Evidence map›Paper›PMID 22253453›Full record

ReviewEuropean journal of heart failure2012

Targeting myocardial substrate metabolism in heart failure: potential for new therapies.

Hossein Ardehali, Hani N Sabbah, Michael A Burke, Satyam Sarma, Peter P Liu, John G F Cleland, Aldo Maggioni, Gregg C Fonarow, E Dale Abel, Umberto Campia and 1 more

Abstract readReview
In one paragraph

Review in European journal of heart failure, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
11.2field-weighted citation impact, top 1% 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

92 citing papers in PubMed, 153 citations in OpenAlex.

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  11. Mechano-energetic uncoupling in heart failure.Nature reviews. Cardiology · 2025
    Review
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  15. Recent advances associated with cardiometabolic remodeling in diabetes-induced heart failure.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  16. Article
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  19. Iron Deficiency and Deranged Myocardial Energetics in Heart Failure.International journal of environmental research and public health · 2022
    Review
  20. Review

32 more citing papers are in PubMed but not listed here.

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

11 authors at 7 institutions in 5 countries.

Hossein ArdehaliDivision of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. h-ardehali@northwestern.edu
Hani N Sabbah
Michael A Burke
Satyam Sarma
Peter P Liu
John G F Cleland
Aldo Maggioni
Gregg C Fonarow
E Dale Abel
Umberto Campia
Mihai Gheorghiade
Northwestern University · USFlorence (Netherlands) · NLHenry Ford Health System · USUniversity of California, Los Angeles · USUniversity of Hull · GBUniversity of Toronto · CAUniversity of Utah · US

Funding

Substrate Selection and Oxidative Stress in Heart FailureP01HL074237 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI SABBAH, HANI N · 2003 to 2013
$19.9M
Small Animal Surgery and HistologyP01HL108795 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOSORDO, DOUGLAS W · 2011 to 2015
$10.7M
Vascular Medicine at Northwestern UniversityK12HL083790 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MCDERMOTT, MARY MCGRAE · 2007 to 2012
$2.5M
Role of the mitochondrial ATP-binding cassette protein-1 in cellular protectionR01HL087149 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ARDEHALI, HOSSEIN · 2007 to 2011
$2.1M
The role of microRNA210 in cardiomyocyte response to ischemia-reperfusionR01HL104181 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ARDEHALI, HOSSEIN · 2011 to 2014
$1.5M
Mechanistic insights into the cardioprotective effects of mABC1 proteinK02HL107448 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ARDEHALI, HOSSEIN · 2011 to 2015
$503k
NHLBI NIH HHS 1P01 HL108795NHLBI NIH HHS K02 HL107448NHLBI NIH HHS K12-HL083790NHLBI NIH HHS P01-HL074237-06NHLBI NIH HHS R01 HL087149NHLBI NIH HHS R01 HL104181
6 · The paper itself

Abstract

The incidence and prevalence of heart failure have increased significantly over the past few decades. Available data suggest that patients with heart failure independent of the aetiology have viable but dysfunctional myocardium that is potentially salvageable. Although a great deal of research effort has focused on characterizing the molecular basis of heart failure, cardiac metabolism in this disorder remains an understudied discipline. It is known that many aspects of cardiomyocyte energetics are altered in heart failure. These include a shift from fatty acid to glucose as a preferred substrate and a decline in the levels of ATP. Despite these demonstrated changes, there are currently no approved drugs that target metabolic enzymes or proteins in heart failure. This is partly due to our limited knowledge of the mechanisms and pathways that regulate cardiac metabolism. Better characterization of these pathways may potentially lead to new therapies for heart failure. Targeting myocardial energetics in the viable and potentially salvageable tissue may be particularly effective in the treatment of heart failure. Here, we will review metabolic changes that occur in fatty acid and glucose metabolism and AMP-activated kinase in heart failure. We propose that cardiac energetics should be considered as a potential target for therapy in heart failure and more research should be done in this area.

Indexed as

AdultAMP-Activated Protein KinasesAnimalsDisease Models, AnimalEnergy MetabolismFatty AcidsGlucoseHeart FailureHumansMiceMyocardiumMyocytes, CardiacAMP-Activated Protein KinasesFatty AcidsGlucose

Identifiers

PMID22253453
PMCPMC3260022
OpenAlexW2091696488

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.