| Literature DB >> 31104495 |
João Pedro Ferreira1,2, Job Verdonschot3,4, Timothy Collier5, Ping Wang4, Anne Pizard1,6, Christian Bär7, Jens Björkman, Alessandro Boccanelli8, Javed Butler9,10,11, Andrew Clark12, John G Cleland13,14, Christian Delles15, Javier Diez16,17,18,19, Nicolas Girerd1, Arantxa González16,17,18, Mark Hazebroek3, Anne-Cécile Huby1, Wouter Jukema20, Roberto Latini21, Joost Leenders22, Daniel Levy23,24, Alexandre Mebazaa25, Harald Mischak26, Florence Pinet27, Patrick Rossignol1, Naveed Sattar28, Peter Sever29, Jan A Staessen30,31, Thomas Thum7,32, Nicolas Vodovar25, Zhen-Yu Zhang30, Stephane Heymans3,33, Faiez Zannad1.
Abstract
Background Identifying the mechanistic pathways potentially associated with incident heart failure (HF) may provide a basis for novel preventive strategies. Methods and Results To identify proteomic biomarkers and the potential underlying mechanistic pathways that may be associated with incident HF defined as the first hospitalization for HF, a nested-matched case-control design was used with cases (incident HF) and controls (without HF) selected from 3 cohorts (>20 000 individuals). Controls were matched on cohort, follow-up time, age, and sex. Two independent sample sets (a discovery set with 286 cases and 591 controls and a replication set with 276 cases and 280 controls) were used to discover and replicate the findings. Two hundred fifty-two circulating proteins in the plasma were studied. Adjusting for the matching variables age, sex, and follow-up time (and correcting for multiplicity of tests), 89 proteins were found to be associated with incident HF in the discovery phase, of which 38 were also associated with incident HF in the replication phase. These 38 proteins pointed to 4 main network clusters underlying incident HF: (1) inflammation and apoptosis, indicated by the expression of the TNF (tumor necrosis factor)-family members; (2) extracellular matrix remodeling, angiogenesis and growth, indicated by the expression of proteins associated with collagen metabolism, endothelial function, and vascular homeostasis; (3) blood pressure regulation, indicated by the expression of natriuretic peptides and proteins related to the renin-angiotensin-aldosterone system; and (4) metabolism, associated with cholesterol and atherosclerosis. Conclusions Clusters of biomarkers associated with mechanistic pathways leading to HF were identified linking inflammation, apoptosis, vascular function, matrix remodeling, blood pressure control, and metabolism. These findings provide important insight on the pathophysiological mechanisms leading to HF. Clinical Trial Registration: URL: https://www.clinicaltrials.gov . Unique identifier: NCT02556450.Entities:
Keywords: apoptosis; atherosclerosis; blood pressure; heart failure; proteomics
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Year: 2019 PMID: 31104495 DOI: 10.1161/CIRCHEARTFAILURE.118.005897
Source DB: PubMed Journal: Circ Heart Fail ISSN: 1941-3289 Impact factor: 8.790