Evidence map›Paper›PMID 31785104›Full record

ArticleHepatology (Baltimore, Md.)2020

Insights From Liver-Humanized Mice on Cholesterol Lipoprotein Metabolism and LXR-Agonist Pharmacodynamics in Humans.

Mirko E Minniti, Matteo Pedrelli, Lise-Lotte Vedin, Anne-Sophie Delbès, Raphaël G P Denis, Katariina Öörni, Claudia Sala, Chiara Pirazzini, Divya Thiagarajan, Harri J Nurmi and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  5. Article
  6. Mice Engrafted with Human Liver Cells.Seminars in liver disease · 2024
    Review
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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

20 authors at 10 institutions in 6 countries.

Mirko E MinnitiDepartment of Laboratory Medicine, Division of Clinical Chemistry, Karolinska Institute, Stockholm, Sweden.ORCID 0000-0002-5476-145X
Matteo PedrelliDepartment of Laboratory Medicine, Division of Clinical Chemistry, Karolinska Institute, Stockholm, Sweden.
Lise-Lotte VedinDepartment of Laboratory Medicine, Division of Clinical Chemistry, Karolinska Institute, Stockholm, Sweden.
Anne-Sophie DelbèsUnit of Functional and Adaptive Biology, Paris Diderot University, Sorbonne Paris Cité, Paris, France.
Raphaël G P DenisUnit of Functional and Adaptive Biology, Paris Diderot University, Sorbonne Paris Cité, Paris, France.
Katariina ÖörniAtherosclerosis Research Laboratory, Wihuri Research Institute, Helsinki, Finland.
Claudia SalaDepartment of Physics and Astronomy, University of Bologna, Bologna, Italy.
Chiara PirazziniInstitute of Neurological Sciences of Bologna, Bologna, Italy.
Divya ThiagarajanDepartment of Laboratory Medicine, Clinical Research Center, Karolinska Institute, Stockholm, Sweden.
Harri J NurmiAtherosclerosis Research Laboratory, Wihuri Research Institute, Helsinki, Finland.
Markus GrompeDepartment of Pediatrics, Oregon Stem Cell Center, Oregon Health and Science University, Portland, OR.
Kevin MillsCenter for Inborn Errors of Metabolism, University College London, London, UK.
Paolo GaragnaniDepartment of Laboratory Medicine, Division of Clinical Chemistry, Karolinska Institute, Stockholm, Sweden.
Ewa C S EllisDepartment of Clinical Science, Intervention and Technology, Division of Surgery, Karolinska Institute at Karolinska University Hospital Huddinge, Stockholm, Sweden.ORCID 0000-0002-3057-5337
Stephen C StromDepartment of Laboratory Medicine, Division of Pathology, Karolinska Institute, Stockholm, Sweden.
Serge H LuquetUnit of Functional and Adaptive Biology, Paris Diderot University, Sorbonne Paris Cité, Paris, France.
Elizabeth M WilsonYecuris Corporation, Tualatin, OR.
John BialYecuris Corporation, Tualatin, OR.
Knut R SteffensenDepartment of Laboratory Medicine, Division of Clinical Chemistry, Karolinska Institute, Stockholm, Sweden.
Paolo PariniDepartment of Laboratory Medicine, Division of Clinical Chemistry, Karolinska Institute, Stockholm, Sweden.
Karolinska Institutet · SEUniversité Paris Cité · FRKarolinska University Hospital · SEYecuris (United States) · USInstitute of Neurological Sciences · ITOregon Health & Science University · USUniversity College London · GBUniversity of Bologna · ITUniversity of Helsinki · FIWihuri Research Institute · FI

Funding

Department of Health
6 · The paper itself

Abstract

BACKGROUND AND

aimsGenetically modified mice have been used extensively to study human disease. However, the data gained are not always translatable to humans because of major species differences. Liver-humanized mice (LHM) are considered a promising model to study human hepatic and systemic metabolism. Therefore, we aimed to further explore their lipoprotein metabolism and to characterize key hepatic species-related, physiological differences. APPROACH AND

resultsFah

conclusionsLHM represent an interesting translatable model of human hepatic and lipoprotein metabolism. Because several metabolic parameters displayed donor dependency, LHM may also be used in studies for personalized medicine.

Indexed as

AnimalsBenzoatesBenzylaminesCholesterolHepatocytesHumansLipoproteinsLiverLiver X ReceptorsMaleMiceMice, KnockoutBenzoatesBenzylaminesCholesterolGW 3965lipoprotein cholesterolLipoproteinsLiver X Receptors

Identifiers

PMID31785104
PMCPMC7496592
OpenAlexW2990720937

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.