Evidence map›Paper›PMID 39668321›Full record

ReviewProbiotics and antimicrobial proteins2025

Gut Dysbiosis and Probiotic Therapy in Chronic Kidney Disease: A Comprehensive Review.

Fernanda Priscila Barbosa Ribeiro, Micaelle Oliveira de Luna Freire, Daniella de Oliveira Coutinho, Marry Aneyts de Santana Cirilo, José Luiz de Brito Alves

Abstract readReview
PubMed Publisher
In one paragraph

Review in Probiotics and antimicrobial proteins, 2025. 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.

  1. Article
  2. Article
  3. Review
  4. Review
  5. A guide to uraemic toxicity.Nature reviews. Nephrology · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Impact of aFoods (Basel, Switzerland) · 2025
    Article
  13. Review
  14. Review
  15. 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

5 authors.

Fernanda Priscila Barbosa RibeiroDepartment of Nutrition, Health Sciences Center, Federal University of Paraíba, Campus I - Jd, Cidade Universitária, João Pessoa, 58051-900, Brazil.ORCID http://orcid.org/0009-0004-3411-2884
Micaelle Oliveira de Luna FreireDepartment of Nutrition, Health Sciences Center, Federal University of Paraíba, Campus I - Jd, Cidade Universitária, João Pessoa, 58051-900, Brazil.ORCID http://orcid.org/0000-0002-4847-0699
Daniella de Oliveira CoutinhoDepartment of Nutrition, Health Sciences Center, Federal University of Paraíba, Campus I - Jd, Cidade Universitária, João Pessoa, 58051-900, Brazil.ORCID http://orcid.org/0009-0002-0375-8389
Marry Aneyts de Santana CiriloDepartment of Physiology and Pharmacology, Federal University of Pernambuco, 50.670-901, Recife, Brazil.ORCID http://orcid.org/0000-0003-1525-7741
José Luiz de Brito AlvesDepartment of Nutrition, Health Sciences Center, Federal University of Paraíba, Campus I - Jd, Cidade Universitária, João Pessoa, 58051-900, Brazil. jose.luiz@academico.ufpb.br.ORCID http://orcid.org/0000-0003-4696-3809

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic kidney disease (CKD) is a multifactorial disease affecting more than 13.4% of the world's population and is a growing public health problem. It is silent in its early stages and leads to irreversible kidney damage as the disease progresses. A key factor in this progression is the bidirectional relationship between CKD and gut dysbiosis, which creates an imbalance that promotes the accumulation of uremic toxins (UTs), contributing to renal fibrosis, endothelial dysfunction, and decreased glomerular filtration rate. In addition, CKD itself exacerbates gut dysbiosis by altering the composition of the gut microbiota (GM) and promoting the growth of pathogenic microorganisms. Therefore, it is crucial to explore new therapeutic strategies, and the use of probiotics and synbiotics has shown promise in modulating the GM. Numerous preclinical studies have shown that the use of probiotics in CKD has a beneficial effect on the kidney by reducing UTs, apoptosis, inflammation, and oxidative stress. Probiotic treatment has also been associated with restoration of intestinal integrity, modulation of microbial composition and diversity, and increased production of short-chain fatty acids (SCFAs). These positive results have also been observed in patients at different stages of CKD, where the use of probiotics and/or synbiotics was able to improve creatinine levels and uremic parameters and alleviate abdominal discomfort, in addition to modulating GM and reducing serum endotoxin levels. Although recent studies have explored the benefits of probiotics in the treatment of CKD, further research is needed to determine their long-term efficacy and clinical relevance. This review focuses on the factors driving gut dysbiosis in CKD, its role in disease progression, and the potential of probiotics as a therapeutic strategy.

Indexed as

DysbiosisGastrointestinal MicrobiomeProbioticsRenal Insufficiency, ChronicAnimalsHumansSynbioticsChronic kidney diseaseGut dysbiosisGut microbiotaProbiotic

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.