM is associated with adipocyte metabolic dysfunction. The ECM regulates adipocyte metabolism. Nondiabetic ECM rescues metabolic dysfunction in DM adipocytes, whereas DM ECM imparts features of metabolic dysfunction to nondiabetic adipocytes. These findings suggest the ECM as a target for manipulating adipose tissue metabolism.

Indexed as

LipogenesisLipolysisAbdominal FatAdipocytesAdultCase-Control StudiesCell Culture TechniquesCell DifferentiationCollagen Type IDiabetes Mellitus, Type 2Extracellular MatrixFemaleGlucoseHumansImmunohistochemistryIntra-Abdominal FatCollagen Type IGlucose

Identifiers

PMID28359093
PMCPMC5460687
OpenAlexW2605374526

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.