Evidence map›Paper›PMID 41462165›Full record

Observational studyBMC nephrology2025

Plasma monocyte chemoattractant protein-1 and the risk of kidney and cardiovascular outcomes in people with chronic kidney disease: results from the BRIGHTEN study.

Tadashi Toyama, Tatsuo Kagimura, Kenichiro Tanabe, Yasunori Iwata, Takashi Wada, Ichiei Narita

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in BMC nephrology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Tadashi ToyamaDepartment of Nephrology, Faculty of Medical Sciences, University of Fukui, Yoshida-gun, Japan. ttoyama@u-fukui.ac.jp.ORCID 0000-0003-0162-6286
Tatsuo KagimuraTranslational Research Center for Medical Innovation, Kobe, Japan.
Kenichiro TanabeTranslational Research Center for Medical Innovation, Kobe, Japan.
Yasunori IwataDepartment of Nephrology and Rheumatology, Kanazawa University, Kanazawa, Japan.
Takashi WadaDepartment of Nephrology and Rheumatology, Kanazawa University, Kanazawa, Japan.
Ichiei NaritaDivision of Clinical Nephrology and Rheumatology, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMonocyte chemoattractant protein-1 (MCP-1) has been implicated in the pathogenesis of chronic kidney disease (CKD); however, its clinical significance in CKD remains unclear. This study investigated the association between plasma MCP-1 levels and kidney and cardiovascular outcomes in patients with CKD.

methodsThis multicenter, prospective, observational analysis used data from the BRIGHTEN study. Participants with anemia and CKD (eGFR < 60 mL/min/1.73 m

resultsThis study included 1,447 participants with advanced CKD (median eGFR 17.9 mL/min/1.73 m²). The group with the lowest MCP-1 level (< 324.5 pg/mL) had the highest baseline eGFR. In the univariable analyses, higher MCP-1 levels were associated with an increased risk of kidney and cardiovascular outcomes (log-rank p < 0.01 and p = 0.03, respectively), although these associations were not significant after multivariable adjustment. Analysis of the annual eGFR decline using a multivariable linear mixed-effects model revealed that higher MCP-1 levels were associated with an additional eGFR decline of approximately 1.0 mL/min/1.73 m

conclusionsIn patients with CKD, higher plasma MCP-1 levels are associated with a more rapid decline in kidney function but not with the composite outcome of kidney failure. MCP-1 was not associated with cardiovascular outcomes or mortality in this population cohort.

Indexed as

Cardiovascular DiseasesChemokine CCL2Renal Insufficiency, ChronicAgedBiomarkersFemaleGlomerular Filtration RateHumansMaleMiddle AgedProspective StudiesRisk FactorsBiomarkersCCL2 protein, humanChemokine CCL2Cardiovascular eventsChronic kidney diseaseKidney function declineMonocyte chemoattractant protein-1Risk prediction

Identifiers

PMID41462165
PMCPMC12751990

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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.