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[Retardation of hemodialysis by recombinant human erythropoietin in patients with chronic kidney disease].

Authors :
Kato F
Takeuchi N
Takenoshita E
Yuasa J
Isaka S
Fujii T
Suzuki S
Irie Y
Ogawa M
Ueda S
Source :
Nihon Jinzo Gakkai shi [Nihon Jinzo Gakkai Shi] 2010; Vol. 52 (1), pp. 58-65.
Publication Year :
2010

Abstract

Unlabelled: Renal anemia is a serious complication of chronic kidney disease (CKD) and accelerates its progress. Recombinant human erythropoietin (rHuEPO) therapy not only improves anemia but also has a renoprotective effect. This study aimed to determine whether treatment with rHuEPO can retard the initiation of hemodialysis (HD) in patients with CKD.<br />Methods: Clinical data of CKD patients who had already been treated with HD were analyzed retrospectively. Twenty-one patients who had received rHuEPO therapy constituted the treated group (EPO(+) group), and twenty-one other patients without rHuEPO constituted the non-treated group (EPO(-) group). The study start-point was the day of kidney function deterioration, judged as CKD stage 5. The end-point of the study was the initiation of HD.<br />Results: During the evaluation period, mean values of hemoglobin (Hb) in the EPO(+) group remained lower than those in the EPO(-) group. Survival analysis limited to the two-year period from the beginning of evaluation showed that the renal survival rate of the EPO(+) group was significantly better than that of the EPO(-) group [EPO(+): 42.1% vs. EPO(-): 12.5%, p<0.05]. Duration of renal survival was 29.8 +/- 4.07 months in the EPO(+) group and 19.1 +/- 3.27 months in the EPO(-) group (p<0.05).<br />Conclusion: Although the mean values of Hb remained lower in the EPO(+) group than in the EPO(-) group during the observation period, the renal survival rate and duration of renal survival in the EPO(+) group were significantly superior than in the EPO(-) group. The study suggests that rHuEPO exerts a renoprotective effect via a mechanism other than the correction of anemia.

Details

Language :
Japanese
ISSN :
0385-2385
Volume :
52
Issue :
1
Database :
MEDLINE
Journal :
Nihon Jinzo Gakkai shi
Publication Type :
Academic Journal
Accession number :
20166543