Evidence map›Paper›PMID 40171160›Full record

ArticleFrontiers in cellular and infection microbiology2025

Disrupted gut microbiota promotes the progression of chronic kidney disease in 5/6 nephrectomy mice by

Fei Chen, Hailin Zhang, Qianqian Wei, Jie Tang, Lixia Yin, Yanan Ban, Qifan Zhou

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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.

Fei ChenBlood Purification Centre, The Affiliated Lianyungang Hospital of Xuzhou Medical University, Lianyungang, China.
Hailin ZhangBlood Purification Centre, The Affiliated Lianyungang Hospital of Xuzhou Medical University, Lianyungang, China.
Qianqian WeiBlood Purification Centre, Lianyungang Clinical College of Nanjing Medical University, Lianyungang, China.
Jie TangNursing Department, Yixing Traditional Chinese Medicine Hospital, Wuxi, China.
Lixia YinBlood Purification Centre, The First People's Hospital of Lianyungang, Lianyungang, China.
Yanan BanBlood Purification Centre, Lianyungang Clinical College of Nanjing Medical University, Lianyungang, China.
Qifan ZhouBlood Purification Centre, The First People's Hospital of Lianyungang, Lianyungang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Our previous study identified differences in the gut microbiota between patients with chronic kidney disease (CKD) and healthy individuals. We observed that antibiotic-treated mice exhibited symptoms similar to those of patients with CKD after receiving a gut microbiota transplant from patients with CKD. Methods: We constructed sham-operated and 5/6 nephrectomy mice as the sham control (SC) and CKD models, respectively. CKD models were divided into a control group (CG) and an intervention group (IG). After 16 weeks of normal feeding, the IG were treated with B. pumilus by oral gavage, while SC and CG were treated with PBS once daily, 5 days per week, for 7 weeks. Fecal samples were collected for 16s rRNA sequencing and metabolomic analysis, kidneys were harvested for histological examination, and the colon was used for RT-PCR analysis. Results: Conclusion: This study shows that changes in the gut microbiota can affect the kidneys through gut metabolism, confirming that the lack of probiotics and the proliferation of harmful bacteria leading to gut microbiota dysbiosis are drivers of CKD progression. Our findings provide a basis for clinical interventions using gut microbes and offer a reference for targeted probiotic therapy.

Indexed as

Bacillus pumilusGastrointestinal MicrobiomeRenal Insufficiency, ChronicAnimalsDisease Models, AnimalDisease ProgressionDysbiosisFecesKidneyMaleMetabolomicsMiceMice, Inbred C57BLNephrectomyProbioticsRNA, Ribosomal, 16SRNA, Ribosomal, 16SB. pumiluschronic kidney diseasedysbiosisgut-kidney axisgut metabolismgut microbiotauremic toxins

Identifiers

PMID40171160
PMCPMC11959065

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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.