Bo Mi Gil

Dr. Bo Mi Gil

orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
4 July 2019 in BMC Pulmonary Medicine
Verified
Journal Article
Open access
PDF file
JLJeong Uk Lim
Jeong Uk Lim
BGBo Mi Gil
Bo Mi Gil
HKHye Seon Kang
Hye Seon Kang
JOJongyeol Oh
Jongyeol Oh
YKYong Hyun Kim
Yong Hyun Kim
SKSoon Seog Kwon
Soon Seog Kwon
Patients with interstitial lung disease (ILD) who show features related to autoimmunity without meeting criteria for a defined connective tissue disease are categorized as interstitial pneumonia with autoimmune features (IPAF). The present study compared clinical characteristics and clinical outcomes of patients with IPAF to patients with connective tissue disease related-interstitial lung disease (CTD-ILD) and patients with idiopathic pulmonary fibrosis (IPF). ILD patients who were consecutively enrolled in a single institution ILD cohort between 2008 and 2015 were evaluated for the study. Clinical data had been prospectively collected, while radiologic imaging and pathologic findings were re-reviewed for the present study. Out of 305 patients with ILD, 54 (17.7%) patients met the classification of IPAF, 175 (57.4%) patients had IPF, and 76 (24.9%) patients were diagnosed with CTD-ILD. Compared to IPF, incidences of acute exacerbations in 1,3 and 5 years were significantly less in the IPAF group (p = 0.022, p = 0.026 and p = 0.007, respectively). From multivariate analysis for mortality, age (p = 0.034, HR 1.022, 95% CI: 1.002–1.044), FVC (p < 0.001, HR 0.970, 95% CI: 0.955–0.984), ILD exacerbation (p = 0.001, HR 2.074, 95% CI: 1.366–3.148), and ILD type (p = 0.047, HR 0.436, 95% CI: 0.192–0.984 (IPAF vs IPF), respectively) showed significant association. Compared to the other ILD groups, IPAF showed distinct clinical characteristics. The IPAF group showed better survival and less episodes of exacerbation when compared to the IPF group.

1 January 2023 in Korean Journal of Radiology
Verified
Journal Article
Open access
PDF file
HHHye Jeon Hwang
Hye Jeon Hwang
HKHyunjong Kim
Hyunjong Kim
JSJoon Beom Seo
Joon Beom Seo
JYJong Chul Ye
Jong Chul Ye
GOGyutaek Oh
Gyutaek Oh
YCYo Won Choi
Yo Won Choi
Hwang HJ, et al. Korean J Radiol. 2023 Aug;24(8):807-820. https://doi.org/10.3348/kjr.2023.0088

23 December 2021 in PLOS ONE
Verified
Journal Article
Open access
PDF file
ELEung Gu Lee
Eung Gu Lee
TLTae-Hee Lee
Tae-Hee Lee
YHYujin Hong
Yujin Hong
JRJiwon Ryoo
Jiwon Ryoo
JHJung Won Heo
Jung Won Heo
YKYong Hyun Kim
Yong Hyun Kim
Background: Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive fibrosing interstitial pneumonia of unknown etiology. In several randomized clinical trials, and in the clinical practice, pirfenidone is used to effectively and safely treat IPF. However, sometimes it is difficult to use the dose of pirfenidone used in clinical trials. This study evaluated the effects of low-dose pirfenidone on IPF disease progression and patient survival in the real-world. Methods: This retrospective, observational study enrolled IPF patients seen at the time of diagnosis at a single center from 2008 to 2018. Longitudinal clinical and laboratory data were prospectively collected. We compared the clinical characteristics, survival, and pulmonary function decline between patients treated and untreated with various dose of pirfenidone. Results: Of 295 IPF patients, 100 (33.9%) received pirfenidone and 195 (66.1%) received no antifibrotic agent. Of the 100 patients who received pirfenidone, 24 (24%), 50 (50%), and 26 (26%), respectively, were given 600, 1200, and 1800 mg pirfenidone daily. The mean survival time was 57.03 ± 3.90 months in the no-antifibrotic drug group and 73.26 ± 7.87 months in the pirfenidone-treated group (p = 0.027). In the unadjusted analysis, the survival of the patients given pirfenidone was significantly better (hazard ratio [HR] = 0.69, 95% confidence interval [CI]: 0.48–0.99, p = 0.04). After adjusting for age, gender, body mass index, and the GAP score [based on gender (G), age (A), and two physiological lung parameters (P)], survival remained better in the patients given pirfenidone (HR = 0.56, 95% CI: 0.37–0.85, p = 0.006). In terms of pulmonary function, the decreases in forced vital capacity (%), forced expiratory volume in 1 s (%) and the diffusing capacity of lung for carbon monoxide (%) were significantly smaller (p = 0.000, p = 0.001, and p = 0.007, respectively) in patients given pirfenidone. Conclusions: Low-dose pirfenidone provided beneficial effects on survival and pulmonary function decline in the real-world practice.

1 June 2019 in Journal of Thoracic Disease
Verified
Journal Article
Closed access
PDF file
YCYangsean Choi
Yangsean Choi
BGBo Mi Gil
Bo Mi Gil
MCMyung Hee Chung
Myung Hee Chung
WYWon Jong Yoo
Won Jong Yoo
NJNa Young Jung
Na Young Jung
JKJeana Kim
Jeana Kim
Background: The purpose of this study was to determine whether semi-automated region of interest (ROI) measurement of CT attenuations of solitary pulmonary nodule (SPN) is an accurate approach in differentiating malignant from benign SPN. Methods: Ninety cases of pathologically proven SPN were retrospectively reviewed. CT attenuations of SPN before and after contrast injection were measured using semi-automated ROI selection method. Attenuations within a range of −100 to 200 Hounsfield units (HU) as soft tissue density range were set. The ROI included the entire SPN regardless of its internal soft tissue contents after automatic elimination of airs, calcific, or bony densities. Results: There were 42 (46.7%) malignant SPN and 48 (53.3%) benign SPN, which were grouped into A (18 tuberculoma, 13 fungus), B (5 focal organizing pneumonia, 5 abscess), and C (7 other benign tumors). The malignant SPN showed significantly higher mean attenuations of enhancement and net-enhancement than all benign SPN (P<0.001). Using the area under the receiver operating characteristic curve (AUC), the cut-off net-enhancement of 15 HU gave 83% sensitivity, 65% specificity and 73% accuracy for predicting malignancy. Malignant SPN (mean 67.9 HU) had significantly higher enhancement than group A (mean 52.6 HU, P<0.001, 95% CI: 8.73, 21.81) and group B (mean 57.0 HU, P=0.025, 95% CI: −1.43, 20.34) while group C showed no significant difference (mean 68.1 HU, P=0.97). Net enhancements were higher in group B (mean 18.8 HU) than in group A (mean 8.8 HU) (P<0.001, 95% CI: 11.8, 23.18). Conclusions: The semi-automated ROI measurement of SPN’s attenuations on CT is an accurate approach in distinguishing indeterminate SPN.

1 January 2025 in Korean Journal of Radiology
Verified
Journal Article
Open access
PDF file
WJWon Gi Jeong
Won Gi Jeong
EHEui Jin Hwang
Eui Jin Hwang
GJGong Yong Jin
Gong Yong Jin
JLJu-Hyung Lee
Ju-Hyung Lee
SKSe Ri Kang
Se Ri Kang
JGJin Mo Goo
Jin Mo Goo
Jeong WG, et al. Korean J Radiol. 2025 Sep;26:e75. https://doi.org/10.3348/kjr.2025.0457

1 August 2024 in Radiology: Cardiothoracic Imaging
Verified
Journal Article
Closed access
BGBo Mi Gil
Bo Mi Gil
SCSuyon Chang
Suyon Chang
KBKyongmin Sarah Beck
Kyongmin Sarah Beck
WLWhal Lee
Whal Lee
HLHye-Jeong Lee
Hye-Jeong Lee
JJJung Im Jung
Jung Im Jung
Purpose To investigate the association between the anomalous aortic origin of the right coronary artery (R-AAOCA) from the left coronary sinus with interarterial course (IAC) found at coronary CT angiography and sudden cardiac death using a large data set from five university hospitals. Materials and Methods From a total of 89 314 CCTA scans (January 2009 to December 2016) that were retrospectively collected, 316 patients with R-AAOCA from the left sinus with IAC were retrospectively collected. After excluding patients with less than 2 years of follow-up, patients who had already undergone cardiovascular surgery or intervention, and patients with arrhythmia or heart failure before undergoing coronary CT angiography, 224 patients were analyzed. Follow-up was terminated upon the occurrence of major adverse cardiovascular events (MACE). Logistic regression was used to identify clinical and radiologic information as independent predictors of MACE. Results The period prevalence of R-AAOCA from the left sinus with IAC was 0.354%. The mean age was 62.03 years, with a male-to-female ratio of 182:134. During follow-up, 19 of 224 patients (8.5%) experienced MACE, but none had sudden cardiac death. Of these cases, only seven (3.13%) were suspected of being due to R-AAOCA from the left sinus with IAC and all of them had unstable angina. Coronary artery disease was significantly associated with MACE (P < .001), while no significant correlation was observed with radiologic features. Conclusion Sudden cardiac death was not associated with R-AAOCA from the left sinus with IAC found at coronary CT angiography. The occurrence of MACE was low, with coronary artery disease being the sole significant predictor of a patient's prognosis. Keywords: Anomalous Aortic Origin of the Right Coronary Artery, Left Coronary Sinus with Interarterial Course, Coronary CT Angiography, Sudden Cardiac Death Supplemental material is available for this article. © RSNA, 2024.