| Trials | |
| Effect of oral sodium bicarbonate supplementation on progression of chronickidney disease in patients with chronic metabolic acidosis: study protocol for arandomized controlled trial (SoBic-Study) | |
| Gere Sunder-Plassmann2  Walter H Hörl2  Alice Schmidt2  Melanie Fraunschiel3  Georg Heinze1  Max Plischke2  Daniel Cejka2  Martina Gaggl2  | |
| [1] Center of Medical Statistics, Informatics and Intelligent Systems, Section ofClinical Biometrics, Medical University of Vienna, Vienna, Austria;Department of Medicine III, Division of Nephrology and Dialysis, MedicalUniversity of Vienna, Vienna, Austria;Center of Medical Statistics, Informatics and Intelligent Systems, Sectionfor Medical Information Management and Imaging, Medical University ofVienna, Vienna, Austria | |
| 关键词: Progression; Acidotic; Acid retention; Acid–base balance; Sodium bicarbonate; Kidney injury; Chronic kidney disease; Metabolic acidosis; | |
| Others : 1093553 DOI : 10.1186/1745-6215-14-196 |
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| received in 2012-11-28, accepted in 2013-06-17, 发布年份 2013 | |
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【 摘 要 】
Background
Overt chronic metabolic acidosis in patients with chronic kidney disease develops after a drop of glomerular filtration rate to less than approximately 25 mL/min/1.73 m2. The pathogenic mechanism seems to be a lack of tubular bicarbonate production, which in healthy individuals neutralizes the acid net production. As shown in several animal and human studies the acidotic milieu alters bone and vitamin D metabolism, induces muscle wasting, and impairs albumin synthesis, aside from a direct alteration of renal tissue by increasing angiotensin II, aldosteron and endothelin kidney levels. Subsequent studies testing various therapeutic approaches in very selected study populations showed that oral supplementation of the lacking bicarbonate halts progression of decline of renal function. However, due to methodological limitations of these studies further investigations are of urgent need to ensure the validity of this therapeutic concept.
Methods/Design
The SoBic-study is a single-center, randomized, controlled, open-label clinical phase IV study performed at the nephrological outpatient service of the Medical University of Vienna. Two-hundred patients classified to CKD stage 3 or 4 with two separate measurements of HCO3- of <21 mmol/L will be 1:1 randomized to either receive a high dose of oral sodium bicarbonate with a serum target HCO3- level of 24 ± 1 mmol/L or receive a rescue therapy of sodium bicarbonate with a serum target level of 20 ± 1 mmol/L. The follow up will be for two years. The primary outcome is the effect of sodium bicarbonate supplementation on renal function measured by means of estimated glomerular filtration rates (4-variable-MDRD-equation) after two years. Secondary outcomes are change in markers of bone metabolism between groups, death rates between groups, and the number of subjects proceeding to renal replacement therapy across groups. Adverse events, such as worsening of arterial hypertension due to the additional sodium consumption, will be accurately monitored.
Discussion
We hypothesize that sufficiently balanced acid–base homeostasis leads to a reduction of decline of renal function in patients with chronic kidney disease. The concept of an exogenous bicarbonate supplementation to substitute the lacking endogenous bicarbonate has existed for a long time, but has never been investigated sufficiently to state clear treatment guidelines.
Trial registration
EUDRACT Number: 2012-001824-36
【 授权许可】
2013 Gaggl et al.; licensee BioMed Central Ltd.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| 20150130164051800.pdf | 599KB | ||
| Figure 2. | 155KB | Image | |
| Figure 1. | 51KB | Image |
【 图 表 】
Figure 1.
Figure 2.
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