Evidence map›Paper›PMID 26194067›Full record

ReviewCytokine2015

IL-1 family members in the pathogenesis and treatment of metabolic disease: Focus on adipose tissue inflammation and insulin resistance.

Dov B Ballak, Rinke Stienstra, Cees J Tack, Charles A Dinarello, Janna A van Diepen

Open access · greenAbstract readReview
In one paragraph

Review in Cytokine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed, 2 pooled it
11.8field-weighted citation impact, top 1% 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

138 citing papers in PubMed, 2 syntheses or guidelines pooled it, 258 citations in OpenAlex.

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78 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

5 authors at 3 institutions in 2 countries.

Dov B BallakDepartment of Medicine, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Integrative Physiology, University of Colorado Boulder, Boulder, CO, USA; Department of Medicine, University of Colorado Denver, Aurora, CO, USA. Electronic address: duby.ballak@radboudumc.nl.
Rinke StienstraDepartment of Medicine, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Human Nutrition, Wageningen University, Wageningen, The Netherlands.
Cees J TackDepartment of Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Charles A DinarelloDepartment of Medicine, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Medicine, University of Colorado Denver, Aurora, CO, USA.
Janna A van DiepenDepartment of Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Radboud University Medical Center · NLRadboud University Nijmegen · NLUniversity of Colorado Denver · US

Funding

Yeast-based HTS Assay Technologies for ProteasesR01AI015614 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DINARELLO, CHARLES ANTHONY · 1985 to 2025
$8.5M
CTL RESPONSE IN ACUTE HIV INFECTIONK08AI001561 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MUKHERJEE, JOIA S · 1998 to 2001
$125k
NIAID NIH HHS AI-1561NIAID NIH HHS R01 AI015614
6 · The paper itself

Abstract

Obesity is characterized by a chronic, low-grade inflammation that contributes to the development of insulin resistance and type 2 diabetes. Cytokines and chemokines produced by immunocompetent cells influence local as well as systemic inflammation and are therefore critical contributors to the pathogenesis of type 2 diabetes. Hence, cytokines that modulate inflammatory responses are emerging as potential targets for intervention and treatment of the metabolic consequences of obesity. The interleukin-1 (IL-1) family of cytokines and receptors are key mediators of innate inflammatory responses and exhibit both pro- and anti-inflammatory functions. During the last decades, mechanistic insights into how the IL-1 family affects the initiation and progression of obesity-induced insulin resistance have increased significantly. Here, we review the current knowledge and understanding, with emphasis on the therapeutic potential of individual members of the IL-1 family of cytokines for improving insulin sensitivity in patients with diabetes.

Indexed as

Adipose TissueDiabetes Mellitus, Type 2HumansInflammationInflammation MediatorsInsulin ResistanceInterleukin-1Interleukin-18Interleukin-1alphaInterleukin-1betaInterleukin 1 Receptor Antagonist ProteinInterleukin-33InterleukinsObesityIL1A protein, humanIL1B protein, humanIL1RN protein, humanIL33 protein, humanIL-38 protein, humanInflammation MediatorsInterleukin-1Interleukin-18Interleukin-1alphaInterleukin-1betaInterleukin 1 Receptor Antagonist ProteinInterleukin-33interleukin 36, humanInterleukinsAdipose tissueInflammationInsulin resistanceInterleukin-1 familyObesity

Identifiers

PMID26194067
PMCPMC4553099
OpenAlexW925051455

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.