Effect of low-density lipoprotein cholesterol on angiotensin II sensitivity - A Randomized trial with fluvastatin

被引:24
作者
van der Linde, Nicole A. J. [1 ]
Sijbrands, Eric J. G. [1 ]
Boomsma, Frans [1 ]
van den Meiracker, Anton H. [1 ]
机构
[1] Erasmus MC, Dept Internal Med & Vasc Med, NL-3000 CA Rotterdam, Netherlands
关键词
angiotensin; blood pressure; cholesterol; hypercholesterolemia; lipoproteins; statins;
D O I
10.1161/01.HYP.0000221223.23028.f1
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Increased angiotensin II (Ang II) sensitivity predisposes to hypertension and plaque instability. Raised low-density lipoprotein cholesterol (LDL-c) may increase Ang II sensitivity, but evidence in humans for this effect of LDL-c is limited. In 28, healthy, nonsmoking subjects, aged 30 +/- 8 years, with familial hypercholesterolemia, we determined the difference in infusion rate of Ang II and norepinephrine required to increase systolic blood pressure by 20 mm Hg (Pd-20) after 4 weeks of placebo and fluvastatin 80 mg daily in a randomized, double-blind, placebocontrolled, crossover study. Before infusions were started, fasting blood samples were taken to measure lipids. After 4 weeks of placebo, the mean LDL-c concentration was 6.3 +/- 1.4 mmol/L. The average decrease of LDL-c was 1.7 +/- 0.7 mmol/L after 4 weeks of fluvastatin (P < 0.001). The mean Pd-20 for Ang II increased by 1.28 ng/kg per minute (95% CI, 2.05 to 0.50; P=0.002) on fluvastatin, corresponding with a 26% decrease in Ang II sensitivity. Ang II sensitivity, however, remained increased compared with normocholesterolemic controls. The Pd-20 values for norepinephrine were unaffected by fluvastatin. The present study in healthy, young subjects with isolated hypercholesterolemia shows an increased sensitivity to Ang II that partly can be restored by LDL-c-lowering therapy. These findings indicate that LDL-c levels directly influence Ang II sensitivity.
引用
收藏
页码:1125 / 1130
页数:6
相关论文
共 34 条
[21]   Soluble intercellular adhesion molecule-1 and interleukin-6 levels reflect endothelial dysfunction in patients with primary hypercholesterolaemia treated with atorvastatin [J].
Nawawi, H ;
Osman, NS ;
Annuar, R ;
Khalid, BAK ;
Yusoff, K .
ATHEROSCLEROSIS, 2003, 169 (02) :283-291
[22]  
Nickenig G, 1997, CIRCULATION, V95, P473
[23]   Should angiotensin II receptor blockers and statins be combined? [J].
Nickenig, G .
CIRCULATION, 2004, 110 (08) :1013-1020
[24]   Hypercholesterolemia is associated with enhanced angiotensin AT(1)-receptor expression [J].
Nickenig, G ;
Jung, O ;
Strehlow, K ;
Zolk, O ;
Linz, W ;
Scholkens, BA ;
Bohm, M .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 272 (06) :H2701-H2707
[25]   Statin-sensitive dysregulated AT1 receptor function and density in hypercholesterolemic men [J].
Nickenig, G ;
Bäumer, AT ;
Temur, Y ;
Kebben, D ;
Jockenhövel, F ;
Böhm, M .
CIRCULATION, 1999, 100 (21) :2131-2134
[26]   SPECTRAL AND SEQUENCE-ANALYSIS OF FINGER BLOOD-PRESSURE VARIABILITY - COMPARISON WITH ANALYSIS OF INTRAARTERIAL RECORDINGS [J].
OMBONI, S ;
PARATI, G ;
FRATTOLA, A ;
MUTTI, E ;
DIRIENZO, M ;
CASTIGLIONI, P ;
MANCIA, G .
HYPERTENSION, 1993, 22 (01) :26-33
[27]   INTERACTIONS BETWEEN ANG-II, SYMPATHETIC NERVOUS-SYSTEM, AND BARORECEPTOR REFLEXES IN REGULATION OF BLOOD-PRESSURE [J].
REID, IA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (06) :E763-E778
[28]   Evidence for a causal role of the renin-angiotensin system in vascular dysfunction associated with insulin resistance [J].
Shinozaki, K ;
Ayajiki, K ;
Nishio, Y ;
Sugaya, T ;
Kashiwagi, A ;
Okamura, T .
HYPERTENSION, 2004, 43 (02) :255-262
[29]   Inhibition of early atherogenesis by losartan in monkeys with diet-induced hypercholesterolemia [J].
Strawn, WB ;
Chappell, MC ;
Dean, RH ;
Kivlighn, S ;
Ferrario, CM .
CIRCULATION, 2000, 101 (13) :1586-1593
[30]   EFFECTS OF PRAVASTATIN ON CARDIOVASCULAR REACTIVITY TO NOREPINEPHRINE AND ANGIOTENSIN-II PATIENTS WITH HYPERCHOLESTEROLEMIA AND SYSTEMIC HYPERTENSION [J].
STRAZNICKY, NE ;
HOWES, LG ;
LAM, W ;
LOIS, WJ .
AMERICAN JOURNAL OF CARDIOLOGY, 1995, 75 (08) :582-586