Evidence map›Paper›PMID 32592090›Full record

ArticleJournal of cardiovascular translational research2021

Therapeutic Targeting of Interleukin-11 Signalling Reduces Pressure Overload-Induced Cardiac Fibrosis in Mice.

Ben Corden, Wei-Wen Lim, Weihua Song, Xie Chen, Nicole S J Ko, Liping Su, Nicole G Z Tee, Eleonora Adami, Sebastian Schafer, Stuart A Cook

Abstract read
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In one paragraph

Article in Journal of cardiovascular translational research, 2021. 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
2.4field-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

14 citing papers in PubMed, 23 citations in OpenAlex.

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  13. Towards precision medicine in heart failure.Nature reviews. Cardiology · 2021
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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

10 authors at 2 institutions in 3 countries.

Ben Corden *National Heart Research Institute Singapore, National Heart Centre Singapore, Singapore, Singapore.ORCID http://orcid.org/0000-0003-2136-2994
Wei-Wen Lim *National Heart Research Institute Singapore, National Heart Centre Singapore, Singapore, Singapore.
Weihua SongNational Heart Research Institute Singapore, National Heart Centre Singapore, Singapore, Singapore.
Xie ChenNational Heart Research Institute Singapore, National Heart Centre Singapore, Singapore, Singapore.
Nicole S J KoCardiovascular and Metabolic Disorders Program, Duke-National University of Singapore Medical School, 8 College Road, Singapore, 169857, Singapore.
Liping SuNational Heart Research Institute Singapore, National Heart Centre Singapore, Singapore, Singapore.
Nicole G Z TeeNational Heart Research Institute Singapore, National Heart Centre Singapore, Singapore, Singapore.
Eleonora AdamiCardiovascular and Metabolic Disorders Program, Duke-National University of Singapore Medical School, 8 College Road, Singapore, 169857, Singapore.
Sebastian SchaferNational Heart Research Institute Singapore, National Heart Centre Singapore, Singapore, Singapore.
Stuart A CookNational Heart Research Institute Singapore, National Heart Centre Singapore, Singapore, Singapore. stuart.cook@duke-nus.edu.sg.
National University of Singapore · SGNational Heart Centre Singapore · SG

Funding

Medical Research Council MC_U120085815
6 · The paper itself

Abstract

There are currently no specific treatments for cardiac fibrosis. We tested the efficacy of a neutralising anti-IL11 antibody (X203) to reduce cardiac fibrosis in two preclinical models: transverse aortic constriction (TAC) and chronic angiotensin II infusion (AngII). In the first model, male C57BL/6J mice were subjected to TAC for 2 weeks. In the second model, mice received continuous angiotensin II for 4 weeks via subcutaneous pump. In both models, mice received either 20 mg/kg of X203 or isotype-control antibody twice-weekly, starting 24 h after surgery. Cardiac fibrosis and extracellular matrix gene expression were assessed by RT-qPCR, Western blot, histology and collagen (hydroxyproline) assays. In both models, X203 significantly reduced pro-fibrotic gene expression and myocardial fibrosis (TAC: 51% reduction in total collagen, P < 0.001, 39% in perivascular fibrosis, P < 0.001; AngII: 17% reduction in total collagen, P = 0.04, 83% in perivascular fibrosis, P < 0.001). Pharmacological targeting of IL11 reduces cardiac fibrosis in preclinical models. Figa Graphical Abstract.

Indexed as

Angiotensin IIAnimalsAntibodies, NeutralizingAortaArterial PressureCardiomyopathiesCollagenConstrictionDisease Models, AnimalFibronectinsFibrosisHydroxyprolineInterleukin-11MaleMiceMice, Inbred C57BLAngiotensin IIAntibodies, NeutralizingCollagenFibronectinsHydroxyprolineInterleukin-11Angiotensin IICardiacFibrosisInterleukin-11Transverse-aortic constriction

Identifiers

PMID32592090
OpenAlexW3038065262

What OpenQuestion holds

Textmetadata
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.