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Initial responsiveness to darbepoetin alfa and its contributing factors in non-dialysis chronic kidney disease patients in Japan.
Hayashi, Terumasa; Kato, Hideki; Tanabe, Kenichiro; Nangaku, Masaomi; Hirakata, Hideki; Wada, Takashi; Sato, Hiroshi; Yamazaki, Yasushi; Masaki, Takao; Kagimura, Tatsuo; Yamamoto, Hiroyasu; Hase, Hiroki; Kamouchi, Masahiro; Imai, Enyu; Mizuno, Kyoichi; Iwasaki, Manabu; Akizawa, Tadao; Tsubakihara, Yoshiharu; Maruyama, Shoichi; Narita, Ichiei.
Afiliação
  • Hayashi T; Department of Kidney Disease and Hypertension, Osaka General Medical Center, Osaka, Japan.
  • Kato H; Division of Nephrology and Endocrinology, The University of Tokyo Graduate School of Medicine, Tokyo, Japan.
  • Tanabe K; Translational Research Center for Medical Innovation, Kobe, Japan.
  • Nangaku M; Division of Nephrology and Endocrinology, The University of Tokyo Graduate School of Medicine, Tokyo, Japan.
  • Hirakata H; Fukuoka Renal Clinic, Fukuoka, Japan.
  • Wada T; Department of Nephrology and Laboratory Medicine, Faculty of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan.
  • Sato H; Division of Clinical Pharmacology and Therapeutics, Tohoku University Graduate School of Pharmaceutical Sciences and Faculty of Pharmaceutical Sciences, Sendai, Japan.
  • Yamazaki Y; Department of Nephrology and Rheumatology, Kagawa Prefectural Central Hospital, Takamatsu, Japan.
  • Masaki T; Department of Nephrology, Hiroshima University Hospital, Hiroshima, Japan.
  • Kagimura T; Translational Research Center for Medical Innovation, Kobe, Japan.
  • Yamamoto H; Division of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
  • Hase H; Division of Nephrology, Toho University Ohashi Medical Center, Tokyo, Japan.
  • Kamouchi M; Department of Health Care Administration and Management, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Imai E; Nakayamadera Imai Clinic, Takarazuka, Japan.
  • Mizuno K; Mitsukoshi Health and Welfare Foundation, Tokyo, Japan.
  • Iwasaki M; School of Data Science, Yokohama City University, Yokohama, Japan.
  • Akizawa T; Division of Nephrology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
  • Tsubakihara Y; Course of Safety Management in Health Care Sciences, Graduate School of Health Care Sciences, Jikei Institute, Osaka, Japan.
  • Maruyama S; Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Narita I; Division of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Sciences, 757 Ichibancho Asahimachidori Chuo-ku, Niigata, 951-8510, Japan. naritai@med.niigata-u.ac.jp.
Clin Exp Nephrol ; 25(2): 110-119, 2021 Feb.
Article em En | MEDLINE | ID: mdl-32949295
ABSTRACT

BACKGROUND:

Hyporesponsiveness to erythropoiesis-stimulating agents (ESAs) is associated with cardiovascular events and poor renal outcome in patients with chronic kidney disease (CKD). This study aimed to investigate the initial responsiveness to darbepoetin alfa (DA) and its contributing factors using the data from the BRIGHTEN.

METHODS:

Of 1980 patients enrolled at 168 facilities, 1695 were included in this analysis [285 patients were excluded mainly due to lack of hemoglobin (Hb) values]. The initial ESA response index (iEResI) was defined as a ratio of Hb changes over 12 weeks after DA administration per weight-adjusted total DA dose and contributing factors to iEResI were analyzed.

RESULTS:

The mean age was 70 ± 12 years (male 58.8%; diabetic nephropathy 27.6%). The median creatinine and mean Hb levels at DA initiation were 2.62 mg/dL and 9.8 g/dL, respectively. The most frequent number of DA administration during 12 weeks was 3 times (41.1%), followed by 4 (15.6%) times with a wide distribution of the total DA dose (15-900 µg). Remarkably, 225 patients (13.3%) did not respond to DA. Multivariate analysis showed that male gender, hypoglycemic agent use, iron supplementation, high eGFR, low Hb, low CRP, low NT-proBNP, and low urinary protein-creatinine ratio were independently associated with better initial response to DA (P = < 0.0001, 0.0108, < 0.0001, 0.0476, < 0.0001, 0.0004, 0.0435, and 0.0009, respectively).

CONCLUSIONS:

Non-responder to DA accounted for 13.3% of patients with non-dialysis CKD. Iron supplementation, low CRP, low NT-proBNP, and less proteinuria were predictive and modifiable factors associated with better initial response to DA.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica / Darbepoetina alfa / Anemia Tipo de estudo: Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica / Darbepoetina alfa / Anemia Tipo de estudo: Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article