1.Clinical Prevalence and Associated Factors of Erectile Dysfunction in Patients Undergoing Haemodialysis.
Lang Chu LAU ; P Ganesan ADAIKAN ; Anantharaman VATHSALA ; Balasubramanian SRILATHA ; Mee Lian WONG ; Chuen Seng TAN ; Xiaodong DENG ; Hersharan Kaur SRAN ; Lee Hwee KOH ; Valerie MA
Annals of the Academy of Medicine, Singapore 2018;47(2):78-81
2.Ministry of Health Clinical Practice Guidelines: Lipids.
E Shyong TAI ; Boon Lock CHIA ; Amber Carla BASTIAN ; Terrance CHUA ; Sally Chih Wei HO ; Teck Siew KOH ; Lip Ping LOW ; Jeannie S TEY ; Kian Keong POH ; Chee Eng TAN ; Peter TING ; Tat Yean THAM ; Sue-Anne TOH ; Rob M van DAM
Singapore medical journal 2017;58(3):155-166
		                        		
		                        			
		                        			The Ministry of Health (MOH) has updated the Clinical Practice Guidelines on Lipids to provide doctors and patients in Singapore with evidence-based treatment for lipids. This article reproduces the introduction and executive summary (with recommendations from the guidelines) from the MOH Clinical Practice Guidelines on Lipids, for the information of SMJ readers. Chapters and page numbers mentioned in the reproduced extract refer to the full text of the guidelines, which are available from the Ministry of Health website: http://www.moh.gov.sg/content/moh_web/healthprofessionalsportal/doctors/guidelines/cpg_medical.html.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Cardiovascular Diseases
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			therapy
		                        			;
		                        		
		                        			Child
		                        			;
		                        		
		                        			Coronary Artery Disease
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			therapy
		                        			;
		                        		
		                        			Decision Support Systems, Clinical
		                        			;
		                        		
		                        			Dyslipidemias
		                        			;
		                        		
		                        			blood
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			therapy
		                        			;
		                        		
		                        			Evidence-Based Medicine
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Kidney Failure, Chronic
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			therapy
		                        			;
		                        		
		                        			Life Style
		                        			;
		                        		
		                        			Lipids
		                        			;
		                        		
		                        			blood
		                        			;
		                        		
		                        			Lipoproteins, LDL
		                        			;
		                        		
		                        			blood
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Practice Guidelines as Topic
		                        			;
		                        		
		                        			Pregnancy
		                        			;
		                        		
		                        			Pregnancy Complications
		                        			;
		                        		
		                        			Risk Assessment
		                        			;
		                        		
		                        			Risk Factors
		                        			;
		                        		
		                        			Singapore
		                        			
		                        		
		                        	
3.Advanced chronic kidney disease: a strong risk factor for Clostridium difficile infection.
Sun Chul KIM ; Min Young SEO ; Jun Yong LEE ; Ki Tae KIM ; Eunjung CHO ; Myung Gyu KIM ; Sang Kyung JO ; Won Yong CHO ; Hyoung Kyu KIM
The Korean Journal of Internal Medicine 2016;31(1):125-133
		                        		
		                        			
		                        			BACKGROUND/AIMS: It has been suggested that chronic kidney disease (CKD) is a risk factor for Clostridium difficile infection (CDI) and is associated with increased mortality among patients infected with C. difficile. However, recent studies of the clinical impact of CKD on CDI in Asians are still insufficient. We sought to determine the relationship between CKD and CDI in a Korean population. METHODS: This was a single-center, retrospective case-control study. In total, 171 patients with CDI were included as cases and 342 age- and gender-matched patients without CDI were used as controls. We compared the prevalence of CKD in the study sample and identified independent risk factors that could predict the development or prognosis of CDI. RESULTS: Independent risk factors for CDI included stage IV to V CKD not requiring dialysis (odds ratio [OR], 2.90) and end-stage renal disease requiring dialysis (OR, 3.34). Patients with more advanced CKD (estimated glomerular filtration rate < 30) and CDI showed higher in-hospital mortality and poorer responses to the initial metronidazole therapy. CONCLUSIONS: More advanced CKD is an independent risk factor for CDI and is associated with higher in-hospital mortality and poor treatment responses in CDI patients. Thus, in CKD patients, careful attention should be paid to the occurrence of CDI and its management to improve the outcome of CDI.
		                        		
		                        		
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Anti-Infective Agents/therapeutic use
		                        			;
		                        		
		                        			Chi-Square Distribution
		                        			;
		                        		
		                        			Clostridium difficile/*pathogenicity
		                        			;
		                        		
		                        			Enterocolitis, Pseudomembranous/diagnosis/drug therapy/*microbiology/mortality
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Hospital Mortality
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Kidney Failure, Chronic/*complications/diagnosis/therapy
		                        			;
		                        		
		                        			Logistic Models
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Metronidazole/therapeutic use
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Multivariate Analysis
		                        			;
		                        		
		                        			Odds Ratio
		                        			;
		                        		
		                        			Prevalence
		                        			;
		                        		
		                        			Renal Dialysis
		                        			;
		                        		
		                        			Renal Insufficiency, Chronic/*complications/diagnosis/mortality/therapy
		                        			;
		                        		
		                        			Republic of Korea/epidemiology
		                        			;
		                        		
		                        			Retrospective Studies
		                        			;
		                        		
		                        			Risk Factors
		                        			;
		                        		
		                        			Treatment Outcome
		                        			
		                        		
		                        	
4.Prevalence of chronic kidney disease-mineral and bone disorder in incident peritoneal dialysis patients and its association with short-term outcomes.
Shen Hui CHUANG ; Hung Chew WONG ; Anantharaman VATHSALA ; Evan LEE ; Priscilla Pei Ching HOW
Singapore medical journal 2016;57(11):603-609
INTRODUCTIONA complex relationship exists between chronic kidney disease-mineral and bone disorder (CKD-MBD) and adverse outcomes among dialysis patients. This study aimed to report the prevalence of CKD-MBD and examine the impact of achieving target CKD-MBD parameters on morbidity and mortality one year after peritoneal dialysis (PD) initiation.
METHODSIn this retrospective cohort study, patients electively initiated on PD were followed up for one year. Laboratory parameters were collected and the prevalence of CKD-MBD 4-6 months after PD initiation was determined based on the Kidney Disease Outcomes Quality Initiative (KDOQI) and Kidney Disease: Improving Global Outcomes (KDIGO) guidelines. Linear regression and Cox proportional hazards model were used to evaluate the effects of achieving CKD-MBD targets 4-6 months after PD initiation on hospitalisation, the incidence of peritonitis or exit-site infections (ESIs), and mortality at one year.
RESULTSThe prevalence of CKD-MBD among the 86 patients in this study was 86.0% (KDOQI) and 54.7% (KDIGO). There was no significant difference in hospitalisation duration between patients who achieved targets and those who did not. Patients who failed to meet all the KDIGO CKD-MBD or calcium serum targets had a higher incidence of peritonitis or ESI. A trend toward shorter time to death was observed among patients who failed to meet the KDIGO phosphorus serum targets.
CONCLUSIONThere was moderate (KDIGO) to high prevalence (KDOQI) of CKD-MBD among the patients. Achievement of all the KDIGO CKD-MBD or calcium serum targets was associated with reduced peritonitis or ESI, while achievement of the KDIGO phosphorus serum targets was associated with improved survival.
Adult ; Aged ; Aged, 80 and over ; Chronic Kidney Disease-Mineral and Bone Disorder ; complications ; epidemiology ; Female ; Humans ; Kidney Failure, Chronic ; complications ; therapy ; Linear Models ; Male ; Middle Aged ; Peritoneal Dialysis ; Prevalence ; Proportional Hazards Models ; Quality Control ; Retrospective Studies ; Treatment Outcome
5.AST-120 Improves Microvascular Endothelial Dysfunction in End-Stage Renal Disease Patients Receiving Hemodialysis.
Jung Hwa RYU ; Mina YU ; Sihna LEE ; Dong Ryeol RYU ; Seung Jung KIM ; Duk Hee KANG ; Kyu Bok CHOI
Yonsei Medical Journal 2016;57(4):942-949
		                        		
		                        			
		                        			PURPOSE: Endothelial dysfunction (ED) is a pivotal phenomenon in the development of cardiovascular disease (CVD) in patients receiving hemodialysis (HD). Indoxyl sulfate (IS) is a known uremic toxin that induces ED in patients with chronic kidney disease. The aim of this study was to investigate whether AST-120, an absorbent of IS, improves microvascular or macrovascular ED in HD patients. MATERIALS AND METHODS: We conducted a prospective, case-controlled trial. Fourteen patients each were enrolled in respective AST-120 and control groups. The subjects in the AST-120 group were treated with AST-120 (6 g/day) for 6 months. Microvascular function was assessed by laser Doppler flowmetry using iontophoresis of acetylcholine (Ach) and sodium nitroprusside (SNP) at baseline and again at 3 and 6 months. Carotid arterial intima-media thickness (cIMT) and flow-mediated vasodilation were measured at baseline and 6 months. The Wilcoxon rank test was used to compare values before and after AST-120 treatment. RESULTS: Ach-induced iontophoresis (endothelium-dependent response) was dramatically ameliorated at 3 months and 6 months in the AST-120 group. SNP-induced response showed delayed improvement only at 6 months in the AST-120 group. The IS level was decreased at 3 months in the AST-120 group, but remained stable thereafter. cIMT was significantly reduced after AST-120 treatment. No significant complications in patients taking AST-120 were reported. CONCLUSION: AST-120 ameliorated microvascular ED and cIMT in HD patients. A randomized study including a larger population will be required to establish a definitive role of AST-120 as a preventive medication for CVD in HD patients.
		                        		
		                        		
		                        		
		                        			Acetylcholine
		                        			;
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Carbon/*therapeutic use
		                        			;
		                        		
		                        			Cardiovascular Diseases/etiology/*prevention & control
		                        			;
		                        		
		                        			Carotid Intima-Media Thickness
		                        			;
		                        		
		                        			Endothelium, Vascular/*physiopathology
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Iontophoresis
		                        			;
		                        		
		                        			Kidney Failure, Chronic/complications/*physiopathology/*therapy
		                        			;
		                        		
		                        			Laser-Doppler Flowmetry
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Microcirculation/physiology
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Nitroprusside
		                        			;
		                        		
		                        			Oxides/*therapeutic use
		                        			;
		                        		
		                        			Prospective Studies
		                        			;
		                        		
		                        			*Renal Dialysis
		                        			;
		                        		
		                        			Young Adult
		                        			
		                        		
		                        	
6.Copeptin in Hemodialysis Patients with Left Ventricular Dysfunction.
Jae Seok KIM ; Jae Won YANG ; Moon Hee CHAI ; Jun Young LEE ; Hyeoncheol PARK ; Youngsub KIM ; Seung Ok CHOI ; Byoung Geun HAN
Yonsei Medical Journal 2015;56(4):976-980
		                        		
		                        			
		                        			PURPOSE: Copeptin has been considered as a useful marker for diagnosis and prediction of prognosis in heart diseases. However, copeptin has not been investigated sufficiently in hemodialysis patients. This study aimed to investigate the general features of copeptin in hemodialysis and to examine the usefulness of copeptin in hemodialysis patients with left ventricular dysfunction (LV dysfunction). MATERIALS AND METHODS: This study included 41 patients on regular hemodialysis. Routine laboratory data and peptides such as the N-terminal of the prohormone brain natriuretic peptide and copeptin were measured on the day of hemodialysis. Body fluid volume was estimated by bioimpedance spectroscopy, and the E/Ea ratio was estimated by echocardiography. RESULTS: Copeptin increased to 171.4 pg/mL before hemodialysis. The copeptin had a positive correlation with pre-dialysis body fluid volume (r=0.314; p=0.04). The copeptin level decreased along with body fluid volume and plasma osmolality during hemodialysis. The copeptin increased in the patients with LV dysfunction more than in those with normal LV function (218.7 pg/mL vs. 77.6 pg/mL; p=0.01). Receiver operating characteristic curve analysis showed that copeptin had a diagnostic value in the hemodialysis patients with LV dysfunction (area under curve 0.737; p=0.02) and that the cut-off value was 125.48 pg/mL (sensitivity 0.7, specificity 0.8, positive predictive value 0.9, negative predictive value 0.6). CONCLUSION: Copeptin increases in hemodialysis patients and is higher in patients with LV dysfunction. We believe that copeptin can be a useful marker for the diagnosis of LV dysfunction in hemodialysis patients.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Biomarkers/blood
		                        			;
		                        		
		                        			Echocardiography
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Glycopeptides/*blood
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Kidney Failure, Chronic/*blood/complications/therapy
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Natriuretic Peptide, Brain/blood
		                        			;
		                        		
		                        			Predictive Value of Tests
		                        			;
		                        		
		                        			Prognosis
		                        			;
		                        		
		                        			ROC Curve
		                        			;
		                        		
		                        			Renal Dialysis/*adverse effects
		                        			;
		                        		
		                        			Sensitivity and Specificity
		                        			;
		                        		
		                        			Ventricular Dysfunction, Left/*blood/complications/*physiopathology
		                        			
		                        		
		                        	
7.Congenital nephrogenic diabetes insipidus with end-stage renal disease.
Hyun Ho RYU ; Jong Hoon CHUNG ; Byung Chul SHIN ; Hyun Lee KIM
The Korean Journal of Internal Medicine 2015;30(2):259-261
		                        		
		                        			
		                        			No abstract available.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			DNA Mutational Analysis
		                        			;
		                        		
		                        			Diabetes Insipidus, Nephrogenic/*complications/diagnosis/genetics/therapy
		                        			;
		                        		
		                        			Disease Progression
		                        			;
		                        		
		                        			Genetic Predisposition to Disease
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Kidney Failure, Chronic/diagnosis/*etiology
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Mutation
		                        			;
		                        		
		                        			Phenotype
		                        			;
		                        		
		                        			Receptors, Vasopressin/genetics
		                        			;
		                        		
		                        			Renal Dialysis
		                        			;
		                        		
		                        			Tomography, X-Ray Computed
		                        			
		                        		
		                        	
8.Cutoff value of serum procalcitonin as a diagnostic biomarker of infection in end-stage renal disease patients.
Wan Soo LEE ; Dae Woong KANG ; Jong Hun BACK ; Hyun Lee KIM ; Jong Hoon CHUNG ; Byung Chul SHIN
The Korean Journal of Internal Medicine 2015;30(2):198-204
		                        		
		                        			
		                        			BACKGROUND/AIMS: Serum procalcitonin (PCT) levels are low in healthy individuals but are elevated in patients with a serious bacterial infection or sepsis. In this study, we examined the ability of serum PCT concentration to diagnose infections in end-stage renal disease (ESRD) patients, and sought to determine an appropriate threshold level. METHODS: Serum PCT levels were measured in ESRD patients on antibiotic therapy for a suspected bacterial infection (ESRD infection [iESRD] group, n = 21), and compared with those of ESRD patients on hemodialysis with no sign of infection (ESRD control [cESRD] group, n = 20). RESULTS: The mean serum PCT concentration of the iESRD group was significantly higher than in the cESRD group (2.95 +/- 3.67 ng/mL vs. 0.50 +/- 0.49 ng/mL, p = 0.006), but serum PCT concentrations did not correlate with severity of infection. The optimized threshold level derived for serum PCT was 0.75 ng/mL, rather than the currently used 0.5 ng/mL; this threshold demonstrated a sensitivity and specificity of 76.2% and 80.0% for infection and 100% and 60.6% for systemic inflammatory response syndrome, respectively, compared with the cutoff of 0.5 ng/mL. CONCLUSIONS: This study suggests that serum PCT at a cutoff value of 0.75 ng/mL is an appropriate indicator of infection in ESRD patients.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Area Under Curve
		                        			;
		                        		
		                        			Bacterial Infections/*blood/complications/*diagnosis/microbiology
		                        			;
		                        		
		                        			Biomarkers/blood
		                        			;
		                        		
		                        			Calcitonin/*blood
		                        			;
		                        		
		                        			Case-Control Studies
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Inflammation Mediators/*blood
		                        			;
		                        		
		                        			Kidney Failure, Chronic/*complications/diagnosis/therapy
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Peritoneal Dialysis
		                        			;
		                        		
		                        			Predictive Value of Tests
		                        			;
		                        		
		                        			Protein Precursors/*blood
		                        			;
		                        		
		                        			ROC Curve
		                        			;
		                        		
		                        			Renal Dialysis
		                        			;
		                        		
		                        			Reproducibility of Results
		                        			;
		                        		
		                        			Up-Regulation
		                        			
		                        		
		                        	
9.Shenshuai Yingyang capsule ameliorates muscle atrophy in rats with chronic renal failure: role of Wnt7a-Akt/mTOR signal pathway.
Ming WANG ; Dongtao WANG ; Yi YIN ; Lu LU ; Ying SHI ; Yanfeng HUANG ; Dexiu CHEN ; Lianbo WEI
Journal of Southern Medical University 2015;35(8):1170-1174
OBJECTIVETo observe the effect of Shenshuai Yingyang Capsule (SSYYJN) in ameliorating muscle atrophy in rats with chronic renal failure (CRF) and explore the role of Wnt7a-Akt/mTOR signal pathway in mediating this effect.
METHODSMale rats were randomly assigned to 5/6 nephrectomy group and sham-operated group, and the former group was further randomly divided into CRF model group, KA group, and SSYYJN group. The size of anterior tibia muscle was examined microscopically with HE staining. Protein synthesis in the soleus muscle was investigated by (14)C-phenylalanine experiment, and the expression of Wnt7a, frizzled-7, phospho-Akt, phospho-mTOR and GAPDH were detected with Western blotting.
RESULTSThe body weight, the wet and dry weight, cross-sectional area, and muscle protein synthesis of the anterior tibia muscles, and expressions of the proteins in the Wnt7a/Akt signaling pathway all increased significantly in SSYYJN and KA groups as compared with those in the model group.
CONCLUSIONSSYYJN can effectively improve muscle atrophy in the rat model of CRF possibly by reversing the reduction in the expressions of Wnt7a/Akt signaling pathway proteins in the skeletal muscles.
Animals ; Capsules ; Drugs, Chinese Herbal ; pharmacology ; Kidney Failure, Chronic ; complications ; Male ; Muscle Proteins ; biosynthesis ; Muscle, Skeletal ; drug effects ; Muscular Atrophy ; drug therapy ; Nephrectomy ; Proto-Oncogene Proteins ; metabolism ; Rats ; Signal Transduction ; TOR Serine-Threonine Kinases ; metabolism ; Wnt Proteins ; metabolism
10.Secondary haemochromatosis in a haemodialysis patient.
Lu CHENG ; Xi TANG ; Ping FU ; Fang LIU
Singapore medical journal 2015;56(7):e124-6
		                        		
		                        			
		                        			A 39-year-old woman with end-stage renal disease, which was maintained on haemodialysis, developed secondary haemochromatosis after receiving blood transfusions and intravenous iron supplementation without sufficient serum ferritin concentration monitoring. The patient received intravenous deferoxamine three times a week, combined with high-dose recombinant human erythropoietin therapy and haemodialysis. After three months, improvements in biochemical indicators and iron overload were noted.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Chelating Agents
		                        			;
		                        		
		                        			chemistry
		                        			;
		                        		
		                        			Erythropoietin
		                        			;
		                        		
		                        			therapeutic use
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Ferritins
		                        			;
		                        		
		                        			blood
		                        			;
		                        		
		                        			Hemochromatosis
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			Hemoglobins
		                        			;
		                        		
		                        			analysis
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Kidney Failure, Chronic
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			therapy
		                        			;
		                        		
		                        			Recombinant Proteins
		                        			;
		                        		
		                        			therapeutic use
		                        			;
		                        		
		                        			Renal Dialysis
		                        			;
		                        		
		                        			adverse effects
		                        			;
		                        		
		                        			Sequence Analysis, DNA
		                        			;
		                        		
		                        			Tomography, X-Ray Computed
		                        			;
		                        		
		                        			Transferrin
		                        			;
		                        		
		                        			chemistry
		                        			;
		                        		
		                        			Transfusion Reaction
		                        			;
		                        		
		                        			Treatment Outcome
		                        			
		                        		
		                        	
            
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