Evidence map›Paper›PMID 36671398›Full record

ArticleBiomolecules2022

Metabolomics and a Breath Sensor Identify Acetone as a Biomarker for Heart Failure.

Patrick A Gladding, Maxine Cooper, Renee Young, Suzanne Loader, Kevin Smith, Erica Zarate, Saras Green, Silas G Villas Boas, Phillip Shepherd, Purvi Kakadiya and 6 more

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

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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

16 authors at 3 institutions in 2 countries.

Patrick A GladdingCardiology Department, Waitemata District Health Board, Auckland 0620, New Zealand.
Maxine CooperCardiology Department, Waitemata District Health Board, Auckland 0620, New Zealand.
Renee YoungCardiology Department, Waitemata District Health Board, Auckland 0620, New Zealand.
Suzanne LoaderCardiology Department, Waitemata District Health Board, Auckland 0620, New Zealand.
Kevin SmithClinical Laboratory, Waitemata District Health Board, Auckland 0622, New Zealand.
Erica ZarateSchool of Biological Science, University of Auckland, Auckland 1010, New Zealand.
Saras GreenSchool of Biological Science, University of Auckland, Auckland 1010, New Zealand.
Silas G Villas BoasSchool of Biological Science, University of Auckland, Auckland 1010, New Zealand.ORCID 0000-0003-0148-5882
Phillip ShepherdGrafton Genomics Ltd., Liggins Institute, University of Auckland, Auckland 1010, New Zealand.
Purvi KakadiyaGrafton Genomics Ltd., Liggins Institute, University of Auckland, Auckland 1010, New Zealand.
Eric ThorstensenLiggins Institute, University of Auckland, Auckland 1010, New Zealand.
Christine KevenLiggins Institute, University of Auckland, Auckland 1010, New Zealand.
Margaret CoeLiggins Institute, University of Auckland, Auckland 1010, New Zealand.
Mia JülligPaper Dog Ltd., Waiheke Island, Auckland 1081, New Zealand.
Edmond ZhangPrecision Driven Health Initiative, Auckland 1021, New Zealand.
Todd T SchlegelKarolinska Institutet, 17177 Stockholm, Sweden.ORCID 0000-0003-1997-3227
University of Auckland · NZWaitemata District Health Board · NZKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMulti-omics delivers more biological insight than targeted investigations. We applied multi-omics to patients with heart failure with reduced ejection fraction (HFrEF).

methods46 patients with HFrEF and 20 controls underwent metabolomic profiling, including liquid/gas chromatography mass spectrometry (LC-MS/GC-MS) and solid-phase microextraction (SPME) volatilomics in plasma and urine. HFrEF was defined using left ventricular global longitudinal strain, ejection fraction and NTproBNP. A consumer breath acetone (BrACE) sensor validated results in n = 73.

results28 metabolites were identified by GCMS, 35 by LCMS and 4 volatiles by SPME in plasma and urine. Alanine, aspartate and glutamate, citric acid cycle, arginine biosynthesis, glyoxylate and dicarboxylate metabolism were altered in HFrEF. Plasma acetone correlated with NT-proBNP (r = 0.59, 95% CI 0.4 to 0.7), 2-oxovaleric and cis-aconitic acid, involved with ketone metabolism and mitochondrial energetics. BrACE > 1.5 ppm discriminated HF from other cardiac pathology (AUC 0.8, 95% CI 0.61 to 0.92,

conclusionBreath acetone discriminated HFrEF from other cardiac pathology using a consumer sensor, but was not cardiac specific.

Indexed as

Heart FailureAcetoneBiomarkersHumansMetabolomicsStroke VolumeAcetoneBiomarkersheart failure with reduced ejection fraction

Identifiers

PMID36671398
PMCPMC9856097
OpenAlexW4313502422

What OpenQuestion holds

Textmetadata
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.