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Predictive Factors for Efficacy of AST-120 Treatment in Diabetic Nephropathy: a Prospective Single-Arm, Open-Label, Multi-Center Study

Authors
Hwang, YC | Kim, SW | Hur, KY | Cha, BS | Kim, IJ | Park, TS | Baik, SH | Yoon, KH | Lee, KW  | Lee, IK | Lee, MK
Citation
Journal of Korean medical science, 34(15). : e117-e117, 2019
Journal Title
Journal of Korean medical science
ISSN
1011-89341598-6357
Abstract
BACKGROUND: Removal of uremic toxins such as indoxyl sulfate by AST-120 is known to improve renal function and delay the initiation of dialysis in patients with advanced chronic kidney disease. However, it is unclear whether the addition of AST-120 to conventional treatments is effective in delaying the progression of renal dysfunction in patients with diabetic nephropathy.
METHODS: A total of 100 patients with type 2 diabetes and renal dysfunction (serum creatinine levels ranging from 1.5 to 3.0 mg/dL) were recruited from eight centers in Korea and treated with AST-120 (6 g/day) for 24 weeks. The primary endpoint was improvement in renal function measured as the gradient of the reciprocal serum creatinine level (1/sCr) over time (i.e., the ratio of 1/sCr time slope for post- to pre-AST-120 therapy). A response was defined as a ratio change of the regression coefficient of 1/sCr RESULTS: Renal function improved in 80.3% of patients (61/76) after 24 weeks of AST-120 treatment. There were no differences between responder and non-responder groups in baseline characteristics except for diastolic blood pressure (73.5 +/- 9.5 mmHg in the responder group vs. 79.3 +/- 11.1 mmHg in the non-responder group: P = 0.046). Serum lipid peroxidation level decreased significantly in the responder group (from 2.25 +/- 0.56 muol/L to 1.91 +/- 0.72 muol/L: P = 0.002) but not in the non-responder group.
CONCLUSION: The addition of AST-120 to conventional treatments may delay the progression of renal dysfunction in diabetic nephropathy. The antioxidant effect of AST-120 might contribute to improvement in renal function.
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DOI
10.3346/jkms.2019.34.e117
PMID
31001934
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Journal Papers > School of Medicine / Graduate School of Medicine > Endocrinology & Metabolism
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