Evidence map›Paper›PMID 24675715›Full record

ArticleInternational journal of obesity (2005)2015

Mapping of the circulating metabolome reveals α-ketoglutarate as a predictor of morbid obesity-associated non-alcoholic fatty liver disease.

E Rodríguez-Gallego, M Guirro, M Riera-Borrull, A Hernández-Aguilera, R Mariné-Casadó, S Fernández-Arroyo, R Beltrán-Debón, F Sabench, M Hernández, D del Castillo and 5 more

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In one paragraph

Article in International journal of obesity (2005), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.6field-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

49 citing papers in PubMed, 85 citations in OpenAlex.

  1. Laparoscopic sleeve gastrectomy altersScientific reports · 2021
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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

15 authors at 5 institutions in 1 country.

E Rodríguez-GallegoUnitat de Recerca Biomèdica, Hospital Universitari Sant Joan, Institut d'Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, Reus, Spain.
M GuirroUnitat de Recerca Biomèdica, Hospital Universitari Sant Joan, Institut d'Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, Reus, Spain.
M Riera-BorrullUnitat de Recerca Biomèdica, Hospital Universitari Sant Joan, Institut d'Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, Reus, Spain.
A Hernández-AguileraUnitat de Recerca Biomèdica, Hospital Universitari Sant Joan, Institut d'Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, Reus, Spain.
R Mariné-CasadóUnitat de Recerca Biomèdica, Hospital Universitari Sant Joan, Institut d'Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, Reus, Spain.
S Fernández-ArroyoUnitat de Recerca Biomèdica, Hospital Universitari Sant Joan, Institut d'Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, Reus, Spain.
R Beltrán-DebónUnitat de Recerca Biomèdica, Hospital Universitari Sant Joan, Institut d'Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, Reus, Spain.
F SabenchServei de Cirurgia General i de l'Aparell Digestiu, Hospital Universitari de Sant Joan de Reus, Universitat Rovira i Virgili, Reus, Spain.
M HernándezServei de Cirurgia General i de l'Aparell Digestiu, Hospital Universitari de Sant Joan de Reus, Universitat Rovira i Virgili, Reus, Spain.
D del CastilloServei de Cirurgia General i de l'Aparell Digestiu, Hospital Universitari de Sant Joan de Reus, Universitat Rovira i Virgili, Reus, Spain.
J A MenendezCatalan Institute of Oncology and Girona Biomedical Research Institute, Girona, Spain.
J CampsUnitat de Recerca Biomèdica, Hospital Universitari Sant Joan, Institut d'Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, Reus, Spain.
R RasCenter for Omics Sciences, Reus, Spain.
L Arola1] Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili. Centre Tecnològic de Nutrició i Salut, Reus, Spain [2] Campus of International Excellence Southern Catalonia, Tarragona, Spain.
J Joven1] Unitat de Recerca Biomèdica, Hospital Universitari Sant Joan, Institut d'Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, Reus, Spain [2] Campus of International Excellence Southern Catalonia, Tarragona, Spain.
Institut de Recerca Biomèdica Catalunya Sud · ESHospital Universitari Sant Joan de Reus · ESCentre for Omic Sciences · ESInstitut Català d'Oncologia · ESTechnological Center of Nutrition and Health · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundObesity severely affects human health, and the accompanying non-alcoholic fatty liver disease (NAFLD) is associated with high morbidity and mortality. Rapid and non-invasive methods to detect this condition may substantially improve clinical care.

methodsWe used liquid and gas chromatography-quadruple time-of-flight-mass spectrometry (LC/GC-QTOF-MS) analysis in a non-targeted metabolomics approach on the plasma from morbidly obese patients undergoing bariatric surgery to gain a comprehensive measure of metabolite levels. On the basis of these findings, we developed a method (GC-QTOF-MS) for the accurate quantification of plasma α-ketoglutarate to explore its potential as a novel biomarker for the detection of NAFLD.

resultsPlasma biochemical differences were observed between patients with and without NAFLD indicating that the accumulation of lipids in hepatocytes decreased β-oxidation energy production, reduced liver function and altered glucose metabolism. The results obtained from the plasma analysis suggest pathophysiological insights that link lipid and glucose disturbances with α-ketoglutarate. Plasma α-ketoglutarate levels are significantly increased in obese patients compared with lean controls. Among obese patients, the measurement of this metabolite differentiates between those with or without NAFLD. Data from the liver were consistent with data from plasma. Clinical utility was assessed, and the results revealed that plasma α-ketoglutarate is a fair-to-good biomarker in patients (n=230). Other common laboratory liver tests used in routine application did not favourably compare.

conclusionPlasma α-ketoglutarate is superior to common liver function tests in obese patients as a surrogate biomarker of NAFLD. The measurement of this biomarker may potentiate the search for a therapeutic approach, may decrease the need for liver biopsy and may be useful in the assessment of disease progression.

Indexed as

MetabolomeBiomarkersChromatography, LiquidDisease ProgressionHumansKetoglutaric AcidsLipid MetabolismMass SpectrometryMetabolomicsNon-alcoholic Fatty Liver DiseaseObesity, MorbidPredictive Value of TestsBiomarkersKetoglutaric Acids

Identifiers

PMID24675715
OpenAlexW2005430136

What OpenQuestion holds

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Registered trials

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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.