Vitamin K-dependent proteins, warfarin, and vascular calcification

被引:197
作者
Danziger, John [1 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Div Renal, Boston, MA USA
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2008年 / 3卷 / 05期
关键词
D O I
10.2215/CJN.00770208
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Vitamin K-dependent proteins (VKDPs) require carboxylation to become biologically active. Although the coagulant factors are the most well-known VKDPs, there are many others with important physiologic roles. Matrix Gla Protein (MGP) and Growth Arrest Specific Gene 6 (Gas-6) are two particularly important VKDPs, and their roles in vascular biology are just beginning to be understood. Both function to protect the vasculature; MGP prevents vascular calcification and Gas-6 affects vascular smooth muscle cell apoptosis and movement. Unlike the coagulant factors, which undergo hepatic carboxylation, MGP and Gas-6 are carboxylated within the vasculature. This peripheral carboxylation process is distinct from hepatic carboxylation, yet both are inhibited by warfarin administration. Warfarin prevents the activation of MGP and Gas-6, and in animals, induces vascular calcification. The relationship of warfarin to vascular calcification in humans is not fully known, yet observational data suggest an association. Given the high risk of vascular calcification in those patients with chronic kidney disease, the importance of understanding warfarin's effect on VKDPs is paramount. Furthermore, recognizing the importance of VKDPs in vascular biology will stimulate new areas of research and offer potential therapeutic interventions.
引用
收藏
页码:1504 / 1510
页数:7
相关论文
共 56 条
[1]  
Anand S, 2007, NEW ENGL J MED, V357, P217
[2]   The physiology of vitamin K nutriture and vitamin K-dependent protein function in atherosclerosis [J].
Berkner, KL ;
Runge, KW .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (12) :2118-2132
[3]   Control of serum phosphorus: implications for coronary artery calcification and calcific uremic arteriolopathy (calciphylaxis) [J].
Block, GA .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2001, 10 (06) :741-747
[4]   Cytochrome P4502C9 (CYP2C9) and vitamin K epoxide reductase (VKORC1) genotypes as determinants of acenocoumarol sensitivity [J].
Bodin, L ;
Verstuyft, C ;
Tregouet, DA ;
Robert, A ;
Dubert, L ;
Funck-Brentano, C ;
Jaillon, P ;
Beaune, P ;
Laurent-Puig, P ;
Becquemont, L ;
Loriot, MA .
BLOOD, 2005, 106 (01) :135-140
[5]   Matrix GLA protein gene polymorphisms: Clinical correlates and cardiovascular mortality in chronic kidney disease patients [J].
Brancaccio, D ;
Biondi, ML ;
Gallieni, M ;
Turri, O ;
Galassi, A ;
Cecchini, F ;
Russo, D ;
Andreucci, V ;
Cozzolino, M .
AMERICAN JOURNAL OF NEPHROLOGY, 2005, 25 (06) :548-552
[6]   Physiological plasma Gas6 levels do not influence platelet aggregation [J].
Clauser, S ;
Bachelot-Iozat, C ;
Fontana, P ;
Gaussem, P ;
Remones, V ;
Aiach, M ;
Borgel, D .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (03) :E22-E22
[7]  
CONLY J, 1994, CLIN INVEST MED, V17, P531
[8]   Mechanisms of vascular calcification [J].
El-Abbadi, Mohga ;
Giachelli, Cecilia M. .
ADVANCES IN CHRONIC KIDNEY DISEASE, 2007, 14 (01) :54-66
[9]   A polymorphism of the human matrix γ-carboxyglutamic acid protein promoter alters binding of an activating protein-1 complex and is associated with altered transcription and serum levels [J].
Farzaneh-Far, A ;
Davies, JD ;
Braam, LA ;
Spronk, HM ;
Proudfoot, D ;
Chan, SW ;
O'Shaughnessy, KM ;
Weissberg, PL ;
Vermeer, C ;
Shanahan, CM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (35) :32466-32473
[10]   Calciphylaxis associated with alcoholic cirrhosis [J].
Ferreres, JR ;
Marcoval, J ;
Bordas, X ;
Moreno, A ;
Muniesa, C ;
Prat, C ;
Peyrí, J .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2006, 20 (05) :599-601