Evidence map›Paper›PMID 40114574›Full record

ArticleEndocrine, metabolic & immune disorders drug targets2026

Akkermansia muciniphila Delays the Progression of Diabetic Nephropathy by Reducing the Accumulation of Uremic Toxins in the Feces and Peripheral Blood

Xixi Song, Mingyan Yao, Jing Zhang, Bo Huang, Xin Li, Mengjuan Zhang, Jingqiu Cui

Abstract read
In one paragraph

Article in Endocrine, metabolic & immune disorders drug targets, 2026. 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

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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. Effect of pasteurizedGut microbes · 2026
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  2. 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.

Xixi SongDepartment of Endocrinology and Metabolism, Tianjin Medical University General Hospital, Tianjin, China
Mingyan YaoDepartment of Endocrinology and Metabolism, Baoding No.1 Central Hospital, Baoding, China
Jing ZhangDepartment of Cardiology, Affiliated Hospital of Hebei University, Hebei, Shijazhuang, China
Bo HuangDepartment of Endocrinology and Metabolism, Tianjin Medical University General Hospital, Tianjin, China
Xin LiDepartment of Endocrinology and Metabolism, Tianjin Medical University General Hospital, Tianjin, China
Mengjuan ZhangDepartment of Endocrinology and Metabolism, Tianjin Medical University General Hospital, Tianjin, China
Jingqiu CuiDepartment of Endocrinology and Metabolism, Tianjin Medical University General Hospital, Tianjin, China

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe pathogenesis of diabetes and diabetic kidney disease (DKD) is closely related to the imbalance of gut microbiota. We aimed to explore whether exogenous Akkermansia muciniphila (A. muciniphila) supplementation affected the progression of DKD.

methodsThe feces from normal subjects, diabetic patients without kidney diseases, and patients with DKD were collected, and the changes in microbial communities were analyzed. A rodent db/db DKD model was also constructed to investigate whether the abundance of A. muciniphila would be altered in response to renal function decline. The measurement of inflammatory cytokines in peripheral blood, fecal short-chain fatty acids (SCFAs), renal histopathology, and Western blot analysis were carried out to further evaluate the effects of A. muciniphila.

resultsThe relative abundance of A. muciniphila was found to be lower in the feces of DKD patients and also in the intestine of DKD mice. After exogenous supplementation of A. muciniphila, the levels of urinary protein, blood urea nitrogen, and creatinine decreased in DKD mice, as well as uremic toxins, trimethylamine-N-oxide (TMAO), p-cresol sulfonate, and indole sulfonate. A. muciniphila supplementation also increased the SCFAs gut production. The supplementation also protected the integrity of the intestinal mucosa by increasing MUC2, occludin, and zona occludens 1 (ZO-1) protein expression in the intestinal wall.

conclusionExogenous supplementation of A. muciniphila improved the imbalance of gut microbiota, reduced systemic inflammation, decreased uremic toxins, and protected the integrity of the intestinal mucosa, thus delaying DKD progression.

Indexed as

Diabetic NephropathiesFecesProbioticsUremic ToxinsAkkermansiaAnimalsDisease ProgressionFemaleGastrointestinal MicrobiomeHumansMaleMiceMice, Inbred C57BLMiddle AgedUremic ToxinsAkkermansia muciniphiladiabetic kidney diseaseGut microbiotauremic toxins.

Identifiers

PMID40114574
PMCPMC13555839

What Socratic holds

Textmetadata
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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 Socratic graph.