Glycemic Control Is a Predictor of Survival for Diabetic Patients on Hemodialysis

  1. Tomoaki Morioka, MD1,
  2. Masanori Emoto, MD1,
  3. Tsutomu Tabata, MD2,
  4. Tetsuo Shoji, MD1,
  5. Hideki Tahara, MD1,
  6. Hiroshi Kishimoto, MD2,
  7. Eiji Ishimura, MD1 and
  8. Yoshiki Nishizawa, MD1
  1. 1Metabolism, Endocrinology, and Molecular Medicine, Department of Internal Medicine, Osaka City University Graduate Medical School, Osaka
  2. 2Department of Internal Medicine, Inoue Hospital, Suita, Japan

    Abstract

    OBJECTIVE—To investigate the impact of glycemic control on the survival of diabetic subjects with end-stage renal disease (ESRD) starting hemodialysis treatment.

    RESEARCH DESIGN AND METHODS—This single-center prospective observational study enrolled 150 diabetic ESRD subjects (109 men and 41 women; age at hemodialysis initiation, 60.5 ± 10.2 years) at start of hemodialysis between January 1989 and December 1997. The subjects were divided into groups according to their glycemic control level at inclusion as follows: good HbA1c <7.5%, n = 93 (group G), and poor HbA1c ≥7.5%, n = 57 (group P); and survival was followed until December 1999, with a mean follow-up period of 2.7 years.

    RESULTS—Group G had better survival than group P (the control group) (P = 0.008). At inclusion, there was no significant difference in age, sex, systolic blood pressure (SBP), BMI, cardio-to-thoracic ratio (CTR) on chest X-ray, and serum creatinine (Cre) or hemoglobin (Hb) levels between the two groups. After adjustment for age and sex, HbA1c was a significant predictor of survival (hazard ratio 1.133 per 1.0% increment of HbA1c, 95% CI 1.028–1.249, P = 0.012), as were Cre and CTR.

    CONCLUSIONS—Good glycemic control (HbA1c <7.5%) predicts better survival of diabetic ESRD patients starting hemodialysis treatment.

    Footnotes

    • Address correspondence and reprint requests to Masanori Emoto, Metabolism, Endocrinology, and Molecular Medicine, Department of Internal Medicine, Osaka City University Graduate Medical School, 1-4-3, Asahi-machi, Abeno-ku, Osaka, Japan, 545-8585. E-mail: memoto{at}med.osaka-cu.ac.jp.

      Received for publication 17 October 2000 and accepted in revised form 19 January 2001.

      A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

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