Evidence map›Paper›PMID 31921154›Full record

ReviewFrontiers in immunology2019

Macrophage Function in the Pathogenesis of Non-alcoholic Fatty Liver Disease: The Mac Attack.

Jarren R Oates, Melanie C McKell, Maria E Moreno-Fernandez, Michelle S M A Damen, George S Deepe, Joseph E Qualls, Senad Divanovic

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Annals of medicine · 2023
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Vsig4Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Article
  19. Article
  20. Customized liver organoids as an advancedInternational journal of biological sciences · 2023
    Review
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

7 authors at 2 institutions in 1 country.

Jarren R OatesDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Melanie C McKellDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Maria E Moreno-FernandezDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Michelle S M A DamenDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
George S DeepeDepartment of Medicine, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Joseph E QuallsDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Senad DivanovicDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati Medical Center · US

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Alexander Miethke · 2007 to 2026
$24.4M
Immunopathogenesis of Non-alcoholic Fatty Liver DiseaseR01DK099222 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Senad Divanovic · 2013 to 2026
$5.6M
L-citrulline and anti-tuberculosis host defenseR01AI116668 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI QUALLS, JOSEPH E · 2016 to 2020
$1.9M
Pathogenesis and therapeutic targeting of immune disordersT32AI118697 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI HILDEMAN, DAVID A · 2016 to 2020
$683k
NIAID NIH HHS R01 AI116668NIAID NIH HHS T32 AI118697NIDDK NIH HHS P30 DK078392NIDDK NIH HHS R01 DK099222
6 · The paper itself

Abstract

Obesity is a prevalent predisposing factor to non-alcoholic fatty liver disease (NAFLD), the most common chronic liver disease in the developed world. NAFLD spectrum of disease involves progression from steatosis (NAFL), to steatohepatitis (NASH), cirrhosis and hepatocellular carcinoma (HCC). Despite clinical and public health significance, current FDA approved therapies for NAFLD are lacking in part due to insufficient understanding of pathogenic mechanisms driving disease progression. The etiology of NAFLD is multifactorial. The induction of both systemic and tissue inflammation consequential of skewed immune cell metabolic state, polarization, tissue recruitment, and activation are central to NAFLD progression. Here, we review the current understanding of the above stated cellular and molecular processes that govern macrophage contribution to NAFLD pathogenesis and how adipose tissue and liver crosstalk modulates macrophage function. Notably, the manipulation of such events may lead to the development of new therapies for NAFLD.

Indexed as

Disease SusceptibilityAnimalsBiomarkersCell MovementCell PlasticityCytokinesDisease ManagementDisease Models, AnimalEnergy MetabolismHumansInflammation MediatorsMacrophagesNon-alcoholic Fatty Liver DiseaseSignal TransductionBiomarkersCytokinesInflammation MediatorscytokinesinflammationmacrophagemetabolismNAFLD

Identifiers

PMID31921154
PMCPMC6922022
OpenAlexW2991270297

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.