Evidence map›Paper›PMID 39186633›Full record

ArticleJornal brasileiro de nefrologia

Skin accumulation of advanced glycation end-products predicts kidney outcomes in type 2 diabetes: results from the Brazilian Diabetes Study.

Joaquim Barreto, Marilia Martins, Cynthia M Borges, Sofia Helena Vitte, Wilson Nadruz Junior, Rodrigo Bueno de Oliveira, Andrei C Sposito

Abstract read
In one paragraph

Article in Jornal brasileiro de nefrologia. 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
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. 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.

Joaquim BarretoUniversidade Estadual de Campinas, Área de Cardiologia, Laboratório de Aterosclerose e Biologia Vascular, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0003-1914-316X
Marilia MartinsUniversidade Estadual de Campinas, Área de Cardiologia, Laboratório de Aterosclerose e Biologia Vascular, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-9982-2260
Cynthia M BorgesUniversidade Estadual de Campinas, Área de Nefrologia, Laboratório para Avaliação do Distúrbio Mineral e Ósseo em Nefrologia, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-4792-0678
Sofia Helena VitteUniversidade Estadual de Campinas, Área de Cardiologia, Laboratório de Aterosclerose e Biologia Vascular, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-7706-6599
Wilson Nadruz JuniorUniversidade Estadual de Campinas, Área de Cardiologia, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-0003-5102
Rodrigo Bueno de OliveiraUniversidade Estadual de Campinas, Área de Nefrologia, Laboratório para Avaliação do Distúrbio Mineral e Ósseo em Nefrologia, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-8273-6200
Andrei C SpositoUniversidade Estadual de Campinas, Área de Cardiologia, Laboratório de Aterosclerose e Biologia Vascular, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0001-7127-2052

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The accumulation of advanced glycation end-products (AGEs) elicits morphofunctional kidney impairment. AGEs levels can be noninvasively estimated by skin autofluorescence (SAF). We explored whether high SAF predicts kidney outcomes in type 2 diabetes (T2D) individuals. The study was conducted as a predefined analysis of the Brazilian Diabetes Study, a prospective single-center cohort of T2D adults. Data from 155 individuals followed for up to 1716 days were considered. The incidence of major adverse kidney events (MAKE) was 9.6%. Individuals with above-median SAF had a higher incidence of MAKEs (4.6% vs. 21%; p = 0.002), with an HR of 3.39 [95% CI: 1.06-10.85; p = 0.040] after adjustment by age and gender. The mean adjusted eGFR change was 1.08 units (SE: 1.15; 95%CI: -1.20, 3.37) in the low SAF and -5.19 units [SE: 1.93; 95%CI: -9.10, -1.29] in the high SAF groups (between-subject difference: F: 5.62, p = 0.019). The high-SAF group had a greater prevalence of rapid decliners than the low-SAF group (36.7% vs. 15.8%; p = 0.028). In conclusion, high SAF was related to increased incidence of MAKEs and faster decline in eGFR among T2D subjects. This should be considered by healthcare providers when identifying individuals more prone to diabetes-related kidney complications.

Indexed as

Diabetes Mellitus, Type 2Glycation End Products, AdvancedSkinAgedBrazilDiabetic NephropathiesFemaleHumansMaleMiddle AgedPrognosisProspective StudiesGlycation End Products, Advanced

Identifiers

PMID39186633
PMCPMC11346773

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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.