Evidence map›Paper›PMID 32921312›Full record

ArticleLipids in health and disease2020

Enrichment of apolipoprotein A-IV and apolipoprotein D in the HDL proteome is associated with HDL functions in diabetic kidney disease without dialysis.

Monique F M Santana, Aécio L A Lira, Raphael S Pinto, Carlos A Minanni, Amanda R M Silva, Maria I B A C Sawada, Edna R Nakandakare, Maria L C Correa-Giannella, Marcia S Queiroz, Graziella E Ronsein and 1 more

Open access · goldAbstract read
In one paragraph

Article in Lipids in health and disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Lifestyles, metabolome and diabetic kidney disease: a cohort study.QJM : monthly journal of the Association of Physicians · 2026
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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

11 authors at 4 institutions in 1 country.

Monique F M SantanaLaboratório de Lípides (LIM-10), Hospital das Clínicas (HCFMUSP) da Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Arnaldo 455, room 3305; CEP, São Paulo, 01246-000, Brazil.
Aécio L A LiraLaboratório de Lípides (LIM-10), Hospital das Clínicas (HCFMUSP) da Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Arnaldo 455, room 3305; CEP, São Paulo, 01246-000, Brazil.
Raphael S PintoLaboratório de Lípides (LIM-10), Hospital das Clínicas (HCFMUSP) da Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Arnaldo 455, room 3305; CEP, São Paulo, 01246-000, Brazil.
Carlos A MinanniLaboratório de Lípides (LIM-10), Hospital das Clínicas (HCFMUSP) da Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Arnaldo 455, room 3305; CEP, São Paulo, 01246-000, Brazil.
Amanda R M SilvaDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo, Brazil.
Maria I B A C SawadaPrograma de Pós-Graduação em Medicina, Universidade Nove de Julho, São Paulo, Brazil.
Edna R NakandakareLaboratório de Lípides (LIM-10), Hospital das Clínicas (HCFMUSP) da Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Arnaldo 455, room 3305; CEP, São Paulo, 01246-000, Brazil.
Maria L C Correa-GiannellaPrograma de Pós-Graduação em Medicina, Universidade Nove de Julho, São Paulo, Brazil.
Marcia S QueirozPrograma de Pós-Graduação em Medicina, Universidade Nove de Julho, São Paulo, Brazil.
Graziella E RonseinDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo, Brazil.
Marisa PassarelliLaboratório de Lípides (LIM-10), Hospital das Clínicas (HCFMUSP) da Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Arnaldo 455, room 3305; CEP, São Paulo, 01246-000, Brazil. m.passarelli@fm.usp.br.ORCID http://orcid.org/0000-0002-9249-4698
Companhia Energética de São Paulo · BRUniversidade Nove de Julho · BRUniversidade de São Paulo · BRHospital Israelita Albert Einstein · BR

Funding

CAPES/CNPq 01Conselho Nacional de Desenvolvimento Científico e Tecnológico 01Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 01FAPESP 2015/21072-5FAPESP 2016/00696-3FAPESP 2016/15603-0FAPESP 2017/07725-1FAPESP 2018/00172-0FAPESP 2018/1845-4Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/21072-5Fundação de Amparo à Pesquisa do Estado de São Paulo 2016/00696-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2016/15603-0Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/007725-1Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/00172-0Fundação de Amparo à Pesquisa do Estado de São Paulo (BR) 2018/18545-4
6 · The paper itself

Abstract

BACKGROUND AND

aimsDiabetic kidney disease (DKD) is associated with lipid derangements that worsen kidney function and enhance cardiovascular (CVD) risk. The management of dyslipidemia, hypertension and other traditional risk factors does not completely prevent CVD complications, bringing up the participation of nontraditional risk factors such as advanced glycation end products (AGEs), carbamoylation and changes in the HDL proteome and functionality. The HDL composition, proteome, chemical modification and functionality were analyzed in nondialysis subjects with DKD categorized according to the estimated glomerular filtration rate (eGFR) and urinary albumin excretion rate (AER).

methodsIndividuals with DKD were divided into eGFR> 60 mL/min/1.73 m

resultsTargeted proteomic analyses quantified 28 proteins associated with HDL in all groups, although only 2 were more highly expressed in the eGFR< 60 + A3 group than in the controls: apolipoprotein D (apoD) and apoA-IV. HDL from the eGFR< 60 + A3 group presented higher levels of total AGEs (20%), pentosidine (6.3%) and carbamoylation (4.2 x) and a reduced ability to remove

conclusionThe increase in apoD and apoA-IV could contribute to counteracting the HDL chemical modification by AGEs and carbamoylation, which contributes to HDL loss of function in well-established DKD.

Indexed as

AgedAged, 80 and overAlbuminuriaApolipoproteins AApolipoproteins DArginineCase-Control StudiesDiabetic NephropathiesFemaleGene ExpressionGlomerular Filtration RateGlycation End Products, AdvancedHumansInterleukin-6KidneyLipopolysaccharidesAPOD protein, humanapolipoprotein A-IVApolipoproteins AApolipoproteins DArginineGlycation End Products, AdvancedIL6 protein, humanInterleukin-6LipopolysaccharidesLipoproteins, HDLLysinepentosidineProteomeTumor Necrosis Factor-alphaAdvanced glycationApolipoprotein A-IVApolipoprotein DAtherosclerosisCarbamoylationDiabetic kidney diseaseHDLProteomics

Identifiers

PMID32921312
PMCPMC7488728
OpenAlexW3086665300

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.