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Correcting anemia and native vitamin D supplementation in kidney transplant recipients: a multicenter, 2 × 2 factorial, open-label, randomized clinical trial.
Obi, Yoshitsugu; Ichimaru, Naotsugu; Sakaguchi, Yusuke; Iwadoh, Kazuhiro; Ishii, Daisuke; Sakai, Ken; Iwami, Daiki; Harada, Hiroshi; Sumida, Keiichi; Sekine, Akinari; Masutani, Kosuke; Akutsu, Naotake; Inoue, Takamitsu; Nishihira, Morikuni; Yoneda, Tatsuo; Ito, Shinichi; Araki, Motoo; Kaimori, Jun-Ya; Yoshida, Katsunori; Satoh, Shigeru; Ubara, Yoshifumi; Isaka, Yoshitaka; Yoshida, Kazunari; Tsubakihara, Yoshiharu; Takahara, Shiro; Hamano, Takayuki.
  • Obi Y; Department of Nephrology, Osaka University Graduate School of Medicine, Suita, Japan.
  • Ichimaru N; Obi Clinic, Osaka, Japan.
  • Sakaguchi Y; Division of Nephrology, University of Tennessee Health Science Center, Memphis, TN, USA.
  • Iwadoh K; Department of Advanced Technology for Transplantation, Osaka University Graduate School of Medicine, Suita, Japan.
  • Ishii D; Department of Inter-Organ Communication Research in Kidney Disease, Osaka University Graduate School of Medicine, Suita, Japan.
  • Sakai K; Department of Surgery III, Tokyo Women's Medical University, Tokyo, Japan.
  • Iwami D; Department of Blood Purification, Tokyo Women's Medical University, Tokyo, Japan.
  • Harada H; Department of Urology, Kitasato University School of Medicine, Sagamihara, Japan.
  • Sumida K; Department of Nephrology, Omori Medical Center, Toho University School of Medicine, Tokyo, Japan.
  • Sekine A; Department of Urology, Hokkaido University, Sapporo, Japan.
  • Masutani K; Division of Renal Surgery and Transplantation, Department of Urology, Jichi Medical University, Shimotsuke, Japan.
  • Akutsu N; Department of Kidney Transplant Surgery, Sapporo City General Hospital, Sapporo, Japan.
  • Inoue T; Division of Nephrology, University of Tennessee Health Science Center, Memphis, TN, USA.
  • Nishihira M; Nephrology Center, Toranomon Hospital Kajigaya, Kawasaki, Japan.
  • Yoneda T; Nephrology Center, Toranomon Hospital Kajigaya, Kawasaki, Japan.
  • Ito S; Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Araki M; Department of Surgery and Clinical Research Center, Chibahigashi National Hospital, National Hospital Organization, Chiba, Japan.
  • Kaimori JY; Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.
  • Yoshida K; Department of Nephrology, Tomishiro Central Hospital, Tomigusuku, Japan.
  • Satoh S; Departments of Urology, Nara Medical University, Kashihara, Nara, Japan.
  • Ubara Y; Sunshine M&D Clinic, Mizuho, Gifu, Japan.
  • Isaka Y; Department of Urology, Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
  • Yoshida K; Department of Advanced Technology for Transplantation, Osaka University Graduate School of Medicine, Suita, Japan.
  • Tsubakihara Y; Department of Inter-Organ Communication Research in Kidney Disease, Osaka University Graduate School of Medicine, Suita, Japan.
  • Takahara S; Departments of Urology, Nara Medical University, Kashihara, Nara, Japan.
  • Hamano T; Center for Kidney Disease and Transplantation, Akita University Hospital, Akita, Japan.
Transpl Int ; 34(7): 1212-1225, 2021 07.
Article en En | MEDLINE | ID: mdl-33884674
ABSTRACT
Anemia and vitamin D deficiency are associated with allograft failure, and hence, are potential therapeutic targets among kidney transplant recipients (KTRs). We conducted a multicenter, two-by-two factorial, open-label, randomized clinical trial to examine the effects of anemia correction and vitamin D supplementation on 2-year change in eGFR among KTRs (CANDLE-KIT). We enrolled 153 patients with anemia and >1-year history of transplantation across 23 facilities in Japan, and randomly assigned them to either a high or low hemoglobin target (>12.5 vs. <10.5 g/dl) and to either cholecalciferol 1000 IU/day or control. This trial was terminated early based on the planned interim intention-to-treat analyses (α = 0.034). Among 125 patients who completed the study, 2-year decline in eGFR was smaller in the high vs. low hemoglobin group (i.e., -1.6 ± 4.5 vs. -4.0 ± 6.9 ml/min/1.73 m2 ; P = 0.021), but did not differ between the cholecalciferol and control groups. These findings were supported by the fully adjusted mixed effects model evaluating the rate of eGFR decline among all 153 participants. There were no significant between-group differences in all-cause death or the renal composite outcome in either arm. In conclusion, aggressive anemia correction showed a potential to preserve allograft kidney function.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante de Riñón / Anemia Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans País como asunto: Asia Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante de Riñón / Anemia Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans País como asunto: Asia Idioma: En Año: 2021 Tipo del documento: Article