Evidence map›Paper›PMID 32029233›Full record

ArticleMolecular metabolism2020

Hepatic ERα accounts for sex differences in the ability to cope with an excess of dietary lipids.

Clara Meda, Mara Barone, Nico Mitro, Federica Lolli, Silvia Pedretti, Donatella Caruso, Adriana Maggi, Sara Della Torre

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
4.8field-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

59 citing papers in PubMed, 86 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Sex Hormones and Metabolic Dysfunction-Associated Steatotic Liver Disease.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Metabolic Messengers: oestradiol.Nature metabolism · 2025
    Review
  13. Review
  14. Sex-specific effects of PNPLA3 I148M.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 1 institution in 1 country.

Clara MedaDepartment of Health Sciences, University of Milan, Italy.
Mara BaroneDepartment of Pharmaceutical Sciences, University of Milan, Italy; Center of Excellence on Neurodegenerative Diseases, University of Milan, Italy.
Nico MitroDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Italy.
Federica LolliDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Italy.
Silvia PedrettiDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Italy.
Donatella CarusoDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Italy.
Adriana MaggiDepartment of Pharmaceutical Sciences, University of Milan, Italy; Center of Excellence on Neurodegenerative Diseases, University of Milan, Italy.
Sara Della TorreDepartment of Pharmaceutical Sciences, University of Milan, Italy; Center of Excellence on Neurodegenerative Diseases, University of Milan, Italy. Electronic address: sara.dellatorre@unimi.it.
University of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAmong obesity-associated metabolic diseases, non-alcoholic fatty liver disease (NAFLD) represents an increasing public health issue due to its emerging association with atherogenic dyslipidemia and cardiovascular diseases (CVDs). The lower prevalence of NAFLD in pre-menopausal women compared with men or post-menopausal women led us to hypothesize that the female-inherent ability to counteract this pathology might strongly rely on estrogen signaling. In female mammals, estrogen receptor alpha (ERα) is highly expressed in the liver, where it acts as a sensor of the nutritional status and adapts the metabolism to the reproductive needs. As in the male liver this receptor is little expressed, we here hypothesize that hepatic ERα might account for sex differences in the ability of males and females to cope with an excess of dietary lipids and counteract the accumulation of lipids in the liver.

methodsThrough liver metabolomics and transcriptomics we analyzed the relevance of hepatic ERα in the metabolic response of males and females to a diet highly enriched in fats (HFD) as a model of diet-induced obesity.

resultsThe study shows that the hepatic ERα strongly contributes to the sex-specific response to an HFD and its action accounts for opposite consequences for hepatic health in males and females.

conclusionThis study identified hepatic ERα as a novel target for the design of sex-specific therapies against fatty liver and its cardio-metabolic consequences.

Indexed as

Diet, High-FatSex CharacteristicsAnimalsEstrogen Receptor alphaFemaleLipidsLiverMaleMiceMice, KnockoutNon-alcoholic Fatty Liver DiseaseEstrogen Receptor alphaLipidsAmino acidsERαEstrogenFatty liverLiver metabolismSex differences

Identifiers

PMID32029233
PMCPMC6957843
OpenAlexW2995121531

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.