Evidence map›Paper›PMID 34320987›Full record

ArticleCardiovascular diabetology2021

A molecular signature for the metabolic syndrome by urine metabolomics.

Chiara Bruzzone, Rubén Gil-Redondo, Marisa Seco, Rocío Barragán, Laura de la Cruz, Claire Cannet, Hartmut Schäfer, Fang Fang, Tammo Diercks, Maider Bizkarguenaga and 13 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Cardiovascular diabetology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  17. A metabolic readout of the urine metabolome of COVID-19 patients.Metabolomics : Official journal of the Metabolomic Society · 2023
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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

23 authors at 7 institutions in 5 countries.

Chiara Bruzzone *Precision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Bizkaia Technology Park, Bld. 800, 48160, Derio, Bizkaia, Spain.
Rubén Gil-Redondo *Precision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Bizkaia Technology Park, Bld. 800, 48160, Derio, Bizkaia, Spain.
Marisa SecoOSARTEN Kooperativa Elkartea, 20500, Arrasate-Mondragón, Spain.
Rocío BarragánDepartment of Preventive Medicine and Public Health, School of Medicine, University of Valencia, 46010, Valencia, Spain.
Laura de la CruzPrecision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Bizkaia Technology Park, Bld. 800, 48160, Derio, Bizkaia, Spain.
Claire CannetBruker Biospin GmbH, Silberstreifen, 76287, Rheinstetten, Germany.
Hartmut SchäferBruker Biospin GmbH, Silberstreifen, 76287, Rheinstetten, Germany.
Fang FangBruker Biospin GmbH, Silberstreifen, 76287, Rheinstetten, Germany.
Tammo DiercksPrecision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Bizkaia Technology Park, Bld. 800, 48160, Derio, Bizkaia, Spain.
Maider BizkarguenagaPrecision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Bizkaia Technology Park, Bld. 800, 48160, Derio, Bizkaia, Spain.
Beatriz González-VallePrecision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Bizkaia Technology Park, Bld. 800, 48160, Derio, Bizkaia, Spain.
Ana LaínPrecision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Bizkaia Technology Park, Bld. 800, 48160, Derio, Bizkaia, Spain.
Arantza Sanz-ParraPrecision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Bizkaia Technology Park, Bld. 800, 48160, Derio, Bizkaia, Spain.
Oscar ColtellCIBER Fisiopatología de la Obesidad y Nutrición, Madrid, Spain.
Ander López de LetonaGetxo Kirolak, Los Chopos Etorbidea, 56, 48992, Getxo, Bizkaia, Spain.
Manfred SpraulBruker Biospin GmbH, Silberstreifen, 76287, Rheinstetten, Germany.
Shelly C LuKarsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Elisabetta BuguianesiGastroenterology Department, University of Turin, Turin, Italy.
Nieves EmbadePrecision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Bizkaia Technology Park, Bld. 800, 48160, Derio, Bizkaia, Spain.
Quentin M AnsteeTranslational & Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
Dolores CorellaDepartment of Preventive Medicine and Public Health, School of Medicine, University of Valencia, 46010, Valencia, Spain.
José M MatoPrecision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Bizkaia Technology Park, Bld. 800, 48160, Derio, Bizkaia, Spain.
Oscar MilletPrecision Medicine and Metabolism Laboratory, CIC bioGUNE, BRTA, CIBERehd, Bizkaia Technology Park, Bld. 800, 48160, Derio, Bizkaia, Spain. director@cicbiogune.es.ORCID 0000-0001-8748-4105
CIC bioGUNE · ESBruker (Germany) · DEUniversitat de València · ESCedars-Sinai Medical Center · USNIHR Newcastle Biomedical Research Centre · GBUniversitat Jaume I · ESUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetabolic syndrome (MetS) is a multimorbid long-term condition without consensual medical definition and a diagnostic based on compatible symptomatology. Here we have investigated the molecular signature of MetS in urine.

methodsWe used NMR-based metabolomics to investigate a European cohort including urine samples from 11,754 individuals (18-75 years old, 41% females), designed to populate all the intermediate conditions in MetS, from subjects without any risk factor up to individuals with developed MetS (4-5%, depending on the definition). A set of quantified metabolites were integrated from the urine spectra to obtain metabolic models (one for each definition), to discriminate between individuals with MetS.

resultsMetS progression produces a continuous and monotonic variation of the urine metabolome, characterized by up- or down-regulation of the pertinent metabolites (17 in total, including glucose, lipids, aromatic amino acids, salicyluric acid, maltitol, trimethylamine N-oxide, and p-cresol sulfate) with some of the metabolites associated to MetS for the first time. This metabolic signature, based solely on information extracted from the urine spectrum, adds a molecular dimension to MetS definition and it was used to generate models that can identify subjects with MetS (AUROC values between 0.83 and 0.87). This signature is particularly suitable to add meaning to the conditions that are in the interface between healthy subjects and MetS patients. Aging and non-alcoholic fatty liver disease are also risk factors that may enhance MetS probability, but they do not directly interfere with the metabolic discrimination of the syndrome.

conclusionsUrine metabolomics, studied by NMR spectroscopy, unravelled a set of metabolites that concomitantly evolve with MetS progression, that were used to derive and validate a molecular definition of MetS and to discriminate the conditions that are in the interface between healthy individuals and the metabolic syndrome.

Indexed as

MetabolomeMetabolomicsProton Magnetic Resonance SpectroscopyAdolescentAdultAgedBiomarkersCase-Control StudiesDisease ProgressionEuropeFemaleHumansMaleMetabolic SyndromeMiddle AgedPredictive Value of TestsBiomarkersMetabolic syndromeNMR-metabolomicsNMR spectroscopyPrecision medicineUrine

Identifiers

PMID34320987
PMCPMC8320177
OpenAlexW3167797199

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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.