1.Identification of susceptibility modules and genes for peri-implantitis compared to periodontitis within the same host environment using weighted gene co-expression network analysis
Ju-Young LEE ; Yeongjoo KIM ; Jung-min OH ; Yun Hak KIM ; Hyun-Joo KIM
Journal of Periodontal & Implant Science 2025;55(3):217-231
Purpose:
This study aimed to identify new susceptibility modules and genes by analyzing the transcriptional profiles of peri-implantitis and periodontitis within the same host environment, using weighted gene co-expression network analysis (WGCNA).
Methods:
Gingival tissue samples were collected from 10 patients, each presenting with both periodontitis and peri-implantitis sites, and were used for RNA sequencing. We conducted WGCNA to identify key modules that showed distinct transcriptional expression profiles between periodontitis and peri-implantitis. Gene Ontology enrichment and Kyoto Encyclopedia of Genes and Genomes pathway analyses were carried out using R software.Genes with an adjusted P value greater than 0.05 were excluded from gene selection using the Pearson correlation method.
Results:
A total of 2,226 regulated genes were identified, and those with similar expression patterns were grouped into 5 color-coded functional modules using WGCNA. Among these, 3 modules showed distinct differences in expression profiles between peri-implantitis and periodontitis. The turquoise and yellow modules were associated with upregulation in periimplantitis, while the blue module was linked to periodontitis. This finding suggests that peri-implantitis and periodontitis have significantly different transcriptional signatures.Over-representation analysis was conducted to explore the component genes of the established modules. The top-ranked genes, selected based on their network connectivity within the modules, were identified using DESeq2 and were considered hub genes.
Conclusions
WGCNA revealed distinct modular gene patterns in peri-implantitis and periodontitis, highlighting transcriptional differences between the 2 conditions. Notably, we identified 10 key genes from each of the 3 modules—the blue module associated with periodontitis-dominant pathways, and the turquoise and yellow modules associated with peri-implantitis-dominant pathways. The hub genes and pathways unveiled in this research are likely key contributors to the progression of peri-implantitis and warrant further exploration as promising candidates.
2.Various Applications of Purse-String Suture and Its Cosmetic Outcome in Cutaneous Surgical Defects
Sujin PARK ; Yeongjoo OH ; Jong Won LEE ; Sooyie CHOI ; Kyoung Ae NAM ; Mi Ryung ROH ; Kee Yang CHUNG
Annals of Dermatology 2023;35(2):100-106
Background:
Purse-string suture is a simple technique to reduce wound size and to achieve complete or partial closure of skin defects.
Objective:
To classify situations in which purse-string sutures can be utilized and to assess the long-term size reduction and cosmetic outcome of the final scar.
Methods:
Patients (93 from Severance hospital and 12 from Gangnam Severance hospital) in whom purse-string sutures were used between January 2015 and December 2019 were retrospectively reviewed. Wound site, final reconstruction method, repair duration, final wound size, and Vancouver scar scale were assessed.
Results:
A total of 105 patients were reviewed. Lesions were located on the trunk (48 [45.7%]), limbs (32 [30.5%]), and face (25 [23.8%]). Mean ratio of wound length/primary defect length was 0.79±0.30. Multilayered purse-string suture showed the shortest duration from excision to final repair (p<0.001) and most effectively minimized the scar size (scar to defect size ratio 0.67±0.23, p=0.002). The average Vancouver scar scale measured at the latest followup visit at least 6 months postoperatively was 1.62, and the risk of hypertrophic scarring was 8.6%. There was no significant difference in the Vancouver scar scale and the risk of hypertrophic scarring between the different surgical method groups.
Conclusion
Purse-string sutures can be utilized in many stages of reconstruction to effectively reduce scar size without compromising the final cosmetic outcome.
3.Angiosarcoma Presenting with a Wide Range of Histopathological Features and Differentiation: A Case Report
Yeongjoo OH ; Hemin LEE ; Sang Kyum KIM ; Sang Ho OH
Korean Journal of Dermatology 2019;57(5):290-291
No abstract available.
Hemangiosarcoma
4.The Role of F-18 FDG PET/CT in Intrahepatic Cholangiocarcinoma
Yeongjoo LEE ; Ie Ryung YOO ; Sun Ha BOO ; Hyoungwoo KIM ; Hye Lim PARK ; Joo Hyun O
Nuclear Medicine and Molecular Imaging 2017;51(1):69-78
PURPOSE: The aim of this study was to evaluate the diagnostic and prognostic role of metabolic parameters of FDG PET/CT in patients with intrahepatic cholangiocarcinoma (ICC).METHODS: From December 2008 to December 2013, 76 FDG PET/CT scans performed for initial staging of ICC in a single institution (57 male and 19 female; mean age 68 ± 9 years) were retrospectively reviewed. Patients with history of other known malignancy were excluded. Detection rates of regional lymph node and distant metastasis by FDG PET/CT were analyzed in comparison with conventional imaging modalities such as CT or MRI. Metabolic parameters including maximum, peak and mean standardized uptake values (SUVmax, SUVpeak, SUVmean), metabolic tumor volume (MTV), total lesion glycolysis (TLG), glucose corrected SUV (SUVgluc), and glucose corrected TLG (TLGgluc) were measured for the primary tumor. Cut-off values for the metabolic parameters were calculated by ROC curve analysis, and used to dichotomize the patient groups. The overall survival time (OS) was calculated and compared using the Cox proportional hazard regression analysis.RESULTS: The median duration of follow-up period was 5.4 months (interquartile range: 1.45~15.45). FDG PET/CT showed higher sensitivity than conventional imagingmodalities in detection of regional node involvement (74.5 % vs. 61.8 %, p = 0.013). In six patients, distant metastasis was identified only by FDG PET/CT. The mean SUVmax, SUVpeak, SUVmean, MTV, and TLG for the primary tumor were 8.2 ± 3.1, 6.8 ± 2.5, 4.0 ± 0.8, 192.7 ± 360.5 cm3, and 823.7 ± 1615.4, respectively. Patients with higher (≥7.3, HR: 4.280, p = 0.001), higher SUVpeak (≥6.5, HR: 2.333, p = 0.020), higher SUVmean (≥3.9, HR: 2.799, p = 0.004), higher SUVgluc (≥8.1, HR: 2.648, p = 0.012), and higher TLGgluc (≥431.6, HR: 2.186, p = 0.030) showed significantly shorter survival time. By multivariate study, operability was an independent prognostic factor for longer survival (HR: 4.113, p= 0.005).CONCLUSION: FDG PET/CT is an important diagnostic imaging tool in the nodal staging and detection of distant metastasis in ICC patients. Metabolic parameters may have a significant role as prognostic factors in patients with ICC.
Cholangiocarcinoma
;
Diagnostic Imaging
;
Female
;
Follow-Up Studies
;
Glucose
;
Glycolysis
;
Humans
;
Lymph Nodes
;
Magnetic Resonance Imaging
;
Male
;
Neoplasm Metastasis
;
Positron-Emission Tomography
;
Positron-Emission Tomography and Computed Tomography
;
Prognosis
;
Retrospective Studies
;
ROC Curve
;
Tumor Burden
5.Giant Cell Tumor of the Rib: Two Cases of F-18 FDG PET/CT Findings
Hye Lim PARK ; Ie Ryung YOO ; Yeongjoo LEE ; Sonya Youngju PARK ; Chan Kwon JUNG
Nuclear Medicine and Molecular Imaging 2017;51(2):182-185
We report two cases of giant cell tumor arising from the rib and their F-18 FDG PET/CT findings. The two patients complained of chest wall pain, and large lobulated soft tissue masses with intense FDG uptake were seen on F-18 FDG PET/CT. A malignant tumor such as osteosarcoma or chondrosarcoma was suspected due to the large size of the mass, bony destruction, and intense FDG uptake. En bloc resection was performed and final pathologic results revealed giant cell tumor of the rib. Giant cell tumor of the rib is very rare, and larger lesions with high FDG uptake can be misdiagnosed as an intrathoracic malignancy arising from the rib, pleura, or chest wall.
Chondrosarcoma
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Giant Cell Tumor of Bone
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Giant Cell Tumors
;
Giant Cells
;
Humans
;
Osteosarcoma
;
Pleura
;
Positron-Emission Tomography and Computed Tomography
;
Ribs
;
Thoracic Wall

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