Augmentation of central arterial pressure in type 1 diabetes

被引:106
作者
Brooks, B
Molyneaux, L
Yue, DK
机构
[1] Royal Prince Alfred Hosp, Ctr Diabet, Camperdown, NSW 2050, Australia
[2] Univ Sydney, Dept Med, Sydney, NSW 2006, Australia
关键词
D O I
10.2337/diacare.22.10.1722
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - Atherosclerosis is more severe in individuals with diabetes. Whether diabetic subjects have accelerated arterial hardening (i.e., arteriosclerosis) is less clear. Arteriosclerosis increases pulse-wave velocity and can augment central arterial pressure due to early wave reflection. The aim of this study was to determine whether subjects with type 1 diabetes had evidence of increased arterial stiffness by using pulse-wave analysis. RESEARCH DESIGN AND METHODS- Radial artery pressure waveforms were obtained noninvasively by applanation tonometry (PWV Medical Blood Pressure Analysis System, Sydney). A central aortic waveform can be derived by using a transfer function used in previous studies during cardiac catheterization. A total of 89 subjects with type 1 diabetes (46 men and 43 women, aged 34.0 +/- 11.0 years, duration of diabetes 13.1 years [interquartile range 5.8-24.3], HbA(1c) 8.2 +/- 1.7%) and 95 control subjects (44 men and 51 women, aged 36.1 +/- 12.0 years) were studied. The central aortic waveform allowed the determination of 1) the aortic augmentation index (AAI), a parameter that reflects the degree to which central arterial pressure is augmented by wave reflection, and 2) the subendocardial viability ratio (SEVR), which is a measure of myocardial perfusion relative to cardiac workload. RESULTS- In multivariate analysis, diabetes was an important determinant of AAI (P = 0.001). The higher AAI was mainly evident in the men, for whom diabetes was a highly significant covariate (P = 0.006); this was not the case for diabetic women (P = 0.2). Nondiabetic men had a lower AAI than nondiabetic women (103.7 +/- 18.6 vs. 117.0 +/- 22.3%, respectively, P = 0.002), but this difference was abolished by diabetes (110.7 +/- 18.5 vs. 116.1 +/- 18.7%, respectively, P = 0.2). Subjects with type 1 diabetes had a significantly lower mean SEVR compared with control subjects (139.2 +/- 28.3 vs. 163.6 +/- 27.4%, respectively P < 0.0001). In multivariate analysis, diabetes was an important determinant of SEVR (P = 0.001). A significant interaction between diabetes and age was evident (P = 0.0001), which suggests that the effect of age is modified by diabetes. CONCLUSIONS - These findings suggest that central systolic blood pressure is increased in relatively young individuals with type 1 diabetes, although myocardial perfusion related to cardiac workload is decreased. These changes can be explained by more rapid pulse-wave velocity resulting from arterial stiffening.
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页码:1722 / 1727
页数:6
相关论文
共 19 条
[1]  
[Anonymous], 1991, JAMA, V265, P3255
[2]   EFFECTS OF AGING ON CHANGING ARTERIAL COMPLIANCE AND LEFT-VENTRICULAR LOAD IN A NORTHERN CHINESE URBAN-COMMUNITY [J].
AVOLIO, AP ;
CHEN, SG ;
WANG, RP ;
ZHANG, CL ;
LI, MF ;
OROURKE, MF .
CIRCULATION, 1983, 68 (01) :50-58
[3]  
BUCKBERG GD, 1972, J THORAC CARDIOV SUR, V64, P669
[4]   EXPERIMENTAL SUBENDOCARDIAL ISCHEMIA IN DOGS WITH NORMAL CORONARY-ARTERIES [J].
BUCKBERG, GD ;
ARCHIE, JP ;
FIXLER, DE ;
HOFFMAN, JIE .
CIRCULATION RESEARCH, 1972, 30 (01) :67-+
[5]  
Chen CH, 1997, CIRCULATION, V95, P1827
[6]   AN ANALYSIS OF THE RELATIONSHIP BETWEEN CENTRAL AORTIC AND PERIPHERAL UPPER LIMB PRESSURE WAVES IN MAN [J].
KARAMANOGLU, M ;
OROURKE, MF ;
AVOLIO, AP ;
KELLY, RP .
EUROPEAN HEART JOURNAL, 1993, 14 (02) :160-167
[7]   NONINVASIVE DETERMINATION OF AGE-RELATED-CHANGES IN THE HUMAN ARTERIAL PULSE [J].
KELLY, R ;
HAYWARD, C ;
AVOLIO, A ;
OROURKE, M .
CIRCULATION, 1989, 80 (06) :1652-1659
[8]   ARTERIAL DILATION AND REDUCED WAVE REFLECTION - BENEFIT OF DILEVALOL IN HYPERTENSION [J].
KELLY, R ;
DALEY, J ;
AVOLIO, A ;
OROURKE, M .
HYPERTENSION, 1989, 14 (01) :14-21
[9]  
Kelly R., 1989, J Vasc Med Biol, V1, P142
[10]   Arterial wall remodelling and stiffness in hypertension: Heterogeneous aspects [J].
London, GM ;
Safar, ME .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1996, 23 (08) :S1-S5