Evidence map›Paper›PMID 35264456›Full record

ArticleJournal of the American Society of Nephrology : JASN2022

Intestinal Bacterial Translocation Contributes to Diabetic Kidney Disease.

Hoang Thuy Linh, Yasunori Iwata, Yasuko Senda, Yukiko Sakai-Takemori, Yusuke Nakade, Megumi Oshima, Shiori Nakagawa-Yoneda, Hisayuki Ogura, Koichi Sato, Taichiro Minami and 12 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 2% of its field
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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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  5. The gut as a central hub for multi-organ crosstalk in aging.Cellular and molecular life sciences : CMLS · 2026
    Review
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  8. Article
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  12. Article
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  14. Salvianolic Acids and Their Pharmacological Promise in Kidney Diseases: A Narrative Review.International journal of nephrology and renovascular disease · 2026
    Review
  15. Article
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  17. Article
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  19. Article
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8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 5 institutions in 1 country.

Hoang Thuy LinhDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.ORCID 0000-0001-7860-5219
Yasunori IwataDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Yasuko SendaDivision of Infection Control, Kanazawa University Hospital, Kanazawa, Japan.
Yukiko Sakai-TakemoriDivision of Infection Control, Kanazawa University Hospital, Kanazawa, Japan.
Yusuke NakadeDivision of Infection Control, Kanazawa University Hospital, Kanazawa, Japan.
Megumi OshimaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.ORCID 0000-0002-4108-5229
Shiori Nakagawa-YonedaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Hisayuki OguraDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Koichi SatoDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Taichiro MinamiDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Shinji KitajimaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Tadashi ToyamaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Yuta YamamuraDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.ORCID 0000-0003-3713-0733
Taro MiyagawaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.ORCID 0000-0003-0186-7362
Akinori HaraDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Miho ShimizuDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.ORCID 0000-0002-7737-935
Kengo FuruichiDivision of Nephrology, Kanazawa Medical University School of Medicine, Kanazawa, Japan.
Norihiko SakaiDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Hiroyuki YamadaDepartment of Nephrology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Katsuhiko AsanumaDepartment of Nephrology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Kouji MatsushimaDivision of Molecular Regulation of Inflammatory and Immune Diseases, Research Institute of Biomedical Sciences, Tokyo University of Science, Tokyo, Japan.
Takashi WadaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Kanazawa University · JPKanazawa University Hospital · JPChiba University · JPKanazawa Medical University · JPTokyo University of Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn recent years, many studies have focused on the intestinal environment to elucidate pathogenesis of various diseases, including kidney diseases. Impairment of the intestinal barrier function, the "leaky gut," reportedly contributes to pathologic processes in some disorders. Mitochondrial antiviral signaling protein (MAVS), a component of innate immunity, maintains intestinal integrity. The effects of disrupted intestinal homeostasis associated with MAVS signaling in diabetic kidney disease remains unclear.

methodsTo evaluate the contribution of intestinal barrier impairment to kidney injury under diabetic conditions, we induced diabetic kidney disease in wild-type and MAVS knockout mice through unilateral nephrectomy and streptozotocin treatment. We then assessed effects on the kidney, intestinal injuries, and bacterial translocation.

resultsMAVS knockout diabetic mice showed more severe glomerular and tubular injuries compared with wild-type diabetic mice. Owing to impaired intestinal integrity, the presence of intestine-derived

conclusionsImpaired MAVS signaling both in the kidney and intestine contributes to the disrupted homeostasis, leading to diabetic kidney disease progression. Controlling intestinal homeostasis may offer a novel therapeutic approach for this condition.

Indexed as

Diabetes Mellitus, ExperimentalDiabetic NephropathiesAnimalsBacterial TranslocationInterleukin-17KidneyMiceMice, KnockoutInterleukin-17bacterial translocationdiabetesdiabetic kidney diseasegut-kidney axisinflammationmicrobiota

Identifiers

PMID35264456
PMCPMC9161796
OpenAlexW4220997028

What OpenQuestion 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 OpenQuestion graph.