Evidence map›Paper›PMID 23332087›Full record

ArticleHepatology research : the official journal of the Japan Society of Hepatology2013

Liver and diabetes. A vicious circle.

Paola Loria, Amedeo Lonardo, Frank Anania

Open access · bronzeAbstract read
In one paragraph

Article in Hepatology research : the official journal of the Japan Society of Hepatology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed, 1 pooled it
8.8field-weighted citation impact, top 2% 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

107 citing papers in PubMed, 1 synthesis or guideline pooled it, 206 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  15. Exploring the Biological Effects of Anti-Diabetic Vanadium Compounds in the Liver, Heart and Brain.Diabetes, metabolic syndrome and obesity : targets and therapy · 2024
    Review
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  19. Observational
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47 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

3 authors at 2 institutions in 2 countries.

Paola LoriaUniversity of Modena and Reggio Emilia, Modena, Italy Emory University School of Medicine, Atlanta, Georgia, USA.
Amedeo Lonardo
Frank Anania
Emory University · USUniversity of Modena and Reggio Emilia · IT

Funding

The Role of Leptin in Liver FibrogenesisR01DK062092 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI ANANIA, FRANK A · 2003 to 2016
$3.9M
Potential Mechanisms of Glucagon-like peptide-1 in Fatty Liver DiseaseR01DK075397 · NIDDK · EMORY UNIVERSITY · PI ANANIA, FRANK A · 2007 to 2010
$1.1M
The Role of Leptin in Liver FibrogenesisR56DK062092 · NIDDK · EMORY UNIVERSITY · PI ANANIA, FRANK A · 2012 to 2012
$207k
NIDDK NIH HHS R01 DK062092NIDDK NIH HHS R01 DK075397NIDDK NIH HHS R56 DK062092
6 · The paper itself

Abstract

The complex and bi-directional relationship linking the liver and diabetes has recently gained intense new interest. This critical review of the published work aims to highlight the most recent basic and clinical data underlying the development of type 2 diabetes, in those with non-alcoholic fatty liver disease. Moreover, the potentially detrimental effects of type 2 diabetes in liver injury are also discussed in each of the two sections of the present paper. Fatty liver and diabetes share insulin resistance as their chief pathogenic determinant. The roles of the hypothalamus, the intestinal microbiome, white adipose tissue and inflammation are discussed in detail. Molecular insights into hepatocyte insulin resistance as the initiator of systemic insulin resistance are also presented with full coverage of the danger of fatty acids. Lipotoxicity, apoptosis, lipoautophagy, endoplasmic reticular stress response and recent developments in genetics are discussed. Closing the circle, special emphasis is given to biochemical pathways and clinical evidence supporting the role of type 2 diabetes as a risk factor for the development of progressive liver disease, including non-alcoholic steatohepatitis, cirrhosis and primary liver cancer. In conclusion, data support non-alcoholic fatty liver disease as a risk factor for the development of type 2 diabetes which is, in turn, a major contributor to progressive liver disease. This pathway leading from fatty liver to type 2 diabetes and back from the latter to the progressive liver disease is a vicious circle.

Identifiers

PMID23332087
PMCPMC3733501
OpenAlexW1541793964

What OpenQuestion holds

Textmetadata
LicenceTDM
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.