Abstract
ABSTRACTBackgroundAnthocyanin-rich blueberry intake is associated with reduced type 2 diabetes and cardiovascular disease (CVD) risk in prospective studies, although long-term randomized controlled trials (RCTs) have not been conducted in at-risk populations.ObjectiveIn the longest-duration RCT to date, we examined the effect of 6-mo blueberry intake on insulin resistance and cardiometabolic function in metabolic syndrome.MethodsA double-blind, parallel RCT (n = 115; age 63 ± 7 y; 68% male; body mass index 31.2 ± 3.0 kg/m2) was conducted, which fed 2 dietarily achievable blueberry intakes [equivalent to 1/2 and 1 cup/d (75/150 g)] compared with matched placebo. Insulin resistance was assessed via the homeostasis model assessment of insulin resistance (primary endpoint) and confirmed by [6-6-2H2]-glucose-labeled, 2-step hyperinsulinemic clamp (n = 20). Clinically relevant cardiometabolic endpoints [including flow-mediated dilatation, augmentation index, lipoprotein status (by nuclear magnetic resonance spectroscopy), and nitric oxide (NO)-related metabolite assay] and anthocyanin metabolism were assessed.ResultsA daily intake of 1 cup of blueberries improved endothelial function (flow-mediated dilatation: +1.45%; 95% CI: 0.83%, 2.1%; P = 0.003), systemic arterial stiffness (augmentation index: –2.24%; 95% CI: –3.97%, –0.61%; P = 0.04) and attenuated cyclic guanosine monophosphate concentrations. In statin nonusers (n = 71), elevated high-density lipoprotein cholesterol (+0.08 mmol/L; P = 0.03), high-density lipoprotein particle density (+0.48n, ×10–6; P = 0.002) and apolipoprotein A-I (+0.05 g/L; P = 0.01) concentrations were observed following the 1-cup/d intervention. Treatment compliance was 94.1% (wrapper returns) and total concentrations of anthocyanin-derived phenolic acid metabolites significantly increased, dose-dependently, in serum and 24-h urine (P < 0.01 and P < 0.001, respectively). Insulin resistance, pulse wave velocity, blood pressure, NO, and overall plasma thiol status were unaffected. Likewise, a half cup per day had no effect on any biomarkers.ConclusionsDespite insulin resistance remaining unchanged we show, to our knowledge, the first sustained improvements in vascular function, lipid status, and underlying NO bioactivity following 1 cup blueberries/d. With effect sizes predictive of 12–15% reductions in CVD risk, blueberries should be included in dietary strategies to reduce individual and population CVD risk. This study was registered at clinicaltrials.gov as NCT02035592.
Highlights
Metabolic syndrome (MetS) affects approximately one-third of Westernized populations and has been widely reported to increase the risk of type 2 diabetes, cardiovascular (CV) disease, and CV-related mortality
Insulin resistance is considered central to the development of MetS, compromised vascular function and dysregulated lipids are integral in the etiology, and worsening, of the condition
We investigated the effects of 6-mo blueberry intake on biomarkers of insulin resistance, vascular function, lipid status, and anthocyanin metabolism in adults with MetS
Summary
Metabolic syndrome (MetS) affects approximately one-third of Westernized populations and has been widely reported to increase the risk of type 2 diabetes, cardiovascular (CV) disease, and CV-related mortality. Identifying effective dietary approaches has clinical relevance throughout MetS progression—as a preventive strategy in nonmedicated individuals, and as an adjunct to those receiving standard pharmacologic therapies Blueberries and their main bioactive constituents (especially the flavonoid subclass, anthocyanins) have been identified as candidates to improve CV-related endpoints and the components of MetS. Prospective studies have shown that higher anthocyanin intakes are associated with lower all-cause mortality [2] and reduced risk of type 2 diabetes [3] and myocardial infarction [4, 5]; with benefits observed for biomarkers including reduced insulin resistance [6] and hypertension [7] and lower weight gain [8]. A half cup per day had no effect on any biomarkers
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