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Featured researches published by Misol Lee.


Blood Purification | 2015

Serum Ferritin Predicts Mortality Regardless of Inflammatory and Nutritional Status in Patients Starting Dialysis: A Prospective Cohort Study

Kyoung Sook Park; Geun Woo Ryu; Jong Hyun Jhee; Hyung Woo Kim; S Park; Sul Lee; Young Eun Kwon; Yung Ly Kim; Han Jak Ryu; Misol Lee; Seung Hyeok Han; Tae Hyun Yoo; Yonhee Kim; Chul-Woo Yang; Nam Ho Kim; Shin-Wook Kang; Jung Tak Park

Background: The impact of serum ferritin on prognosis in patients starting hemodialysis (HD) is not fully elucidated. Methods: A prospective cohort of 946 incident HD patients from 26 dialysis centers in Korea was selected for this study. Patients were divided into tertiles according to natural logarithm (Ln) ferritin concentrations. Results: During a median follow-up of 39 months, 88 (9.3%) patients died. Multivariate Cox proportional hazard analysis demonstrated that Ln ferritin was independently associated with an increase in cardiovascular mortality risk (hazard ratio (HR) 1.604, 95% CI 1.040-2.474, p = 0.033), infection-related mortality risk (HR 1.916, 95% CI 1.056-3.476, p = 0.032), and all-cause mortality risk (HR 1.547, 95% CI 1.156-2.069, p = 0.003). Conclusion: Serum ferritin levels at the time of HD commencement were a significant independent risk factor for mortality regardless of systemic inflammation and nutritional status. Therefore, elevated serum ferritin levels could be an effective indicator for prognosis.


The American Journal of Clinical Nutrition | 2017

High dietary phosphorus density is a risk factor for incident chronic kidney disease development in diabetic subjects: a community-based prospective cohort study

Chang Yun Yoon; Jung Tak Park; Jong Hyun Jhee; Juhwan Noh; Youn Kyung Kee; Changhwan Seo; Misol Lee; Min Uk Cha; Hyoungnae Kim; Seohyun Park; Hae Ryong Yun; Su Young Jung; Seung Hyeok Han; Tae Hyun Yoo; Shin-Wook Kang

Background: High serum phosphorus concentrations are associated with an increased risk of cardiovascular disease and progression of chronic kidney disease (CKD). However, the relation between dietary phosphorus intake and CKD development has not been well evaluated.Objective: In this study, we investigated the impact of dietary phosphorus density on the development of incident CKD in a cohort of subjects with normal renal function.Design: Data were retrieved from the Korean Genome and Epidemiology Study, a prospective community-based cohort study. The study cohort consisted of subjects aged 40-69 y, who were followed up biennially from 2001 to 2014. A total of 873 subjects with diabetes mellitus (DM) and 5846 subjects without DM (non-DM) were included in the final analysis. The primary endpoint was incident CKD, defined as a composite of estimated glomerular filtration rate <60 mL · min-1 · 1.73 m-2 and/or the development of proteinuria.Results: In the DM and non-DM groups, the mean ages of the participants were 55.6 ± 8.7 and 51.4 ± 8.6 y, the numbers of male subjects were 454 (52.0%) and 2784 (47.6%), and the mean estimated glomerular filtration rates were 91.6 ± 14.0 and 94.5 ± 14.0 mL · min-1 · 1.73 m-2, respectively. The mean values of dietary phosphorus density, defined as the ratio of a single-day dietary phosphorus amount to the total daily calorie intake, were 0.51 ± 0.08 mg/kcal in the DM group and 0.51 ± 0.07 mg/kcal in the non-DM group. During the follow-up, CKD newly developed in 283 (32.4%) and 792 subjects (13.5%) in the DM and non-DM groups, respectively. When the subjects were divided into quartiles according to the dietary phosphorus density in each group, the highest quartile was significantly associated with the development of incident CKD by multiple Cox proportional hazard analysis in the DM group (P = 0.02) but not in the non-DM group (P = 0.72).Conclusions: High dietary phosphorus density is associated with an increased risk of CKD development in DM patients with normal renal function. The causality in this association needs to be tested in a randomized controlled trial.


Kidney research and clinical practice | 2017

Body mass index is inversely associated with mortality in patients with acute kidney injury undergoing continuous renal replacement therapy

Hyoungnae Kim; Joohwan Kim; Changhwan Seo; Misol Lee; Min-Uk Cha; Su-Young Jung; Jong Hyun Jhee; Seohyun Park; Hae-Ryong Yun; Youn Kyung Kee; Chang-Yun Yoon; Hyung Jung Oh; Jung Tak Park; Tae Ik Chang; Tae-Hyun Yoo; Shin-Wook Kang; and Seung Hyeok Han

Background Many epidemiologic studies have reported on the controversial concept of the obesity paradox. The presence of acute kidney injury (AKI) can accelerate energy-consuming processes, particularly in patients requiring continuous renal replacement therapy (CRRT). Thus, we aimed to investigate whether obesity can provide a survival benefit in this highly catabolic condition. Methods We conducted an observational study in 212 patients who had undergone CRRT owing to various causes of AKI between 2010 and 2014. The study end point was defined as death that occurred within 30 days after the initiation of CRRT. Results Patients were categorized into three groups according to tertiles of body mass index (BMI). During ≥30 days after the initiation of CRRT, 39 patients (57.4%) in the highest tertile died, as compared with 58 patients (78.4%) in the lowest tertile (P = 0.02). In a multivariable analysis adjusted for cofounding factors, the highest tertile of BMI was significantly associated with a decreased risk of death (hazard ratio [HR], 0.57; 95% confidence interval [CI], 0.37–0.87; P = 0.01). This significant association remained unaltered for 60-day (HR, 0.64; 95% CI, 0.43–0.94; P = 0.03) and 90-day mortality (HR, 0.66; 95% CI, 0.44–0.97; P = 0.03). Conclusion This study showed that a higher BMI confer a survival benefit over a lower BMI in AKI patients undergoing CRRT.


Kidney International | 2017

High and low sodium intakes are associated with incident chronic kidney disease in patients with normal renal function and hypertension

Chang Yun Yoon; Juhwan Noh; Jinae Lee; Youn Kyung Kee; Changhwan Seo; Misol Lee; Min Uk Cha; Hyoungnae Kim; Seohyun Park; Hae Ryong Yun; Su Young Jung; Jong Hyun Jhee; Seung Hyeok Han; Tae Hyun Yoo; Shin-Wook Kang; Jung Tak Park

The association between salt intake and renal outcome in subjects with preserved kidney function remains unclear. Here we evaluated the effect of sodium intake on the development of chronic kidney disease (CKD) in a prospective cohort of people with normal renal function. Data were obtained from the Korean Genome and Epidemiology Study, a prospective community-based cohort study while sodium intake was estimated by a 24-hour dietary recall Food Frequency Questionnaire. A total of 3,106 individuals with and 4,871 patients without hypertension were analyzed with a primary end point of CKD development [a composite of estimated glomerular filtration rate (eGFR) under 60 mL/min/1.73 m2 and/or development of proteinuria during follow-up]. The median ages were 55 and 47 years, the proportions of males 50.9% and 46.3%, and the median eGFR 92 and 96 mL/min/1.73 m2 in individuals with and without hypertension, respectively. During a median follow-up of 123 months in individuals with hypertension and 140 months in those without hypertension, CKD developed in 27.8% and 16.5%, respectively. After adjusting for confounders, multiple Cox models indicated that the risk of CKD development was significantly higher in people with hypertension who consumed less than 2.08 g/day or over 4.03 g/day sodium than in those who consumed between 2.93-4.03 g/day sodium. However, there was no significant difference in the incident CKD risk among each quartile of people without hypertension. Thus, both high and low sodium intakes were associated with increased risk for CKD, but this relationship was only observed in people with hypertension.


Korean Circulation Journal | 2016

Remnant Pacemaker Lead Tips after Lead Extractions in Pacemaker Infections

Daehoon Kim; Yong Soo Baek; Misol Lee; Jae Sun Uhm; Hui Nam Pak; Moon Hyoung Lee; Boyoung Joung

Complete hardware removal is recommended in the case of patients with cardiovascular implantable electronic device (CIED) infections. However, the complete extraction of chronically implanted leads is not always achieved. The outcomes and optimal management of CIED infections with retained material after lead extractions have not been elucidated. In this case report, we present five patients with CIED infections with remnant lead tips even after lead extractions. Two patients had localized pocket infections, and were managed with antibiotics for a period of more than two weeks. The other three patients had infective endocarditis, and were managed with antibiotics for a period of more than four weeks. In one patient, the lead tip migrated to the right pulmonary artery, but did not produce any symptoms or complications. Only one of five patients experienced a resurgence of an infection.


Peritoneal Dialysis International | 2015

Is It Beneficial to Convert to a Neutral-pH Bicarbonate/Lactate-Buffered PD Solution in Long-Term CAPD Patients? A Single-Center Prospective Study.

Tae Hyun Yoo; Misol Lee; Hyung Jung Oh; Jung Tak Park; Seung Hyeok Han; Shin-Wook Kang; Dong-Hoo Han

We assumed that hydrothorax was due to the malpositioned peritoneal catheter. Peritoneal dialysis was stopped and the right peritoneal catheter was removed and a new left-sided catheter was inserted at the same time. Peritoneal dialysis was restarted after 1 month of catheter replacement with progressive increase of volume exchange. The chest X-ray did not show any recurrence of the pleural effusion up to 2 months later. Hydrotorax is an infrequent PD mechanical complication of PD (1). It usually occurs early after starting PD treatment (less than 30 days), and it is associated with an increase in intra-abdominal pressure in patients with congenital defects of the diaphragm muscle. It appears more commonly in females and in the r ight hemithorax. On very rare occasions, it has been related to peritonitis episodes (2–3). Treatment consists of peritoneal rest, temporary or definitive transference to HD, pleurodesis or surgical repair of the diaphragm defect (4). Our patient developed a late-onset right peritoneal-pleural leak in clear temporal relationship with a right malpositioned catheter which resolved after removing it. There has been no recurrence of pleural effusion since resuming PD and no surgical repair was required. We propose catheter malposition as a new cause of hydrothorax in PD.


The American Journal of Medicine | 2018

Effects of Coffee Intake on Incident Chronic Kidney Disease: Community-Based Prospective Cohort Study

Jong Hyun Jhee; Ki Heon Nam; Seong Yeong An; Min-Uk Cha; Misol Lee; Seohyun Park; Hyoungnae Kim; Hae-Ryong Yun; Youn Kyung Kee; Jung Tak Park; Tae-Ik Chang; Ea Wha Kang; Tae-Hyun Yoo; Shin-Wook Kang; Seung Hyeok Han

BACKGROUND Drinking coffee can raise public health problems, but the association between coffee and kidney disease is unknown. We studied whether coffee intake can affect the development of chronic kidney disease in the general population. METHODS We analyzed 8717 subjects with normal renal function recruited from the Korean Genome and Epidemiology Study (KoGES) cohort. Based on a food frequency questionnaire, coffee consumption was categorized into 5 groups: 0 per week, <1 cup per week, 1-6 cups per week, 1 cup per day, and ≥2 cups per day. The primary outcome was incident chronic kidney disease, defined as an estimated glomerular filtration rate <60 mL/min/1.73 m2. RESULTS The mean age (standard deviation) of study subjects was 52.0 (8.8) years, and 47.8% were male. Among the subjects, 52.8% were daily coffee consumers. During a mean follow-up of 11.3 (range, 5.9-11.5) years, 9.5% of participants developed chronic kidney disease. The incident chronic kidney disease occurred less in daily coffee consumers. Unadjusted hazard ratios (HRs) was significantly lower in daily coffee consumers. In multivariable Cox model even after adjustment of blood pressure, hypertension, cardiovascular disease, diabetes, and amount of daily intake for caffeine-containing foods such as tea and chocolate, coffee consumers with 1 cup per day (HR, 0.76; 95% confidence interval, 0.63-0.92) and ≥2 cups per day (HR, 0.80; 95% confidence interval, 0.65-0.98) were associated with a lower risk of chronic kidney disease development than nondrinkers. Time-averaged and time-varying Cox models yielded similar results. The rates of decline in glomerular filtration were lower in daily coffee consumers. CONCLUSIONS Our findings suggest that daily coffee intake is associated with decreased risk of the development of chronic kidney disease.


Kidney research and clinical practice | 2017

Fatty liver associated with metabolic derangement in patients with chronic kidney disease: A controlled attenuation parameter study

Chang Yun Yoon; Misol Lee; Seung Up Kim; Hyunsun Lim; Tae Ik Chang; Youn Kyung Kee; Seung Gyu Han; In Mee Han; Young Eun Kwon; Kyoung Sook Park; Mi Jung Lee; Jung Tak Park; Seung Hyeok Han; Sang Hoon Ahn; Shin-Wook Kang; Tae Hyun Yoo

Background Hepatic steatosis measured with controlled attenuation parameter (CAP) using transient elastography predicts metabolic syndrome in the general population. We investigated whether CAP predicted metabolic syndrome in chronic kidney disease patients. Methods CAP was measured with transient elastography in 465 predialysis chronic kidney disease patients (mean age, 57.5 years). Results The median CAP value was 239 (202–274) dB/m. In 195 (41.9%) patients with metabolic syndrome, diabetes mellitus was more prevalent (105 [53.8%] vs. 71 [26.3%], P < 0.001), with significantly increased urine albumin-to-creatinine ratio (184 [38–706] vs. 56 [16–408] mg/g Cr, P = 0.003), high sensitivity C-reactive protein levels (5.4 [1.4–28.2] vs. 1.7 [0.6–9.9] mg/L, P < 0.001), and CAP (248 [210–302] vs. 226 [196–259] dB/m, P < 0.001). In multiple linear regression analysis, CAP was independently related to body mass index (β = 0.742, P < 0.001), triglyceride levels (β = 2.034, P < 0.001), estimated glomerular filtration rate (β = 0.316, P = 0.001), serum albumin (β = 1.386, P < 0.001), alanine aminotransferase (β = 0.064, P = 0.029), and total bilirubin (β = −0.881, P = 0.009). In multiple logistic regression analysis, increased CAP was independently associated with increased metabolic syndrome risk (per 10 dB/m increase; odds ratio, 1.093; 95% confidence interval, 1.009–1.183; P = 0.029) even after adjusting for multiple confounding factors. Conclusion Increased CAP measured with transient elastography significantly correlated with and could predict increased metabolic syndrome risk in chronic kidney disease patients.


Scientific Reports | 2018

Circulating Fibroblast Growth Factor-23 Levels are Associated with an Increased Risk of Anemia Development in Patients with Nondialysis Chronic Kidney Disease

Ki Heon Nam; Hyoungnae Kim; Seong Yeong An; Misol Lee; Min Uk Cha; Jung Tak Park; Tae Hyun Yoo; Kyu Beck Lee; Yeong Hoon Kim; Su Ah Sung; Joongyub Lee; Shin-Wook Kang; Kyu Hun Choi; Curie Ahn; Seung Hyeok Han

Fibroblast growth factor-23 (FGF23) is an established biomarker of adverse outcomes in patients with chronic kidney disease (CKD). Several cross-sectional studies have suggested a possible association between FGF23 and anemia in these patients. In this large-scale prospective cohort study, we investigated this relationship and examined whether high FGF23 levels increase the risk of incident anemia. This prospective longitudinal study included 2,089 patients from the KoreaN cohort study for Outcome in patients With CKD. Anemia was defined as hemoglobin level <13.0 g/dl (men) and <12.0 g/dl (women). Log-transformed FGF23 significantly correlated with hepcidin but inversely correlated with iron profiles and hemoglobin. Multivariate logistic regression showed that log-transformed FGF23 was independently associated with anemia (odds ratio [OR], 1.14; 95% confidence interval [CI], 1.04–1.24, P = 0.01). Among 1,164 patients without anemia at baseline, 295 (25.3%) developed anemia during a median follow-up of 21 months. In fully adjusted multivariable Cox models, the risk of anemia development was significantly higher in the third (hazard ratio [HR], 1.66; 95% CI, 1.11–2.47; P = 0.01) and fourth (HR, 1.84; 95% CI, 1.23–2.76; P = 0.001) than in the first FGF23 quartile. In conclusion, high serum FGF23 levels were associated with an increased risk for anemia in patients with nondialysis CKD.


QJM: An International Journal of Medicine | 2018

Microscopic hematuria is a risk factor of incident chronic kidney disease in the Korean general population: a community-based prospective cohort study

Hyoungnae Kim; Misol Lee; Min-Uk Cha; Ky-Youb Nam; Seong Yeong An; Soon-Jung Park; Jong Hyun Jhee; Hae-Ryong Yun; Y. K. Kee; Jung Tak Park; Tae Hyun Yoo; Shin-Wook Kang; Seung Hyeok Han

Background Although asymptomatic microscopic hematuria (MH) is a common finding in clinical practice, its long-term outcome remains unknown. Aim This study evaluated the clinical implication of MH in the general population using a large-scale long-term longitudinal cohort database. Methods This study included 8719 participants from the Korean Genome and Epidemiology Study between 2001 and 2014. MH was defined as ≥5 red blood cells per high-power field in random urinalysis without evidence of pyuria. The primary study outcome measure was incident chronic kidney disease (CKD), defined as estimated glomerular filtration rate <60 ml min-1⋅1.73⋅m-2. Results During a median follow-up of 11.7 years, CKD occurred in 677 (7.8%) subjects. In Cox regression after adjustment for multiple confounders, subjects with MH had a significantly higher risk of incident CKD than those without [hazard ratio (HR) 1.45, 95% confidence interval (CI) 1.12-1.87; P = 0.005]. Isolated MH without proteinuria was also a risk factor of incident CKD (HR 1.37, 95% CI 1.04-1.79; P = 0.023) and the risk was further increased in MH with concomitant proteinuria (HR 5.41, 95% CI 2.54-11.49; P < 0.001). In propensity score matching analysis after excluding subjects with proteinuria, multi-variable stratified Cox regression analysis revealed that subjects with isolated MH had a significantly higher risk of incident CKD than those without (HR 1.83, 95% CI 1.14-2.94; P = 0.012). Conclusion The presence of MH is associated with an increased risk of incident CKD in the general population. Therefore, attentive follow-up is warranted in persons with MH for early detection of CKD.

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