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Vol. 22, Suppl. 2, 2004   

Free Abstract     Article (References)     Article (PDF 136 KB)     

9th Annual Conference of the Japanese Society for Hemodiafiltration in Conjunction with the International Symposium on Hemodiafiltration Therapy
August 30-31, 2003, Kanagawa, Japan
Selected Papers
Editor: Akihiro C. Yamashita, Kanagawa


Luncheon Seminar

Effect of Hemodiafiltration against Radical Stress in the Course of Blood Purification
Tadashi Tomo, Kazuhiro Matsuyama, Masaru Nasu

Second Department of Internal Medicine, Oita University, Faculty of Medicine, Hazama, Japan

Address of Corresponding Author

Blood Purif 2004;22 (Suppl. 2):72-77 (DOI: 10.1159/000081879)


 goto top of page Key Words

  • Hemodiafiltration
  • Hydroperoxide radical
  • Hydroxy radical
  • Advanced glycation end products

 goto top of page Abstract

The involvement of radical stress has been suggested as a cause for complications in patients on dialysis, such as arteriosclerosis, dialysis-related amyloidosis, etc. It has been reported that the increase in radical stress is not only seen in renal failure, but that its amplified effect is also seen in the process of blood purification. Our group has reported on the radical stress-reducing effect of HDF. We performed four types of blood purification (HD; on-line HDF; pre, on-line HDF; post, P/P HDF) in patients on maintenance dialysis using the polysulfone (APS) dialyzer. The change in radical related markers such as pentosidine (total, free) and CML (total, free), and the CTL/Cr ratio, and the hydroperoxide radicals were studied. In HDF (post, pre), the amplification rate of hydroperoxide radicals was significantly low, whereas the reduction rate of CTL/Cr ratio as index for hydroxy radicals was significantly higher in on-line HDF than in HD. Both the total CML and T-pentosidine increased in HD but showed a decrease in HDF. As HDF uses large amounts of replacement solution, the following effects can be expected: (a) suppression of the amplification of hydroperoxide radicals and suppression of the amplification of hydroxy radicals, and (b) suppression of fat oxidation by AGEs themselves. These antiradical stress effects are presumed to be exerted by effective removal of radical carrier protein, denatured protein, and complement protein in HDF, by dilution of radicals by massive use of replacement solution, and by the sequential reduction of the excitation and amplification effects.

Copyright © 2004 S. Karger AG, Basel


 goto top of page Author Contacts

Tadashi Tomo
Second Department of Internal Medicine, Faculty of Medicine, Oita University
Idaigaoka 1-1, Hazama-machi
Oita 879-5593 (Japan)
Tel. +81 97 586 5804, Fax +81 97 549 4245, E-Mail tomo@med.oita-u.ac.jp


 goto top of page Article Information

Number of Print Pages : 6
Number of Figures : 8, Number of Tables : 0, Number of References : 13

 
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