Evidence map›Paper›PMID 39125267›Full record

ArticleNutrients2024

Extracellular Vesicles Modulate Liver Cells Viability and Reactive Oxygen Species in Patients Following a Very Low-Calorie Ketogenic Diet.

Francesco Balestra, Roberto Negro, Maria De Luca, Nicoletta Depalo, Federica Rizzi, Giorgia Panzetta, Valentina Arrè, Rita Mastrogiacomo, Sergio Coletta, Dolores Stabile and 7 more

Abstract read
In one paragraph

Article in Nutrients, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
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

17 authors.

Francesco BalestraLaboratory of Molecular Medicine, National Institute of Gastroenterology IRCCS "S. de Bellis", Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.ORCID 0009-0009-8853-3533
Roberto NegroLaboratory of Personalized Medicine, National Institute of Gastroenterology IRCCS "S. de Bellis", Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.
Maria De LucaLaboratory of Molecular Medicine, National Institute of Gastroenterology IRCCS "S. de Bellis", Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.ORCID 0000-0002-7827-7742
Nicoletta DepaloInstitute for Chemical-Physical Processes, Italian National Research Council (IPCF)-CNR SS Bari, Via Orabona 4, 70125 Bari, Italy.ORCID 0000-0002-2107-2762
Federica RizziInstitute for Chemical-Physical Processes, Italian National Research Council (IPCF)-CNR SS Bari, Via Orabona 4, 70125 Bari, Italy.ORCID 0000-0001-8891-4218
Giorgia PanzettaLaboratory of Molecular Medicine, National Institute of Gastroenterology IRCCS "S. de Bellis", Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.
Valentina ArrèLaboratory of Personalized Medicine, National Institute of Gastroenterology IRCCS "S. de Bellis", Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.
Rita MastrogiacomoInstitute for Chemical-Physical Processes, Italian National Research Council (IPCF)-CNR SS Bari, Via Orabona 4, 70125 Bari, Italy.ORCID 0009-0007-2184-9205
Sergio ColettaDepartment of Pathology, National Institute of Gastroenterology IRCCS "S. de Bellis", Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.ORCID 0000-0003-3359-7010
Dolores StabileDepartment of Pathology, National Institute of Gastroenterology IRCCS "S. de Bellis", Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.
Pasqua Letizia PesoleDepartment of Pathology, National Institute of Gastroenterology IRCCS "S. de Bellis", Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.ORCID 0000-0003-4675-2075
Nicole CerabinoCenter of Nutrition for the Research and the Care of Obesity and Metabolic Diseases, National Institute of Gastroenterology IRCCS "S. de Bellis", Via Turi 27, 70013 Castellana Grotte, Italy.
Martina Di ChitoCenter of Nutrition for the Research and the Care of Obesity and Metabolic Diseases, National Institute of Gastroenterology IRCCS "S. de Bellis", Via Turi 27, 70013 Castellana Grotte, Italy.
Endrit ShahiniGastroenterology Unit, National Institute of Gastroenterology IRCCS "S. de Bellis", Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.
Gianluigi GiannelliScientific Direction, National Institute of Gastroenterology IRCCS "S. de Bellis", Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.ORCID 0000-0002-5140-8060
Giovanni De PergolaCenter of Nutrition for the Research and the Care of Obesity and Metabolic Diseases, National Institute of Gastroenterology IRCCS "S. de Bellis", Via Turi 27, 70013 Castellana Grotte, Italy.ORCID 0000-0003-0020-3273
Maria Principia ScavoLaboratory of Molecular Medicine, National Institute of Gastroenterology IRCCS "S. de Bellis", Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.ORCID 0000-0002-0812-4441

Funding

Governo Italiano RC2024Italian Ministry of Health RC 2024
6 · The paper itself

Abstract

The VLCKD is a diet recognized to promote rapid fat mobilization and reduce inflammation, hepatic steatosis, and liver fibrosis. Extracellular vesicles (EVs) mediate cell-to-cell communication. The aim of the study is to investigate the role of circulating EVs in cell proliferation, ketone bodies, and ROS production in patients on an 8-week VLCKD regimen. Participants were classified as responders (R) or non-responders (NR) to VLCKD treatment based on their fibroscan results. In vitro experiments with the hepatic cell lines HEPA-RG (normal hepatocytes) and LX-2 (stellate cells) were conducted to investigate the effects of circulating EVs on cell viability, ROS production, and ketone body presence. The findings reveal a notable reduction in cell viability in both cell lines when treated with exosomes (EXOs). In contrast, treatment with microvesicles (MVs) did not appear to affect cell viability, which remained unchanged. Additionally, the levels of ketone bodies measured in urine were not consistently correlated with the reduction of fibrosis in responders (R). Similarly, an increase in ketone bodies was observed in non-responders (NR), which was also not aligned with the expected reduction in fibrosis. This inconsistency stands in stark contrast to the levels of Reactive Oxygen Species (ROS), which exhibited a clear and consistent pattern in accordance with the dietary intervention. Finally, in this preliminary study, ROS has been identified as a potential diet adherence marker for VLCKD patients; the ROS levels reliably follow the progression of the fibrosis response, providing a more accurate reflection of the therapeutic effects.

Indexed as

Cell SurvivalDiet, KetogenicExtracellular VesiclesHepatocytesKetone BodiesReactive Oxygen SpeciesAdultCell LineExosomesFemaleHumansLiver CirrhosisMaleMiddle AgedKetone BodiesReactive Oxygen Speciescell proliferationextracellular vesiclesliver fibrosisROSVLCKD

Identifiers

PMID39125267
PMCPMC11314450

What Socratic holds

Textmetadata
LicenceCC BY
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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.