Evidence map›Paper›PMID 38166933›Full record

ArticleNutrition & metabolism2024

Deficiency of Trex1 leads to spontaneous development of type 1 diabetes.

Jiang-Man Zhao, Zhi-Hui Su, Qiu-Ying Han, Miao Wang, Xin Liu, Jing Li, Shao-Yi Huang, Jing Chen, Xiao-Wei Li, Xia-Ying Chen and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nutrition & metabolism, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

16 authors at 3 institutions in 1 country.

Jiang-Man ZhaoNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Zhi-Hui SuNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Qiu-Ying HanNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Miao WangNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Xin LiuNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Jing LiBeijing Tongren Eye Center, Beijing Tongren Hospital of Capital Medical University, Beijing, 100730, China.
Shao-Yi HuangNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Jing ChenNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Xiao-Wei LiNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Xia-Ying ChenNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Zeng-Lin GuoNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Shuai JiangNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Jie PanNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Tao LiNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China.
Wen XueNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China. wxue@xmail.ncba.ac.cn.
Tao ZhouNanhu Laboratory, National Center of Biomedical Analysis, Beijing, 100850, China. tzhou@ncba.ac.cn.
National Center of Biomedical Analysis · CNZhejiang University · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundType 1 diabetes is believed to be an autoimmune condition, characterized by destruction of insulin-producing cells, due to the detrimental inflammation in pancreas. Growing evidences have indicated the important role of type I interferon in the development of type 1 diabetes.

methodsTrex1-deficient rats were generated by using CRISPR-Cas9. The fasting blood glucose level of rat was measured by a Roche Accuchek blood glucose monitor. The levels of insulin, islet autoantibodies, and interferon-β were measured using enzyme-linked immunosorbent assay. The inflammatory genes were detected by quantitative PCR and RNA-seq. Hematein-eosin staining was used to detect the pathological changes in pancreas, eye and kidney. The pathological features of kidney were also detected by Masson trichrome and periodic acid-Schiff staining. The distribution of islet cells, immune cells or ssDNA in pancreas was analyzed by immunofluorescent staining.

resultsIn this study, we established a Trex1-deletion Sprague Dawley rat model, and unexpectedly, we found that the Trex1

conclusionsOur study links the DNA-induced chronic inflammation to the pathogenesis of type 1 diabetes, and also provides an animal model for type 1 diabetes studies.

Indexed as

TREX1Type 1 diabetesType I interferon

Identifiers

PMID38166933
PMCPMC10763031
OpenAlexW4390509478

What OpenQuestion holds

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LicenceCC BY
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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.