1.Age-Group Related Cohort Effects on the Association between Age at Menarche and Metabolic Syndrome among Korean Premenopausal Women
Korean Journal of Family Medicine 2019;40(4):280-281
No abstract available.
Cohort Effect
;
Cohort Studies
;
Female
;
Humans
;
Menarche
2.Efficacy of Dose-Escalated Radiotherapy for Recurrent Colorectal Cancer.
Sunmi JO ; Yunseon CHOI ; Sung Kwang PARK ; Jin Young KIM ; Hyun Jung KIM ; Yun Han LEE ; Won Yong OH ; Heunglae CHO ; Ki Jung AHN
Annals of Coloproctology 2016;32(2):66-72
PURPOSE: This study aimed to evaluate the effects of radiotherapy (RT) on progression-free survival (PFS) for patients with recurrent colorectal cancer. METHODS: We reviewed the records of 22 patients with recurrent colorectal cancer treated with RT between 2008 and 2014. The median radiation dose for recurrent disease was 57.6 Gy (range, 45-75.6 Gy). Patients were divided into 2 groups according to the type of RT: patients underwent RT without previous history of irradiation (n = 14) and those treated with secondary RT (reirradiation: n = 8) at the time of recurrence. RESULTS: The median follow-up period was 24.9 months (range, 4.5-66.6 months). Progression was observed in 14 patients (including 8 with loco-regional failure and 9 with distant metastases). Distant metastases were related to the RT dose (<70 Gy, P = 0.031). The 2-year loco-regional control (LRC), PFS, and overall survival (OS) rates were 74.6%, 45.1%, and 82.0%, respectively. The LRC rate was not different between the patients treated with RT for the first time and those treated with reirradiation (P = 0.101, 2-year LRC 79.5% vs. 41.7%). However, reirradiation was related to poor PFS (P = 0.022) and OS (P = 0.002). An escalated RT dose (≥70 Gy) was associated with a higher PFS (P = 0.014, 2-year PFS 63.5% vs. 20.8%). CONCLUSION: Salvage RT for locally recurrent colorectal cancer can be offered when surgery is impossible. Dose-escalated RT shows a possible benefit in reducing the risk of progression.
Colorectal Neoplasms*
;
Disease-Free Survival
;
Follow-Up Studies
;
Humans
;
Neoplasm Metastasis
;
Radiotherapy*
;
Rectal Neoplasms
;
Recurrence
3.The microbiome of the lung and its extracellular vesicles in nonsmokers, healthy smokers and COPD patients.
Hyun Jung KIM ; You Sun KIM ; Kang Hyun KIM ; Jun Pyo CHOI ; Yoon Keun KIM ; Sunmi YUN ; Lokesh SHARMA ; Charles S DELA CRUZ ; Jae Seung LEE ; Yeon Mok OH ; Sang Do LEE ; Sei Won LEE
Experimental & Molecular Medicine 2017;49(4):e316-
Chronic obstructive pulmonary disease (COPD) is a chronic inflammatory disease, and bacterial infection plays a role in its pathogenesis. Bacteria secrete nanometer-sized extracellular vesicles (EVs), which may induce more immune dysfunction and inflammation than the bacteria themselves. We hypothesized that the microbiome of lung EVs might have distinct characteristics depending on the presence of COPD and smoking status. We analyzed and compared the microbiomes of 13 nonsmokers with normal spirometry, 13 smokers with normal spirometry (healthy smokers) and 13 patients with COPD by using 16S ribosomal RNA gene sequencing of surgical lung tissue and lung EVs. Subjects were matched for age and sex in all groups and for smoking levels in the COPD and healthy smoker groups. Each group included 12 men and 1 woman with the same mean age of 65.5 years. In all groups, EVs consistently showed more operational taxonomic units (OTUs) than lung tissue. In the healthy smoker and COPD groups, EVs had a higher Shannon index and a lower Simpson index than lung tissue and this trend was more prominent in the COPD group. Principal component analysis (PCA) showed clusters based on sample type rather than participants' clinical characteristics. Stenotrophomonas, Propionibacterium and Alicyclobacillus were the most commonly found genera. Firmicutes were highly present in the EVs of the COPD group compared with other samples or groups. Our analysis of the lung microbiome revealed that the bacterial communities present in the EVs and in the COPD group possessed distinct characteristics with differences in the OTUs, diversity indexes and PCA clustering.
Alicyclobacillus
;
Bacteria
;
Bacterial Infections
;
Extracellular Vesicles*
;
Female
;
Firmicutes
;
Humans
;
Inflammation
;
Lung*
;
Male
;
Microbiota*
;
Passive Cutaneous Anaphylaxis
;
Principal Component Analysis
;
Propionibacterium
;
Pulmonary Disease, Chronic Obstructive*
;
RNA, Ribosomal, 16S
;
Smoke
;
Smoking
;
Spirometry
;
Stenotrophomonas