Evidence map›Paper›PMID 36227003›Full record

Observational studyJournal of diabetes investigation2023

Metabolic signatures of β-cell destruction in type 1 diabetes.

Shinsuke Noso, Naru Babaya, Yoshihisa Hiromine, Yasunori Taketomo, Fumimaru Niwano, Sawa Yoshida, Hiroshi Ikegami

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Journal of diabetes investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Genetics of type-1 diabetes.Diabetology international · 2024
    Review
  5. Article
  6. 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 at 1 institution in 1 country.

Shinsuke NosoDepartment of Endocrinology, Metabolism and Diabetes, Kindai University Faculty of Medicine, Osaka, Japan.ORCID https://orcid.org/0000-0002-0943-8450
Naru BabayaDepartment of Endocrinology, Metabolism and Diabetes, Kindai University Faculty of Medicine, Osaka, Japan.ORCID https://orcid.org/0000-0003-2466-1228
Yoshihisa HiromineDepartment of Endocrinology, Metabolism and Diabetes, Kindai University Faculty of Medicine, Osaka, Japan.ORCID https://orcid.org/0000-0002-7317-236X
Yasunori TaketomoDepartment of Endocrinology, Metabolism and Diabetes, Kindai University Faculty of Medicine, Osaka, Japan.ORCID https://orcid.org/0000-0003-1366-2049
Fumimaru NiwanoDepartment of Endocrinology, Metabolism and Diabetes, Kindai University Faculty of Medicine, Osaka, Japan.ORCID https://orcid.org/0000-0003-4673-9401
Sawa YoshidaDepartment of Endocrinology, Metabolism and Diabetes, Kindai University Faculty of Medicine, Osaka, Japan.ORCID https://orcid.org/0000-0002-3538-9779
Hiroshi IkegamiDepartment of Endocrinology, Metabolism and Diabetes, Kindai University Faculty of Medicine, Osaka, Japan.ORCID https://orcid.org/0000-0001-8808-4605
Kindai University · JP

Funding

Manpei Suzuki Diabetes Foundation Research grantMinistry of Education, Culture, Sports, Science and Technology Grants-in-Aid for Scientific Research, 17K09852Ministry of Education, Culture, Sports, Science and Technology Grants-in-Aid for Scientific Research, 21K08589
6 · The paper itself

Abstract

AIMS/

introductionIn the development of type 1 diabetes, metabolites are significantly altered and might be involved in β-cell destruction and protection. We aimed to identify new metabolic markers of β-cell destruction in type 1 diabetes patients. MATERIALS AND

methodsA total of 33 participants were recruited for this cross-sectional observational study: 23 with type 1 diabetes, seven with type 2 diabetes and three healthy controls. Those with type 1 diabetes were further subdivided into three groups: new-onset, microsecretors and complete lack of endogenous insulin in type 1 diabetes.

resultsMetabolomic analysis identified a total of 737 peaks, and partial least square analysis was successful in discriminating between the three groups of type 1 diabetes. Among the factor loadings discriminating type 1 diabetes, 3-phenylpropionic acid (r = 0.80, P = 4.7E

conclusionsIn the present study, metabolic signatures were shown to be useful in identifying type 1 diabetes at different clinical stages, and 3-phenylpropionic acid and hypotaurine are novel biomarkers for identifying new-onset type 1 diabetes, suggesting the involvement of the gut bacterial environment, anti-oxidant mechanisms through the hypotaurine-taurine pathway and methylated deoxyribonucleic acid fragmentation in the process of β-cell destruction.

Indexed as

Diabetes Mellitus, Type 1Diabetes Mellitus, Type 25-MethylcytosineCross-Sectional StudiesHumansMetabolomeMetabolomicsPhenylpropionatesTaurine3-phenylpropionic acid5-MethylcytosinehypotaurinePhenylpropionatesTaurineMetabolomeType 1 diabetesβ-cell

Identifiers

PMID36227003
PMCPMC9807153
OpenAlexW4304957541

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.