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Circulation. 2004;109:2885-2889
Published online before print May 24, 2004, doi: 10.1161/01.CIR.0000129304.98566.D8
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Right arrow Endothelium/vascular type/nitric oxide

(Circulation. 2004;109:2885-2889.)
© 2004 American Heart Association, Inc.


Clinical Investigation and Reports

Determinants of Arterial Nitrate-Mediated Dilatation in Children

Role of Oxidized Low-Density Lipoprotein, Endothelial Function, and Carotid Intima-Media Thickness

Mikko J. Järvisalo, MD, PhD; Terho Lehtimäki, MD, PhD; Olli T. Raitakari, MD, PhD

From the Department of Clinical Physiology and Turku PET Centre (M.J.J., O.T.R.), Turku University Hospital, and the Research Centre of Applied and Preventive Cardiovascular Medicine (M.J.J.), University of Turku, and the Laboratory of Atherosclerosis Genetics (T.L.), Department of Clinical Chemistry, Centre for Laboratory Medicine, Tampere University Hospital and University of Tampere, Finland.

Correspondence to Mikko J Järvisalo, Turku PET Centre, Turku University Hospital, Kiinamyllynkatu 4-8, FIN-20520 Turku, Finland. E-mail mikko.jarvisalo{at}utu.fi

Received December 8, 2003; revision received February 27, 2004; accepted March 4, 2004.

Background— Impaired arterial dilatation response to nitroglycerin has been observed in adults with risk factors for atherosclerosis and in patients with established atherosclerotic disease. This defect parallels changes in vascular endothelial function and may be attributed to increased oxidative stress. Because atherosclerosis begins in childhood, we examined the correlates of nitrate-mediated dilatation (NMD) in children, including brachial artery endothelial function, oxidized LDL, and carotid artery intima-media thickness (IMT).

Methods and Results— Brachial artery flow-mediated endothelium-dependent dilatation (FMD) and nitrate-mediated smooth muscle function, IMT of the carotid bulb, and brachial artery and oxidized LDL were measured in 142 children (mean age, 11 years; range, 8 to 17 years), including 87 healthy children, 41 diabetic children, and 14 children with familial hypercholesterolemia. NMD correlated directly with FMD (r=0.46, P<0.001) and inversely with brachial artery baseline diameter (r=–0.36, P<0.001), age (r=–0.25, P=0.003), body mass index (r=–0.31, P<0.001), diabetes (r=–0.22, P=0.008), oxidized LDL (r=–0.18, P=0.045), and IMT (r=–0.33, P<0.001). In a multivariate regression model, the significant correlates for NMD were FMD response (ß=0.003, P<0.001), brachial artery diameter (ß=–0.03, P=0.01), oxidized LDL (ß=–0.07, P=0.02), and IMT (ß=–0.15, P=0.03).

Conclusions— Reduced endothelial function, increased oxidative stress, and preclinical carotid atherosclerosis are independent determinants of impaired NMD in children. These data thus suggest that primary nitrate tolerance occurs in children at risk for atherosclerosis.


Key Words: arteries • diabetes mellitus • endothelium • nitroglycerin • pediatrics




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