Impaired secretion of parathyroid hormone is coherent to diabetic hemodialyzed patients

Diabetic bone disease is characterized by low bone turnover resulting from impaired secretion of parathyroid hormone (PTH). However, it was suggested that the difference in duration of hemodialysis (HD) therapy and age of patients between HD patients with and without diabetes mellitus (DM) may be re...

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Veröffentlicht in:American journal of kidney diseases 2001-10, Vol.38 (4), p.S139-S142
Hauptverfasser: Inaba, Masaaki, Okuno, Senji, Nagasue, Kyoko, Otoshi, Tatsuyuki, Kurioka, Yasuko, Maekawa, Kiyoshi, Kumeda, Yasuro, Imanishi, Yasuo, Ishimura, Eiji, Ohta, Tomohiro, Morii, Hirotoshi, Kim, Masao, Nishizawa, Yoshiki
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Sprache:eng
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Zusammenfassung:Diabetic bone disease is characterized by low bone turnover resulting from impaired secretion of parathyroid hormone (PTH). However, it was suggested that the difference in duration of hemodialysis (HD) therapy and age of patients between HD patients with and without diabetes mellitus (DM) may be responsible for a significant reduction in serum intact PTH (iPTH) level in HD patients with DM. The present study showed that although such major factors affecting PTH secretion as age, sex, HD duration, and serum calcium, phosphate, and magnesium levels did not differ significantly between HD patients with and without DM, serum iPTH levels were still significantly lower in HD patients with than without DM. Among biochemical markers for bone metabolism, serum levels of intact osteocalcin (iOC) and deoxypyridinoline (DPD) were significantly lower in HD patients with than without DM, whereas serum bone-specific alkaline phosphatase, pyridinoline, and β-crosslaps did not differ significantly between the two groups of patients. In summary, our findings indicate that PTH secretion may be significantly impaired in HD patients with DM compared with those without DM, and serum iOC and DPD are bone markers sensitive enough to detect low bone turnover in HD patients with DM. © 2001 by the National Kidney Foundation, Inc.
ISSN:0272-6386
1523-6838
DOI:10.1053/ajkd.2001.27423