Evidence map›Paper›PMID 32066202›Full record

ArticleNMR in biomedicine2020

Increasing mitochondrial ATP synthesis with butyrate normalizes ADP and contractile function in metabolic heart disease.

Marcello Panagia, Huamei He, Tomas Baka, David R Pimentel, Dominique Croteau, Markus M Bachschmid, James A Balschi, Wilson S Colucci, Ivan Luptak

Open access · greenAbstract read
In one paragraph

Article in NMR in biomedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 26 citations in OpenAlex.

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  9. Gut-heart axis: cardiac remodeling and heart failure in the context of inflammatory bowel disease and dysbiosis.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Review
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  13. International journal of medical sciences · 2025
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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

9 authors at 2 institutions in 2 countries.

Marcello PanagiaMyocardial Biology Unit, Boston University School of Medicine, Boston, Massachusetts.
Huamei HePhysiological NMR Core Laboratory, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Tomas BakaMyocardial Biology Unit, Boston University School of Medicine, Boston, Massachusetts.
David R PimentelMyocardial Biology Unit, Boston University School of Medicine, Boston, Massachusetts.
Dominique CroteauMyocardial Biology Unit, Boston University School of Medicine, Boston, Massachusetts.
Markus M BachschmidVascular Biology Section, Boston University School of Medicine, Boston, Massachusetts.
James A BalschiPhysiological NMR Core Laboratory, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Wilson S ColucciMyocardial Biology Unit, Boston University School of Medicine, Boston, Massachusetts.
Ivan LuptakMyocardial Biology Unit, Boston University School of Medicine, Boston, Massachusetts.ORCID 0000-0001-7498-7694
Boston University · USBrigham and Women's Hospital · US

Funding

Oxidative Stress in Myocardial Remodeling and FailureR01HL064750 · NHLBI · BOSTON MEDICAL CENTER · PI COLUCCI, WILSON S. · 2001 to 2018
$5.0M
Redox Control of Hepatic Lipid MetabolismR01DK103750 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BACHSCHMID, MARKUS MICHAEL · 2015 to 2019
$1.8M
Multiplexed Imaging of Energy Metabolism in Murine Models of Heart FailureK08HL123744 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI PANAGIA, MARCELLO · 2014 to 2018
$767k
Active transmembrane water cycling kinetics: A Cellular Metabolic 1H MR BiomarkerR21EB014414 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI BALSCHI, JAMES ALVIN · 2013 to 2014
$491k
NHLBI PROTEOMICS INITIATIVE-N01HV28178N01HV028178 · HV · BOSTON UNIVERSITY MEDICAL CAMPUS · PI COSTELLO, CATHERINE E. · 2002 to 2006
–
STRUCTURAL CHARACTERIZATION OF THE APOPROTEIN E RECEPTORR01HL028178 · NHLBI · J. DAVID GLADSTONE INSTITUTES · PI INNERARITY, THOMAS L. · 1986 to 1988
–
NHLBI NIH HHS K08 HL123744NHLBI NIH HHS N01 HV028178NHLBI NIH HHS R01 HL064750NIBIB NIH HHS R21 EB014414NIDDK NIH HHS R01 DK103750
6 · The paper itself

Abstract

Metabolic heart disease (MHD), which is strongly associated with heart failure with preserved ejection fraction, is characterized by reduced mitochondrial energy production and contractile performance. In this study, we tested the hypothesis that an acute increase in ATP synthesis, via short chain fatty acid (butyrate) perfusion, restores contractile function in MHD. Isolated hearts of mice with MHD due to consumption of a high fat high sucrose (HFHS) diet or on a control diet (CD) for 4 months were studied using

Indexed as

Adenosine DiphosphateAdenosine TriphosphateAnimalsButyratesCardiovascular DiseasesEnergy MetabolismHemodynamicsHydrolysisMagnetic Resonance SpectroscopyMaleMetabolic DiseasesMice, Inbred C57BLMitochondria, HeartMyocardial ContractionThermodynamicsAdenosine DiphosphateAdenosine TriphosphateButyratesATP synthesiscontractile functionheart failuremetabolic syndromemetabolismmitochondrianuclear magnetic resonance spectroscopy

Identifiers

PMID32066202
PMCPMC7165026
OpenAlexW3007849673

What OpenQuestion holds

Textmetadata
LicenceTDM
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.