Evidence map›Paper›PMID 35712257›Full record

ArticleFrontiers in endocrinology2022

ASK1-Interacting Protein 1 Acts as a Novel Predictor of Type 2 Diabetes.

Zhigao Song, Cong Chen, Jipei He, Bixia Liu, Weidong Ji, Liangping Wu, Li He

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Therapeutic Potential of Myricitrin in aMolecules (Basel, Switzerland) · 2025
    Article
  4. Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Zhigao SongCenter for Translational Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Cong ChenCenter for Translational Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Jipei HeDepartment of Metabolic Surgery, Your Doctor Medical Group, Guangzhou, China.
Bixia LiuCenter for Translational Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Weidong JiCenter for Translational Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Liangping WuDepartment of Metabolic Surgery, Your Doctor Medical Group, Guangzhou, China.
Li HeCenter for Translational Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
The First Affiliated Hospital, Sun Yat-sen University · CNGuangzhou University · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes (T2D) mellitus is a chronic inflammatory disease characterized with high secretion of tumor necrosis factor (TNF)-α, but the regulatory pathway of TNF-α production in T2D has not been fully elucidated. ASK1-interacting protein 1 (AIP1) is a signaling scaffold protein that modulates several pathways associated with inflammation. In this study, we aimed to investigate the role of AIP1 in T2D development. Our results revealed that AIP1 was downregulated in omental adipose tissue (OAT) of obese patients with T2D compared with that in obese patients. In addition, Pearson's correlation test showed that AIP1 was negatively correlated with the homeostatic model assessment for insulin resistance (HOMA-IR, r = -0.4829) and waist-to-hip ratio (r = -0.2614), which are major clinical indexes of T2D. As revealed by the proteomic analysis, immunohistochemistry, and ELISA, the OAT and the serum of obese patients with T2D presented high inflammatory status. And the increased inflammatory factors TNF-α and C-reactive protein C (CRP) in the serum of obese patients with T2D showed a positive correlation with HOMA-IR (TNF-α, r = 0.4728; CRP, r = 0.5522). Interestingly, AIP1 deficiency in adipocytes facilitated TNF-α secretion and retarded glucose uptake. Mechanistically,

Indexed as

Diabetes Mellitus, Type 2Insulin Resistanceras GTPase-Activating ProteinsHumansObesityp38 Mitogen-Activated Protein KinasesProteomicsTumor Necrosis Factor-alphaDAB2IP protein, humanp38 Mitogen-Activated Protein Kinasesras GTPase-Activating ProteinsTumor Necrosis Factor-alphaadipose inflammationAIP1insulin resistancetype 2 diabetesvisceral adipose

Identifiers

PMID35712257
PMCPMC9196954
OpenAlexW4281625571

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.