Evidence map›Paper›PMID 30260562›Full record

ArticleAging cell2018

Effects of aging on liver microcirculatory function and sinusoidal phenotype.

Raquel Maeso-Díaz, Martí Ortega-Ribera, Anabel Fernández-Iglesias, Diana Hide, Leticia Muñoz, Amelia J Hessheimer, Sergi Vila, Rubén Francés, Constantino Fondevila, Agustín Albillos and 5 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

84 citing papers in PubMed, 161 citations in OpenAlex.

  1. Article
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  7. Role of cellular senescence in hepatic diseases (Review).International journal of molecular medicine · 2025
    Review
  8. Article
  9. Liver, ageing and disease.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  10. Review
  11. Stem cell-based therapeutic strategies for liver aging.Liver research (Beijing, China) · 2025
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. A CommonOxidative medicine and cellular longevity · 2025
    Article

24 more citing papers are in PubMed but not listed here.

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

15 authors at 7 institutions in 4 countries.

Raquel Maeso-DíazLiver Vascular Biology Research Group, Barcelona Hepatic Hemodynamic Laboratory, IDIBAPS Biomedical Research Institute, University of Barcelona Medical School, Barcelona, Spain.
Martí Ortega-RiberaLiver Vascular Biology Research Group, Barcelona Hepatic Hemodynamic Laboratory, IDIBAPS Biomedical Research Institute, University of Barcelona Medical School, Barcelona, Spain.
Anabel Fernández-IglesiasLiver Vascular Biology Research Group, Barcelona Hepatic Hemodynamic Laboratory, IDIBAPS Biomedical Research Institute, University of Barcelona Medical School, Barcelona, Spain.
Diana HideLiver Vascular Biology Research Group, Barcelona Hepatic Hemodynamic Laboratory, IDIBAPS Biomedical Research Institute, University of Barcelona Medical School, Barcelona, Spain.
Leticia MuñozBiomedical Research Networking Center in Hepatic and Digestive Diseases (CIBEREHD), Madrid, Spain.
Amelia J HessheimerBiomedical Research Networking Center in Hepatic and Digestive Diseases (CIBEREHD), Madrid, Spain.
Sergi VilaLiver Vascular Biology Research Group, Barcelona Hepatic Hemodynamic Laboratory, IDIBAPS Biomedical Research Institute, University of Barcelona Medical School, Barcelona, Spain.
Rubén FrancésBiomedical Research Networking Center in Hepatic and Digestive Diseases (CIBEREHD), Madrid, Spain.
Constantino FondevilaBiomedical Research Networking Center in Hepatic and Digestive Diseases (CIBEREHD), Madrid, Spain.
Agustín AlbillosBiomedical Research Networking Center in Hepatic and Digestive Diseases (CIBEREHD), Madrid, Spain.
Carmen PeraltaBiomedical Research Networking Center in Hepatic and Digestive Diseases (CIBEREHD), Madrid, Spain.
Jaime BoschLiver Vascular Biology Research Group, Barcelona Hepatic Hemodynamic Laboratory, IDIBAPS Biomedical Research Institute, University of Barcelona Medical School, Barcelona, Spain.
Frank TackeDept of Medicine III, University Hospital Aachen, Aachen, Germany.
Victoria C CoggerCentre for Education and Research on Ageing & ANZAC Research Institute, University of Sydney and Concord Hospital, Sydney, Australia.
Jordi Gracia-SanchoLiver Vascular Biology Research Group, Barcelona Hepatic Hemodynamic Laboratory, IDIBAPS Biomedical Research Institute, University of Barcelona Medical School, Barcelona, Spain.ORCID 0000-0001-7736-4089
Centro de Investigación Biomédica en Red · ESInstitut d'Investigacions Biomèdiques de Barcelona · ESUniversidad de Alcalá · ESUniversity Hospital of Bern · CHFundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana · ESThe University of Sydney · AUUniversitätsklinikum Aachen · DE

Funding

CERCA Program from the Generalitat de CatalunyaEuropean Union FEDER FundsInstituto de Salud Carlos III CD15/00050Instituto de Salud Carlos III FIS PI14/00029Instituto de Salud Carlos III FIS PI17/00012Instituto de Salud Carlos III iPFIS IFI15/00037Instituto de Salud Carlos III iPFIS IFI16/00016"una manera de hacer Europa,"
6 · The paper itself

Abstract

The socioeconomic and medical improvements of the last decades have led to a relevant increase in the median age of worldwide population. Although numerous studies described the impact of aging in different organs and the systemic vasculature, relatively little is known about liver function and hepatic microcirculatory status in the elderly. In this study, we aimed at characterizing the phenotype of the aged liver in a rat model of healthy aging, particularly focusing on the microcirculatory function and the molecular status of each hepatic cell type in the sinusoid. Moreover, major findings of the study were validated in young and aged human livers. Our results demonstrate that healthy aging is associated with hepatic and sinusoidal dysfunction, with elevated hepatic vascular resistance and increased portal pressure. Underlying mechanisms of such hemodynamic disturbances included typical molecular changes in the cells of the hepatic sinusoid and deterioration in hepatocyte function. In a specific manner, liver sinusoidal endothelial cells presented a dysfunctional phenotype with diminished vasodilators synthesis, hepatic macrophages exhibited a proinflammatory state, while hepatic stellate cells spontaneously displayed an activated profile. In an important way, major changes in sinusoidal markers were confirmed in livers from aged humans. In conclusion, our study demonstrates for the first time that aging is accompanied by significant liver sinusoidal deregulation suggesting enhanced sinusoidal vulnerability to chronic or acute injuries.

Indexed as

MicrocirculationAgingAnimalsBacterial TranslocationEndothelial CellsGene Expression Regulation, DevelopmentalHemodynamicsHepatic Stellate CellsHepatocytesImmunity, InnateInflammationLiverMaleModels, AnimalPhenotypeRats, Wistar

Identifiers

PMID30260562
PMCPMC6260924
OpenAlexW2892020139

What OpenQuestion holds

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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 OpenQuestion graph.