Evidence map›Paper›PMID 36016933›Full record

ArticleFrontiers in immunology2022

Identification of nine signature proteins involved in periodontitis by integrated analysis of TMT proteomics and transcriptomics.

Wei Liu, Wei Qiu, Zhendong Huang, Kaiying Zhang, Keke Wu, Ke Deng, Yuanting Chen, Ruiming Guo, Buling Wu, Ting Chen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
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

11 authors at 4 institutions in 1 country.

Wei LiuShenzhen Stomatology Hospital (Pingshan), Southern Medical University, Shenzhen, China.
Wei QiuDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Zhendong HuangDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Kaiying ZhangDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Keke WuDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Ke DengShanghai Key Laboratory of Stomatology, Department of Oral Implantology, Shanghai Ninth People Hospital, National Center of Stomatology, National Clinical Research Center of Oral Diseases, School of Medicine, College of Stomatology, Shanghai Jiao Tong University, Shanghai, China.
Yuanting ChenDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Ruiming GuoDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Buling WuShenzhen Stomatology Hospital (Pingshan), Southern Medical University, Shenzhen, China.
Ting ChenDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Fuchun FangDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Nanfang Hospital · CNSouthern Medical University · CNShanghai Jiao Tong University · CNStomatology Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, there are many researches on signature molecules of periodontitis derived from different periodontal tissues to determine the disease occurrence and development, and deepen the understanding of this complex disease. Among them, a variety of omics techniques have been utilized to analyze periodontitis pathology and progression. However, few accurate signature molecules are known and available. Herein, we aimed to screened and identified signature molecules suitable for distinguishing periodontitis patients using machine learning models by integrated analysis of TMT proteomics and transcriptomics with the purpose of finding novel prediction or diagnosis targets. Differential protein profiles, functional enrichment analysis, and protein-protein interaction network analysis were conducted based on TMT proteomics of 15 gingival tissues from healthy and periodontitis patients. DEPs correlating with periodontitis were screened using LASSO regression. We constructed a new diagnostic model using an artificial neural network (ANN) and verified its efficacy based on periodontitis transcriptomics datasets (GSE10334 and GSE16134). Western blotting validated expression levels of hub DEPs. TMT proteomics revealed 5658 proteins and 115 DEPs, and the 115 DEPs are closely related to inflammation and immune activity. Nine hub DEPs were screened by LASSO, and the ANN model distinguished healthy from periodontitis patients. The model showed satisfactory classification ability for both training (AUC=0.972) and validation (AUC=0.881) cohorts by ROC analysis. Expression levels of the 9 hub DEPs were validated and consistent with TMT proteomics quantitation. Our work reveals that nine hub DEPs in gingival tissues are closely related to the occurrence and progression of periodontitis and are potential signature molecules involved in periodontitis.

Indexed as

PeriodontitisProteomicsBiomarkersHumansProtein Interaction MapsTranscriptomeBiomarkersartificial neural networkinflammation and immune responseperiodontitissignature proteinsTMT proteomicstranscriptomics

Identifiers

PMID36016933
PMCPMC9397367
OpenAlexW4290772555

What Socratic 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 Socratic graph.