Evidence map›Paper›PMID 34694461›Full record

SynthesisMolecular genetics and genomics : MGG2022

Identification of novel genome-wide pleiotropic associations with oral inflammatory traits.

Yanjiao Jin, Jie Yang, Shuyue Zhang, Xuefeng Shi, Jin Li, Songlin Wang

Abstract readMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in Molecular genetics and genomics : MGG, 2022. 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
0.3field-weighted citation impact, top 40% 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, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

6 authors at 3 institutions in 2 countries.

Yanjiao Jin *Salivary Gland Disease Center and Molecular Laboratory for Gene Therapy and Tooth Regeneration, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction, Capital Medical University School of Stomatology, Beijing, 100050, China.
Jie Yang *Department of Cell Biology, Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Shuyue ZhangDepartment of Cell Biology, Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Xuefeng ShiTianjin Key Laboratory of Ophthalmology and Visual Science, Tianjin Eye Hospital, Tianjin, 300020, China. shixf_tmu@163.com.
Jin LiDepartment of Cell Biology, Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China. jli01@tmu.edu.cn.ORCID http://orcid.org/0000-0001-7024-3591
Songlin WangSalivary Gland Disease Center and Molecular Laboratory for Gene Therapy and Tooth Regeneration, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction, Capital Medical University School of Stomatology, Beijing, 100050, China. slwang@ccmu.edu.cn.
Capital Medical University · CNTianjin Medical University · CNTianjin Medical University Eye Hospital · CN

Funding

scientific and technological research grant of tianjin health commission 2013KZ118
6 · The paper itself

Abstract

Oral inflammatory diseases (OIDs) are a group of dental diseases with multiple clinical manifestations that impact the majority of the world's population. Many studies have investigated the associations between individual OID traits and genomic variants, but whether pleiotropic loci are shared by oral inflammatory traits remains poorly understood. Here, we conducted multitrait joint analyses based on the summary statistics of genome-wide association studies (GWASs) of five dental traits from the UK Biobank. Among these genome-wide significant loci, two were novel for both painful gums and toothache. We identified causal variants at each novel locus, and functional annotation based on multiomics data suggested IL10 and IL12A/TRIM59 as potential candidate genes at the novel pleiotropic loci. Subsequent analyses of pathway enrichment and protein-protein interaction networks suggested the involvement of the candidate genes in immune regulation. In conclusion, our results uncover novel pleiotropic loci for OID traits and highlight the importance of immune regulation in the pathogenesis of OIDs. These findings will enhance our understanding of the pathogenesis of OIDs and be beneficial for risk screening, prevention, and the development of novel drugs targeting the immune regulation of OIDs.

Indexed as

Genetic PleiotropyCohort StudiesGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansInflammationIntracellular Signaling Peptides and ProteinsMouth DiseasesPhenotypePolymorphism, Single NucleotideQuantitative Trait, HeritableQuantitative Trait LociStomatitisStomatognathic DiseasesTripartite Motif ProteinsUnited KingdomIntracellular Signaling Peptides and ProteinsTRIM59 protein, humanTripartite Motif ProteinsGenome-wide association studiesImmunityInflammationMultitrait joint analysisOral diseasesPleiotropic loci

Identifiers

PMID34694461
OpenAlexW3210876202

What OpenQuestion holds

Textmetadata
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.