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Wiley InterScience

Therapeutic Apheresis and Dialysis

Therapeutic Apheresis and Dialysis

Volume 8 Issue 6, Pages 474 - 479

Published Online: 16 Dec 2004

Journal compilation © 2009 International Society for Apheresis


Published on behalf of the International Society for Apheresis, the Japanese Society for Apheresis and the Japanese Society for Dialysis Therapy
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Bio-Intact Parathyroid Hormone and Intact Parathyroid Hormone in Hemodialysis Patients With Secondary Hyperparathyroidism Receiving Intravenous Calcitriol Therapy
Akira Fujimori 1 , Makoto Sakai 2 , Kunihiko Yoshiya 3 , Jeongsoo Shin 4 , Jong-Il Kim 5 , Yoko Inaba 6 , Takashi Miyamoto 7 , Seishi Inoue,8 and Masafumi Fukagawa 9*
  1 Konan Hospital, Kobe,
  2 Takasago Municipal Hospital, Takasago,
  3 Hara Genito-urinary Hospital, Kobe,
  4 Motomachi HD Clinic, Kobe,
  5 Hidaka Hospital, Hidaka-cho,
  6 Shinsuma Hospital, Kobe,
  7 Miyamoto Clinic, Nishinomiya, Hyogo,
  8 Sumiyoshigawa Hospital, Kobe,
  9 Division of Nephrology and Dialysis Center, Kobe University School of Medicine, Kobe, Japan.
Correspondence to  Dr Akira Fujimori, Department of Artificial Kidney, Konan Hospital, 1-5-16, Kamokogahara, Higashinada-ku, Kobe 658-0064, Japan. Email: louie@kcc.zaq.ne.jp

  *for the Kobe Parathyroid and Bone Forum.

Copyright 2004 International Society for Apheresis
KEYWORDS
Bio-Intact parathyroid hormone • bone-specific alkaline phosphatase • calcitriol • intact-parathyroid hormone • secondary hyperparathyroidism

ABSTRACT

Abstract: Intact parathyroid hormone (iPTH) assay has been the most widely used for the diagnosis of secondary hyperparathyroidism and evaluation of vitamin D therapy. However, 1–84 PTH assay might be a better diagnostic tool since iPTH detects not only 1–84 PTH but also large C-terminal fragments, which would antagonize PTH action. Therefore, we conducted a multicenter study to evaluate the clinical usefulness of a newly developed immunochemiluminometric assay for 1–84 PTH, Bio-Intact PTH (BiPTH). Thirty-five uremic patients with secondary hyperparathyroidism participated in the study. Intravenous calcitriol therapy was continued for 12 months. iPTH and bone-specific alkaline phosphatase (BAP) were monitored at each dialysis center to control the dose of calcitriol. Serum and plasma samples were collected from each center and both iPTH and BiPTH were measured using Allegro-Lite assay reagents from Nichols Institute Diagnostics (San Clemente, CA, USA). Intravenous calcitriol suppressed iPTH after 1 month as well as BiPTH. Bone-specific alkaline phosphatase decreased after 3 months. A high degree of correlation between Nichols iPTH and BiPTH (y = 0.3913 × + 19.517, r = 0.9561) was demonstrated with a BiPTH/iPTH ratio of approximately 0.44. Significant correlation between BAP and iPTH, or between BAP and BiPTH was not observed. Our limited data failed to demonstrate the superiority of BiPTH to iPTH. Therefore, further investigations would be necessary to examine the relationship between BiPTH and bone histomorphometry.


Received March 2004; revised June 2004.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1774-9987.2004.00189.x About DOI

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