Evidence map›Paper›PMID 32830215›Full record

ArticleEuropace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology2020

Assessment of causality of natriuretic peptides and atrial fibrillation and heart failure: a Mendelian randomization study in the FINRISK cohort.

Bastiaan Geelhoed, Christin S Börschel, Teemu Niiranen, Tarja Palosaari, Aki S Havulinna, Césaire J K Fouodo, Markus O Scheinhardt, Stefan Blankenberg, Pekka Jousilahti, Kari Kuulasmaa and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 4 pooled it
2.1field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 4 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  4. Pooled it
  5. Article
  6. Article
  7. The Genetic Polymorphisms ofInternational journal of molecular sciences · 2025
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  9. A proteomic analysis of atrial fibrillation in a prospective longitudinal cohort (AGES-Reykjavik study).Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2023
    Article
  10. Plasma angiopoietin-2 and its association with heart failure in patients with atrial fibrillation.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2023
    Article
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  15. BNP and Precision Medicine: Tip of an Iceberg.JACC. Basic to translational science · 2021
    Article
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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

13 authors at 3 institutions in 2 countries.

Bastiaan GeelhoedDepartment of General and Interventional Cardiology, University Heart Centre Hamburg, Martinistr. 52, 20246 Hamburg, Germany.
Christin S BörschelDepartment of General and Interventional Cardiology, University Heart Centre Hamburg, Martinistr. 52, 20246 Hamburg, Germany.
Teemu NiiranenFinnish Institute for Health and Welfare, THL, Helsinki, Finland.
Tarja PalosaariFinnish Institute for Health and Welfare, THL, Helsinki, Finland.
Aki S HavulinnaFinnish Institute for Health and Welfare, THL, Helsinki, Finland.
Césaire J K FouodoInstitute of Medical Biometry and Statistics, University of Lübeck, University Medical Centre Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Markus O ScheinhardtInstitute of Medical Biometry and Statistics, University of Lübeck, University Medical Centre Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Stefan BlankenbergDepartment of General and Interventional Cardiology, University Heart Centre Hamburg, Martinistr. 52, 20246 Hamburg, Germany.
Pekka JousilahtiFinnish Institute for Health and Welfare, THL, Helsinki, Finland.
Kari KuulasmaaFinnish Institute for Health and Welfare, THL, Helsinki, Finland.
Tanja ZellerDepartment of General and Interventional Cardiology, University Heart Centre Hamburg, Martinistr. 52, 20246 Hamburg, Germany.
Veikko SalomaaFinnish Institute for Health and Welfare, THL, Helsinki, Finland.
Renate B SchnabelDepartment of General and Interventional Cardiology, University Heart Centre Hamburg, Martinistr. 52, 20246 Hamburg, Germany.
Finnish Institute for Health and Welfare · FIUniversität Hamburg · DEUniversity of Lübeck · DE

Funding

Medical Research Council G0601463
6 · The paper itself

Abstract

aimsNatriuretic peptides are extensively studied biomarkers for atrial fibrillation (AF) and heart failure (HF). Their role in the pathogenesis of both diseases is not entirely understood and previous studies several single-nucleotide polymorphisms (SNPs) at the NPPA-NPPB locus associated with natriuretic peptides have been identified. We investigated the causal relationship between natriuretic peptides and AF as well as HF using a Mendelian randomization approach. METHODS AND

resultsN-terminal pro B-type natriuretic peptide (NT-proBNP) (N = 6669), B-type natriuretic peptide (BNP) (N = 6674), and mid-regional pro atrial natriuretic peptide (MR-proANP) (N = 6813) were measured in the FINRISK 1997 cohort. N = 30 common SNPs related to NT-proBNP, BNP, and MR-proANP were selected from studies. We performed six Mendelian randomizations for all three natriuretic peptide biomarkers and for both outcomes, AF and HF, separately. Polygenic risk scores (PRSs) based on multiple SNPs were used as genetic instrumental variable in Mendelian randomizations. Polygenic risk scores were significantly associated with the three natriuretic peptides. Polygenic risk scores were not significantly associated with incident AF nor HF. Most cardiovascular risk factors showed significant confounding percentages, but no association with PRS. A causal relation except for small causal betas is unlikely.

conclusionIn our Mendelian randomization approach, we confirmed an association between common genetic variation at the NPPA-NPPB locus and natriuretic peptides. A strong causal relationship between natriuretic peptides and incidence of AF as well as HF at the community-level was ruled out. Therapeutic approaches targeting natriuretic peptides will therefore very likely work through indirect mechanisms.

Indexed as

Atrial FibrillationHeart FailureAdultAtrial Natriuretic FactorBiomarkersCohort StudiesFemaleHumansMaleMendelian Randomization AnalysisMiddle AgedNatriuretic Peptide, BrainNatriuretic PeptidesPeptide FragmentsAtrial Natriuretic FactorBiomarkersNatriuretic Peptide, BrainNatriuretic PeptidesPeptide FragmentsAtrial fibrillationEpidemiologyHeart failureMendelian randomizationNatriuretic peptides

Identifiers

PMID32830215
PMCPMC7544535
OpenAlexW3080549140

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.