Relation between plasma fibroblast growth factor-23, serum fetuin-A levels and coronary artery calcification evaluated by multislice computed tomography in patients with normal kidney function

被引:73
作者
Roos, Marcel [1 ]
Lutz, Jens [1 ]
Salmhofer, Hermann [1 ,2 ]
Luppa, Peter [3 ]
Knauss, Amelie [3 ]
Braun, Siegmund [4 ]
Martinof, Stefan [5 ]
Schoemig, Albert [6 ]
Heemann, Uwe [1 ]
Kastrati, Adnan [6 ]
Hausleiter, Joerg [6 ]
机构
[1] Tech Univ Munich, Klinikum Rechts Isar, Dept Nephrol, Nephrol Abt, D-81675 Munich, Germany
[2] Paracelsus Med Univ, Univ Klin Innere Med 1, Salzburg, Austria
[3] Tech Univ Munich, Klinikum Rechts Isar, Inst Klin Chem & Pathobiochem, D-8000 Munich, Germany
[4] Deutsch Herzzentrum Munich, Inst Lab Med, Munich, Germany
[5] Deutsch Herzzentrum Munich, Klin Radiol & Nukl Med, Munich, Germany
[6] Deutsch Herzzentrum Munich, Klin Herz & Kreislauferkrankungen, Munich, Germany
关键词
D O I
10.1111/j.1365-2265.2007.03074.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To examine the correlation of plasma fibroblast growth factor (FGF)-23 and serum fetuin A levels with the coronary artery calcification score (CACS) in patients with normal kidney function. Background Vascular calcification is an active process that may be aggravated by hyperphosphataemia and hypercalcaemia. FGF-23 and human fetuin-A have been associated with calcifying arteriosclerosis in renal failure. Plasma FGF-23 was identified as an independent factor negatively associated with peripheral vascular calcification. Fetuin-A acts as a systemic inhibitor of ectopic calcification in dialysis patients and can be correlated to the survival of these patients. Very few data exists on the role of FGF-23 and fetuin-A in coronary calcification of patients without impaired kidney function. Materials and methods Sixty-four patients, 21 females and 43 males, were subjected to 64-slice coronary computed tomography (CT) to evaluate coronary artery calcification (CAC). Plasma intact FGF-23 was determined by ELISA. Serum fetuin-A concentration were evaluated nephelometrically. Results Mean plasma FGF-23 level was 20.4 +/- 9.1 pg/ml and serum fetuin-A was 0.46 +/- 0.09 g/l. There was no correlation between FGF-23 (P = 0.777) and fetuin-A (P = 0.767) levels and the CACS. No correlation was found between the presence of noncalcified plaques and coronary artery stenosis (CAS) >= 50%, and FGF-23 (P = 0.313 and P = 0.775) and fetuin-A levels (P = 0.601 and P = 0.659). Conclusion Plasma intact FGF-23 and serum fetuin-A concentration do not correlate with the CACS, the grade of stenosis or presence of noncalcified plaques of the coronary arteries in patients with normal kidney function.
引用
收藏
页码:660 / 665
页数:6
相关论文
共 33 条
[1]  
BENET P, 2005, HUMAN MOL GENE, V14, P385, DOI DOI 10.1093/HMG/DDI034
[2]  
Boström K, 2000, CRIT REV EUKAR GENE, V10, P151
[3]   Serum fetuin-A levels link inflammation and cardiovascular calcification in hemodialysis patients [J].
Cozzolino, Mario ;
Galassi, Andrea ;
Biondi, Maria Luisa ;
Turri, Olivia ;
Papagni, Sergio ;
Mongelli, Nicola ;
Civita, Luigi ;
Gallieni, Maurizio ;
Brancaccio, Diego .
AMERICAN JOURNAL OF NEPHROLOGY, 2006, 26 (05) :423-429
[4]   Pathophysiological mechanisms of vascular calcification in end-stage renal disease [J].
Davies, MR ;
Hruska, KA .
KIDNEY INTERNATIONAL, 2001, 60 (02) :472-479
[5]  
FIORE CE, 2006, ATHEROSCLEROSIS, DOI DOI 10.1016/J.ATHER0SCLER0SIS.2006.08.052)
[6]   Role of fibroblast growth factor 23 in health and in chronic kidney disease [J].
Fukagawa, M ;
Nii-Kono, T ;
Kazama, JJ .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2005, 14 (04) :325-329
[7]   Vascular calcification mechanisms [J].
Giachelli, CM .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2004, 15 (12) :2959-2964
[8]  
GIACHELLI CM, 2001, VASCULAR S1, V1, pS34
[9]   Peripheral arterial disease: Morbidity and mortality implications [J].
Golomb, Beatrice A. ;
Dang, Tram T. ;
Criqui, Michael H. .
CIRCULATION, 2006, 114 (07) :688-699
[10]   Vascular calcification in chronic kidney disease [J].
Goodman, WG ;
London, G ;
Amann, K ;
Block, GA ;
Giachelli, C ;
Hruska, KA ;
Ketteler, M ;
Levin, A ;
Massy, Z ;
McCarron, DA ;
Raggi, P ;
Shanahan, CM ;
Yorioka, N .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2004, 43 (03) :572-579