Evidence map›Paper›PMID 25623940›Full record

ReviewHamostaseologie2015

Tissue factor pathways linking obesity and inflammation.

W Ruf, F Samad

Abstract readReview
In one paragraph

Review in Hamostaseologie, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. The plasminogen receptor Plg-RJournal of thrombosis and haemostasis : JTH · 2022
    Article
  7. Review
  8. Abdominal Obesity, Adipokines and Non-communicable Diseases.The Journal of steroid biochemistry and molecular biology · 2020
    Review
  9. Article
  10. Article
  11. Adipogenesis: A Necessary but Harmful Strategy.International journal of molecular sciences · 2019
    Review
  12. Article
  13. Article
  14. Observational
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

2 authors at 1 institution in 1 country.

W RufWolfram Ruf, M.D., Professor, Department of Immunology and Microbial Science, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, Mail stop: SP258, Tel. 858/784-2748, Fax -8480, E-mail: ruf@uni-mainz.de, ruf@scripps.edu.
F Samad
Scripps Research Institute · US

Funding

THROMBUS FORMATION IN BABOONSP01HL031950 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI GRIFFIN, JOHN H · 1985 to 2015
$29.4M
TF Signaling in Systemic InflammationR01HL077753 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI RUF, WOLFRAM · 2004 to 2011
$3.6M
Therapeutic Opportunities of Targeting Tissue Factor Signaling in ObesityR01HL104232 · NHLBI · TORREY PINES INST FOR MOLECULAR STUDIES · PI SAMAD, FAHUMIYA · 2011 to 2014
$2.4M
Ceramide and cardiovascular risk in obesityR01HL071146 · NHLBI · TORREY PINES INST FOR MOLECULAR STUDIES · PI SAMAD, FAHUMIYA · 2004 to 2008
$2.2M
NHLBI NIH HHS HL104232NHLBI NIH HHS HL31950NHLBI NIH HHS HL71146NHLBI NIH HHS HL77753NHLBI NIH HHS P01 HL031950NHLBI NIH HHS R01 HL071146NHLBI NIH HHS R01 HL077753NHLBI NIH HHS R01 HL104232
6 · The paper itself

Abstract

Obesity is a major cause for a spectrum of metabolic syndrome-related diseases that include insulin resistance, type 2 diabetes, and steatosis of the liver. Inflammation elicited by macrophages and other immune cells contributes to the metabolic abnormalities in obesity. In addition, coagulation activation following tissue factor (TF) upregulation in adipose tissue is frequently found in obese patients and particularly associated with diabetic complications. Genetic and pharmacological evidence indicates that TF makes significant contributions to the development of the metabolic syndrome by signaling through G protein-coupled protease activated receptors (PARs). Adipocyte TF-PAR2 signaling contributes to diet-induced obesity by decreasing metabolism and energy expenditure, whereas hematopoietic TF-PAR2 signaling is a major cause for adipose tissue inflammation, hepatic steatosis and inflammation, as well as insulin resistance. In the liver of mice on a high fat diet, PAR2 signaling increases transcripts of key regulators of gluconeogenesis, lipogenesis and inflammatory cytokines. Increased markers of hepatic gluconeogenesis correlate with decreased activation of AMP-activated protein kinase (AMPK), a known regulator of these pathways and a target for PAR2 signaling. Clinical markers of a TF-induced prothrombotic state may thus indicate a risk in obese patient for developing complications of the metabolic syndrome.

Indexed as

AnimalsHumansImmunologic FactorsInflammationMetabolic SyndromeModels, ImmunologicalObesityReceptor, PAR-2Signal TransductionThromboplastinImmunologic FactorsReceptor, PAR-2ThromboplastinPARsTF

Identifiers

PMID25623940
PMCPMC4516700
OpenAlexW2099408369

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.