Structural and functional changes in peripheral vasculature of Fabry patients

被引:57
作者
Kalliokoski, Riikka J. [1 ]
Kalliokoski, Kari K.
Penttinen, Maila
Kantola, Ilkka
Leino, Aila
Viikari, Jorma S.
Simell, Olli
Nuutila, Pirjo
Raitakari, Olli T.
机构
[1] Univ Turku, Turku PET Ctr, FIN-20520 Turku, Finland
[2] Univ Turku, Dept Med, FIN-20520 Turku, Finland
[3] Univ Turku, Dept Pediat, FIN-20520 Turku, Finland
[4] Univ Turku, Dept Clin Physiol, FIN-20520 Turku, Finland
[5] Univ Turku, Dept Pediat, Clin Genet Unit, FIN-20520 Turku, Finland
[6] Univ Turku, Cent Hosp, Dept Clin Chem, FIN-20520 Turku, Finland
[7] Natl Publ Hlth Inst, Dept Hlth & Funct Capac, Populat Res Lab, Turku, Finland
基金
芬兰科学院;
关键词
D O I
10.1007/s10545-006-0340-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Fabry disease is a lysosomal storage disorder due to deficient alpha-galactosidase A activity, which leads to glycosphingolipid accumulation especially in vascular smooth-muscle and endothelial cells. Little is known about the effects of Fabry disease on peripheral artery function and structure. Therefore, we aimed to further characterize the peripheral vascular structural and functional changes in Fabry disease. Methods and results: We measured structural and functional vascular parameters, including intima-media thickness (IMT) of brachial and carotid arteries and abdominal aorta, carotid and aortic compliance, and brachial artery flow-mediated dilatation (FMD) in 17 Fabry patients and 34 healthy controls matched for age, sex and smoking. Carotid IMT (0.64 +/- 0.15 vs 0.57 +/- 0.12 mm), brachial IMT (1.02 +/- 0.25 vs 0.74 +/- 0.18 mm), and aortic IMT (0.31 +/- 0.09 vs 0.26 +/- 0.04 mm) were significantly increased, and brachial FMD was significantly impaired (6.3 +/- 5.0 vs 9.7 +/- 3.9%) in Fabry patients compared to healthy controls (p < 0.05 in all comparisons after adjustments for age, LDL-cholesterol, and systolic blood pressure). No differences were observed in arterial compliance between the groups. Conclusions: These data suggest that Fabry disease affects arterial function and structure by disturbing peripheral endothelial function and promoting intima-media thickening.
引用
收藏
页码:660 / 666
页数:7
相关论文
共 48 条
[41]  
Pfeilschifter J, 2000, NEWS PHYSIOL SCI, V15, P11
[42]   NON-INSULIN-DEPENDENT DIABETES-MELLITUS AND FASTING GLUCOSE AND INSULIN CONCENTRATIONS ARE ASSOCIATED WITH ARTERIAL STIFFNESS INDEXES - THE ARIC STUDY [J].
SALOMAA, V ;
RILEY, W ;
KARK, JD ;
NARDO, C ;
FOLSOM, AR .
CIRCULATION, 1995, 91 (05) :1432-1443
[43]  
SCHIFFMANN R, 2005, VIRCHOWS ARCH, V29, P1
[44]   PERIPHERAL HEMODYNAMICS IN PATIENTS WITH FABRYS-DISEASE [J].
SEINO, Y ;
VYDEN, JK ;
PHILIPPART, M .
AMERICAN HEART JOURNAL, 1983, 105 (05) :783-787
[45]   Postischemic cutaneous hyperperfusion in the presence of forearm hypoperfusion suggests sympathetic vasomotor dysfunction in Fabry disease [J].
Stemper, B ;
Hilz, MJ .
JOURNAL OF NEUROLOGY, 2003, 250 (08) :970-976
[46]   Large-artery elastic properties in young men -: Relationships to serum lipoproteins and oxidized low-density lipoproteins [J].
Toikka, JO ;
Niemi, P ;
Ahotupa, M ;
Niinikoski, H ;
Viikari, JSA ;
Rönnemaa, T ;
Hartiala, JJ ;
Raitakari, OT .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (02) :436-441
[47]   Presence of increased stiffness of the common carotid artery and endothelial dysfunction in severely obese children: a prospective study [J].
Tounian, P ;
Aggoun, Y ;
Dubern, B ;
Varille, V ;
Guy-Grand, B ;
Sidi, D ;
Girardet, JP ;
Bonnet, D .
LANCET, 2001, 358 (9291) :1400-1404
[48]  
VANCE DE, 1975, J BIOL CHEM, V250, P8119