Evidence map›Paper›PMID 29314251›Full record

ArticleJournal of clinical laboratory analysis2018

Clinical and hematological data to group different chronic kidney disease patients: A practical approach to establish different groups of patients.

Vinícius B Péterle, Jéssica de O Souza, Fernanda de O Busato, Frederico J Eutrópio, Gisele de A P da Costa, David N Olivieri, Carlos E Tadokoro

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 100% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

7 authors at 3 institutions in 2 countries.

Vinícius B PéterlePrograma de Pós-Graduação em Ciências Farmacêuticas, Universidade Vila Velha, Vila Velha, Brazil.
Jéssica de O SouzaPrograma de Pós-Graduação em Ciências Farmacêuticas, Universidade Vila Velha, Vila Velha, Brazil.
Fernanda de O BusatoLaboratory of Immunobiology, Universidade Vila Velha, Vila Velha, Brazil.
Frederico J EutrópioInstituto Capixaba de Ciências e Administração, Vitória, Brazil.
Gisele de A P da CostaPrograma de Pós-Graduação em Ecologia de Ecossistemas, Universidade Vila Velha, Vila Velha, Brazil.
David N OlivieriEscuela Superior de Ingeniería Informatica, University of Vigo, Vigo, Spain.
Carlos E TadokoroPrograma de Pós-Graduação em Ciências Farmacêuticas, Universidade Vila Velha, Vila Velha, Brazil.ORCID http://orcid.org/0000-0002-7874-5657
Universidade Vila Velha · BRInstituto Capixaba de Pesquisa, Assistência Técnica e Extensão Rural · BRUniversidade de Vigo · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic kidney disease (CKD) is the convergent point of several pathological processes, and its evolution is insidious and characterized by a progressive and irreversible loss of kidney function. This impaired function induces the accumulation of uremic toxins and individuals with terminal CKD often have altered physiological responses, including a persistent state of immuno-suppression and development of diseases. A better characterization and stratification of these patients with CKD in different immuno-compromised groups would contribute to more effective and personalized treatments. The focus of this study was to use two parameters to stratify patients with CKD into four separate groups that are representative of different immunological status.

methodsPatients with CKD were chosen randomly and stratified into four separate groups according to the period of time receiving dialysis treatment and leukocyte blood counts. The amount of apoptotic CD4 T cells were measured in each group of patients, and clinical/hematological parameters were correlated by multivariate analysis with each group.

resultsObservations reveal that one of the four groups of patients with CKD (group 3) had more apoptotic CD4 T cells than the other group; this group also had an increased malnutrition inflammation score (MIS), an elevated Kt/V, and a higher incidence of smoking.

conclusionA simple two-parameter-based stratification strategy could be used to design effective immunological therapies that differentiate the degrees of immuno-suppression across groups of patients with CKD.

Indexed as

ApoptosisCD4-Positive T-LymphocytesDisease ProgressionFemaleFlow CytometryHematologic TestsHumansImmune ToleranceKidneys, ArtificialLeukocytesMaleMultivariate AnalysisRenal Insufficiency, ChronicStatistics as TopicapoptosisCD4 T cellshemodialysisimmuno-suppressionmultivariate analysissmoking

Identifiers

PMID29314251
PMCPMC6817195
OpenAlexW2782001361

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.