Evidence map›Paper›PMID 39961689›Full record

ArticleRenal failure2025

Plasma brain-derived neurotrophic factor before hemodialysis reduces the risk of depression in patients with chronic renal failure.

Juan Antonio Suárez-Cuenca, Nuri Perla Campos-Nolasco, Ernesto Rodríguez-Ayala, Ana Daniela Zepeda-Làmbarry, Marta Georgina Ochoa-Madrigal, Diana Maldonado-Tapia, Eduardo Vera-Gómez, Alejandro Hernández-Patricio, Gustavo Martínez-Torres, Yareni Bernal-Figueroa and 4 more

Abstract read
In one paragraph

Article in Renal failure, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

14 authors.

Juan Antonio Suárez-CuencaLaboratorio de Metabolismo Experimental e Investigación Clínica, División de Investigación, Centro Médico Nacional "20 de Noviembre", Mexico City, Mexico.
Nuri Perla Campos-NolascoUnidad de Hemodialisis, Clínica de Especialidades "Dr. Alberto Pisanty Ovadia", Mexico City, Mexico.
Ernesto Rodríguez-AyalaFacultad de Medicina, Universidad Anáhuac México Norte, Estado de México, Mexico.
Ana Daniela Zepeda-LàmbarryServicio de Psiquiatría Médica, Centro Médico Nacional "20 de Noviembre" ISSSTE; Mexico City, Mexico.
Marta Georgina Ochoa-MadrigalServicio de Psiquiatría Médica, Centro Médico Nacional "20 de Noviembre" ISSSTE; Mexico City, Mexico.
Diana Maldonado-TapiaUnidad de Hemodialisis, Centro Médico Nacional "20 de Noviembre", Mexico City, Mexico.
Eduardo Vera-GómezLaboratorio de Metabolismo Experimental e Investigación Clínica, División de Investigación, Centro Médico Nacional "20 de Noviembre", Mexico City, Mexico.
Alejandro Hernández-PatricioLaboratorio de Metabolismo Experimental e Investigación Clínica, División de Investigación, Centro Médico Nacional "20 de Noviembre", Mexico City, Mexico.
Gustavo Martínez-TorresLaboratorio de Metabolismo Experimental e Investigación Clínica, División de Investigación, Centro Médico Nacional "20 de Noviembre", Mexico City, Mexico.
Yareni Bernal-FigueroaLaboratorio de Metabolismo Experimental e Investigación Clínica, División de Investigación, Centro Médico Nacional "20 de Noviembre", Mexico City, Mexico.
Juan Antonio Pineda-JuárezCoordinación de Investigación, Centro Médico Nacional "20 de Noviembre", Mexico City, Mexico.
José Gutiérrez-SalinasLaboratorio de Bioquímica y Medicina Experimental, División de Investigación Biomédica, Centro Médico Nacional "20 de Noviembre", Mexico City, Mexico.
Christian Gabriel Toledo-LozanoCoordinación de Investigación, Centro Médico Nacional "20 de Noviembre", Mexico City, Mexico.
Silvia GarcíaLaboratorio de Metabolismo Experimental e Investigación Clínica, División de Investigación, Centro Médico Nacional "20 de Noviembre", Mexico City, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeurotrophins are related with depressive disorders. Significant neurotrophins variations occur during renal replacement therapy, but whether peri-hemodialysis availability is associated with depression in patients with Chronic Kidney Disease (CKD) is yet unclear.

aimTo determine dynamic concentrations of neurotrophins in the peri-hemodialysis range and their association with depressive symptoms in patients with CKD.

methodsPre-, and post-hemodialysis plasma concentrations of brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF), as well as their plasma clearance rates, were determined (multiplexing) in patients with stage 5 CKD. Depressive symptoms, as assessed by the Beck Depression Inventory-II (BDI-II), were determined. Finally, the bioavailability of BDNF and NGF was related to the score of depressive symptoms.

resultsFifty-three patients were divided according to depressive symptoms. Pre-hemodialysis plasma BDNF was lower in patients with depressive disorder; whereas basal BDNF value >220 pg/mL independently reduced the risk for depressive disorder (Odds Ratio 0.23,

conclusionHigher plasma BDNF before hemodialysis reduces the risk of mild depression in patients with CKD under renal replacement therapy.

Indexed as

Brain-Derived Neurotrophic FactorDepressionKidney Failure, ChronicRenal DialysisAdultAgedFemaleHumansMaleMiddle AgedNerve Growth FactorRisk FactorsBDNF protein, humanBrain-Derived Neurotrophic FactorNerve Growth Factorchronic renal failuredepressionhemodialysisPlasma brain-derived neurotrophic factor

Identifiers

PMID39961689
PMCPMC11834812

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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.