Evidence map›Paper›PMID 36161905›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Leptin treatment has vasculo-protective effects in lipodystrophic mice.

Paulina Elena Stürzebecher, Susan Kralisch, Marie Ruth Schubert, Vanina Filipova, Annett Hoffmann, Fabiana Oliveira, Bilal N Sheikh, Matthias Blüher, Alexander Kogel, Markus Scholz and 9 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

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  14. Adipokines in atherosclerosis: unraveling complex roles.Frontiers in cardiovascular medicine · 2023
    Review
  15. Article
  16. Leptin treatment has vasculo-protective effects in lipodystrophic mice.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Article
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

19 authors at 6 institutions in 2 countries.

Paulina Elena StürzebecherKlinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, 04103, Germany.ORCID 0000-0001-5297-7137
Susan KralischMedical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, 04103, Germany.
Marie Ruth SchubertKlinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, 04103, Germany.
Vanina FilipovaKlinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, 04103, Germany.ORCID 0000-0003-0854-4750
Annett HoffmannMedical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, 04103, Germany.
Fabiana OliveiraHelmholtz Institute for Metabolic, Obesity and Vascular Research (HI-MAG) of the Helmholtz Zentrum München at the University of Leipzig and University Hospital Leipzig, Leipzig, 04103, Germany.
Bilal N SheikhHelmholtz Institute for Metabolic, Obesity and Vascular Research (HI-MAG) of the Helmholtz Zentrum München at the University of Leipzig and University Hospital Leipzig, Leipzig, 04103, Germany.ORCID 0000-0002-1970-6236
Matthias BlüherMedical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, 04103, Germany.ORCID 0000-0003-0208-2065
Alexander KogelKlinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, 04103, Germany.ORCID 0000-0002-1842-4480
Markus ScholzInstitute for Medical Informatics, Statistics and Epidemiology, Medical Faculty, University of Leipzig, Leipzig, 04107, Germany.
Karoline Elizabeth KokotKlinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, 04103, Germany.ORCID 0000-0002-8130-4289
Stephan ErbeKlinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, 04103, Germany.ORCID 0000-0003-0139-8981
Jasmin Marga KneuerKlinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, 04103, Germany.ORCID 0000-0003-0273-3614
Thomas EbertMedical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, 04103, Germany.ORCID 0000-0003-1683-9276
Mathias FasshauerInstitute of Nutritional Science, Justus-Liebig-University, Giessen, 35390, Germany.
Konstanze MiehleMedical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, 04103, Germany.
Ulrich LaufsKlinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, 04103, Germany.ORCID 0000-0003-2620-9323
Anke TönjesMedical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, 04103, Germany.
Jes-Niels BoeckelKlinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, 04103, Germany.
University Hospital Leipzig · DEHelmholtz Zentrum München · DEJustus-Liebig-Universität Gießen · DEKarolinska Institutet · SELeipzig University · DEUniversitätsklinikum Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipodystrophy syndromes (LDs) are characterized by loss of adipose tissue, metabolic complications such as dyslipidemia, insulin resistance, and fatty liver disease, as well as accelerated atherosclerosis. As a result of adipose tissue deficiency, the systemic concentration of the adipokine leptin is reduced. A current promising therapeutic option for patients with LD is treatment with recombinant leptin (metreleptin), resulting in reduced risk of mortality. Here, we investigate the effects of leptin on endothelial to mesenchymal transition (EndMT), which impair the functional properties of endothelial cells and promotes atherogenesis in LD. Leptin treatment reduced inflammation and TGF-β2-induced expression of mesenchymal genes and prevented impairment of endothelial barrier function. Treatment of lipodystrophic- and atherosclerosis-prone animals (Ldlr

Indexed as

Endothelial CellsEpithelial-Mesenchymal TransitionGrowth Differentiation Factor 15LeptinLipodystrophyAnimalsAtherosclerosisMiceTransforming Growth Factor beta2Gdf15 protein, mouseGrowth Differentiation Factor 15LeptinTransforming Growth Factor beta2atherosclerosisEndMTGDF15leptinlipodystrophy

Identifiers

PMID36161905
PMCPMC9546548
OpenAlexW4297251023

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.