Abstract | BACKGROUND: METHODS: In 20 patients with SHPT resistant to maxacalcitol (OCT) intravenously administered, all detectably enlarged parathyroid glands were treated by percutaneous maxacalcitol injection therapy (PMIT) under ultrasonographic guidance consecutively 6 times, which was followed by OCT that was intravenously administered. The clinical effects of PMIT were evaluated based on the changes in the serum intact-PTH, adjusted Ca, phosphorus, and bone marker levels, and the parathyroid gland volume determined by ultrasonography. Morphologic examination, apoptosis analysis, and PTH mRNA expression level determination by reverse transcription-polymerase chain reaction (RT-PCR) using parathyroid tissues obtained by a biopsy technique were performed. RESULTS: PMIT and subsequent intravenous OCT administrations significantly decreased the serum intact-PTH level and parathyroid gland volume for at least 12 weeks after PMIT without major complications. Parathyroid tissues obtained after PMIT exhibited some partial defects of parathyroid cells, a marked increase in the number of the terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling (TUNEL)-positive cells, the ladder formation determined by DNA electrophoresis, and the decrease in the PTH mRNA expression level. CONCLUSION: PMIT is effective and safe for the treatment of refractory SHPT, and a locally high level of OCT suppresses PTH secretion and regresses parathyroid hyperplasia, which is involved in the induction of apoptosis of parathyroid cells.
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Authors | Kazuhiro Shiizaki, Ikuji Hatamura, Shigeo Negi, Nobuhiko Narukawa, Masahide Mizobuchi, Toshifumi Sakaguchi, Akira Ooshima, Tadao Akizawa |
Journal | Kidney international
(Kidney Int)
Vol. 64
Issue 3
Pg. 992-1003
(Sep 2003)
ISSN: 0085-2538 [Print] United States |
PMID | 12911549
(Publication Type: Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Parathyroid Hormone
- RNA, Messenger
- Calcitriol
- maxacalcitol
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Topics |
- Administration, Cutaneous
- Adult
- Aged
- Apoptosis
(drug effects)
- Calcitriol
(administration & dosage, analogs & derivatives)
- Female
- Humans
- Hyperparathyroidism, Secondary
(drug therapy, pathology)
- Hyperplasia
- Injections, Intralesional
- Male
- Middle Aged
- Parathyroid Glands
(drug effects, pathology)
- Parathyroid Hormone
(genetics)
- RNA, Messenger
(metabolism)
- Reverse Transcriptase Polymerase Chain Reaction
- Uremia
(drug therapy, pathology, physiopathology)
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