1.Changes of QT Dispersion in Hemodialysis Patients after Administrating Zhigancao Decoction ().
Yan-Qing TONG ; Min SUN ; Chun-Jie HU ; Dong-Kai ZHAO
Chinese journal of integrative medicine 2018;24(8):627-631
OBJECTIVETo observe the alteration of QT dispersion (QTd) and QTc dispersion (QTcd) in hemodialysis patients after oral administration of Zhigancao Decoction (, Roasted Licorice Decoction, RLD).
METHODSTo investigate the alteration of QTd and QTcd in 68 routine hemodialysis patients before and after hemodialysis with 12-lead electrocardiogram (ECG) after orally administrated RLD for 4 weeks. Blood was also taken for measurement of plasma electrolytes, liver function, renal function, hemoglobin (Hgb) and hematocrit (HCT).
RESULTSAfter hemodialysis, QTd and QTcd were prolonged evidently; the difference was significant between before and after hemodialysis (P<0.05). After RLD orally administrated for 4 weeks, QTd and QTcd only slightly increased after dialysis compared with pre-dialysis (P>0.05). The QTd and QTcd of the post-therapy-post-dialysis decreased significantly compared with the pre-therapy-post-dialysis (P<0.05). There were no other significant changes in other variables (post-therapy-pre-dialysis vs. pre-therapy-pre-dialysis, or post-therapy-post-dialysis vs. pre-therapy-post-dialysis;P>0.05). After therapy, the number of patients with supraventricular arrhythmia, occasional ventricular premature beat and multiple ventricular premature beat were decreased from 15 to 4, 10 to 2 and 7 to 1, respectively.
CONCLUSIONRLD therapy not only lowered the increased QTd and QTcd after hemodialysis, but also displayed a safety profile.
Adult ; Aged ; Demography ; Drugs, Chinese Herbal ; administration & dosage ; therapeutic use ; Electrocardiography ; Female ; Humans ; Kidney Failure, Chronic ; drug therapy ; physiopathology ; Male ; Middle Aged ; Renal Dialysis
2.Research progress of the uremic toxin indoxyl sulfate in cardiovascular complication of end-stage renal diseases.
Chu-Chu GUO ; Wei-Wei XIA ; Ai-Hua ZHANG
Acta Physiologica Sinica 2018;70(6):657-662
Cardiovascular disease is one of the most common complications and the main cause of death in patients with chronic kidney disease. Uremic toxins are the primary cause of cardiovascular disease in renal insufficiency. In patients with chronic kidney disease, the protein-bound uremic toxins represented by indoxyl sulfate are difficult to be removed by conventional dialysis and are extremely toxic. In recent years, studies have confirmed that the occurrence of cardiovascular disease induced by chronic kidney disease is closely related to the accumulation of indoxyl sulfate. Indoxyl sulfate can induce oxidative stress to cause endothelial injury, smooth muscle cell proliferation and migration, and promote the occurrence of atherosclerosis, thereby affecting multiple systems throughout the body. This article reviews the research progress of uremic toxin indoxyl sulfate in end-stage renal diseases associated cardiovascular diseases.
Cardiovascular Diseases
;
complications
;
physiopathology
;
Humans
;
Indican
;
toxicity
;
Kidney Failure, Chronic
;
complications
;
physiopathology
;
Oxidative Stress
;
Toxins, Biological
;
toxicity
3.The Impact of Diabetes Mellitus on Vascular Biomarkers in Patients with End-Stage Renal Disease.
Jeonggeun MOON ; Chan Joo LEE ; Sang Hak LEE ; Seok Min KANG ; Donghoon CHOI ; Tae Hyun YOO ; Sungha PARK
Yonsei Medical Journal 2017;58(1):75-81
PURPOSE: Diabetes mellitus (DM) is the most common cause of end-stage renal disease (ESRD) and an important risk factor for cardiovascular (CV) disease. We investigated the impact of DM on subclinical CV damage by comprehensive screening protocol in ESRD patients. MATERIALS AND METHODS: Echocardiography, coronary computed tomography angiogram, 24-h ambulatory blood pressure monitoring, and central blood pressure with pulse wave velocity (PWV) were performed in 91 ESRD patients from the Cardiovascular and Metabolic disease Etiology Research Center-HIgh risk cohort. RESULTS: The DM group (n=38) had higher systolic blood pressure than the non-DM group (n=53), however, other clinical CV risk factors were not different between two groups. Central aortic systolic pressure (148.7±29.8 mm Hg vs. 133.7±27.0 mm Hg, p= 0.014), PWV (12.1±2.7 m/s vs. 9.4±2.1 m/s, p<0.001), and early mitral inflow to early mitral annulus velocity (16.7±6.4 vs. 13.7±5.9, p=0.026) were higher in the DM group. Although the prevalence of coronary artery disease (CAD) was not different between the DM and the non-DM group (95% vs. 84.4%, p=0.471), the severity of CAD was higher in the DM group (p=0.01). In multivariate regression analysis, DM was an independent determinant for central systolic pressure (p=0.011), PWV (p<0.001) and the prevalence of CAD (p=0.046). CONCLUSION: Diabetic ESRD patients have higher central systolic pressure and more advanced arteriosclerosis than the non-DM control group. These findings suggest that screening for subclinical CV damage may be helpful for diabetic ESRD patients.
Aged
;
Aorta
;
Biomarkers
;
Blood Pressure/physiology
;
Blood Pressure Monitoring, Ambulatory
;
Coronary Artery Disease/diagnostic imaging/*physiopathology
;
Diabetes Mellitus/*physiopathology
;
Diabetic Nephropathies/physiopathology
;
Echocardiography
;
Female
;
Humans
;
Kidney Failure, Chronic/*physiopathology
;
Male
;
Middle Aged
;
Pulse Wave Analysis
;
Regression Analysis
;
Risk Factors
;
Systole/physiology
4.Vascular Calcification: Current Genetics Underlying This Complex Phenomenon.
Nonanzit PÉREZ-HERNÁNDEZ ; Gad APTILON-DUQUE ; Ruben BLACHMAN-BRAUN ; Gilberto VARGAS-ALARCÓN ; Adrián Asael RODRÍGUEZ-CORTÉS ; Shely AZRAD-DANIEL ; Rosalinda POSADAS-SÁNCHEZ ; José Manuel RODRÍGUEZ-PÉREZ
Chinese Medical Journal 2017;130(9):1113-1121
OBJECTIVEVascular calcification is the consequence of the complex interaction between genetic, environmental, and vascular factors, which ultimately lead to the deposition of calcium in the tunica intima (atherosclerotic calcification) or tunica media (Mönckenberg's sclerosis). Vascular calcification is also closely related to other pathologies, such as diabetes mellitus, dyslipidemia, and chronic kidney disease. It has been concluded that the degree of vascular calcification may vary from person to person, even if the associated pathologies and environmental factors are the same. Therefore, this suggests an important genetic contribution to the development of vascular calcification. This review aimed to find the most recent evidence about vascular calcification pathophysiology regarding the genetic aspects and molecular pathways.
DATA SOURCESWe conducted an exhaustive search in Scopus, EBSCO, and PubMed with the keywords "genetics and vascular calcification", "molecular pathways, genetic and vascular calcification" and included the main articles from January 1995 up to August 2016. We focused on the most recent evidence about vascular calcification pathophysiology regarding the genetic aspects and molecular pathways.
STUDY SELECTIONThe most valuable published original and review articles related to our objective were selected.
RESULTSVascular calcification is a multifactorial disease; thus, its pathophysiology cannot be explained by a single specific factor, rather than by the result of the association of several genetic variants, molecular pathway interactions, and environmental factors that promote its development.
CONCLUSIONAlthough several molecular aspects of this mechanism have been elucidated, there is still a need for a better understanding of the factors that predispose to this disease.
Diabetes Mellitus ; metabolism ; physiopathology ; Dyslipidemias ; metabolism ; physiopathology ; Humans ; Kidney Failure, Chronic ; metabolism ; physiopathology ; Renal Insufficiency, Chronic ; metabolism ; physiopathology ; Tunica Intima ; metabolism ; physiopathology ; Tunica Media ; metabolism ; physiopathology ; Vascular Calcification ; metabolism ; physiopathology
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.The Impact of Hemodialysis and Arteriovenous Access Flow on Extracranial Hemodynamic Changes in End-Stage Renal Disease Patients.
Sarah CHUNG ; Hye Seon JEONG ; Dae Eun CHOI ; Hee Jung SONG ; Young Gi LIM ; Joo Yeon HAM ; Ki Ryang NA ; Kang Wook LEE
Journal of Korean Medical Science 2016;31(8):1239-1245
In this study, we characterized cerebral blood flow changes by assessment of blood flow parameters in neck arteries using carotid duplex ultrasonography and predictive factors for these hemodynamic changes. Hemodynamic variables were measured before and during hemodialysis in 81 patients with an arteriovenous access in their arm. Hemodialysis produced significant lowering in peak systolic velocity and flow volume of neck arteries and calculated total cerebral blood flow (1,221.9 ± 344.9 [before hemodialysis] vs. 1,085.8 ± 319.2 [during hemodialysis], P < 0.001). Effects were greater in vessels on the same side as the arteriovenous access and these changes were influenced by arteriovenous access flow during hemodialysis, both in the CCA (r = -0.277, P = 0.015) and the VA (r = -0.239, P = 0.034). The change of total cerebral blood flow during hemodialysis was independently related with age, presence of diabetes, and systemic blood pressure.
Aged
;
Carotid Arteries/diagnostic imaging
;
Cerebrovascular Circulation/*physiology
;
Dizziness/etiology
;
Female
;
Hemodynamics/*physiology
;
Humans
;
Kidney Failure, Chronic/*physiopathology
;
Male
;
Middle Aged
;
Renal Dialysis
;
Risk Factors
;
Ultrasonography, Doppler, Duplex
7.The Impact of Hemodialysis and Arteriovenous Access Flow on Extracranial Hemodynamic Changes in End-Stage Renal Disease Patients.
Sarah CHUNG ; Hye Seon JEONG ; Dae Eun CHOI ; Hee Jung SONG ; Young Gi LIM ; Joo Yeon HAM ; Ki Ryang NA ; Kang Wook LEE
Journal of Korean Medical Science 2016;31(8):1239-1245
In this study, we characterized cerebral blood flow changes by assessment of blood flow parameters in neck arteries using carotid duplex ultrasonography and predictive factors for these hemodynamic changes. Hemodynamic variables were measured before and during hemodialysis in 81 patients with an arteriovenous access in their arm. Hemodialysis produced significant lowering in peak systolic velocity and flow volume of neck arteries and calculated total cerebral blood flow (1,221.9 ± 344.9 [before hemodialysis] vs. 1,085.8 ± 319.2 [during hemodialysis], P < 0.001). Effects were greater in vessels on the same side as the arteriovenous access and these changes were influenced by arteriovenous access flow during hemodialysis, both in the CCA (r = -0.277, P = 0.015) and the VA (r = -0.239, P = 0.034). The change of total cerebral blood flow during hemodialysis was independently related with age, presence of diabetes, and systemic blood pressure.
Aged
;
Carotid Arteries/diagnostic imaging
;
Cerebrovascular Circulation/*physiology
;
Dizziness/etiology
;
Female
;
Hemodynamics/*physiology
;
Humans
;
Kidney Failure, Chronic/*physiopathology
;
Male
;
Middle Aged
;
Renal Dialysis
;
Risk Factors
;
Ultrasonography, Doppler, Duplex
8.Epidemiology of acute kidney injury in Chinese critical patients.
Ying LEI ; Sheng NIE ; Dan-Hua SUN ; Wei BIN ; Xin XU
Journal of Southern Medical University 2016;36(6):744-750
OBJECTIVETo investigate the epidemiological profile of acute kidney injury (AKI) in the Chinese critical patients.
METHODSThe hospitalization data and serum creatinine data of critically ill adult patients were collected from 9 regional central hospitals across China in 2013. Kidney Disease Improving Global Outcomes (KDIGO 2012) criteria was used to define and stage AKI. The demographic characteristics of the patients, comorbidities, stage of AKI, in-hospital outcomes and risk factors were retrospectively analyzed.
RESULTSOf the total of 14 305 critically ill patients included in the study, 4298 (30.04%) were identified to have AKI, including 2240 (52.1%) in stage 1, 845 (19.7%) in stage 2, and 1213 (28.2%) in stage 3. The in-hospital mortality rate was 16.7% (716/4298) and the odds ratio for death was 7.59 (95%CI 6.54-8.79, P<0.001). The length of hospital stay, daily cost, and mortality rate were associated with the stage of AKI. Multivariate analysis identified chronic kidney disease (OR=5.45, 95%CI: 4.71-6.32, P<0.001), extra-renal organ failure (OR=12.57, 95%CI: 11.24-14.07, P<0.001), shock (OR=2.44, 95%CI: 2.01-2.96, P<0.001) and cardiac surgery (OR=5.96, 95%CI: 5.16-6.87, P<0.001) as the independent risk factors for AKI. Only 5.4% of the AKI patients whose serum creatinine change met the KDIGO criteria during hospitalization received the diagnosis of AKI upon discharge.
CONCLUSIONAKI is common in critically ill patients and associated with high mortality rates and poor outcomes. The stage of AKI is related with the in-hospital outcomes of the patients. Chronic kidney disease, extra-renal organ failure, shock and cardiac surgery are the major risk factors for AKI in these patients. Missed diagnosis occurs in most of the AKI cases, which urges more awareness of the condition in the critically ill patients during hospitalization.
Acute Kidney Injury ; epidemiology ; Adult ; Cardiac Surgical Procedures ; China ; Critical Illness ; Hospital Mortality ; Humans ; Kidney ; physiopathology ; Kidney Function Tests ; Length of Stay ; Multiple Organ Failure ; epidemiology ; Odds Ratio ; Renal Insufficiency, Chronic ; epidemiology ; Retrospective Studies ; Risk Factors ; Shock ; epidemiology
9.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
10.Benefits of a Continuous Ambulatory Peritoneal Dialysis (CAPD) Technique with One Icodextrin-Containing and Two Biocompatible Glucose-Containing Dialysates for Preservation of Residual Renal Function and Biocompatibility in Incident CAPD Patients.
Hye Eun YOON ; Yoon Kyung CHANG ; Seok Joon SHIN ; Bum Soon CHOI ; Byung Soo KIM ; Cheol Whee PARK ; Ho Cheol SONG ; Sun Ae YOON ; Dong Chan JIN ; Yong Soo KIM
Journal of Korean Medical Science 2014;29(9):1217-1225
In a prospective randomized controlled study, the efficacy and safety of a continuous ambulatory peritoneal dialysis (CAPD) technique has been evaluated using one icodextrin-containing and two glucose-containing dialysates a day. Eighty incident CAPD patients were randomized to two groups; GLU group continuously using four glucose-containing dialysates (n=39) and ICO group using one icodextrin-containing and two glucose-containing dialysates (n=41). Variables related to residual renal function (RRF), metabolic and fluid control, dialysis adequacy, and dialysate effluent cancer antigen 125 (CA125) and interleukin 6 (IL-6) levels were measured. The GLU group showed a significant decrease in mean renal urea and creatinine clearance (-Delta1.2+/-2.9 mL/min/1.73 m2, P=0.027) and urine volume (-Delta363.6+/-543.0 mL/day, P=0.001) during 12 months, but the ICO group did not (-Delta0.5+/-2.7 mL/min/1.73 m2, P=0.266; -Delta108.6+/-543.3 mL/day, P=0.246). Peritoneal glucose absorption and dialysate calorie load were significantly lower in the ICO group than the GLU group. The dialysate CA125 and IL-6 levels were significantly higher in the ICO group than the GLU group. Dialysis adequacy, beta2-microglobulin clearance and blood pressure did not differ between the two groups. The CAPD technique using one icodextrin-containing and two glucose-containing dialysates tends to better preserve RRF and is more biocompatible, with similar dialysis adequacy compared to that using four glucose-containing dialysates in incident CAPD patients. [Clincal Trial Registry, ISRCTN23727549]
Adult
;
Aged
;
CA-125 Antigen/analysis
;
Creatinine/urine
;
Dialysis Solutions/*therapeutic use
;
Female
;
Glomerular Filtration Rate
;
Glucans/*therapeutic use
;
Glucose/*therapeutic use
;
Humans
;
Interleukin-6/analysis
;
Kidney/physiopathology
;
Kidney Failure, Chronic/*therapy
;
Male
;
Membrane Proteins/analysis
;
Middle Aged
;
Peritoneal Dialysis
;
Peritoneal Dialysis, Continuous Ambulatory
;
Urea/urine

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