Evidence map›Paper›PMID 36854740›Full record

ArticleCommunications biology2023

Abnormal proliferation of gut mycobiota contributes to the aggravation of Type 2 diabetes.

Li Bao, Ying Zhang, Guoying Zhang, Dechun Jiang, Dan Yan

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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  18. Targeting metabolic pathways: a novel therapeutic direction for type 2 diabetes.Frontiers in cellular and infection microbiology · 2023
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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

5 authors at 3 institutions in 1 country.

Li BaoDepartment of Pharmacy, Beijing Shijitan Hospital, Capital Medical University, No.10 Tieyi-Road, Haidian District, 100038, Beijing, China.
Ying ZhangBeijing Key Laboratory of Bio-characteristic Profiling for Evaluation of Rational Drug Use, No.10 Tieyi-Road, Haidian District, 100038, Beijing, China.
Guoying ZhangBiomedical Innovation Center, Beijing Shijitan Hospital, Capital Medical University, No.10 Tieyi-Road, Haidian District, 100038, Beijing, China.
Dechun JiangDepartment of Pharmacy, Beijing Shijitan Hospital, Capital Medical University, No.10 Tieyi-Road, Haidian District, 100038, Beijing, China.
Dan YanBeijing Key Laboratory of Bio-characteristic Profiling for Evaluation of Rational Drug Use, No.10 Tieyi-Road, Haidian District, 100038, Beijing, China. danyan@ccmu.edu.cn.ORCID 0000-0003-2985-3798
Capital Medical University · CNBeijing Friendship Hospital · CNNational Medical Products Administration · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82073741
6 · The paper itself

Abstract

Type 2 diabetes (T2D) constitutes a worldwide health threat, and the underlying mechanism for the development and progression of T2D is complex and multifactorial. During the last decade, gut commensal bacteria have been found to play a crucial role in the regulation of T2D and related metabolic disorders. However, as a considerable component in gut microbiome, the relationship between mycobiota and T2D and related metabolic disorders remains unclear. As a proof-of-concept, we observed that the ablation of the commensal fungi in mice can protect HFD (High fat diet) induced insulin resistance and related metabolic disorders. Both ITS2 (internal transcribed spacer 2) sequencing and culture-dependent analysis show the enrichment of Candida albicans in samples from individuals with T2D (Chinese Clinical Trial Registry, ChiCTR2100042049). Repopulation with C. albicans in HFD mice accelerated insulin resistance and related disorders. Mechanically, we found the β-glucan from C. albicans mirrored the deteriorating effect of C. albicans through the dectin-1 dependent pathway. Our current findings support that gut mycobiota play an important role in the progress of T2D and indicated the preventing of gut mycobiota is a promising strategy to alleviate insulin resistance and related metabolic dysfunctions.

Indexed as

Diabetes Mellitus, Type 2Gastrointestinal MicrobiomeMycobiomeAnimalsCandida albicansCell ProliferationHumansInsulin ResistanceMice

Identifiers

PMID36854740
PMCPMC9974954
OpenAlexW4322720214

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.