Literature DB >> 24720404

Impacts of recombinant human erythropoietin treatment during predialysis periods on the progression of chronic kidney disease in a large-scale cohort study (Co-JET study).

Tadao Akizawa1, Akira Saito, Fumitake Gejyo, Masashi Suzuki, Yoshiki Nishizawa, Yasuhiko Tomino, Yoshiharu Tsubakihara, Takashi Akiba, Hideki Hirakata, Yuzo Watanabe, Hideki Kawanishi, Masami Bessho, Yukio Udagawa, Kotonari Aoki, Yukari Uemura, Yasuo Ohashi.   

Abstract

The effect of recombinant human erythropoietin (rHuEPO) treatment on the progression of chronic kidney disease (CKD) has not been fully evaluated in Japan. We therefore retrospectively evaluated this in a sub-cohort of a prospective multicenter study to investigate optimal hemoglobin (Hb) level of CKD patients on hemodialysis (HD) treated with rHuEPO; Japan Erythropoietin Treatment Study for Target Hb and Survival (JET study). Effect of rHuEPO treatment during predialysis period to delay initiation of HD was retrospectively assessed in 2434 patients from the JET study comparing groups with and without rHuEPO treatment. The assessment was done by Cox proportional hazards regression analysis and inverse probability-weighted (IPW) analysis to adjust for time-dependent confounders. The weights used in the IPW analysis were calculated using a logistic model that included baseline confounders and time-dependent variables. During the predialysis period, 71.7% (1746 patients) were treated with rHuEPO (mean Hb level of 8.7 g/dL at initiation of rHuEPO treatment). Covariates significantly associated with initiation of rHuEPO treatment were Hb level, serum creatinine level, age, diabetes, cardiac insufficiency, and hypertension. The adjusted hazard ratio for time until HD initiation under rHuEPO treatment was 0.272 (95% CI, 0.223-0.331; P < 0.001) in the Cox analysis and 0.63 (95% CI, 0.53-0.76; P < 0.0001) in the IPW analysis. This retrospective study suggests that rHuEPO treatment during the predialysis period has preventive effects on the progression of CKD although further prospective investigation on the efficacy is needed.
© 2013 The Authors. Therapeutic Apheresis and Dialysis © 2013 International Society for Apheresis.

Entities:  

Keywords:  Anemia; Chronic kidney disease; Erythropoietin; Inverse probability-weighted Cox model; Observational cohort study; Predialysis

Mesh:

Substances:

Year:  2013        PMID: 24720404     DOI: 10.1111/1744-9987.12066

Source DB:  PubMed          Journal:  Ther Apher Dial        ISSN: 1744-9979            Impact factor:   1.762


  4 in total

1.  Impact of hemoglobin levels on renal and non-renal clinical outcomes differs by chronic kidney disease stages: the Gonryo study.

Authors:  Tae Yamamoto; Mariko Miyazaki; Masaaki Nakayama; Gen Yamada; Masato Matsushima; Mistuhiro Sato; Toshinobu Sato; Yoshio Taguma; Hiroshi Sato; Sadayoshi Ito
Journal:  Clin Exp Nephrol       Date:  2015-10-30       Impact factor: 2.801

2.  Association between the Hemoglobin Level and Cardiothoracic Ratio in Patients on Incident Dialysis.

Authors:  Takasuke Asakawa; Nobuhiko Joki; Yuri Tanaka; Toshihide Hayashi; Hiroki Hase; Yasuhiro Komatsu; Ryoichi Ando; Masato Ikeda; Daijo Inaguma; Toshifumi Sakaguchi; Toshio Shinoda; Fumihiko Koiwa; Shigeo Negi; Toshihiko Yamaka; Takashi Shigematsu
Journal:  Cardiorenal Med       Date:  2014-10-17       Impact factor: 2.041

3.  A Comparative Study of the Hemoglobin-Maintaining Effects Between Epoetin-β Pegol and Darbepoetin-α in Patients with Chronic Kidney Disease During 3 Months Before Dialysis Initiation.

Authors:  Satoru Oka; Yoko Obata; Kenta Torigoe; Miki Torigoe; Shinichi Abe; Kumiko Muta; Yuki Ota; Mineaki Kitamura; Satoko Kawasaki; Misaki Hirose; Tadashi Uramatsu; Hiroshi Yamashita; Hideyuki Arai; Hiroshi Mukae; Tomoya Nishino
Journal:  Drugs R D       Date:  2017-09

4.  Haemoglobin concentration and survival of haemodialysis patients before and after experiencing cardiovascular disease: a cohort study from Japanese dialysis outcomes and practice pattern study (J-DOPPS).

Authors:  Ryo Kido; Tadao Akizawa; Shunichi Fukuhara
Journal:  BMJ Open       Date:  2019-09-05       Impact factor: 2.692

  4 in total

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