Vasculoprotective Effects of Dietary Cocoa Flavanols in Patients on Hemodialysis: A Double-Blind, Randomized, Placebo-Controlled Trial

被引:44
|
作者
Rassaf, Tienush [1 ]
Rammos, Christos [1 ]
Hendgen-Cotta, Ulrike B. [1 ]
Heiss, Christian [1 ]
Kleophas, Werner [2 ]
De Hanna, Frank [2 ]
Floege, Juergen [3 ]
Hetzel, Gerd R. [2 ]
Kelm, Malte [1 ,4 ]
机构
[1] Univ Hosp Dusseldorf, Dept Med, Div Cardiol Pulmonol & Vasc Med, Fac Med, Dusseldorf, Germany
[2] DaVita Renal Ctr Dusseldorf, Dusseldorf, Germany
[3] Univ Aachen, Dept Nephrol, Rheinish Westphalian Tech High Sch, Aachen, Germany
[4] Univ Hosp Dusseldorf, Fac Med, Cardiovasc Res Inst Dusseldorf CARID, Dusseldorf, Germany
关键词
STAGE RENAL-DISEASE; CORONARY-ARTERY-DISEASE; CHRONIC KIDNEY-DISEASE; ENDOTHELIAL FUNCTION; CARDIOVASCULAR EVENTS; VASCULAR FUNCTION; OXIDATIVE STRESS; NITRIC-OXIDE; RICH COCOA; DIALYSIS PATIENTS;
D O I
10.2215/CJN.05560515
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 and objectives Hemodialysis (HD) per se entails vascular dysfunction in patients with ESRD. Endothelial dysfunction is a key step in atherosclerosis and is characterized by impaired flow-mediated dilation (FMD). Interventional studies have shown that cocoa flavanol (CF)-rich supplements improve vascular function. Aim of this study was to investigate the effect of flavanol-rich bioactive food ingredients on acute and chronic HD-induced vascular dysfunction in ESRD. Design, setting, participants, & measurements We conducted a randomized, double-blind, placebo-controlled trial from 2012 to 2013. Fifty-seven participants were enrolled, ingested CF-rich beverages (900 mg CF per study day), and were compared with those ingesting CF-free placebo. This included (1) a baseline cross over acute study to determine safety and efficacy of CF and (2) a subsequent chronic parallel group study with a 30-day follow-up period to study effects of CF on HD-mediated vascular dysfunction entailing (3) an acute substudy during HD in flavanol-naive patients and (4) an acute on chronic study during HD. Primary and secondary outcome measures included changes in FMD and hemodynamics. Results CF ingestion was well tolerated. Acute ingestion improved FMD by 53% (3.2 +/- 0.6% to 4.8 +/- 0.9% versus placebo, 3.2 +/- 0.7% to 3.3 +/- 0.8%; P<0.001), with no effects on BP or heart rate. A 30-day ingestion of CF led to an increase in baseline FMD by 18% (3.4 +/- 0.9% to 3.9 +/- 0.8% versus placebo, 3.5 +/- 0.7% to 3.5 +/- 0.7%; P<0.001), with reduced diastolic BP (73 +/- 12 to 69 +/- 11 mmHg versus placebo, 70 +/- 11. to 73 +/- 13 mmHg; P=0.03) and increased heart rate (70 +/- 12 to 74 +/- 13 bpm versus placebo, 75 +/- 15 to 74 +/- 13 bpm; P=0.01). No effects were observed for placebo. Acute ingestion of CF during HD alleviated HD induced vascular dysfunction (3.4 +/- 0.9% to 2.7 +/- 0.6% versus placebo, 3.5 +/- 0.7% to 2.0 +/- 0.6%; P<0.001). This effect was sustained throughout the study (acute on chronic, 3.9 +/- 0.9% to 3.0 +/- 0.7% versus placebo, 3.5 +/- 0.7% to 2.2 +/- 0.6; P=0.01). Conclusions Dietary CF ingestion mitigates acute HD-induced and chronic endothelial dysfunction in patients with ESRD and thus, improves vascular function in this high-risk population. Larger clinical trials are warranted to test whether this translates into an improved cardiovascular prognosis in patients with ESRD.
引用
收藏
页码:108 / 118
页数:11
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