Evidence mapPaperPMID 38635405Full record

ArticleThe Journal of clinical endocrinology and metabolism2025

Effects of Hypertriglyceridemia With or Without NEFA Elevation on β-cell Function and Insulin Clearance and Sensitivity.

Domenico Tricò, Eleni Rebelos, Brenno Astiarraga, Simona Baldi, Tiziana Scozzaro, Luca Sacchetta, Martina Chiriacò, Andrea Mari, Ele Ferrannini, Elza Muscelli and 1 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

6 citing papers in PubMed, 8 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 5 institutions in 4 countries.

Domenico TricòDepartment of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.ORCID 0000-0002-7633-1346
Eleni RebelosDepartment of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.ORCID 0000-0003-3050-8692
Brenno AstiarragaHospital Universitari Joan XXIII de Tarragona, Institut d'Investigació Sanitària Pere Virgili (IISPV), 43005 Tarragona, Spain.
Simona BaldiDepartment of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.
Tiziana ScozzaroDepartment of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.
Luca SacchettaDepartment of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.
Martina ChiriacòDepartment of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.
Andrea MariInstitute of Neuroscience, National Research Council, 35127 Padua, Italy.
Ele FerranniniInstitute of Clinical Physiology, National Research Council, 56124 Pisa, Italy.
Elza MuscelliDepartment of Internal Medicine, University of Campinas, 13083-887 Campinas, Brazil.ORCID 0000-0001-6979-3553
Andrea NataliDepartment of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.
University of Pisa · ITInstituto de Salud Carlos III · ESIstituto di Fisiologia Clinica · ITNeuroscience Institute · ITUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

European Foundation for the Study of Diabetes
6 · The paper itself

Abstract

contextHypertriglyceridemia is a risk factor for developing type 2 diabetes (T2D) and might contribute to its pathogenesis either directly or through elevation of nonesterified fatty acids (NEFAs).

objectiveThis study aimed at comparing the glucometabolic effects of acute hypertriglyceridemia alone or combined with NEFA elevation in subjects without diabetes.

methodsTwenty-two healthy lean volunteers underwent 5-hour intravenous infusions of either saline or Intralipid, without (n = 12) or with heparin (I + H; n = 10) to activate the release of NEFAs. Oral glucose tolerance tests (OGTTs) were performed during the last 3 hours of infusion. Insulin sensitivity, insulin secretion rate (ISR), model-derived β-cell function, and insulin clearance were measured after 2 hours of lipid infusion and during the OGTTs.

resultsIn fasting conditions, both lipid infusions increased plasma insulin and ISR and reduced insulin clearance without affecting plasma glucose and insulin sensitivity. These effects on insulin and ISR were more pronounced for I + H than Intralipid alone. During the OGTT, the lipid infusions markedly impaired glucose tolerance, increased plasma insulin and ISR, and decreased insulin sensitivity and clearance, without significant group differences. Intralipid alone inhibited glucose-stimulated insulin secretion (ie, β-cell glucose sensitivity) and increased β-cell potentiation, whereas I + H had neutral effects on these β-cell functions.

conclusionIn healthy nonobese subjects, mild acute hypertriglyceridemia directly reduces glucose tolerance and insulin sensitivity and clearance, and has selective and opposite effects on β-cell function that are neutralized by NEFAs. These findings provide new insight into plausible biological signals that generate and sustain insulin resistance and chronic hyperinsulinemia in the development of T2D.

Indexed as

Fatty Acids, NonesterifiedHypertriglyceridemiaInsulinInsulin ResistanceInsulin-Secreting CellsAdultBlood GlucoseDiabetes Mellitus, Type 2EmulsionsFat Emulsions, IntravenousFemaleGlucose Tolerance TestHumansInsulin SecretionMalePhospholipidsBlood GlucoseEmulsionsFat Emulsions, IntravenousFatty Acids, NonesterifiedInsulinPhospholipidsSoybean Oilsoybean oil, phospholipid emulsionhypertriglyceridemiainsulin clearanceinsulin secretioninsulin sensitivitynonesterified fatty acidsoral glucose tolerancetype 2 diabetes

Identifiers

PMID38635405
PMCPMC11918624
OpenAlexW4394912120

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.