Evidence map›Paper›PMID 24751397›Full record

ArticleAging2014

Increased hepatic CD36 expression with age is associated with enhanced susceptibility to nonalcoholic fatty liver disease.

Fareeba Sheedfar, Miranda My Sung, Marcela Aparicio-Vergara, Niels J Kloosterhuis, Maria Eugenia Miquilena-Colina, Javier Vargas-Castrillón, Maria Febbraio, René L Jacobs, Alain de Bruin, Manlio Vinciguerra and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

64 citing papers in PubMed, 105 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. HepaticiScience · 2023
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. The role of aging in cancer.Molecular oncology · 2022
    Article
  18. Article
  19. A Transcriptomic Response toInternational journal of molecular sciences · 2022
    Article
  20. Review

4 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

14 authors at 6 institutions in 5 countries.

Fareeba SheedfarUniversity of Groningen, University Medical Center Groningen, Molecular Genetics, Groningen, The Netherlands.
Miranda My Sung
Marcela Aparicio-Vergara
Niels J Kloosterhuis
Maria Eugenia Miquilena-Colina
Javier Vargas-Castrillón
Maria Febbraio
René L Jacobs
Alain de Bruin
Manlio Vinciguerra
Carmelo García-Monzón
Marten H Hofker
Jason Rb Dyck
Debby P Y Koonen
University of Alberta · CAUniversity of Groningen · NLHospital Universitario Santa Cristina · ESThe Royal Free Hospital · GBUniversity Medical Center Groningen · NLUtrecht University · NL

Funding

Canadian Institutes of Health Research MOP125973
6 · The paper itself

Abstract

CD36 has been associated with obesity and diabetes in human liver diseases, however, its role in age-associated nonalcoholic fatty liver disease (NAFLD) is unknown. Therefore, liver biopsies were collected from individuals with histologically normal livers (n=30), and from patients diagnosed with simple steatosis (NAS; n=26). Patients were divided into two groups according to age and liver biopsy samples were immunostained for CD36. NAFLD parameters were examined in young (12-week) and middle-aged (52-week) C57BL/6J mice, some fed with chow-diet and some fed with low-fat (LFD; 10% kcal fat) or high-fat diet (HFD; 60% kcal fat) for 12-weeks. CD36 expression was positively associated with age in individuals with normal livers but not in NAS patients. However, CD36 was predominantly located at the plasma membrane of hepatocytes in aged NAS patients as compared to young. In chow-fed mice, aging, despite an increase in hepatic CD36 expression, was not associated with the development of NAFLD. However, middle-aged mice did exhibit the development of HFD-induced NAFLD, mediated by an increase of CD36 on the membrane. Enhanced CD36-mediated hepatic fat uptake may contribute to an accelerated progression of NAFLD in mice and humans. Therapies to prevent the increase in CD36 expression and/or CD36 from anchoring at the membrane may prevent the development of NAFLD.

Indexed as

AdultAgedAgingAnimalsCD36 AntigensCell MembraneFemaleHepatocytesHumansImmunoblottingImmunohistochemistryLiverMaleMiceMice, Inbred C57BLMiddle AgedCD36 Antigens

Identifiers

PMID24751397
PMCPMC4032795
OpenAlexW2111913630

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.