Evidence map›Paper›PMID 31316299›Full record

ArticleMediators of inflammation2019

Long Pentraxin 3 as a Broader Biomarker for Multiple Risk Factors in End-Stage Renal Disease: Association with All-Cause Mortality.

Maria João Valente, Susana Rocha, Susana Coimbra, Cristina Catarino, Petronila Rocha-Pereira, Elsa Bronze-da-Rocha, José Gerardo Oliveira, José Madureira, João Carlos Fernandes, Maria do Sameiro-Faria and 3 more

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

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  5. Impact ofBiomedicines · 2024
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  12. Inflammatory biomarkers in staging of chronic kidney disease: elevated TNFR2 levels accompanies renal function decline.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
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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 1 country.

Maria João ValenteUCIBIO, REQUIMTE, Laboratório de Bioquímica, Faculdade de Farmácia da Universidade do Porto, Porto, Portugal.ORCID https://orcid.org/0000-0001-6162-2426
Susana RochaUCIBIO, REQUIMTE, Laboratório de Bioquímica, Faculdade de Farmácia da Universidade do Porto, Porto, Portugal.
Susana CoimbraUCIBIO, REQUIMTE, Laboratório de Bioquímica, Faculdade de Farmácia da Universidade do Porto, Porto, Portugal.ORCID https://orcid.org/0000-0001-8411-8038
Cristina CatarinoUCIBIO, REQUIMTE, Laboratório de Bioquímica, Faculdade de Farmácia da Universidade do Porto, Porto, Portugal.
Petronila Rocha-PereiraUCIBIO, REQUIMTE, Laboratório de Bioquímica, Faculdade de Farmácia da Universidade do Porto, Porto, Portugal.
Elsa Bronze-da-RochaUCIBIO, REQUIMTE, Laboratório de Bioquímica, Faculdade de Farmácia da Universidade do Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-3571-2513
José Gerardo OliveiraClínica de Hemodiálise do Porto, Porto, Portugal.
José MadureiraNefroServe, Centro de Hemodiálise de Nossa Senhora Da Franqueira, Barcelos, Portugal.
João Carlos FernandesNefroServe, Clínica de Hemodiálise de Viana do Castelo, Viana do Castelo, Portugal.
Maria do Sameiro-FariaUCIBIO, REQUIMTE, Laboratório de Bioquímica, Faculdade de Farmácia da Universidade do Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-8061-9289
Vasco MirandaClínica de Hemodiálise de Gondomar, Gondomar, Portugal.
Luís BeloUCIBIO, REQUIMTE, Laboratório de Bioquímica, Faculdade de Farmácia da Universidade do Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-3941-6850
Alice Santos-SilvaUCIBIO, REQUIMTE, Laboratório de Bioquímica, Faculdade de Farmácia da Universidade do Porto, Porto, Portugal.ORCID https://orcid.org/0000-0002-2565-3169
Universidade do Porto · PTPolytechnic Institute of Viana do Castelo · PTUniversity of Beira Interior · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persistent inflammation in end-stage renal disease (ESRD) patients is known to underlie the progression of chronic kidney disease and to be associated with multiple risk factors including malnutrition, atherosclerosis, and cardiovascular disease (CVD). The acute-phase protein pentraxin 3 (PTX3) has a proven potential as a local inflammatory biomarker, but its clinical utility in ESRD remains unclear. Circulating levels of PTX3 and classical inflammatory mediators, including the clinical prototypical C-reactive protein (CRP), were assessed in 246 ESRD patients on dialysis and analysed in relation to the lipid profile, adipokine levels, and nutritional, cardiac, and renal fibrosis markers. Occurrence of deaths was recorded for the following year. Contrarily to the classical inflammatory markers, PTX3 levels were negatively correlated with nutritional markers and associated with a less atherogenic lipid profile. Levels of the cardiac and renal fibrosis markers and of the oxidized LDL/LDL-C ratio were found to be independent determinants of PTX3 concentration. When comparing inflammatory mediators, the increase in the PTX3 levels was the only predictor of all-cause mortality in dialysis patients in a survival model adjusted to all markers under study, other than the inflammatory ones, besides common confounding factors in dialysis. Data support the clinical applicability of PTX3 as a broader inflammatory biomarker than the classical ones, presenting a close association with inflammation, malnutrition, CVD, and renal fibrosis and a great potential to predict all-cause mortality in dialysis patients. The pleiotropic character of PTX3 may be of clinical relevance, and it could be targeted to ameliorate the high morbidity and mortality associated with ESRD.

Indexed as

AgedAged, 80 and overBiomarkersCardiovascular DiseasesCase-Control StudiesC-Reactive ProteinDisease ProgressionFemaleHumansInflammationKidney Failure, ChronicMaleMiddle AgedPentraxinsPortugalRenal DialysisBiomarkersC-Reactive ProteinPentraxinsSerum Amyloid P-Component

Identifiers

PMID31316299
PMCPMC6604294
OpenAlexW2952902032

What OpenQuestion holds

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LicenceCC BY
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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.