Evidence map›Paper›PMID 30175272›Full record

ArticleJACC. Basic to translational science2018

Fatty Acids Prevent Hypoxia-Inducible Factor-1α Signaling Through Decreased Succinate in Diabetes.

Michael S Dodd, Maria da Luz Sousa Fialho, Claudia N Montes Aparicio, Matthew Kerr, Kerstin N Timm, Julian L Griffin, Joost J F P Luiken, Jan F C Glatz, Damian J Tyler, Lisa C Heather

Open access · goldAbstract read
In one paragraph

Article in JACC. Basic to translational science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
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  15. Targeting hypoxia and thrombospondin-2 in diabetic wound healing.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  16. Unraveling the Roles of HIF-1, HO-1, GLUT-1 and GLUT-4 in Myocardial Protection.International journal of drug discovery and pharmacology · 2024
    Article
  17. Molecular Basis of Cardiomyopathies in Type 2 Diabetes.International journal of molecular sciences · 2024
    Review
  18. Review
  19. Observational
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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

10 authors at 3 institutions in 2 countries.

Michael S DoddDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Maria da Luz Sousa FialhoDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Claudia N Montes AparicioDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Matthew KerrDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Kerstin N TimmDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Julian L GriffinDepartment of Biochemistry and MRC Human Nutrition Research, University of Cambridge, Cambridge, United Kingdom.
Joost J F P LuikenDepartment of Molecular Genetics, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, the Netherlands.
Jan F C GlatzDepartment of Molecular Genetics, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, the Netherlands.
Damian J TylerDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Lisa C HeatherDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
University of Oxford · GBMaastricht University · NLUniversity of Cambridge · GB

Funding

British Heart Foundation FS/10/002/28078British Heart Foundation FS/14/17/30634British Heart Foundation FS/16/7/31843British Heart Foundation FS/17/58/33072Medical Research Council MC_UP_A090_1006Medical Research Council MR/P011705/1
6 · The paper itself

Abstract

Hypoxia-inducible factor (HIF)-1α is essential following a myocardial infarction (MI), and diabetic patients have poorer prognosis post-MI. Could HIF-1α activation be abnormal in the diabetic heart, and could metabolism be causing this? Diabetic hearts had decreased HIF-1α protein following ischemia, and insulin-resistant cardiomyocytes had decreased HIF-1α-mediated signaling and adaptation to hypoxia. This was due to elevated fatty acid (FA) metabolism preventing HIF-1α protein stabilization. FAs exerted their effect by decreasing succinate concentrations, a HIF-1α activator that inhibits the regulatory HIF hydroxylase enzymes. In vivo and in vitro pharmacological HIF hydroxylase inhibition restored HIF-1α accumulation and improved post-ischemic functional recovery in diabetes.

Indexed as

ANOVA, analysis of varianceBSA, bovine serum albumincardiovascular diseasediabetesDMF, dimethyl fumarateDMOG, dimethyloxalylglycineFA, fatty acidfatty acidsFIH, factor inhibiting hypoxia-inducible factorHIF-1αHIF, hypoxia-inducible factorhypoxiai.p., intraperitonealIR, insulin resistance/resistantmetabolismMI, myocardial infarctionPHD, prolyl hydroxylase domainSSO, sulfo-N-succinimidyl oleate

Identifiers

PMID30175272
PMCPMC6115650
OpenAlexW2889120321

What OpenQuestion holds

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LicenceCC BY
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.