Evidence map›Paper›PMID 37734903›Full record

ArticleBMJ open diabetes research & care2023

Circulating metabolites improve the prediction of renal impairment in patients with type 2 diabetes.

Vincenzo Trischitta, Mario Mastroianno, Maria Giovanna Scarale, Cornelia Prehn, Lucia Salvemini, Andrea Fontana, Jerzy Adamski, Francesco Paolo Schena, Salvatore De Cosmo, Massimiliano Copetti and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open diabetes research & care, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 5 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

11 authors at 3 institutions in 3 countries.

Vincenzo TrischittaResearch Unit of Diabetes and Endocrine Diseases, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy c.menzaghi@operapadrepio.it vincenzo.trischitta@uniroma1.it.
Mario MastroiannoScientific Direction, Fondazione IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo, Italy.
Maria Giovanna ScaraleResearch Unit of Diabetes and Endocrine Diseases, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.ORCID 0000-0003-1769-6246
Cornelia PrehnInstitute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
Lucia SalveminiResearch Unit of Diabetes and Endocrine Diseases, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Andrea FontanaUnit of Biostatistics, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Jerzy AdamskiInstitute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
Francesco Paolo SchenaRecerch Center, Fondazione Schena, Bari, Italy.
Salvatore De CosmoUnit of Internal Medicine, IRCCS Casa Sollievo della Sofferenza San Giovanni Rotondo, Foggia, Italy.
Massimiliano CopettiUnit of Biostatistics, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.ORCID 0000-0002-7960-5947
Claudia MenzaghiResearch Unit of Diabetes and Endocrine Diseases, Istituti di Ricovero e Cura a Carattere Scientifico Ospedale Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy c.menzaghi@operapadrepio.it vincenzo.trischitta@uniroma1.it.ORCID 0000-0002-7438-8955
Casa Sollievo della Sofferenza · ITHelmholtz Zentrum München · DENational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionLow glomerular filtration rate (GFR) is a leading cause of reduced lifespan in type 2 diabetes. Unravelling biomarkers capable to identify high-risk patients can help tackle this burden. We investigated the association between 188 serum metabolites and kidney function in type 2 diabetes and then whether the associated metabolites improve two established clinical models for predicting GFR decline in these patients. RESEARCH DESIGN AND

methodsTwo cohorts comprising 849 individuals with type 2 diabetes (discovery and validation samples) and a follow-up study of 575 patients with estimated GFR (eGFR) decline were analyzed.

resultsTen metabolites were independently associated with low eGFR in the discovery sample, with nine of them being confirmed also in the validation sample (ORs range 1.3-2.4 per 1SD, p values range 1.9×10

conclusionsFurther studies are needed to validate our findings in larger cohorts of different clinical, environmental and genetic background.

Indexed as

Diabetes Mellitus, Type 2CarnitineFollow-Up StudiesGlomerular Filtration RateHumansKynurenineCarnitineKynureninetiglylcarnitineBiomarkersDiabetes Mellitus, Type 2InflammationKidney Diseases

Identifiers

PMID37734903
PMCPMC10514631
OpenAlexW4386923551

What OpenQuestion holds

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LicenceCC BY-NC
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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.