The role of calcimimetics in the treatment of hyperparathyroidism

被引:47
作者
Wuethrich, R. P.
Martin, D.
Bilezikian, J. P.
机构
[1] Univ Zurich Hosp, Clin Nephrol, CH-8091 Zurich, Switzerland
[2] Amgen Inc, Thousand Oaks, CA 91320 USA
[3] Columbia Univ, Coll Phys & Surg, New York, NY USA
关键词
calcimimetics; cinacalcet; primary hyperparathyroidism; secondary hyperparathyroidism; tertiary hyperparathyroidism; SENSING RECEPTOR EXPRESSION; PARATHYROID-HORMONE LEVELS; RENAL-TRANSPLANT PATIENTS; NORMALIZES SERUM-CALCIUM; SECONDARY HYPERPARATHYROIDISM; CINACALCET HCL; NPS R-568; HEMODIALYSIS-PATIENTS; MORTALITY RISK; DOUBLE-BLIND;
D O I
10.1111/j.1365-2362.2007.01874.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Calcimimetics reduce serum levels of parathyroid hormone (PTH) and calcium, with a leftward shift in the set-point for calcium-regulated PTH secretion. The aim of this publication is to review the data available for calcimimetics in primary, secondary and tertiary hyperparathyroidism (HPT). Parathyroidectomy (PTX) is currently the only curative treatment for primary HPT, and recommended for patients with moderate-to-severe disease, as defined by a 2002 National Institute's of Health summary statement. In general, patients with primary HPT not meeting these surgical criteria, as well as those with contraindication or refusal for surgery, are monitored for signs and symptoms of primary HPT. There are currently no non-surgical therapies approved for use in primary HPT, although bisphosphonates are used in some patients, in an effort to control serum calcium levels. Calcimimetics decrease PTH and calcium levels and are a potential alternative for patients contraindicated for PTX, or who have failed previous PTX and have recurrent primary HPT. Secondary HPT develops early in chronic kidney disease and is present virtually in all patients with end-stage renal disease (ESRD). Secondary HPT is a progressive disease and is associated with several systemic complications, including renal osteodystrophy, soft tissue and vascular calcifications, and adverse cardiovascular outcomes. In ESRD patients, calcimimetics were shown to simultaneously reduce PTH, calcium, phosphate and calcium x phosphate product. In addition, observational analyses of use of calcimimetics in the ESRD population have shown a reduction of important clinical outcomes. In renal allograft recipients with tertiary HPT and hypercalcaemia, calcimimetics are a promising treatment option to control the parameters of calcium phosphate metabolism and may be a valid alternative to PTX. Based on its unique mechanism of action, the calcimimetic cinacalcet may play a role in the medical treatment of primary and tertiary forms of HPT, in addition to the registered indication for the treatment of secondary HPT.
引用
收藏
页码:915 / 922
页数:8
相关论文
共 64 条
[1]  
BILEZIKIAN J P, 1991, Journal of Bone and Mineral Research, V6, pS85
[2]   Summary statement from a workshop on asymptomatic primary hyperparathyroidism: A perspective for the 21st century [J].
Bilezikian, JP ;
Potts, JT ;
El-Hajj Fuleihan, G ;
Kleerekoper, M ;
Neer, R ;
Peacock, M ;
Rastad, J ;
Silverberg, SJ ;
Udelsman, R ;
Wells, SA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (12) :5353-5361
[3]   Clinical practice - Asymptomatic primary hyperparathyroidism [J].
Bilezikian, JP ;
Silverberg, SJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (17) :1746-1751
[4]   Cinacalcet for secondary hyperparathyroidism in patients receiving hemodialysis [J].
Block, GA ;
Martin, KJ ;
de Francisco, ALM ;
Turner, SA ;
Avram, MM ;
Suranyi, MG ;
Hercz, G ;
Cunningham, J ;
Abu-Alfa, AK ;
Messa, P ;
Coyne, DW ;
Locatelli, F ;
Cohen, RM ;
Evenepoel, P ;
Moe, SM ;
Fournier, A ;
Braun, J ;
McCary, LC ;
Zani, VJ ;
Olson, KA ;
Drüeke, TB ;
Goodman, WG .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (15) :1516-1525
[5]   Mineral metabolism, mortality, and morbidity in maintenance hemodialysis [J].
Block, GA ;
Klassen, PS ;
Lazarus, JM ;
Ofsthun, N ;
Lowrie, EG ;
Chertow, GM .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2004, 15 (08) :2208-2218
[6]   Association of serum phosphorus and calcium x phosphate product with mortality risk in chronic hemodialysis patients: A national study [J].
Block, GA ;
Hulbert-Shearon, TE ;
Levin, NW ;
Port, FK .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 31 (04) :607-617
[7]   ESTROGEN REPLACEMENT DECREASES THE SET POINT OF PARATHYROID-HORMONE STIMULATION BY CALCIUM IN NORMAL POSTMENOPAUSAL WOMEN [J].
BOUCHER, A ;
DAMOUR, P ;
HAMEL, L ;
FUGERE, P ;
GASCONBARRE, M ;
LEPAGE, R ;
STEMARIE, LG .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 68 (04) :831-836
[8]   Decreased calcium-sensing receptor expression in hyperplastic parathyroid glands of uremic rats: Role of dietary phosphate [J].
Brown, AJ ;
Ritter, CS ;
Finch, JL ;
Slatopolsky, EA .
KIDNEY INTERNATIONAL, 1999, 55 (04) :1284-1292
[9]   Calcium Receptor and Regulation of Parathyroid Hormone Secretion [J].
Brown E.M. .
Reviews in Endocrine and Metabolic Disorders, 2000, 1 (4) :307-315
[10]  
Canaud Bernard, 2006, Hemodial Int, V10 Suppl 1, pS5, DOI 10.1111/j.1542-4758.2006.01183.x