Statin therapy improves brachial artery endothelial function in nephrotic syndrome

被引:47
作者
Dogra, GK
Watts, GF
Herrmann, S
Thomas, MAB
Irish, AB
机构
[1] Royal Perth Hosp, Univ Dept Med, Dept Nephrol, Perth, WA 6847, Australia
[2] Univ Western Australia, Dept Med, Perth, WA 6009, Australia
[3] Univ Western Australia, Western Australian Heart Res Inst, Perth, WA 6009, Australia
基金
英国医学研究理事会;
关键词
nephrosis; HMGCoA reductase inhibitors; dyslipidemia; cardiovascular disease; proteinuria; end-stage renal disease;
D O I
10.1046/j.1523-1755.2002.00483.x
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
Background. Patients with nephrotic syndrome have impaired endothelial function probably related to dyslipidemia. This study evaluated the effects of statin therapy on dyslipidemia and endothelial function in patients with nephrotic syndrome. Methods. A sequential, open-label study of the effects of statins on endothelial dysfunction in 10 nephrotic patients treated with an angiotensin-converting enzyme (ACE) inhibitor or angiotensin II (Ang II) receptor antagonist. Endothelial function was assessed at baseline, after 12 weeks of treatment with statins, and after an 8-week washout. Brachial artery endothelial function was measured as post-ischemic flow-mediated dilation (FMD) using ultrasonography. Endothelium-independent, glyceryl trinitrate-mediated vasodilation (GTNMD) also was measured. Results. Serum lipids were significantly lower following statin: total cholesterol mean 8.2 +/- 0.4 (standard error) mmol/L versus 5.2 +/- 0.3 mmol/L, triglycerides 2.6 +/- 0.4 mmol/L versus 1.6 +/- 0.2 mmol/L, non-HDL-cholesterol 6.7 +/- 0.4 mmol/L versus 3.7 +/- 0.2 mmol/L (all P < 0.001). There was a trend to an increase in serum albumin (31.0 +/- 1.3 g/L vs. 33.8 +/- 1.5 g/L; P = 0.078) and FMD improved significantly following treatment (3.7 +/- 1.1% vs. 7.0 +/- 0.8%, P < 0.01). After washout, FMD deteriorated significantly to 3.5 +/- 1.4% (P < 0.05) versus week 12 FMD. GTNMD was unchanged. In multivariate regression, reduction in non-high-density lipoprotein (HDL)-cholesterol (beta - 0.736, P = 0.027) and increase in serum albumin (beta 0.723, P = 0.028), but not the on-treatment level of non-HDL-cholesterol, were significant independent predictors of improvement in FMD after adjusting for change in resting brachial artery diameter. Changes in serum lipoprotein and albumin concentrations off treatment were not associated with deterioration in FMD. Conclusion. Statin therapy significantly improves dyslipidemia and brachial artery endothelial function in patients with nephrotic syndrome. Improvement in brachial artery endothelial function may be in part related to a non-lipid effect of statins. The findings also suggest a role for dyslipidemia in endothelial dysfunction and the risk for cardiovascular disease in nephrotic syndrome.
引用
收藏
页码:550 / 557
页数:8
相关论文
共 43 条
[1]   Long-term follow-up of patients with mild coronary artery disease and endothelial dysfunction [J].
Al Suwaidi, J ;
Hamasaki, S ;
Higano, ST ;
Nishimura, RA ;
Holmes, DR ;
Lerman, A .
CIRCULATION, 2000, 101 (09) :948-954
[2]   Effect of statin therapy on C-reactive protein levels - The Pravastatin Inflammation/CRP Evaluation (PRINCE): A randomized trial and cohort study [J].
Albert, MA ;
Danielson, E ;
Rifai, N ;
Ridker, PM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (01) :64-70
[3]   Sustained long-term improvement of arterial endothelial function in heterozygous familial hypercholesterolemia patients treated with simvastatin [J].
Alonso, R ;
Mata, P ;
De Andres, R ;
Villacastin, BP ;
Martínez-González, J ;
Badimon, L .
ATHEROSCLEROSIS, 2001, 157 (02) :423-429
[4]   CLOSE RELATION OF ENDOTHELIAL FUNCTION IN THE HUMAN CORONARY AND PERIPHERAL CIRCULATIONS [J].
ANDERSON, TJ ;
UEHATA, A ;
GERHARD, MD ;
MEREDITH, IT ;
KNAB, S ;
DELAGRANGE, D ;
LIEBERMAN, EH ;
GANZ, P ;
CREAGER, MA ;
YEUNG, AC ;
SELWYN, AP .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1995, 26 (05) :1235-1241
[5]  
Cameron J., 1998, OXFORD TXB CLIN NEPH, P461
[6]   NONINVASIVE DETECTION OF ENDOTHELIAL DYSFUNCTION IN CHILDREN AND ADULTS AT RISK OF ATHEROSCLEROSIS [J].
CELERMAJER, DS ;
SORENSEN, KE ;
GOOCH, VM ;
SPIEGELHALTER, DJ ;
MILLER, OI ;
SULLIVAN, ID ;
LLOYD, JK ;
DEANFIELD, JE .
LANCET, 1992, 340 (8828) :1111-1115
[7]  
Daniel V, 1997, CLIN NEPHROL, V47, P289
[8]   Methods and endpoint issues in clinical development of lipid-acting agents with pleiotropic effects [J].
Davignon, J .
AMERICAN JOURNAL OF CARDIOLOGY, 1998, 81 (8A) :17F-23F
[9]   Increased VLDL in nephrotic patients results from a decreased catabolism while increased LDL results from increased synthesis [J].
de Sain-van der Velden, M ;
Kaysen, GA ;
Barrett, HA ;
Stellaard, F ;
Gadellaa, MM ;
Voorbij, HA ;
Reijngoud, DJ ;
Rabelink, TJ .
KIDNEY INTERNATIONAL, 1998, 53 (04) :994-1001
[10]   The atherogenic lipoprotein phenotype: small dense LDL and lipoprotein remnants in nephrotic range proteinuria [J].
Deighan, CJ ;
Caslake, MJ ;
McConnell, M ;
Boulton-Jones, JM ;
Packard, CJ .
ATHEROSCLEROSIS, 2001, 157 (01) :211-220