Intact PTH assay overestimates true 1-84 PTH levels after maxacalcitol therapy in dialysis patients with secondary hyperparathyroidism

被引:17
作者
Kazama, JJ
Omori, K
Higuchi, N
Takahashi, N
Ito, Y
Maruyama, H
Narita, I
Cantor, TL
Gao, P
Gejyo, F
机构
[1] Niigata Univ Med Hosp, Div Intens Care Med, Niigata, Japan
[2] Niigata Univ, Grad Sch Med & Dent Sci, Div Clin Nephrol & Rheumatol, Niigata, Japan
[3] Scantibodies Lab Inc, Santee, CA USA
关键词
estimation; intact parathyroid hormone assay; maxacalcitol; 1-84 parathyroid hormone; secondary hyperparathyroidism;
D O I
10.1093/ndt/gfh038
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. Although the so-called intact parathyroid hormone (iPTH) assay detects not only true 1-84 PTH (1-84PTH) but also large C-terminal PTH fragments, it remains inconclusive whether the 1-84PTH assay is more useful in clinical practice. Previous studies have shown that;the results of these two PTH assays in dialysis patients are closely correlated. Methods. Chronic dialysis patients whose plasma iPTH levels were >400pg/ml were selected for inclusion in the present study. Following a 4 week wash-out time during which all vitamin D administration was halted, maxacalcitol was intravenously injected at the end of dialysis sessions three times per week for 24 weeks, at an initial dosage of 10 mug. Results. Ninety-seven patients with secondary hyperparathyroidism were included in our analysis. Their serum calcium levels were elevated from the start levels while phosphate levels remained unchanged. The plasma 1-84PTH levels constantly declined throughout the 24 weeks. Although the patients' plasma 1-84PTH and iPTH levels were closely correlated with each other both at the beginning of the study and after 24 weeks of maxacalcitol therapy, the ratio of 1-84PTH/iPTH consistently decreased throughout the study period (P < 0.01). The changes in the ratio were significantly correlated with changes in serum calcium levels. Conclusions. Twenty-four weeks of intravenous maxacalcitol injection therapy significantly reduced the 1-84PTH/iPTH ratio. Estimated 1-84PTH levels from iPTH levels using a conversion formula obtained before the treatment were 21.0 +/- 20.4% higher than measured 1-84PTH levels after the therapy. Thus, iPTH measurement has a potential risk to overestimate 1-84PTH levels when evaluating the efficacy of maxacalcitol therapy in dialysis patients with secondary hyperparathyroidism.
引用
收藏
页码:892 / 897
页数:6
相关论文
共 19 条
[11]   Improved assessment of bone turnover by the PTH-(1-84) large C-PTH fragments ratio in ESRD patients [J].
Monier-Faugere, MC ;
Geng, ZP ;
Mawad, H ;
Friedler, RM ;
Gao, P ;
Cantor, TL ;
Malluche, HH .
KIDNEY INTERNATIONAL, 2001, 60 (04) :1460-1468
[12]   Synthetic carboxyl-terminal fragments of parathyroid hormone (PTH) decrease ionized calcium concentration in rats by acting on a receptor different from the PTH/PTH-related peptide receptor [J].
Nguyen-Yamamoto, L ;
Rousseau, L ;
Brossard, JH ;
Lepage, R ;
D'Amour, P .
ENDOCRINOLOGY, 2001, 142 (04) :1386-1392
[13]   PREDICTIVE VALUE OF SERUM PARATHYROID-HORMONE LEVELS FOR BONE TURNOVER IN PATIENTS ON CHRONIC MAINTENANCE DIALYSIS [J].
QI, QL ;
MONIERFAUGERE, MC ;
GENG, ZP ;
MALLUCHE, HH .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1995, 26 (04) :622-631
[14]   Influence of PTH assay methodology on differential diagnosis of renal bone disease [J].
Reichel, H ;
Esser, A ;
Roth, HJ ;
Schmidt-Gayk, H .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2003, 18 (04) :759-768
[15]   Is there an optimal parathyroid hormone level in end-stage renal failure: the lower the better? [J].
Sakhaee, K .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2001, 10 (03) :421-427
[16]   Similar predictive value of bone turnover using first- and second-generation immunometric PTH assays in pediatric patients treated with peritoneal dialysis [J].
Salusky, IB ;
Goodman, WG ;
Kuizon, BD ;
Lavigne, JR ;
Zahranik, RJ ;
Gales, B ;
Wang, HJ ;
Elashoff, RM ;
Jüppner, H .
KIDNEY INTERNATIONAL, 2003, 63 (05) :1801-1808
[17]   New analogs of vitamin D3 [J].
Slatopolsky, E ;
Dusso, A ;
Brown, A .
KIDNEY INTERNATIONAL, 1999, 56 :S46-S51
[18]   A novel mechanism for skeletal resistance in uremia [J].
Slatopolsky, E ;
Finch, J ;
Clay, P ;
Martin, D ;
Sicard, G ;
Singer, G ;
Gao, P ;
Cantor, T ;
Dusso, A .
KIDNEY INTERNATIONAL, 2000, 58 (02) :753-761
[19]   Effect of 22-oxacalcitriol on bone histology of hemodialyzed patients with severe secondary hyperparathyroidism [J].
Tsukamoto, Y ;
Hanaoka, M ;
Matsuo, T ;
Saruta, T ;
Nomura, M ;
Takahashi, Y .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 35 (03) :458-464