6.Up-to-Date Knowledge on Osteoporosis Treatment Selection in Postmenopausal Women
Hye Gyeong JEONG ; Min Kyung KIM ; Hee Jeung LIM ; Seul Ki KIM
Journal of Menopausal Medicine 2022;28(3):85-91
The concept of a super-aged society has led to a steady increase in the average lifespan and hence, interest in a healthy life has increased. Aging is a major risk factor for many diseases, including osteoporosis. Osteoporotic fractures have a significant impact on the quality of life of the elderly and hence, it is pivotal to provide effective treatment of osteoporosis after menopause. Osteoporosis requires proper management and the treatment must be centered on long-term goals. New drugs with diverse mechanisms have been developed for treating osteoporosis. Current management of osteoporosis generally focuses on the importance of risk-based strategies to maximize the effectiveness of existing treatments and mitigate potential negative side-effects. Additionally, there is a need for sequential treatment of osteoporosis in the future. This review discusses the dynamic strategies for osteoporosis treatment and the importance of long-term management in postmenopausal women.
7.Isolation and Characterization of Extracellular Vesicle from Mesenchymal Stem Cells of the Epidural Fat of the Spine
Soo-Eun SUNG ; Min-Soo SEO ; Kyung-Ku KANG ; Joo-Hee CHOI ; Si-Joon LEE ; Ju-Hyeon LIM ; Seung Yun YANG ; Seul-Ki KIM ; Gun Woo LEE
Asian Spine Journal 2022;16(2):153-161
Methods:
In this study, we isolated the exosomes using the tangential flow filtration (TFF) system with exosome-depleted fetal bovine serum and performed the characterization tests via western blotting, reverse transcription–polymerase chain reaction, nanoparticle tracking analysis (NTA), and transmission electron microscopy.
Results:
In transmission electron microscopy, the exosome had a diameter of approximately 100–200 nm and had a spherical shape, whereas in the NTA, the exosome had an average diameter of 142.8 nm with a concentration of 1.27×1010 particles/mL. The flow cytometry analysis showed the expression of CD63 and CD81. The western blotting analysis showed the positive markers.
Conclusions
These findings showed that isolating the exosomes via TFF resulted in high-quality EF-MSC exosome yield. Further studies with exosomes from EF-MSC are needed to evaluate the function and role of the EF tissue.
8.Pictorial Review of Mediastinal Masses with an Emphasis on Magnetic Resonance Imaging
Jin Wang PARK ; Won Gi JEONG ; Jong Eun LEE ; Hyo-jae LEE ; So Yeon KI ; Byung Chan LEE ; Hyoung Ook KIM ; Seul Kee KIM ; Suk Hee HEO ; Hyo Soon LIM ; Sang Soo SHIN ; Woong YOON ; Yong Yeon JEONG ; Yun-Hyeon KIM
Korean Journal of Radiology 2021;22(1):139-154
Magnetic resonance imaging (MRI) has become a crucial tool for evaluating mediastinal masses considering that several lesions that appear indeterminate on computed tomography and radiography can be differentiated on MRI. Using a three-compartment model to localize the mass and employing a basic knowledge of MRI, radiologists can easily diagnose mediastinal masses. Here, we review the use of MRI in evaluating mediastinal masses and present the images of various mediastinal masses categorized using the International Thymic Malignancy Interest Group’s three-compartment classification system. These masses include thymic hyperplasia, thymic cyst, pericardial cyst, thymoma, mediastinal hemangioma, lymphoma, mature teratoma, bronchogenic cyst, esophageal duplication cyst, mediastinal thyroid carcinoma originating from ectopic thyroid tissue, mediastinal liposarcoma, mediastinal pancreatic pseudocyst, neurogenic tumor, meningocele, and plasmacytoma.
9.Importance and utilization frequency of essential competencies of Korean physical therapists
Junghyun CHOI ; Taeyoung OH ; Jae Seop OH ; Wootaek LIM ; Jeonhyeong LEE ; Seul Ki HAN ; Yun Sang PARK ; Hyeok Gyu KWON ; Chang Sik AHN
Journal of Educational Evaluation for Health Professions 2020;17():24-
10.Shprintzen–Goldberg syndrome with a novel missense mutation of SKI in a 6-month-old boy
Min Jin JEON ; Seul Gi PARK ; Man Jin KIM ; Byung Chan LIM ; Ki Joong KIM ; Jong Hee CHAE ; Soo Yeon KIM
Journal of Genetic Medicine 2020;17(1):43-46
The Shprintzen–Goldberg syndrome (SGS) is an extremely rare genetic disorder caused by heterozygous variant in SKI . SGS is characterized by neurodevelopmental impairment with skeletal anomaly. Recognition of SGS is sometimes quite challenging in practice because it has diverse clinical features involving skeletal, neurological, and cardiovascular system. Here we report a case of a 6-month-old boy who initially presented with developmental delay and marfanoid facial features including prominent forehead, hypertelorism, high arched palate and retrognathia. He showed motor developmental delay since birth and could not control his head at the time of first evaluation. His height was above 2 standard deviation score. Arachnodactyly, hypermobility of joints, skin laxity, and pectus excavatum were also noted. Sequencing for FBN1 was negative, however, a novel missense variant, c.350G>A in SKI was identified by sequential whole exome sequencing. To our knowledge, this is the first case with SGS with phenotypic features of SGS overlapping with those of the Marfan syndrome, diagnosed by next generation sequencing in Korea.

Result Analysis
Print
Save
E-mail