Evidence map›Paper›PMID 33959903›Full record

ArticleAdvances in experimental medicine and biology2021

Kidney Diseases: The Age of Molecular Markers.

Glaucia Luciano da Veiga, Beatriz da Costa Aguiar Alves, Matheus Moreira Perez, Joyce Regina Raimundo, Jéssica Freitas de Araújo Encinas, Neif Murad, Fernando Luiz Affonso Fonseca

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In one paragraph

Article in Advances in experimental medicine and biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Contemporary Perspectives on Chronic Renal Disorders.Chronic diseases and translational medicine · 2025
    Review
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 2 institutions in 1 country.

Glaucia Luciano da VeigaDivision of Clinical Analysis, Centro Universitário Saúde ABC, Santo André, Brazil. grlveiga@gmail.com.
Beatriz da Costa Aguiar AlvesDivision of Clinical Analysis, Centro Universitário Saúde ABC, Santo André, Brazil.
Matheus Moreira PerezDivision of Clinical Analysis, Centro Universitário Saúde ABC, Santo André, Brazil.
Joyce Regina RaimundoDivision of Clinical Analysis, Centro Universitário Saúde ABC, Santo André, Brazil.
Jéssica Freitas de Araújo EncinasDivision of Clinical Analysis, Centro Universitário Saúde ABC, Santo André, Brazil.
Neif MuradCardiology Department, Centro Universitário Saúde ABC, Santo André, Brazil.
Fernando Luiz Affonso FonsecaDivision of Clinical Analysis, Centro Universitário Saúde ABC, Santo André, Brazil.
Faculdade de Medicina do ABC · BRUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kidney diseases are conditions that increase the morbidity and mortality of those afflicted. Diagnosis of these conditions is based on parameters such as the glomerular filtration rate (GFR), measurement of serum and urinary creatinine levels and equations derived from these measurements (Wasung, Chawla, Madero. Clin Chim Acta 438:350-357, 2015). However, serum creatinine as a marker for measuring renal dysfunction has its limitations since it is altered in several other physiological situations, such as in patients with muscle loss, after intense physical exercise or in people on a high protein diet (Riley, Powers, Welch. Res Q Exerc Sport 52(3):339-347, 1981; Juraschek, Appel, Anderson, Miller. Am J Kidney Dis 61(4):547-554, 2013). Besides the fact that serum creatinine is a marker that indicates glomerular damage, it is necessary the discovery of new biomarkers that reflect not only glomerular damage but also tubular impairment. Recent advances in Molecular Biology have led to the generation or identification of new biomarkers for kidney diseases such as: Acute Kidney Failure (AKI), chronic kidney disease (CKD), nephritis or nephrotic syndrome. There are recent markers that have been used to aid in diagnosis and have been shown to be more sensitive and specific than classical markers, such as neutrophil gelatinase associated lipocalin (NGAL) or kidney injury molecule-1 (KIM-1) (Wasung, Chawla, Madero. Clin Chim Acta 438:350-357, 2015; George, Gounden. Adv Clin Chem 88:91-119, 2019; Han, Bailly, Abichandani, Thadhani, Bonventre. Kidney Int 62(1):237-244, 2002; Fontanilla, Han. Expert Opin Med Diagn 5(2):161-173, 2011). However, early diagnostic biomarkers are still necessary to assist the intervention and monitor of the progression of these conditions.

Indexed as

Acute Kidney InjuryLipocalinsAcute-Phase ProteinsBiomarkersCreatinineGlomerular Filtration RateHumansProto-Oncogene ProteinsAcute-Phase ProteinsBiomarkersCreatinineLipocalinsProto-Oncogene ProteinsBiomarkersEarly diagnosticKidney disease

Identifiers

PMID33959903
OpenAlexW3157900533

What OpenQuestion holds

Textmetadata
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.