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Distinct Pathological Pathways in Patients With Heart Failure and Diabetes.

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journal contribution
posted on 2020-03-12, 15:15 authored by Jasper Tromp, Adriaan A Voors, Abhinav Sharma, João P Ferreira, Wouter Ouwerkerk, Hans L Hillege, Karla A Gomez, Kenneth Dickstein, Stefan D Anker, Marco Metra, Chim C Lang, Leong L Ng, Pim van der Harst, Dirk J van Veldhuisen, Peter van der Meer, Carolyn SP Lam, Faiez Zannad, Iziah E Sama
OBJECTIVES:The aims of this study were to compare the characteristics of patients with and without diabetes and to use network analyses to compare biomarker profiles and associated pathways in patients with diabetes compared with those without diabetes, which might offer new avenues for potential therapeutic targets. BACKGROUND:Diabetes adversely affects clinical outcomes and complicates treatment in patients with heart failure (HF). A clear understanding of the pathophysiological processes associated with type 2 diabetes in HF is lacking. METHODS:Network and pathway over-representation analyses were performed to identify unique pathological pathways in patients with and without diabetes using 92 biomarkers from different pathophysiological domains measured in plasma samples from 1,572 patients with HF (31% with diabetes) with reduced ejection fraction (left ventricular ejection fraction <40%). The results were validated in an independent cohort of 729 patients (30% with diabetes). RESULTS:Biomarker profiles were first compared between patients with HF with and without diabetes. Patients with diabetes showed higher levels of galectin-4, growth differentiation factor 15, and fatty acid binding protein 4 and lower levels of paraoxonase 3. Network analyses were then performed, revealing that epidermal growth factor receptor and galectin-3 were the most prominent connecting proteins. Translation of these networks to biologic pathways revealed that diabetes was associated with inflammatory response and neutrophil degranulation. Diabetes conferred worse outcomes after correction for an established risk model (hazard ratio: 1.20; 95% confidence interval: 1.01 to 1.42). CONCLUSIONS:Concomitant diabetes in patients with HF with reduced ejection fraction is associated with distinct pathophysiological pathways related to inflammation, protein phosphorylation, and neutrophil degranulation. These data support the evaluation of anti-inflammatory therapeutic approaches, epidermal growth factor receptor in particular, for patients with HF and diabetes.

Funding

BIOSTAT-CHF was funded by the European Commission (FP7-242209-BIOSTAT-CHF; and EudraCT 2010-020808-29). Additional funding was provided by Roche Diagnostics.

History

Citation

JACC: Heart Failure, Volume 8, Issue 3, March 2020, Pages 234-242

Author affiliation

Department of Cardiovascular Sciences

Version

  • AM (Accepted Manuscript)

Published in

JACC: Heart failure

Volume

8

Issue

3

Pagination

234-242

Publisher

Elsevier

issn

2213-1779

eissn

2213-1787

Acceptance date

2019-11-06

Copyright date

2020

Publisher version

https://www.sciencedirect.com/science/article/abs/pii/S2213177919308686#kwrds0010

Spatial coverage

United States

Language

eng

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