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pmid:37051594

Discovering genetic linkage between periodontitis and type 1 diabetes: A bioinformatics study.

Junqi Liu · Bo Zhang · Guanyin Zhu · Chenlu Liu · Shuangcheng Wang · Zhihe Zhao

Frontiers in genetics · 2023 doi:10.3389/fgene.2023.1147819

Paper

complete

Experiment

complete

Data

partial

Analysis

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title
Discovering genetic linkage between periodontitis and type 1 diabetes: A bioinformatics study.
doi
10.3389/fgene.2023.1147819
pmid
37051594
authors array · 6 items
[0]
Junqi Liu
[1]
Bo Zhang
[2]
Guanyin Zhu
[3]
Chenlu Liu
[4]
Shuangcheng Wang
[5]
Zhihe Zhao
journal
Frontiers in genetics
year
2023
abstract
Background: Relationship between periodontitis (PD) and type 1 diabetes (T1D) has been reported, but the detailed pathogenesis requires further elucidation. This study aimed to reveal the genetic linkage between PD and T1D through bioinformatics analysis, thereby providing novel insights into scientific research and clinical treatment of the two diseases. Methods: PD-related datasets (GSE10334, GSE16134, GSE23586) and T1D-related datasets(GSE162689)were downloaded from NCBI Gene Expression Omnibus (GEO). Following batch correction and merging of PD-related datasets as one cohort, differential expression analysis was performed (adjusted p-value <0.05 and ∣log2 fold change| > 0.5), and common differentially expressed genes (DEGs) between PD and T1D were extracted. Functional enrichment analysis was conducted via Metascape website. The protein-protein interaction (PPI) network of common DEGs was generated in The Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) database. Hub genes were selected by Cytoscape software and validated by receiver operating characteristic (ROC) curve analysis. Results: 59 common DEGs of PD and T1D were identified. Among these DEGs, 23 genes were commonly upregulated, and 36 genes were commonly downregulated in both PD- and T1D-related cohorts. Functional enrichment analysis indicated that common DEGs were mainly enriched in tube morphogenesis, supramolecular fiber organization, 9 + 0 non-motile cilium, plasma membrane bounded cell projection assembly, glomerulus development, enzyme-linked receptor protein signaling pathway, endochondral bone morphogenesis, positive regulation of kinase activity, cell projection membrane and regulation of lipid metabolic process. After PPI construction and modules selection, 6 hub genes (CD34, EGR1, BBS7, FMOD, IGF2, TXN) were screened out and expected to be critical in linking PD and T1D. ROC analysis showed that the AUC values of hub genes were all greater than 70% in PD-related cohort and greater than 60% in T1D-related datasets. Conclusion: Shared molecular mechanisms between PD and T1D were revealed in this study, and 6 hub genes were identified as potential targets in treating PD and T1D.
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To identify the DEGs between disease and normal samples, the “limma” package and “DESeq2” package in R language software were used for PD- and T1D-related datasets respectively.
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sections[4] "2.2 Identification of DEGs" paragraph 2
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To identify the DEGs between disease and normal samples, the “limma” package and “DESeq2” package in R language software were used for PD- and T1D-related datasets respectively.
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number (s) can be found in the article/Supplementary Material.
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The analysis identified 59 common differentially expressed genes between periodontitis and type 1 diabetes and selected six hub genes: CD34, EGR1, BBS7, FMOD, IGF2, and TXN.
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59 common DEGs of PD and T1D were identified.
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sections[11] "3.3 PPI network construction and hub genes selection" paragraph 2
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6 hub genes were identified in this study: CD34, EGR1, BBS7, FMOD, IGF2, TXN.
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The analysis identified 59 common differentially expressed genes between periodontitis and type 1 diabetes and selected six hub genes: CD34, EGR1, BBS7, FMOD, IGF2, and TXN.
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[199]
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[202]
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[203]
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[205]
GSM404210
[206]
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[208]
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[209]
GSM404214
[210]
GSM404215
[211]
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[212]
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GSM404221
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GSM404222
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[223]
GSM404228
[224]
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GSM404230
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[230]
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[231]
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[233]
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[234]
GSM404239
[235]
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[237]
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[238]
GSM404243
[239]
GSM404244
[240]
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[241]
GSM404246
[242]
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[243]
GSM404248
[244]
GSM404249
[245]
GSM404250
[246]
GSM404251
[247]
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[248]
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[249]
GSM404254
[250]
GSM404255
[251]
GSM404256
[252]
GSM404257
[253]
GSM404258
[254]
GSM404259
[255]
GSM404260
[256]
GSM404261
[257]
GSM404262
[258]
GSM404263
[259]
GSM404264
[260]
GSM404265
[261]
GSM404266
[262]
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[263]
GSM404268
[264]
GSM404269
[265]
GSM404270
[266]
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[267]
GSM404272
[268]
GSM404273
[269]
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[270]
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[271]
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[272]
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[273]
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[274]
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[275]
GSM404280
[276]
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[277]
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[278]
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[279]
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[282]
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[283]
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[284]
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[286]
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[287]
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[290]
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[291]
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[292]
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[293]
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[294]
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[295]
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[296]
GSM404301
[297]
GSM404302
[298]
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[299]
GSM404304
[300]
GSM404305
[301]
GSM404306
[302]
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[303]
GSM404308
[304]
GSM404309
[305]
GSM404310
[306]
GSM404311
[307]
GSM404312
[308]
GSM404313
[309]
GSM404314
sample_count
310
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Bacterial Correlates of Gingival Gene Expression
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[3] object · 15 fields
id
data:geo:GSE162689
role
raw
format
geo-series
media_type
application/vnd.ncbi.geo-series+json
uri
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE162689
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE162689
version
null
note
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number (s) can be found in the article/Supplementary Material.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number (s) can be found in the article/Supplementary Material.
access_statement_kind
data_availability_statement
sample_accessions array · 59 items
[0]
GSM4957182
[1]
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[2]
GSM4957184
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GSM4957186
[5]
GSM4957187
[6]
GSM4957188
[7]
GSM4957189
[8]
GSM4957190
[9]
GSM4957191
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[12]
GSM4957194
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GSM4957195
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GSM4957196
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GSM4957198
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GSM4957199
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GSM4957200
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GSM4957201
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[22]
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GSM4957205
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GSM4957210
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GSM4957211
[30]
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GSM4957219
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GSM4957220
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[40]
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[41]
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[42]
GSM4957224
[43]
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[44]
GSM4957226
[45]
GSM4957227
[46]
GSM4957228
[47]
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[48]
GSM4957230
[49]
GSM4957231
[50]
GSM4957232
[51]
GSM4957233
[52]
GSM4957234
[53]
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[54]
GSM4957236
[55]
GSM4957237
[56]
GSM4957238
[57]
GSM4957239
[58]
GSM4957240
sample_count
59
group_sizes
null
group_sizes_basis
null
platform
24014
taxon
Homo sapiens
title
A histological and transcriptional characterization of the pancreatic acinar tissue in type 1 diabetes
resolution_checked_at
2026-11-01T18:06:43Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[4] object · 15 fields
id
data:geo:GSE23586
role
raw
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geo-series
media_type
application/vnd.ncbi.geo-series+json
uri
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE23586
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE23586
version
null
note
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number (s) can be found in the article/Supplementary Material.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number (s) can be found in the article/Supplementary Material.
access_statement_kind
data_availability_statement
sample_accessions array · 6 items
[0]
GSM578529
[1]
GSM578530
[2]
GSM578531
[3]
GSM578532
[4]
GSM578533
[5]
GSM578534
sample_count
6
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Altered gene expressions of leukocyte transendothelial migration and cell communication pathways in periodontitis-affected gingival tissues
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 8 items
[0]
asset:data:geo:GSE10334 not downloaded
[1]
asset:data:geo:GSE10334 licence not read
[2]
asset:data:geo:GSE16134 not downloaded
[3]
asset:data:geo:GSE16134 licence not read
[4]
asset:data:geo:GSE162689 not downloaded
[5]
asset:data:geo:GSE162689 licence not read
[6]
asset:data:geo:GSE23586 not downloaded
[7]
asset:data:geo:GSE23586 licence not read
analysis object · 4 fields
state
complete
methods array · 5 items
[0] object · 10 fields
id
method-1
family
differential_expression
specific
deseq2
label
Differential expression analysis
dsl_operations array · 3 items
[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
count_matrix_with_condition
evidence object · 3 fields
score
1
band
verbatim
quote
To identify the DEGs between disease and normal samples, the “limma” package and “DESeq2” package in R language software were used for PD- and T1D-related datasets respectively.
[1] object · 10 fields
id
method-2
family
differential_expression
specific
limma_voom
label
Differential expression analysis
dsl_operations array · 3 items
[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
count_matrix_with_condition
evidence object · 3 fields
score
0.8
band
high
quote
limma
[2] object · 10 fields
id
method-3
family
network_analysis
specific
ppi_network
label
Network / pathway analysis
dsl_operations array · 3 items
[0]
build_graph
[1]
centrality_scores
[2]
pathway_enrich
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
edge_list
evidence object · 3 fields
score
0.7
band
medium
quote
protein-protein interaction
[3] object · 10 fields
id
method-4
family
genetic_association
specific
linkage
label
Genetic association (GWAS / linkage / MR)
dsl_operations array · 3 items
[0]
gwas_locus_scan
[1]
mr_estimate
[2]
linkage_scan
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
genotype_phenotype_table
evidence object · 3 fields
score
0.7
band
medium
quote
genetic linkage
[4] object · 10 fields
id
method-5
family
diagnostic_evaluation
specific
roc
label
Diagnostic test evaluation
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[0]
confusion_counts
[1]
roc_curve
[2]
sensitivity_specificity
[3]
solve_confusion_matrix
[4]
classification_metrics
[5]
published_precision_envelope
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
reference_standard_and_test
evidence object · 3 fields
score
0.7
band
medium
quote
ROC analysis
targets array · 0 items
gaps array · 0 items
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
label
Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
true
required_operations array · 3 items
[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
missing_operations array · 0 items
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: deseq2.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R1
reachable
true
accessions array · 4 items
[0]
GSE10334
[1]
GSE16134
[2]
GSE23586
[3]
GSE162689
resolved_accessions array · 4 items
[0]
GSE10334
[1]
GSE16134
[2]
GSE23586
[3]
GSE162689
statements array · 1 item
[0]
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number (s) can be found in the article/Supplementary Material.
basis
The paper names GSE10334, GSE16134, GSE23586, GSE162689 in NCBI Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 3 items
[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
assets array · 2 items
[0]
source:pmid:37051594
[1]
data:geo:GSE10334
steps array · 1 item
[0]
run_analysis
must_build object · 5 fields
dsl_operations array · 0 items
converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE10334
gaps array · 0 items
review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T18:36:17Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
16728
completion_tokens
1497
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128
stages array · 1 item
[0] object · 4 fields
id
extraction
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complete
reader
MiniMax-M3.1-Flash
provider
minimax
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review.independent_reader
[1]
review.machine_critique
[2]
review.human_critique
execution object · 5 fields
state
absent
status
not_run
mode
null
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gaps array · 1 item
[0]
execution.not_run
provenance object · 7 fields
entities array · 3 items
[0] object · 3 fields
id
pmid:37051594
type
paper
label
pmid:37051594
[1] object · 3 fields
id
source:pmid:37051594
type
manuscript
label
PMID 37051594 full text
[2] object · 3 fields
id
data:geo:GSE10334
type
dataset
label
GEO GSE10334
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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[0] object · 3 fields
id
pmid:37051594
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paper
label
pmid:37051594
[1] object · 3 fields
id
source:pmid:37051594
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manuscript
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PMID 37051594 full text
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id
data:geo:GSE10334
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dataset
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GEO GSE10334
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agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-37051594
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extraction
used array · 1 item
[0]
source:pmid:37051594
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE10334
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accession_resolution
used array · 1 item
[0]
data:geo:GSE10334
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
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Corpus assay engine
[1] object · 3 fields
id
agent:minimax-reader
type
software
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MiniMax literature reader
source_run_id
reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
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ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:37051594
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sha256:b9da10d908503026fe3c1e631ee332fe66c5a5aff8a1cea62ff30a18d4ad3bd5
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null
gaps array · 12 items
[0]
asset:data:geo:GSE10334 licence not read
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[3]
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[4]
asset:data:geo:GSE162689 licence not read
[5]
asset:data:geo:GSE162689 not downloaded
[6]
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[7]
asset:data:geo:GSE23586 not downloaded
[8]
execution.not_run
[9]
review.human_critique
[10]
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[11]
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assays array · 1 item
[0] object · 11 fields
role
analysis
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differential_expression
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f2132e96ae6c7a4e
required_operations array · 3 items
[0]
normalise_counts
[1]
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[2]
fdr_bh
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supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
To identify the DEGs between disease and normal samples, the “limma” package and “DESeq2” package in R language software were used for PD- and T1D-related datasets respectively.
order_basis
analysis_only
id
assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37051594", "kind": "science-record", "revision": 4, "content_hash": "sha256:52c28a2ec6d6e1a34dea2ff3154459e2d6d816a04f2b01f90f6d1445c1693678", "created_at": "2026-11-01T19:01:42Z", "updated_at": "2026-11-01T22:51:41Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Discovering genetic linkage between periodontitis and type 1 diabetes: A bioinformatics study.", "doi": "10.3389/fgene.2023.1147819", "pmid": "37051594", "authors": ["Junqi Liu", "Bo Zhang", "Guanyin Zhu", "Chenlu Liu", "Shuangcheng Wang", "Zhihe Zhao"], "journal": "Frontiers in genetics", "year": 2023, "abstract": "Background: Relationship between periodontitis (PD) and type 1 diabetes (T1D) has been reported, but the detailed pathogenesis requires further elucidation. This study aimed to reveal the genetic linkage between PD and T1D through bioinformatics analysis, thereby providing novel insights into scientific research and clinical treatment of the two diseases. Methods: PD-related datasets (GSE10334, GSE16134, GSE23586) and T1D-related datasets(GSE162689)were downloaded from NCBI Gene Expression Omnibus (GEO). Following batch correction and merging of PD-related datasets as one cohort, differential expression analysis was performed (adjusted p-value <0.05 and ∣log2 fold change| > 0.5), and common differentially expressed genes (DEGs) between PD and T1D were extracted. Functional enrichment analysis was conducted via Metascape website. The protein-protein interaction (PPI) network of common DEGs was generated in The Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) database. Hub genes were selected by Cytoscape software and validated by receiver operating characteristic (ROC) curve analysis. Results: 59 common DEGs of PD and T1D were identified. Among these DEGs, 23 genes were commonly upregulated, and 36 genes were commonly downregulated in both PD- and T1D-related cohorts. Functional enrichment analysis indicated that common DEGs were mainly enriched in tube morphogenesis, supramolecular fiber organization, 9 + 0 non-motile cilium, plasma membrane bounded cell projection assembly, glomerulus development, enzyme-linked receptor protein signaling pathway, endochondral bone morphogenesis, positive regulation of kinase activity, cell projection membrane and regulation of lipid metabolic process. After PPI construction and modules selection, 6 hub genes (CD34, EGR1, BBS7, FMOD, IGF2, TXN) were screened out and expected to be critical in linking PD and T1D. ROC analysis showed that the AUC values of hub genes were all greater than 70% in PD-related cohort and greater than 60% in T1D-related datasets. Conclusion: Shared molecular mechanisms between PD and T1D were revealed in this study, and 6 hub genes were identified as potential targets in treating PD and T1D.", "claims": [{"id": "claim-method", "statement": "To identify the DEGs between disease and normal samples, the “limma” package and “DESeq2” package in R language software were used for PD- and T1D-related datasets respectively.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37051594", "locator": "sections[4] \"2.2 Identification of DEGs\" paragraph 2", "quote": "To identify the DEGs between disease and normal samples, the “limma” package and “DESeq2” package in R language software were used for PD- and T1D-related datasets respectively."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. 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The names of the repository/repositories and accession number (s) can be found in the article/Supplementary Material."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The analysis identified 59 common differentially expressed genes between periodontitis and type 1 diabetes and selected six hub genes: CD34, EGR1, BBS7, FMOD, IGF2, and TXN.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37051594", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "59 common DEGs of PD and T1D were identified."}, {"asset": "source:pmid:37051594", "locator": "sections[11] \"3.3 PPI network construction and hub genes selection\" paragraph 2", "quote": "6 hub genes were identified in this study: CD34, EGR1, BBS7, FMOD, IGF2, TXN."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The analysis identified 59 common differentially expressed genes between periodontitis and type 1 diabetes and selected six hub genes: CD34, EGR1, BBS7, FMOD, IGF2, and TXN.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:37051594"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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