Evidence map›Paper›PMID 34827701›Full record

ArticleBiomolecules2021

Differences in the Biomarker Profile of De Novo Acute Heart Failure versus Decompensation of Chronic Heart Failure.

Sylwia Nawrocka-Millward, Jan Biegus, Magdalena Hurkacz, Mateusz Guzik, Marta Rosiek-Biegus, Ewa Anita Jankowska, Piotr Ponikowski, Robert Zymliński

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 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

8 authors at 1 institution in 1 country.

Sylwia Nawrocka-MillwardInstitute of Heart Diseases, University Hospital, 50-556 Wroclaw, Poland.ORCID 0000-0003-0980-493X
Jan BiegusInstitute of Heart Diseases, University Hospital, 50-556 Wroclaw, Poland.ORCID 0000-0001-9977-7722
Magdalena HurkaczDepartment of Clinical Pharmacology, Medical University, 50-556 Wroclaw, Poland.ORCID 0000-0003-0846-3168
Mateusz GuzikInstitute of Heart Diseases, University Hospital, 50-556 Wroclaw, Poland.
Marta Rosiek-BiegusDepartment of Internal Medicine, Pneumology and Allergology, Medical University, 50-369 Wroclaw, Poland.ORCID 0000-0003-4839-446X
Ewa Anita JankowskaInstitute of Heart Diseases, University Hospital, 50-556 Wroclaw, Poland.
Piotr PonikowskiInstitute of Heart Diseases, University Hospital, 50-556 Wroclaw, Poland.
Robert ZymlińskiInstitute of Heart Diseases, University Hospital, 50-556 Wroclaw, Poland.
Wroclaw Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The perception of acute heart failure (AHF) as a single entity is increasingly outdated, as distinct patient profiles can be discerned. Key heart failure (HF) studies have previously highlighted the difference in both the course and prognosis of de novo AHF and acute decompensated chronic HF (ADHF). Accordingly, distinct AHF profiles with differing underlying pathophysiologies of disease progression can be shown. We compared a range of selected biomarkers in order to better describe the profile of de novo AHF and ADHF, including the inter alia-serum lactate, bilirubin, matrix metallopeptidase 9 (MMP-9), follistatin, intercellular adhesion molecule 1 (ICAM-1), lipocalin and galectin-3. The study comprised 248 AHF patients (de novo = 104), who were followed up for one year. The biomarker data of the de novo AHF and ADHF profiles was then compared in order to link biomarkers to their prognosis. Our study demonstrated that, although there are similarities between each patient profile, key biomarker differences do exist-predominantly in terms of NTproBNP, serum lactate, bilirubin, ICAM-1, follistatin, ferritin and sTfR (soluble transferrin receptor). ADHF tended to have compromised organ function and higher risks of both one-year mortality and composite endpoint (one-year mortality or rehospitalization for heart failure) hazard ratios (HR) (95% CI): 3.4 (1.8-6.3) and 2.8 (1.6-4.6), respectively, both

Indexed as

BiomarkersHeart FailureAcute DiseaseAgedAged, 80 and overChronic DiseaseFemaleGalectin 3HumansIntercellular Adhesion Molecule-1MaleMatrix Metalloproteinase 9Middle AgedPrognosisBiomarkersGalectin 3Intercellular Adhesion Molecule-1Matrix Metalloproteinase 9acute decompensated chronic HFbiomarkersde novo AHFheart failure

Identifiers

PMID34827701
PMCPMC8615401
OpenAlexW3214139439

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.