Key result
Energy intake-restricted weight loss increased brachial artery flow-mediated dilation by 30% (P=0.01) and peak forearm blood flow by 26% (P<0.05) in overweight or obese adults.
Why the study?
Does energy intake-restricted weight loss alone improve conduit and resistance artery endothelial function in overweight or obese adults?
RCT (n=40)
Does energy intake-restricted weight loss alone improve conduit and resistance artery endothelial function in overweight or obese adults?
p-value: p=0.01
Energy intake-restricted weight loss alone improves peripheral conduit and resistance artery endothelial function in overweight and obese adults, mediated by increased NO bioavailability.
Supports energy-restricted weight loss to improve endothelial function in overweight adults; reinforces RCT evidence for lifestyle interventions on vascular health.
Obesity is associated with vascular endothelial dysfunction, as indicated by impaired endothelium-dependent dilation. Presently there is no direct evidence that energy intake-restricted weight loss alone improves conduit or resistance artery endothelium-dependent dilation, the mechanisms involved, or whether improvements differ with patient age. A total of 40 overweight or obese (body mass index: >or=25<40 kg/m(2)) nondiabetic men and women aged 21 to 69 years completed 12 weeks of reduced energy intake (n=26; 15 male) or attention control (n=14; 9 male) and 4 weeks of weight maintenance (randomized trial). Energy intake restriction reduced estimated total energy intake (33%), body weight (10.5%), total and abdominal body fat, plasma leptin, oxidized low-density lipoprotein, and improved several metabolic risk factors. Brachial artery flow-mediated dilation was increased by 30% (6.0+/-0.7% versus 7.9+/-0.7%Delta; P=0.01; n=17). Peak forearm blood flow during intrabrachial artery infusion of acetylcholine was increased by 26% (16.8+/-1.4 versus 21.1+/-1.9 mL/100 mL per minute; P<0.05; n=15); this was inversely related to the reduction in the abdominal visceral:subcutaneous fat ratio (r=-0.46; P<0.05) and was abolished by inhibition of NO synthesis with N(G)-monomethyl-L-arginine. Improvements in endothelium-dependent dilation were not related to age: mean increases in subjects >50 years of age were similar to or greater than those <50 years of age. Energy intake-restricted weight loss alone is an effective intervention for improving peripheral conduit and resistance artery endothelial function in young and older overweight/obese adults. The improvements in resistance artery function are mediated by an increase in NO bioavailability and are related to reductions in abdominal visceral fat.
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Pierce et al. (2008) conducted an RCT in Overweight or obesity (n=40). Reduced energy intake vs. Attention control was evaluated on Brachial artery flow-mediated dilation (p=0.01). Energy intake-restricted weight loss increased brachial artery flow-mediated dilation by 30% (P=0.01) and peak forearm blood flow by 26% (P<0.05) in overweight or obese adults.
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