Evidence map›Paper›PMID 30912310›Full record

ArticleESC heart failure2019

Bone marrow and plasma FGF-23 in heart failure patients: novel insights into the heart-bone axis.

Beatrice von Jeinsen, Kateryna Sopova, Lars Palapies, David M Leistner, Stephan Fichtlscherer, Florian H Seeger, Jörg Honold, Stefanie Dimmeler, Birgit Aßmus, Andreas M Zeiher and 1 more

Open access · goldAbstract read
In one paragraph

Article in ESC heart failure, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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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

11 authors at 1 institution in 2 countries.

Beatrice von JeinsenDivision of Cardiology, Department of Internal Medicine III, Goethe University Frankfurt, Frankfurt, Germany.
Kateryna SopovaDivision of Cardiology, Department of Internal Medicine III, Goethe University Frankfurt, Frankfurt, Germany.
Lars PalapiesDivision of Cardiology, Department of Internal Medicine III, Goethe University Frankfurt, Frankfurt, Germany.
David M LeistnerDivision of Cardiology, Department of Internal Medicine III, Goethe University Frankfurt, Frankfurt, Germany.
Stephan FichtlschererDivision of Cardiology, Department of Internal Medicine III, Goethe University Frankfurt, Frankfurt, Germany.
Florian H SeegerDivision of Cardiology, Department of Internal Medicine III, Goethe University Frankfurt, Frankfurt, Germany.
Jörg HonoldDivision of Cardiology, Department of Internal Medicine III, Goethe University Frankfurt, Frankfurt, Germany.
Stefanie DimmelerInstitute for Cardiovascular Regeneration, Goethe University Frankfurt, Frankfurt, Germany.
Birgit AßmusDivision of Cardiology, Department of Internal Medicine III, Goethe University Frankfurt, Frankfurt, Germany.
Andreas M ZeiherDivision of Cardiology, Department of Internal Medicine III, Goethe University Frankfurt, Frankfurt, Germany.
Till KellerDivision of Cardiology, Department of Internal Medicine III, Goethe University Frankfurt, Frankfurt, Germany.ORCID 0000-0002-0895-6491
Goethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsFibroblast growth factor 23 (FGF-23) is known to be elevated in patients with congestive heart failure (CHF). As FGF-23 is expressed in the bone but can also be expressed in the myocardium, the origin of serum FGF-23 in CHF remains unclear. It is also unclear if FGF-23 expressed in the bone is associated with outcome in CHF. The aim of the present study was to investigate FGF-23 levels measured in bone marrow plasma (FGF-23-BM) and in peripheral blood (FGF-23-P) in CHF patients to gain further insights into the heart-bone axis of FGF-23 expression. We also investigated possible associations between FGF-23-BM as well as FGF-23-P and outcome in CHF patients. METHODS AND

resultsWe determined FGF-23-P and FGF-23-BM levels in 203 CHF patients (85% male, mean age 61.3 years) with a left ventricular ejection fraction (LVEF) ≤45% and compared them with those of 48 healthy controls (48% male, mean age 39.2 years). We investigated the association between FGF-23-BM and FGF-23-P with all-cause mortality in CHF patients, 32 events, median follow-up 1673 days, interquartile range [923, 1828]. FGF-23-P (median 60.3 vs. 22.0 RU/mL, P < 0.001) and FGF-23-BM (median 130.7 vs. 93.1 RU/mL, P < 0.001) levels were higher in CHF patients compared with healthy controls. FGF-23-BM levels were significantly higher than FGF-23-P levels in both CHF patients and in healthy controls (P < 0.001). FGF-23-P and FGF-23-BM correlated significantly with LVEF (r = -0.37 and r = -0.33, respectively), N terminal pro brain natriuretic peptide levels (r = 0.57 and r = 0.6, respectively), New York Heart Association status (r = 0.28 and r = 0.25, respectively), and estimated glomerular filtration rate (r = -0.43 and r = -0.41, respectively) (P for all <0.001) and were independently associated with all-cause mortality in CHF patients after adjustment for LVEF, estimated glomerular filtration rate, New York Heart Association status, and N terminal pro brain natriuretic peptide, hazard ratio 2.71 [confidence interval: 1.18-6.20], P = 0.018, and hazard ratio 2.80 [confidence interval: 1.19-6.57], P = 0.018, respectively.

conclusionsIn CHF patients, FGF-23 is elevated in bone marrow plasma and is independently associated with heart failure severity and all-cause mortality. The failing heart seems to interact via FGF-23 within a heart-bone axis.

Indexed as

Heart FailureAdultBone MarrowFemaleFibroblast Growth Factor-23Fibroblast Growth FactorsGlucuronidaseHumansKlotho ProteinsMaleMiddle AgedPrognosisRetrospective StudiesRisk AssessmentTreatment OutcomeFGF23 protein, humanFibroblast Growth Factor-23Fibroblast Growth FactorsGlucuronidaseKlotho ProteinsFibroblast growth factorHeart failureOutcomeRisk prediction

Identifiers

PMID30912310
PMCPMC6487718
OpenAlexW2923097976

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.