Evidence map›Paper›PMID 27895822›Full record

ArticleWorld journal of diabetes2016

Linagliptin alleviates fatty liver disease in diabetic

Svetlana V Michurina, Irina Ju Ishenko, Vadim V Klimontov, Sergey A Archipov, Natalia E Myakina, Marina A Cherepanova, Eugenii L Zavjalov, Galina V Koncevaya, Vladimir I Konenkov

Open access · diamondAbstract read
In one paragraph

Article in World journal of diabetes, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Observational
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  9. Unexpected metabolic disorders induced by endocrine disruptors inProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
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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

9 authors at 2 institutions in 2 countries.

Svetlana V MichurinaSvetlana V Michurina, Irina Ju Ishenko, Sergey A Archipov, Laboratory of Functional Morphology, Scientific Institute of Clinical and Experimental Lymphology, 630060 Novosibirsk, Russia.
Irina Ju IshenkoSvetlana V Michurina, Irina Ju Ishenko, Sergey A Archipov, Laboratory of Functional Morphology, Scientific Institute of Clinical and Experimental Lymphology, 630060 Novosibirsk, Russia.
Vadim V KlimontovSvetlana V Michurina, Irina Ju Ishenko, Sergey A Archipov, Laboratory of Functional Morphology, Scientific Institute of Clinical and Experimental Lymphology, 630060 Novosibirsk, Russia.
Sergey A ArchipovSvetlana V Michurina, Irina Ju Ishenko, Sergey A Archipov, Laboratory of Functional Morphology, Scientific Institute of Clinical and Experimental Lymphology, 630060 Novosibirsk, Russia.
Natalia E MyakinaSvetlana V Michurina, Irina Ju Ishenko, Sergey A Archipov, Laboratory of Functional Morphology, Scientific Institute of Clinical and Experimental Lymphology, 630060 Novosibirsk, Russia.
Marina A CherepanovaSvetlana V Michurina, Irina Ju Ishenko, Sergey A Archipov, Laboratory of Functional Morphology, Scientific Institute of Clinical and Experimental Lymphology, 630060 Novosibirsk, Russia.
Eugenii L ZavjalovSvetlana V Michurina, Irina Ju Ishenko, Sergey A Archipov, Laboratory of Functional Morphology, Scientific Institute of Clinical and Experimental Lymphology, 630060 Novosibirsk, Russia.
Galina V KoncevayaSvetlana V Michurina, Irina Ju Ishenko, Sergey A Archipov, Laboratory of Functional Morphology, Scientific Institute of Clinical and Experimental Lymphology, 630060 Novosibirsk, Russia.
Vladimir I KonenkovSvetlana V Michurina, Irina Ju Ishenko, Sergey A Archipov, Laboratory of Functional Morphology, Scientific Institute of Clinical and Experimental Lymphology, 630060 Novosibirsk, Russia.
Institute of Clinical and Experimental Lymphology · RUInstitute of Cytology and Genetics · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo study the effects of linagliptin on the structural signs of non-alcoholic fatty liver disease (NAFLD) in

methodsMale diabetic

resultsIn 18-wk-old diabetic mice, liver steatosis (predominantly microvesicular and mediovesicular steatosis) was accompanied by dilation of the roots of the lymphatic system, interlobular blood vessels and bile canaliculi. Compared to saline-treated mice, linagliptin-treated mice exhibited a reduction in the mean numeral densities of hepatocytes with lipid droplets (92.4% ± 1.7%

conclusionThe DPP4 inhibitor linagliptin alleviates liver steatosis and structural changes in the hepatic microvasculature and lymphatic roots in a model of NAFLD in diabetic

Indexed as

DiabetesDipeptidyl peptidase 4LinagliptinNon-alcoholic fatty liver diseaseObesity

Identifiers

PMID27895822
PMCPMC5107713
OpenAlexW2550915286

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.