Jae Myung Yu
Hallym University
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Featured researches published by Jae Myung Yu.
Diabetes Research and Clinical Practice | 2008
Hye Jin Yoo; Hyonggin An; Soyeon Park; Ohk Hyun Ryu; Honggon Kim; J.A. Seo; Eun-Gyoung Hong; D.H. Shin; Y.H. Kim; Suhyun Kim; Kyung Mook Choi; Inkeun Park; Jae Myung Yu; S. H. Baik
OBJECTIVE The use of a real time continuous glucose monitoring system (RT-CGM) was studied as a behavior modification tool and the effectiveness of a RT-CGM in glucose control for patients with type 2 diabetes was determined. METHODS We conducted a prospective, open-label, randomized, controlled clinical trial in 65 patients with poorly controlled type 2 diabetes (8.0</=HbA1c</=10%) over a 3-month period. The intervention group was monitored monthly with a RT-CGM (three days at a time for 3 months) and the control group continued self-monitoring blood glucose (SMBG) at least four times a week for 3 months. RESULTS The HbA1c of the RT-CGM group was significantly reduced after 12 weeks compared with the SMBG group (9.1+/-1.0% to 8.0+/-1.2% vs. 8.7+/-0.7% to 8.3+/-1.1%, respectively; P=0.004). In the RT-CGM group, there was a significant reduction in total daily calorie intake, weight, body mass index (BMI), and postprandial glucose level, and a significant increase in total exercise time per week after 3 months. CONCLUSIONS We demonstrated that the RT-CGM was useful in modifying a patients diet and exercise habits and could induce better glycemic control than SMBG for patients with type 2 diabetes.
Diabetic Medicine | 2010
Seung-Hyun Ko; Hyuk-Sang Kwon; Jae Myung Yu; S. H. Baik; Ie Byung Park; Ji Hye Lee; Kyung Soo Ko; Jung Hyun Noh; Deog-Yoon Kim; Chong Hwa Kim; Ji Oh Mok; T.S. Park; Hyun-Shik Son; Bong-Yun Cha
Diabet. Med. 27, 1033–1040 (2010)
Journal of International Medical Research | 2010
Jae Myeong Lee; Jong Hyun Kim; Hyun-Shik Son; Eun Gyoung Hong; Jae Myung Yu; Kyung Ah Han; Kyung-Wan Min; Sang-Ah Chang
Evaluating increasing circulating adiponectin levels is becoming an important strategy in the prevention of diabetes mellitus and cardiovascular events. This study was designed to investigate the effect of the angiotensin II receptor blocker valsartan on blood adiponectin levels and insulin sensitivity in patients with type 2 diabetes and mild-to-moderate hypertension. A total of 91 Korean patients were treated with 80 mg/day valsartan for 4 weeks followed by 160 mg/day for a further 8 weeks. Blood pressure, adiponectin levels and metabolic parameters were measured before and after treatment. The homeostasis model assessment of insulin resistance (HOMA-IR) was calculated as an insulin sensitivity index. Valsartan significantly decreased mean blood pressure and increased circulating adiponectin levels. There were no differences in metabolic parameters, including HOMA-IR, glycosylated haemoglobin and lipid levels before and after treatment. These results indicated that valsartan increases circulating adiponectin levels, but does not change insulin sensitivity in patients with type 2 diabetes and mild-to-moderate hypertension.
Diabetes & Metabolism Journal | 2011
Ji-Hyun Kim; Su Jin Oh; Jung Min Lee; Eun Gyoung Hong; Jae Myung Yu; Kyung Ah Han; Kyung Wan Min; Hyun Shik Son; Sang Ah Chang
Background Hypertension and type 2 diabetes mellitus are major risk factors for cardiovascular disease. This study analyzed the changes in central aortic waveforms and pulse wave velocity as well as related parameters after treatment with valsartan, an angiotensin II type 1 receptor blocker, in patients with type 2 diabetes and hypertension. Methods We used pulse wave analysis to measure central aortic waveform in a total of 98 subjects. In 47 of these patients, pulse wave velocity measurements were obtained before and after 12 weeks of treatment with valsartan. Results In the central aortic waveform analysis, the aortic pulse pressure and augmentation index were significantly decreased after valsartan treatment, as was the aortic pulse wave velocity. Factors contributing to the improvement in pulse wave velocity were the fasting blood glucose and haemoglobin A1c levels. Conclusion Short-term treatment with valsartan improves arterial stiffness in patients with type 2 diabetes and hypertension, and the glucose status at baseline was associated with this effect.
Yonsei Medical Journal | 2016
Sung Hoon Yu; Jae Myung Yu; Hyung Joon Yoo; Seong Jin Lee; Dong Hyun Kang; Young Jung Cho; Doo Man Kim
Purpose Proliferation of vascular smooth muscle cells (VSMCs) plays a crucial role in atherosclerosis. Rutin is a major representative of the flavonol subclass of flavonoids and has various pharmacological activities. Currently, data are lacking regarding its effects on VSMC proliferation induced by intermittent hyperglycemia. Here, we demonstrate the effects of rutin on VSMC proliferation and migration according to fluctuating glucose levels. Materials and Methods Primary cultures of male Otsuka Long-Evans Tokushima Fatty (OLETF) rat VSMCs were obtained from enzymatically dissociated rat thoracic aortas. VSMCs were incubated for 72 h with alternating normal (5.5 mmol/L) and high (25.0 mmol/L) glucose media every 12 h. Proliferation and migration of VSMCs, the proliferative molecular pathway [including p44/42 mitogen-activated protein kinases (MAPK), mitogen-activated protein kinase kinase 1/2 (MEK1/2), p38 MAPK, phosphoinositide 3-kinase (PI3K), c-Jun N-terminal protein kinase (JNK), nuclear factor kappa B (NF-κB), and Akt], the migratory pathway (big MAPK 1, BMK1), reactive oxygen species (ROS), and apoptotic pathway were analyzed. Results We found enhanced proliferation and migration of VSMCs when cells were incubated in intermittent high glucose conditions, compared to normal glucose. These effects were lowered upon rutin treatment. Intermittent treatment with high glucose for 72 h increased the expression of phospho-p44/42 MAPK (extracellular signal regulated kinase 1/2, ERK1/2), phospho-MEK1/2, phospho-PI3K, phospho-NF-κB, phospho-BMK1, and ROS, compared to treatment with normal glucose. These effects were suppressed by rutin. Phospho-p38 MAPK, phospho-Akt, JNK, and apoptotic pathways [B-cell lymphoma (Bcl)-xL, Bcl-2, phospho-Bad, and caspase-3] were not affected by fluctuations in glucose levels. Conclusion Fluctuating glucose levels increased proliferation and migration of OLETF rat VSMCs via MAPK (ERK1/2), BMK1, PI3K, and NF-κB pathways. These effects were inhibited by the antioxidant rutin.
Arteriosclerosis, Thrombosis, and Vascular Biology | 2016
Sang Man Jin; Kyung Ah Han; Jae Myung Yu; Tae Seo Sohn; Sung Hee Choi; Choon Hee Chung; Ie Byung Park; Eun-Jung Rhee; Sei Hyun Baik; Tae Sun Park; In-Kyu Lee; Seung-Hyun Ko; You Cheol Hwang; Bong Soo Cha; Hyoung Woo Lee; Moon Suk Nam; Moon Kyu Lee
Objective— To determine the effect of probucol on urine albumin excretion in type 2 diabetes mellitus patients with albuminuria using angiotensin-converting enzyme inhibitors or angiotensin receptor blockers. Approach and Results— This was a 16-week, phase II, randomized, placebo-controlled, parallel-group study in type 2 diabetes mellitus patients with a urinary albumin/creatinine ratio of ≥300 mg/g using angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, conducted in 17 tertiary referral hospitals. Eligible patients were randomized to probucol 250 mg/d (n=44), probucol 500 mg/d (n=41), and placebo (n=41) groups in a ratio of 1:1:1 after block randomization procedures, keeping the treatment assignment blinded to the investigators, patients, and study assistants. The primary end point was change in the geometric mean of urinary albumin/creatinine ratio from baseline to week 16 (ClinicalTrials.gov identifier NCT01726816). The study was started on November 8, 2012, and completed on March 24, 2014. The least squares mean change±SE from baseline in urinary albumin/creatinine ratio at week 16 was −7.2±639.5 mg/g in the probucol 250 mg/d group (n=43; P=0.2077 versus placebo group), 9.3±587.4 mg/g in the probucol 500 mg/d group (n=40; P=0.1975 versus placebo group), and 259.0±969.1 mg/g in the placebo group (n=41). Although the majority of subjects were on statins, probucol treatment significantly lowered total cholesterol and low-density lipoprotein cholesterol levels. QT prolongation occurred in one and two subjects in control and probucol 250 mg/d groups, respectively. Conclusions— Four months of probucol up to 500 mg/d failed to reduce urinary albumin excretion.
Journal of Diabetes and Its Complications | 2018
Shinje Moon; Jung Hwan Park; Jae Myung Yu; Moon-Ki Choi; Hyung Joon Yoo
AIMS The aim of this study was to evaluate ethnic- and sex-specific associations between DM and hearing impairment. METHODS For this cross-sectional study using National Health and Nutrition Examination Survey in the U.S. and Korea, the total number of eligible participants included was 7081 in the U.S. and 15,704 in Korea. Hearing impairment was defined as a pure tone threshold level ≥ 25 dB. Multivariate logistic regression analysis was conducted, adjusting for age, sex, race/ethnicity, socioeconomic status, body mass index, noise exposure, smoking, hypertension, and dyslipidemia. RESULTS The association between DM and hearing impairment was found to be sex-specific. The multivariate adjusted ORs of high-frequency impairment were 0.843 (95% CI, 0.524-1.356) in American men, and 1.073 (95% CI, 0.835-1.379) in Korean men, while the ORs in women from U.S. and Korea were 1.911 (95% CI, 1.244-2.935) and 1.421 (95% CI, 1.103-1.830), respectively. A subgroup analysis of each race/ethnicity among the U.S. adults showed similar results. In contrast to high-frequency impairment, there was no significant association between low-frequency impairment and DM in both men and women. CONCLUSION Our results suggest that DM is associated with hearing impairment in only women, irrespective of race/ethnicity groups.
Korean Diabetes Journal | 2009
Hae Ri Lee; Jae Myung Yu; Moon-Gi Choi; Hyung Joon Yoo; Eun-Gyoung Hong
Journal of Korean Endocrine Society | 2006
Hyun Won Shin; In Kyung Jeong; Goo Yeong Cho; Cheul Young Choi; Jong Yeop Kim; Yeong Je Chae; Min Ho Cho; Byung Wan Lee; Seong Jin Lee; Chul Young Park; Eun Gyoung Hong; Hyeon Kyu Kim; Doo Man Kim; Jae Myung Yu; Sung Hee Ihm; Moon Ki Choi; Hyung Joon Yoo; Sung Woo Park
Endocrinology and Metabolism | 2005
Hyeon Kyu Kim; Min Ho Cho; Choel Young Park; Seong Jin Lee; Gi Weon Oh; In Kyung Jeong; Eun Gyung Hong; Sung Hee Ihm; D.J. Kim; Jae Myung Yu; Moon Gi Choi; Hyung Joon Yoo; Sung Woo Park; Jin Hwan Kim; Young Soo Rho