Unknown

Dataset Information

0

The p38 mitogen activated protein kinase inhibitor losmapimod in chronic obstructive pulmonary disease patients with systemic inflammation, stratified by fibrinogen: A randomised double-blind placebo-controlled trial.


ABSTRACT:

Background

Cardiovascular disease is a major cause of morbidity and mortality in COPD patients. Systemic inflammation associated with COPD, is often hypothesised as a causal factor. p38 mitogen-activated protein kinases play a key role in the inflammatory pathogenesis of COPD and atherosclerosis.

Objectives

This study sought to evaluate the effects of losmapimod, a p38 mitogen-activated protein kinase (MAPK) inhibitor, on vascular inflammation and endothelial function in chronic obstructive pulmonary disease (COPD) patients with systemic inflammation (defined by plasma fibrinogen >2·8g/l).

Methods

This was a randomised, double-blind, placebo-controlled, Phase II trial that recruited COPD patients with plasma fibrinogen >2.8g/l. Participants were randomly assigned by an online program to losmapimod 7·5mg or placebo tablets twice daily for 16 weeks. Pre- and post-dose 18F-Fluorodeoxyglucose positron emission tomography co-registered with computed tomography (FDG PET/CT) imaging of the aorta and carotid arteries was performed to quantify arterial inflammation, defined by the tissue-to-blood ratio (TBR) from scan images. Endothelial function was assessed by brachial artery flow-mediated dilatation (FMD).

Results

We screened 160 patients, of whom, 36 and 37 were randomised to losmapimod or placebo. The treatment effect of losmapimod compared to placebo was not significant, at -0·05 for TBR (95% CI: -0·17, 0·07), p = 0·42, and +0·40% for FMD (95% CI: -1·66, 2·47), p = 0·70. The frequency of adverse events reported was similar in both treatment groups.

Conclusions

In this plasma fibrinogen-enriched study, losmapimod had no effect on arterial inflammation and endothelial function at 16 weeks of treatment, although it was well tolerated with no significant safety concerns. These findings do not support the concept that losmapimod is an effective treatment for the adverse cardiovascular manifestations of COPD.

SUBMITTER: Fisk M 

PROVIDER: S-EPMC5863984 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

altmetric image

Publications

The p38 mitogen activated protein kinase inhibitor losmapimod in chronic obstructive pulmonary disease patients with systemic inflammation, stratified by fibrinogen: A randomised double-blind placebo-controlled trial.

Fisk Marie M   Cheriyan Joseph J   Mohan Divya D   Forman Julia J   Mäki-Petäjä Kaisa M KM   McEniery Carmel M CM   Fuld Jonathan J   Rudd James H F JHF   Hopkinson Nicholas S NS   Lomas David A DA   Cockcroft John R JR   Tal-Singer Ruth R   Polkey Michael I MI   Wilkinson Ian B IB  

PloS one 20180322 3


<h4>Background</h4>Cardiovascular disease is a major cause of morbidity and mortality in COPD patients. Systemic inflammation associated with COPD, is often hypothesised as a causal factor. p38 mitogen-activated protein kinases play a key role in the inflammatory pathogenesis of COPD and atherosclerosis.<h4>Objectives</h4>This study sought to evaluate the effects of losmapimod, a p38 mitogen-activated protein kinase (MAPK) inhibitor, on vascular inflammation and endothelial function in chronic o  ...[more]

Similar Datasets

| S-EPMC5625047 | biostudies-literature
| S-EPMC4830812 | biostudies-literature
| S-EPMC4552301 | biostudies-literature
| S-EPMC9664350 | biostudies-literature
| S-EPMC8575949 | biostudies-literature
| S-EPMC4428223 | biostudies-literature
| S-EPMC7524480 | biostudies-literature
| S-EPMC3690763 | biostudies-literature
| S-EPMC3327889 | biostudies-literature
| S-EPMC6234472 | biostudies-other