Evidence map›Paper›PMID 38911067›Full record

ArticleMedComm2024

Integrin αM promotes macrophage alternative M2 polarization in hyperuricemia-related chronic kidney disease.

Jing Liu, Fan Guo, Xiaoting Chen, Ping Fu, Liang Ma

Abstract read
In one paragraph

Article in MedComm, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

5 authors.

Jing LiuDivision of Nephrology, Institute of Kidney Diseases West China Hospital of Sichuan University Chengdu China.ORCID https://orcid.org/0000-0001-8802-0783
Fan GuoDivision of Nephrology, Institute of Kidney Diseases West China Hospital of Sichuan University Chengdu China.
Xiaoting ChenAnimal Experimental Center West China Hospital of Sichuan University Chengdu China.
Ping FuDivision of Nephrology, Institute of Kidney Diseases West China Hospital of Sichuan University Chengdu China.
Liang MaDivision of Nephrology, Institute of Kidney Diseases West China Hospital of Sichuan University Chengdu China.ORCID https://orcid.org/0000-0001-8327-7969

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperuricemia is an essential risk factor in chronic kidney disease (CKD), while urate-lowering therapy to prevent or delay CKD is controversial. Alternatively activated macrophages in response to local microenvironment play diverse roles in kidney diseases. Here, we aim to investigate whether and how macrophage integrin αM (ITGAM) contributes to hyperuricemia-related CKD. In vivo, we explored dynamic characteristics of renal tissue in hyperuricemia-related CKD mice. By incorporating transcriptomics and phosphoproteomics data, we analyzed gene expression profile, hub genes and potential pathways. In vitro, we validated bioinformatic findings under different conditions with interventions corresponding to core nodes. We found that hyperuricemia-related CKD was characterized by elevated serum uric acid levels, impaired renal function, activation of macrophage alternative (M2) polarization, and kidney fibrosis. Integrated bioinformatic analyses revealed

Indexed as

chronic kidney diseasehyperuricemiaintegrin αMmacrophage M2 polarization

Identifiers

PMID38911067
PMCPMC11193137

What OpenQuestion holds

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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.