Evidence map›Paper›PMID 29251807›Full record

ArticleEuropean journal of heart failure2018

Proteomic diversity of high-density lipoprotein explains its association with clinical outcome in patients with heart failure.

Johanna Elisabeth Emmens, Donald J L Jones, Thong H Cao, Daniel C S Chan, Simon P R Romaine, Paulene A Quinn, Stefan D Anker, John G Cleland, Kenneth Dickstein, Gerasimos Filippatos and 11 more

Open access · bronzeAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in European journal of heart failure, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 36 citations in OpenAlex.

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  10. HDL, heart disease, and the lung.Journal of lipid research · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 16 institutions in 10 countries.

Johanna Elisabeth EmmensDepartment of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Donald J L JonesDepartment of Cancer Studies, University of Leicester, Leicester Royal Infirmary, Leicester, UK.
Thong H CaoDepartment of Cardiovascular Sciences, University of Leicester, NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Daniel C S ChanDepartment of Cardiovascular Sciences, University of Leicester, NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Simon P R RomaineDepartment of Cardiovascular Sciences, University of Leicester, NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Paulene A QuinnDepartment of Cardiovascular Sciences, University of Leicester, NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Stefan D AnkerDivision of Cardiology and Metabolism - Heart Failure, Cachexia and Sarcopenia, Department of Cardiology (CVK); and Berlin-Brandenburg Center for Regenerative Therapies (BCRT), Deutsches Zentrum für Herz-Kreislauf-Forschung (DZHK) Berlin, Charité Universitätsmedizin Berlin, Germany.
John G ClelandNational Heart and Lung Institute, Royal Brompton and Harefield Hospitals, Imperial College, London, UK.
Kenneth DicksteinUniversity of Bergen, Bergen, Norway.
Gerasimos FilippatosNational and Kapodistrian University of Athens, School of Medicine, Heart Failure Unit, Department of Cardiology, Athens University Hospital Attikon, Athens, Greece.
Hans L HillegeDepartment of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Chim C LangSchool of Medicine Centre for Cardiovascular and Lung Biology, Division of Medical Sciences, University of Dundee, Ninewells Hospital & Medical School, Dundee, UK.
Piotr PonikowskiDepartment of Heart Diseases, Wroclaw Medical University, and Cardiology Department, Military Hospital, Wroclaw, Poland.
Nilesh J SamaniDepartment of Cardiovascular Sciences, University of Leicester, NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
Dirk J van VeldhuisenDepartment of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Faiz ZannadInserm CIC 1433, Université de Lorrain, CHU de Nancy, Nancy, France.
Aeilko H ZwindermanDepartment of Epidemiology, Biostatistics and Bioinformatics, Academic Medical Centre, Amsterdam, The Netherlands.
Marco MetraInstitute of Cardiology, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
Rudolf A de BoerDepartment of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Adriaan A VoorsDepartment of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Leong L NgDepartment of Cardiovascular Sciences, University of Leicester, NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.
University Medical Center Groningen · NLNIHR Leicester Cardiovascular Biomedical Research Unit · GBUniversity of Groningen · NLUniversity of Leicester · GBAmsterdam UMC Location University of Amsterdam · NLBerlin-Brandenburger Centrum für Regenerative Therapien · DEGlenfield Hospital · GBImperial College London · GBInserm · FRLeicester Royal Infirmary · GBNational and Kapodistrian University of Athens · GRNIHR Leicester Biomedical Research Centre · GBNinewells Hospital · GBSurgical Specialties (Canada) · CAUniversity of Bergen · NOWroclaw Medical University · PL

Funding

British Heart Foundation FS/12/30/29474British Heart Foundation FS/15/10/31223
6 · The paper itself

Abstract

aimsPreviously, low high-density lipoprotein (HDL) cholesterol was found to be one of the strongest predictors of mortality and/or heart failure (HF) hospitalisation in patients with HF. We therefore performed in-depth investigation of the multifunctional HDL proteome to reveal underlying pathophysiological mechanisms explaining the association between HDL and clinical outcome. METHODS AND

resultsWe selected a cohort of 90 HF patients with 1:1 cardiovascular death/survivor ratio from BIOSTAT-CHF. A novel optimised protocol for selective enrichment of lipoproteins was used to prepare plasma. Enriched lipoprotein content of samples was analysed using high resolution nanoscale liquid chromatography-mass spectrometry-based proteomics, utilising a label free approach. Within the HDL proteome, 49 proteins significantly differed between deaths and survivors. An optimised model of 12 proteins predicted death with 76% accuracy (Nagelkerke R

conclusionThis study shows marked differences in composition of the HDL proteome between HF survivors and deaths. The strongest differences were seen in proteins reflecting crosslinking of actin filaments and alveolar capillary membrane function, posing potential pathophysiological mechanisms underlying the association between HDL and clinical outcome in HF.

Indexed as

AgedBiomarkersCause of DeathFemaleHeart FailureHumansLipoproteins, HDLMalePrognosisProteomeProteomicsRisk AssessmentSurvival RateUnited KingdomBiomarkersLipoproteins, HDLProteomeHeart failureHigh-density lipoproteinProteome

Identifiers

PMID29251807
OpenAlexW2783929973

What OpenQuestion holds

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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.