Determination of the elimination half-life of fibroblast growth factor-23

被引:126
作者
Khosravi, Azarmindokht
Cutler, Carolee M.
Kelly, Marilyn H.
Chang, Richard
Royal, Richard E.
Sherry, Richard M.
Wodajo, Felasfa M.
Fedarko, Neal S.
Collins, Michael T.
机构
[1] Natl Inst Dent & Craniofacial Res, Skeletal Clin Studies Unit, Craniofacial & Skeletal Dis Branch, NIH, Bethesda, MD 20892 USA
[2] NCI, Dept Radiol, Mark O Hatfield Clin Ctr, NIH,Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[3] NCI, Surg Branch, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[4] Georgetown Univ, Dept Orthoped & Pediat, Washington, DC USA
[5] Johns Hopkins Univ, Dept Med, Div Geriatr Med & Gerontol, Baltimore, MD 21224 USA
关键词
D O I
10.1210/jc.2006-2865
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Tumor-induced osteomalacia (TIO) is a rare paraneoplastic disease caused by mesenchymal tumors that secrete fibroblast growth factor-23 (FGF-23), a newly-described vitamin D and phosphate-regulating hormone. Surgical removal of the tumor, the ectopic source of circulating FGF-23, offers the opportunity to determine the elimination half-life of FGF-23. Objective: The aim of the study was to determine the elimination half-life of FGF-23. Patients/Methods: The tumors were removed from three patients with TIO, and serum samples were taken every 30 min for up to 72 h after the operation. FGF-23 was measured by both a C-terminal/intact assay and an intact assay, and the elimination half-life was determined by one phase exponential decay methodology. Setting: The Mark O. Hatfield Clinical Research Center of the National Institutes of Health, a tertiary referral clinical research center, was the setting for the study. Results: The elimination life of FGF-23 as determined by C-terminal/intact and intact assays was 46 +/- 12 and 58 +/- 34 min, respectively. Conclusions: The plasma half-life of serum FGF-23 is in the range of 46-58 min.
引用
收藏
页码:2374 / 2377
页数:4
相关论文
共 29 条
[1]   Transgenic mice overexpressing human fibroblast growth factor 23 (R176Q) delineate a putative role for parathyroid hormone in renal phosphate wasting disorders [J].
Bai, XY ;
Miao, DS ;
Li, JR ;
Goltzman, D ;
Karaplis, AC .
ENDOCRINOLOGY, 2004, 145 (11) :5269-5279
[2]   Post-transplant hypophosphatemia:: Tertiary 'hyper-phosphatoninism'? [J].
Bhan, I. ;
Shah, A. ;
Holmes, J. ;
Isakova, T. ;
Gutierrez, O. ;
Burnett, S-A ;
Jueppner, H. ;
Wolf, M. .
KIDNEY INTERNATIONAL, 2006, 70 (08) :1486-1494
[3]   ASSESSMENT OF PHOSPHATE REABSORPTION [J].
BIJVOET, OLM ;
MORGAN, DB ;
FOURMAN, P .
CLINICA CHIMICA ACTA, 1969, 26 (01) :15-+
[4]   INHIBITION OF RENAL PHOSPHATE-TRANSPORT BY A TUMOR PRODUCT IN A PATIENT WITH ONCOGENIC OSTEOMALACIA [J].
CAI, Q ;
HODGSON, SF ;
KAO, PC ;
LENNON, VA ;
KLEE, GG ;
ZINSMIESTER, AR ;
KUMAR, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (23) :1645-1649
[5]   Fibroblast growth factor-23 is regulated by lα,25-dihydroxyvitamin D [J].
Collins, MT ;
Lindsay, JR ;
Jain, A ;
Kelly, MH ;
Cutler, CM ;
Weinstein, LS ;
Liu, J ;
Fedarko, NS ;
Winer, KK .
JOURNAL OF BONE AND MINERAL RESEARCH, 2005, 20 (11) :1944-1950
[6]   Tumors associated with oncogenic osteomalacia express genes important in bone and mineral metabolism [J].
De Beur, SMJ ;
Finnegan, RB ;
Vassiliadis, J ;
Cook, B ;
Barberio, D ;
Estes, S ;
Manavalan, P ;
Petroziello, J ;
Madden, SL ;
Cho, JY ;
Kumar, R ;
Levine, MA ;
Schiavi, SC .
JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 (06) :1102-1110
[7]  
Dennis JW, 1999, BIOESSAYS, V21, P412, DOI 10.1002/(SICI)1521-1878(199905)21:5<412::AID-BIES8>3.0.CO
[8]  
2-5
[9]   Tumor-Induced Osteomalacia [J].
Drezner M.K. .
Reviews in Endocrine and Metabolic Disorders, 2001, 2 (2) :175-186
[10]   Most osteomalacia-associated mesenchymal tumors are a single histopathologic entity - An analysis of 32 cases and a comprehensive review of the literature [J].
Folpe, AL ;
Fanburg-Smith, JC ;
Billings, SD ;
Bisceglia, M ;
Bertoni, F ;
Cho, JY ;
Econs, MJ ;
Inwards, CY ;
de Beur, SMJ ;
Mentzel, T ;
Montgomery, E ;
Michal, M ;
Miettinen, M ;
Mills, SE ;
Reith, JD ;
O'Connell, JX ;
Rosenberg, AE ;
Rubin, BP ;
Sweet, DE ;
Vinh, TN ;
Wold, LE ;
Wehrli, BM ;
White, FKE ;
Zaino, RJ ;
Weiss, SW .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2004, 28 (01) :1-30