Evidence map›Paper›PMID 32410391›Full record

ArticleESC heart failure2020

Circulating protein biomarkers predict incident hypertensive heart failure independently of N-terminal pro-B-type natriuretic peptide levels.

Celine Fernandez, Jaana Rysä, Kristoffer Ström, Jan Nilsson, Gunnar Engström, Marju Orho-Melander, Heikki Ruskoaho, Olle Melander

Open access · goldAbstract read
In one paragraph

Article in ESC heart failure, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
1.1field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 12 citations in OpenAlex.

  1. Pooled it
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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

8 authors at 3 institutions in 2 countries.

Celine FernandezDepartment of Clinical Sciences, Malmö, Lund University, Lund, Sweden.
Jaana RysäSchool of Pharmacy, Faculty of Health Sciences, University of Eastern Finland, Kuopio, Finland.
Kristoffer StrömDepartment of Clinical Sciences, Malmö, Lund University, Lund, Sweden.
Jan NilssonDepartment of Clinical Sciences, Malmö, Lund University, Lund, Sweden.
Gunnar EngströmDepartment of Clinical Sciences, Malmö, Lund University, Lund, Sweden.
Marju Orho-MelanderDepartment of Clinical Sciences, Malmö, Lund University, Lund, Sweden.
Heikki RuskoahoDrug Research Program, Division of Pharmacology and Pharmacotherapy, University of Helsinki, Helsinki, Finland.
Olle MelanderDepartment of Clinical Sciences, Malmö, Lund University, Lund, Sweden.
Lund University · SEUniversity of Eastern Finland · FIUniversity of Helsinki · FI

Funding

Academy of Finland 266661Academy of Finland 276747Åke Wiberg FoundationAlbert Påhlsson Research FoundationCrafoord Research FoundationErnhold Lundström Research FoundationEuropean Research Council 649021Finnish Foundation for Cardiovascular ResearchGöran Gustafsson FoundationKnut and Alice Wallenberg FoundationLinneus Foundation for the Lund University Diabetes CenterNovo Nordisk FoundationRegion SkåneRoyal Physiographic Society in LundSigrid Jusélius FoundationSkåne University HospitalSwedish Diabetes FoundationSwedish Foundation for Strategic Research IRC15-0067Swedish Heart and Lung FoundationSwedish Research Council
6 · The paper itself

Abstract

aimsHypertension is the leading cause for the development of heart failure (HF). Here, we aimed to identify cardiomyocyte stretch-induced circulating biomarkers for predicting hypertension-associated HF. METHODS AND

resultsCirculating levels of 149 proteins were measured by proximity extension assay at baseline examination in 4742 individuals from the Malmö Diet and Cancer study. Protein levels were compared with stretch-activated gene expression changes in cultured neonatal rat ventricular myocytes (NRVMs) in response to 1-48 h of mechanical stretch. We also studied the association between protein levels and hypertension and HF incidence using respectively binary logistic and Cox regressions. Levels of 35 proteins were differentially expressed after Bonferroni correction in incident HF vs. control (P < 3.4E-4). Growth differentiation factor-15 (GDF-15), interleukin-6 (IL-6), IL-1 receptor type 1, and urokinase plasminogen activator surface receptor had corresponding mRNA levels up-regulated by stretch in NRVMs at all time points (P < 0.05). These four proteins were individually associated with increased risk of HF after age and sex adjustment [hazard ratio (HR) per standard deviation: 1.19 ≤ HR ≤ 1.49, P ≤ 4.90E-3]. GDF-15 and IL-6 were associated with HF independently of each other (1.22 ≤ HR ≤ 1.33, P ≤ 0.001). In subjects with hypertension, these associations remained significant after further adjustment for N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels (1.23 ≤ HR ≤ 1.45, P ≤ 0.001). A higher fasting value of a GDF-15, IL-6 score aggregate was associated with increased risk of hypertensive HF after adjustment for all traditional risk factors for HF and NT-proBNP (HR = 1.31, P = 2.19E-4).

conclusionsCardiomyocyte mRNA levels of GDF-15 and IL-6 are consistently up-regulated by stretch, and their circulating protein levels predict HF in hypertensive subjects independently of NT-proBNP during long-term follow-up. Our results encourage further studies on lower blood pressure goals in hypertensive subjects with high GDF-15 and IL-6, and interventions targeted at stretch-induced cardiomyocyte expressed biomarkers.

Indexed as

Heart FailureHypertensionAnimalsBiomarkersNatriuretic Peptide, BrainPeptide FragmentsRatsBiomarkersNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)CardiomyocyteHeart failureHypertensionProspective cohortProtein panel

Identifiers

PMID32410391
PMCPMC7373917
OpenAlexW3025758804

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.