Evidence map›Paper›PMID 35582668›Full record

ReviewWorld journal of diabetes2022

Gut microbiota and diabetic kidney diseases: Pathogenesis and therapeutic perspectives.

Jia-Ran Lin, Zi-Ting Wang, Jiao-Jiao Sun, Ying-Ying Yang, Xue-Xin Li, Xin-Ru Wang, Yue Shi, Yuan-Yuan Zhu, Rui-Ting Wang, Mi-Na Wang and 3 more

Abstract readReview
In one paragraph

Review in World journal of diabetes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
–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

32 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  17. Molecular Therapeutics for Diabetic Kidney Disease: An Update.International journal of molecular sciences · 2024
    Review
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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

13 authors.

Jia-Ran LinGraduate School, Beijing University of Chinese Medicine, Beijing 100029, China.
Zi-Ting WangDepartment of Environmental Medicine, Karolinska Institutet, Stockholm 17165, Sweden.
Jiao-Jiao SunFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing 100029, China.
Ying-Ying YangClinical Research Center, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University, Shanghai 201204, China.
Xue-Xin LiDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm 17121, Sweden.
Xin-Ru WangDepartment of Acupuncture and Moxibustion, First Clinical Medical College, Beijing University of Chinese Medicine, Beijing 100029, China.
Yue ShiSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing 100029, China.
Yuan-Yuan ZhuFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing 100029, China.
Rui-Ting WangDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100029, China.
Mi-Na WangGraduate School, Beijing University of Chinese Medicine, Beijing 100029, China.
Fei-Yu XieSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China.
Peng WeiSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China.
Ze-Huan LiaoSchool of Biological Sciences, Nanyang Technological University, Singapore 637551, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic kidney disease (DKD) is one of the major chronic complications of diabetes mellitus (DM), as well as a main cause of end-stage renal disease. Over the last few years, substantial research studies have revealed a contributory role of gut microbiota in the process of DM and DKD. Metabolites of gut microbiota like lipopolysaccharide, short-chain fatty acids, and trimethylamine N-oxide are key mediators of microbial-host crosstalk. However, the underlying mechanisms of how gut microbiota influences the onset and progression of DKD are relatively unknown. Besides, strategies to remodel the composition of gut microbiota or to reduce the metabolites of microbiota have been found recently, representing a new potential remedial target for DKD. In this mini-review, we will address the possible contribution of the gut microbiota in the pathogenesis of DKD and its role as a therapeutic target.

Indexed as

DiabetesDiabetic kidney diseaseGut microbiotaInsulin resistancePathogenesisTherapeutic targets

Identifiers

PMID35582668
PMCPMC9052008

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.