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Feasible kidney donation with living marginal donors, including diabetes mellitus.
Yoshinaga, Kasumi; Araki, Motoo; Wada, Koichiro; Sekito, Takanori; Watari, Shogo; Maruyama, Yuki; Mitsui, Yosuke; Sadahira, Takuya; Kubota, Risa; Nishimura, Shingo; Edamura, Kohei; Kobayashi, Yasuyuki; Tanabe, Katsuyuki; Takeuchi, Hidemi; Kitagawa, Masashi; Kitamura, Shinji; Wada, Jun; Watanabe, Masami; Watanabe, Toyohiko; Nasu, Yasutomo.
Afiliación
  • Yoshinaga K; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Araki M; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Wada K; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Sekito T; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Watari S; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Maruyama Y; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Mitsui Y; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Sadahira T; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Kubota R; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Nishimura S; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Edamura K; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Kobayashi Y; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Tanabe K; Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Takeuchi H; Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Kitagawa M; Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Kitamura S; Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Wada J; Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Watanabe M; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Watanabe T; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
  • Nasu Y; Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan.
Immun Inflamm Dis ; 9(3): 1061-1068, 2021 09.
Article en En | MEDLINE | ID: mdl-34102025
ABSTRACT

OBJECTIVES:

To compare the donor outcomes of living donor kidney transplantation between standard donors (SDs) and marginal donors (MDs) including diabetic patients (MD + DM).

METHODS:

MDs were defined according to Japanese guideline criteria (a) age >70-years, (b) blood pressure ≤130/80 mmHg on hypertension medicine, (c) body mass index >25 to ≤32 kg/m2 , (d) 24-h creatinine clearance ≥70 to <80 ml/min/1.73 m2 , and (e) hemoglobin A1c > 6.2 or ≤6.5 with oral diabetic medicine. Fifty-three of 114 donors were MDs. We compared donor kidney functions until 60 months postoperatively.

RESULTS:

No kidney function parameters were different between SDs and MDs. When comparing SD and MD + DM, MD + DM had a lower postoperative eGFR (48 vs. 41 (1 (month), p = .02), 49 vs. 40 (12, p < .01), 48 vs. 42 (24, p = .04), 47 vs. 38 (36, p = .01)) and the percentage of residual eGFR (SD vs. MD + DM 63 vs. 57 (1 (month), p < .01), 63 vs. 57 (2, p < .01), 64 vs. 56 (12, p < .01), 63 vs. 57 (24, p < .01), 63 vs. 52 (36, p = .02)). However, when MD with a single risk factor of DM was compared to SD, the difference disappeared. Nine out of 12 (75%) MD + DM had ≥2 risk factors.

CONCLUSIONS:

Although long-term observation of donor kidney function is necessary, careful MD + DM selection had the potential to expand the donor pool.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trasplante de Riñón / Diabetes Mellitus Tipo de estudio: Risk_factors_studies Límite: Aged / Humans Idioma: En Revista: Immun Inflamm Dis Año: 2021 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trasplante de Riñón / Diabetes Mellitus Tipo de estudio: Risk_factors_studies Límite: Aged / Humans Idioma: En Revista: Immun Inflamm Dis Año: 2021 Tipo del documento: Article País de afiliación: Japón