Evidence map›Paper›PMID 42091203›Full record

ArticleBMJ open diabetes research & care2026

Acylcarnitines and prediction of renal function decline in type 2 diabetes.

Vincenzo Trischitta, Andrea Fontana, Hetal Shah, Mario Mastroianno, Cornelia Prehn, Salvatore De Cosmo, Jerzy Adamski, Massimiliano Copetti, Alessandro Doria, Claudia Menzaghi

Abstract read
In one paragraph

Article in BMJ open diabetes research & care, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Vincenzo TrischittaResearch Unit of Diabetes and Endocrine Diseases, Fondazione Casa Sollievo della Sofferenza IRCCS, San Giovanni Rotondo, Italy.ORCID http://orcid.org/0000-0003-1174-127X
Andrea FontanaUnit of Biostatistics, Fondazione Casa Sollievo della Sofferenza IRCCS, San Giovanni Rotondo, Italy.ORCID http://orcid.org/0000-0002-6660-5315
Hetal ShahGenetics and Epidemiology, Joslin Diabetes Center, Boston, Massachusetts, USA.ORCID http://orcid.org/0000-0002-3685-4572
Mario MastroiannoScientific Direction, Fondazione Casa Sollievo della Sofferenza IRCCS, San Giovanni Rotondo, Italy.ORCID http://orcid.org/0000-0003-3218-1646
Cornelia PrehnResearch Unit Molecular Endocrinology and Metabolism, Helmholtz Zentrum München Deutsches Forschungszentrum für Gesundheit und Umwelt, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-1274-4715
Salvatore De CosmoUnit of Internal Medicine, Fondazione Casa Sollievo della Sofferenza IRCCS, San Giovanni Rotondo, Italy.
Jerzy AdamskiInstitute of Experimental Genetics, Helmholtz Center Munich German Research Center for Environmental Health, Neuherberg, Germany.ORCID http://orcid.org/0000-0001-9259-0199
Massimiliano CopettiUnit of Biostatistics, Fondazione Casa Sollievo della Sofferenza IRCCS, San Giovanni Rotondo, Italy.ORCID http://orcid.org/0000-0002-7960-5947
Alessandro DoriaGenetics and Epidemiology, Joslin Diabetes Center, Boston, Massachusetts, USA.ORCID http://orcid.org/0000-0002-3830-4304
Claudia MenzaghiResearch Unit of Diabetes and Endocrine Diseases, Fondazione Casa Sollievo della Sofferenza IRCCS, San Giovanni Rotondo, Italy c.menzaghi@operapadrepio.it.ORCID http://orcid.org/0000-0002-7438-8955

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe comprehensively investigated whether serum acylcarnitine levels are associated with and predict the decline of glomerular filtration rate (GFR) in type 2 diabetes. RESEARCH DESIGN AND

methodsTwo cohorts of patients with type 2 diabetes were investigated: a subset of the aggregate Gargano Mortality Study (aGMS, n=575; 9 years of median follow-up; mean age=60.9±9.8; mean diabetes duration=11.6±9.3) as a discovery set from Italy. A sample from the Joslin Kidney Study (JKS, n=252; 10 years of median follow-up; mean age=57.8±5.6; mean diabetes duration=14.2±7.6) was used as an independent validation set with different environmental and ethnic background for some associated metabolites in the aGMS. MAIN OUTCOME: estimated GFR (eGFR) change over time (mL/min/1.73 m

resultsEleven out of the 40 acylcarnitines (by the AbsoluteIDQTM p180 Kit, BIOCRATES) were significantly associated with the rate of eGFR decline after Bonferroni correction. All 11 molecules were internally validated (p<0.05). Most of these associations survived the adjustment for several confounders, including age, sex, smoking habit, body mass index, glycated hemoglobin, disease duration, albumin excretion rate, triglycerides, low-density lipoprotein and statins treatment (p<0.05). Tiglylcarnitine and methylglutarylcarnitine, but not tetradecenoylcarnitine and hexadecenoylcarnitine, were also associated with eGFR decline in the JKS (p<0.05). Using multivariable least absolute shrinkage and selection operator regression analysis, methylglutarylcarnitine, hydroxyvalerylcarnitine, hexenoylcarnitine, decadienylcarnitine, dodecanedioylcarnitine, tetradecadienylcarnitine were independently associated with kidney function decline. The pairwise correlation among these ranged from -0.02 to 0.55. An acylcarnitine score comprising these six molecules improved discrimination (p<0.01) and reclassification (p<0.001) of two clinical prediction models of GFR decline in diabetes.

conclusionsIn patients with type 2 diabetes, four short, three medium and four long-chain acylcarnitines are associated with the rate of kidney function decline. Adding the acylcarnitine score to clinical prediction models improves the identification of individuals who are at greater risk of progression to kidney failure.

Indexed as

BiomarkersCarnitineDiabetes Mellitus, Type 2Diabetic NephropathiesGlomerular Filtration RateAgedDisease ProgressionFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisacylcarnitineBiomarkersCarnitineBiomarkersDiabetes Mellitus, Type 2Kidney DiseasesPreventive Medicine

Identifiers

PMID42091203
PMCPMC13150908

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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.