1.Genotypic analysis of zoonotic Enterocytozoon bieneusi in wild deer in Korea
Gyeonguk NOH ; Haeseung LEE ; Seung-Hun LEE ; Min-Goo SEO ; Kyoo-Tae KIM ; Junho LEE ; Kaifa NAZIM ; Sang Joon PARK ; Man Hee RHEE ; Dongmi KWAK
Parasites, Hosts and Diseases 2024;62(4):484-489
Enterocytozoon bieneusi is an important microsporidian protozoa that causes intestinal disorders in humans. We collected 191 fecal samples from roadkill deer carcasses, among which 13 (6.8%) showed positive reaction for E. bieneusi by polymerase chain reaction assay. Phylogenetic analysis revealed 6 distinct genotypes, 1 of which was novel. All genotypes belonged to Group 1, which has low host specificity, indicating possible transmission through sylvatic cycle. E. bieneusi infection was predominant in female deer (p<0.05).
2.Genotypic analysis of zoonotic Enterocytozoon bieneusi in wild deer in Korea
Gyeonguk NOH ; Haeseung LEE ; Seung-Hun LEE ; Min-Goo SEO ; Kyoo-Tae KIM ; Junho LEE ; Kaifa NAZIM ; Sang Joon PARK ; Man Hee RHEE ; Dongmi KWAK
Parasites, Hosts and Diseases 2024;62(4):484-489
Enterocytozoon bieneusi is an important microsporidian protozoa that causes intestinal disorders in humans. We collected 191 fecal samples from roadkill deer carcasses, among which 13 (6.8%) showed positive reaction for E. bieneusi by polymerase chain reaction assay. Phylogenetic analysis revealed 6 distinct genotypes, 1 of which was novel. All genotypes belonged to Group 1, which has low host specificity, indicating possible transmission through sylvatic cycle. E. bieneusi infection was predominant in female deer (p<0.05).
3.Genotypic analysis of zoonotic Enterocytozoon bieneusi in wild deer in Korea
Gyeonguk NOH ; Haeseung LEE ; Seung-Hun LEE ; Min-Goo SEO ; Kyoo-Tae KIM ; Junho LEE ; Kaifa NAZIM ; Sang Joon PARK ; Man Hee RHEE ; Dongmi KWAK
Parasites, Hosts and Diseases 2024;62(4):484-489
Enterocytozoon bieneusi is an important microsporidian protozoa that causes intestinal disorders in humans. We collected 191 fecal samples from roadkill deer carcasses, among which 13 (6.8%) showed positive reaction for E. bieneusi by polymerase chain reaction assay. Phylogenetic analysis revealed 6 distinct genotypes, 1 of which was novel. All genotypes belonged to Group 1, which has low host specificity, indicating possible transmission through sylvatic cycle. E. bieneusi infection was predominant in female deer (p<0.05).
4.Genotypic analysis of zoonotic Enterocytozoon bieneusi in wild deer in Korea
Gyeonguk NOH ; Haeseung LEE ; Seung-Hun LEE ; Min-Goo SEO ; Kyoo-Tae KIM ; Junho LEE ; Kaifa NAZIM ; Sang Joon PARK ; Man Hee RHEE ; Dongmi KWAK
Parasites, Hosts and Diseases 2024;62(4):484-489
Enterocytozoon bieneusi is an important microsporidian protozoa that causes intestinal disorders in humans. We collected 191 fecal samples from roadkill deer carcasses, among which 13 (6.8%) showed positive reaction for E. bieneusi by polymerase chain reaction assay. Phylogenetic analysis revealed 6 distinct genotypes, 1 of which was novel. All genotypes belonged to Group 1, which has low host specificity, indicating possible transmission through sylvatic cycle. E. bieneusi infection was predominant in female deer (p<0.05).
5.Genotypic analysis of zoonotic Enterocytozoon bieneusi in wild deer in Korea
Gyeonguk NOH ; Haeseung LEE ; Seung-Hun LEE ; Min-Goo SEO ; Kyoo-Tae KIM ; Junho LEE ; Kaifa NAZIM ; Sang Joon PARK ; Man Hee RHEE ; Dongmi KWAK
Parasites, Hosts and Diseases 2024;62(4):484-489
Enterocytozoon bieneusi is an important microsporidian protozoa that causes intestinal disorders in humans. We collected 191 fecal samples from roadkill deer carcasses, among which 13 (6.8%) showed positive reaction for E. bieneusi by polymerase chain reaction assay. Phylogenetic analysis revealed 6 distinct genotypes, 1 of which was novel. All genotypes belonged to Group 1, which has low host specificity, indicating possible transmission through sylvatic cycle. E. bieneusi infection was predominant in female deer (p<0.05).
6.Guidelines for the Surgical Management of Oral Cancer: Korean Society of Thyroid-Head and Neck Surgery
Young hoon JOO ; Jae keun CHO ; Bon seok KOO ; Minsu KWON ; Seong keun KWON ; Soon young KWON ; Min su KIM ; Jeong kyu KIM ; Heejin KIM ; Innchul NAM ; Jong lyel ROH ; Young min PARK ; Il seok PARK ; Jung je PARK ; Sung chan SHIN ; Soon hyun AHN ; Seongjun WON ; Chang hwan RYU ; Tae mi YOON ; Giljoon LEE ; Doh young LEE ; Myung chul LEE ; Joon kyoo LEE ; Jin choon LEE ; Jae yol LIM ; Jae won CHANG ; Jeon yeob JANG ; Man ki CHUNG ; Yuh seok JUNG ; Jae gu CHO ; Yoon seok CHOI ; Jeong seok CHOI ; Guk haeng LEE ; Phil sang CHUNG
Clinical and Experimental Otorhinolaryngology 2019;12(2):107-144
Korean Society of Thyroid-Head and Neck Surgery appointed a Task Force to provide guidance on the implementation of a surgical treatment of oral cancer. MEDLINE databases were searched for articles on subjects related to “surgical management of oral cancer” published in English. Results were restricted to systematic reviews, randomized control trials/controlled clinical trials, and observational studies. The quality of evidence was rated with use RoBANS (Risk of Bias Assessment Tool for Nonrandomized Studies) and AMSTAR (A Measurement Tool to Assess the Methodological Quality of Systematic Reviews). Evidence-based recommendations for practice were ranked according to the American College of Physicians grading system. Additional directives are provided as expert opinions and Delphi questionnaire when insufficient evidence existed. The Committee developed 68 evidence-based recommendations in 34 categories intended to assist clinicians and patients and counselors, and health policy-makers. Proper surgical treatment selection for oral cancer, which is directed by patient- and subsite-specific factors, remains the greatest predictor of successful treatment outcomes. These guidelines are intended for use in conjunction with the individual patient's treatment goals.
Advisory Committees
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Bias (Epidemiology)
;
Carcinoma, Squamous Cell
;
Counseling
;
Expert Testimony
;
Humans
;
Mouth Neoplasms
;
Neck
;
Republic of Korea
7.Selective Cannabinoid Receptor-1 Agonists Regulate Mast Cell Activation in an Oxazolone-Induced Atopic Dermatitis Model.
Gaewon NAM ; Se Kyoo JEONG ; Bu Man PARK ; Sin Hee LEE ; Hyun Jong KIM ; Seung Phil HONG ; Beomjoon KIM ; Bong Woo KIM
Annals of Dermatology 2016;28(1):22-29
BACKGROUND: Many inflammatory mediators, including various cytokines (e.g. interleukins and tumor necrosis factor [TNF]), inflammatory proteases, and histamine are released following mast cell activation. However, the endogenous modulators for mast cell activation and the underlying mechanism have yet to be elucidated. Endogenous cannabinoids such as palmitoylethanolamide (PEA) and N-arachidonoylethanolamine (anandamide or AEA), were found in peripheral tissues and have been proposed to possess autacoid activity, implying that cannabinoids may downregulate mast cell activation and local inflammation. OBJECTIVE: In order to investigate the effect of cannabinoid receptor-1 (CB1R) agonists on mast cell activation, AEA-derived compounds were newly synthesized and evaluated for their effect on mast cell activation. METHODS: The effects of selected compounds on FcepsilonRI-induced histamine and beta-hexosaminidase release were evaluated in a rat basophilic leukemia cell line (RBL-2H3). To further investigate the inhibitory effects of CB1R agonist in vivo, an oxazolone-induced atopic dermatitis mouse model was exploited. RESULTS: We found that CB1R inhibited the release of inflammatory mediators without causing cytotoxicity in RBL-2H3 cells and that CB1R agonists markedly and dose-dependently suppressed mast cell proliferation indicating that CB1R plays an important role in modulating antigen-dependent immunoglobulin E (IgE)-mediated mast cell activation. We also found that topical application of CB1R agonists suppressed the recruitment of mast cells into the skin and reduced the level of blood histamine. CONCLUSION: Our results indicate that CB1R agonists down-regulate mast cell activation and may be used for relieving inflammatory symptoms mediated by mast cell activation, such as atopic dermatitis, psoriasis, and contact dermatitis.
Animals
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Basophils
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beta-N-Acetylhexosaminidases
;
Cannabinoid Receptor Agonists
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Cannabinoids
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Cell Line
;
Cytokines
;
Dermatitis, Atopic*
;
Dermatitis, Contact
;
Histamine
;
Immunoglobulin E
;
Immunoglobulins
;
Inflammation
;
Interleukins
;
Leukemia
;
Mast Cells*
;
Mice
;
Peptide Hydrolases
;
Psoriasis
;
Rats
;
Skin
;
Tumor Necrosis Factor-alpha
8.Extracorporeal Membrane Oxygenation Support in Adult Patients with Hematologic Malignancies and Severe Acute Respiratory Failure.
Tai Sun PARK ; You Na OH ; Sang Bum HONG ; Chae Man LIM ; Younsuck KOH ; Je Hwan LEE ; Jung Hee LEE ; Kyoo Hyung LEE ; Jin Won HUH
Korean Journal of Critical Care Medicine 2016;31(3):243-250
BACKGROUND: Administering extracorporeal membrane oxygenation (ECMO) to critically ill patients with acute respiratory distress syndrome has substantially increased over the last decade, however administering ECMO to patients with hematologic malignancies may carry a particularly high risk. Here, we report the clinical outcomes of patients with hematologic malignancies and severe acute respiratory failure who were treated with ECMO. METHODS: We performed a retrospective review of the medical records of patients with hematologic malignancies and severe acute respiratory failure who were treated with ECMO at the medical intensive care unit of a tertiary referral hospital between March 2010 and April 2015. RESULTS: A total of 15 patients (9 men; median age 45 years) with hematologic malignancies and severe acute respiratory failure received ECMO therapy during the study period. The median values of the Acute Physiology and Chronic Health Evaluation II score, Murray Lung Injury Score, and Respiratory Extracorporeal Membrane Oxygenation Survival Prediction Score were 29, 3.3, and -2, respectively. Seven patients received venovenous ECMO, whereas 8 patients received venoarterial ECMO. The median ECMO duration was 2 days. Successful weaning of ECMO was achieved in 3 patients. Hemorrhage complications developed in 4 patients (1 pulmonary hemorrhage, 1 intracranial hemorrhage, and 2 cases of gastrointestinal bleeding). The longest period of patient survival was 59 days after ECMO initiation. No significant differences in survival were noted between venovenous and venoarterial ECMO groups (10.0 vs. 10.5 days; p = 0.56). CONCLUSIONS: Patients with hematologic malignancies and severe acute respiratory failure demonstrate poor outcomes after ECMO treatment. Careful and appropriate selection of candidates for ECMO in these patients is necessary.
Adult*
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APACHE
;
Critical Illness
;
Extracorporeal Membrane Oxygenation*
;
Hematologic Neoplasms*
;
Hemorrhage
;
Humans
;
Intensive Care Units
;
Intracranial Hemorrhages
;
Lung Injury
;
Male
;
Medical Records
;
Respiratory Distress Syndrome, Adult
;
Respiratory Insufficiency*
;
Retrospective Studies
;
Tertiary Care Centers
;
Weaning
9.Extracorporeal Membrane Oxygenation Support in Adult Patients with Hematologic Malignancies and Severe Acute Respiratory Failure
Tai Sun PARK ; You Na OH ; Sang Bum HONG ; Chae Man LIM ; Younsuck KOH ; Je Hwan LEE ; Jung Hee LEE ; Kyoo Hyung LEE ; Jin Won HUH
The Korean Journal of Critical Care Medicine 2016;31(3):243-250
BACKGROUND: Administering extracorporeal membrane oxygenation (ECMO) to critically ill patients with acute respiratory distress syndrome has substantially increased over the last decade, however administering ECMO to patients with hematologic malignancies may carry a particularly high risk. Here, we report the clinical outcomes of patients with hematologic malignancies and severe acute respiratory failure who were treated with ECMO. METHODS: We performed a retrospective review of the medical records of patients with hematologic malignancies and severe acute respiratory failure who were treated with ECMO at the medical intensive care unit of a tertiary referral hospital between March 2010 and April 2015.
Adult
;
APACHE
;
Critical Illness
;
Extracorporeal Membrane Oxygenation
;
Hematologic Neoplasms
;
Hemorrhage
;
Humans
;
Intensive Care Units
;
Intracranial Hemorrhages
;
Lung Injury
;
Male
;
Medical Records
;
Respiratory Distress Syndrome, Adult
;
Respiratory Insufficiency
;
Retrospective Studies
;
Tertiary Care Centers
;
Weaning
10.Correlation between Heart Rate Variability and Sleep Structure in Primary Insomnia.
Sang Jin LEE ; Doo Heum PARK ; Jaehak YU ; Seung Ho RYU ; Ji Hyeon HA ; Man Kyoo SONG
Sleep Medicine and Psychophysiology 2010;17(1):21-27
OBJECTIVES: It is well established that primary insomnia affects the activity of autonomic nervous system. We tried to know how the activity of autonomic nervous system during night sleep changes by analyzing correlation between heart rate variability (HRV) index and the variables related with sleep structure in primary insomnia. METHODS: Thirty three subjects (mean age:36.2+/-14.2 years, male:female=15:18) who were diagnosed with primary insomnia were selected for the study. Nocturnal polysomnography (NPSG) was carried out on each subject and correlation was analyzed between high frequency/low frequency ratio (LF/HF ratio), one of HRV indices and the variables related with sleep structure which were calculated from NPSG. RESULTS: When age and sex were controlled, LF/HF ratio showed negative correlations with slow wave sleep and stage 2 sleep, respectively (r(p)=-0.43, p=0.01;r(p)=-0.37, p=0.04). On the other hands LF/HF ratio showed a positive correlation with arousal index (r(p)=0.65, p<0.001). The activity of autonomic nervous system responded differentially depending on the change of sleep structure in primary insomnia. Especially the increase of arousal index and the decrease of slow wave sleep and stage 2 sleep which are the components of non-REM sleep provoked hyperactivity of sympathetic nervous system. CONCLUSION: This study suggests that the typical change of sleep structure in primary insomnia can negatively impact on cardiovascular system.
Arousal
;
Autonomic Nervous System
;
Cardiovascular System
;
Hand
;
Heart
;
Heart Rate
;
Polysomnography
;
Sleep Initiation and Maintenance Disorders

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