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1.
Arzneimittelforschung ; 54(9): 538-44, 2004.
Article in English | MEDLINE | ID: mdl-15500200

ABSTRACT

A new maintenance fluid containing sodium acetate as the base component and electrolytes (Veen 3G, test preparation) for a maximum of 24 h was infused to 15 patients hospitalized for renal biopsies and requiring intravenous supplements of water, electrolytes and energy because oral or enteric ingestion was inadequate or impossible. A physical examination, blood chemistry tests and urinalysis were performed, and the global improvement rating was obtained by scoring the effects on a) maintenance of cardiovascular hemodynamics (systolic blood pressure), b) blood glucose control (blood glucose level), c) utilization of sugar (free fatty acids, total ketone bodies), d) maintenance of serum electrolytes, e) amount of sugar excreted in the urine and f) maintenance of urinary volume. The results were excellent or good in all of the 15 patients analyzed. The test agent was not the direct cause of any adverse events or abnormal changes in laboratory findings, and no safety-related problems were observed in any of the patients. These results indicated that the test preparation used in this study is a clinically useful and highly safe fluid agent.


Subject(s)
Biopsy/methods , Electrolytes/chemistry , Glomerulonephritis/pathology , Kidney/pathology , Pharmaceutic Aids/chemistry , Sodium Acetate/chemistry , Adult , Blood Glucose/metabolism , Blood Pressure/physiology , Chronic Disease , Electrolytes/blood , Energy Metabolism/drug effects , Female , Glycosuria/urine , Humans , Male , Middle Aged , Pharmaceutical Solutions
2.
Metabolism ; 53(10): 1382-6, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15375799

ABSTRACT

Atherosclerosis is the major cause of morbidity and mortality in patients with type 2 diabetes, and pioglitazone has been reported to have anti-inflammatory and potential antiatherogenic effects. The aim of the present study was to determine whether pioglitazone, glibenclamide, or voglibose affects carotid intima-media thickness (IMT), pulse wave velocity (PWV), and urinary albumin excretion (UAE) in normotensive type 2 diabetic nephropathy patients. Forty-five normotensive type 2 diabetes patients with microalbuminuria were randomized to 12-month treatment with pioglitazone (30 mg/d, n = 15), glibenclamide (5 mg/d, n = 15), or voglibose (0.6 mg/d, n = 15). Pre- and posttreatment UAE, PWV, and IMT values were compared between treatment groups and a group of age-matched healthy control subjects (n = 30). Pretreatment PWV, IMT, and UAE values differed little between the 3 groups, but UAE was greater in the 45 type 2 diabetes patients (132.5 +/- 36.4 microg/min) than in the control subjects (6.2 +/- 1.8 microg/min, P < .001). IMT (0.76 +/- 0.12 mm) was significantly greater in the diabetics than in the controls (0.60 +/- 0.08 mm, P < .01). PWV (1,840 +/- 320 cm/s) was also significantly greater in the diabetics than in the controls (1,350 +/- 225 cm/s, P < .01). After 6 and 12 months, UAE, IMT, and PWV in the pioglitazone treatment group were significantly lower than those in the glibenclamide treatment group and voglibose treatment group (UAE: 6 months, P < .05 and 12 months, P < .01; IMT and PWV: 6 months, P < .05 and 12 months, P < .05). Pioglitazone, but not glibenclamide or voglibose, appears to be effective in reducing UAE, IMT, and PWV in normotensive type 2 diabetes patients with microalbuminuria.


Subject(s)
Carotid Arteries/pathology , Diabetes Mellitus, Type 2/drug therapy , Diabetes Mellitus, Type 2/pathology , Hypoglycemic Agents/therapeutic use , Inositol/analogs & derivatives , Thiazolidinediones/therapeutic use , Albuminuria/prevention & control , Blood Pressure/drug effects , Blood Urea Nitrogen , Creatinine/blood , Double-Blind Method , Enzyme Inhibitors/pharmacology , Female , Glycated Hemoglobin/metabolism , Humans , Inositol/pharmacology , Male , Middle Aged , Pioglitazone , Protein Precursors/metabolism , Sulfonylurea Compounds/pharmacology
3.
Kidney Blood Press Res ; 26(3): 185-91, 2003.
Article in English | MEDLINE | ID: mdl-12886046

ABSTRACT

BACKGROUND: Hemodialysis patients manifest accelerated atherosclerosis. Hemodialysis is associated with oxidative stress, which can be partially prevented with the use of a vitamin E-coated dialyzer. Adsorption of low-density lipoprotein (LDL) has been applied in the treatment of arteriosclerosis obliterans (ASO). The aim of the present study was to determine whether the vitamin E-coated dialyzer and/or LDL apheresis affects carotid atherosclerosis in hemodialysis patients with ASO. METHODS: Thirty hemodialysis patients with ASO were divided into four treatment groups: treatment with conventional cellulose or synthetic membranes (group A, n = 12), treatment with vitamin E-coated membrane (group B, n = 7), treatment with conventional membrane and LDL apheresis (group C, n = 6), and treatment with vitamin E-coated membrane and LDL apheresis (group D, n = 5). Carotid artery intima-media thickness (IMT) and arterial stiffness assessed by pulse wave velocity (PWV), plasma C-reactive protein (CRP) and interleukin (IL)-6 were measured before and 10 weeks after treatment and compared between groups. All values were referred to measurements after LDL apheresis. RESULTS: IMT and PWV, plasma CRP and IL-6 showed little change in group A throughout the experimental period. These decreased slightly from the baseline value in group B, but the change was not significant. In group C, IMT decreased from 1.12 +/- 0.24 to 1.02 +/- 0.18 mm (p < 0.05), and PWV decreased from 2,266 +/- 380 to 1,968 +/- 342 cm/s (p < 0.05). Plasma CRP and IL-6 concentrations also decreased significantly compared with baseline (p < 0.05). In group D, IMT decreased from 1.18 +/- 0.26 to 0.92 +/- 0.18 mm (p < 0.01), and PWV decreased from 2,284 +/- 390 to 1,786 +/- 284 cm/s (p < 0.01). Plasma CRP and IL-6 levels also decreased significantly compared with baseline (p < 0.01). CONCLUSION: These data suggest that LDL apheresis and the vitamin E-coated membrane dialysis in combination may prevent further progression of atherosclerosis in hemodialysis patients with ASO.


Subject(s)
Antioxidants/therapeutic use , Arteriosclerosis Obliterans/prevention & control , Arteriosclerosis/prevention & control , Blood Component Removal , Carotid Arteries/pathology , Lipoproteins, LDL/blood , Membranes, Artificial , Renal Dialysis/adverse effects , Vitamin E/therapeutic use , Anticholesteremic Agents/therapeutic use , Aorta, Thoracic/pathology , Aorta, Thoracic/physiology , Arteriosclerosis/complications , Arteriosclerosis Obliterans/complications , Blood Pressure/physiology , C-Reactive Protein/metabolism , Female , Humans , Interleukin-6/metabolism , Kidney Failure, Chronic/complications , Kidney Failure, Chronic/therapy , Lipoproteins, LDL/isolation & purification , Male , Middle Aged
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