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Serum Uric Acid Levels and Risk for Vascular Diseases in Patients with Metabolic Syndrome JESPER HJORTNAES, ALE ALGRA, JOBIEN OLIJHOEK, MARGRIET HUISMAN, JOHANNES JACOBS, YOLANDA van der GRAAF, and FRANK VISSEREN, for the SMART Study Group
ABSTRACT. Methods. A nested case-cohort study of 431 patients with 220 cases with a new vascular event during followup, originating from the Second Manifestations of Arterial Disease (SMART) study. All patients had manifest vascular diseases, consisting of cerebral, coronary, or peripheral artery disease or abdominal aortic aneurysm. The relationship of SUA with the metabolic syndrome was analyzed with linear regression and adjusted for age, sex, creatinine clearance, and alcohol and diuretic use. The relationship of SUA levels with new vascular disease was investigated with Cox regression and adjusted for age and sex. Results. The metabolic syndrome was present in 50% of patients. SUA levels were higher in 214 patients with the metabolic syndrome than in 217 patients without (0.36 ± 0.08 mmol/l vs 0.32 ± 0.09 mmol/l). SUA concentrations increased with the number of components of the metabolic syndrome (0.30 mmol/l to 0.38 mmol/l) adjusted for age, sex, creatinine clearance, and alcohol and diuretic use. Increased SUA concentrations were independently associated with risk for vascular events in patients without the metabolic syndrome (age and sex adjusted hazard ratio 2.4, 95% CI 1.0–5.5), in contrast to patients with the metabolic syndrome (adjusted hazard ratio 1.9, 95% CI 1.0–3.9). Conclusion. Elevated SUA levels are strongly associated with the metabolic syndrome, yet are not an independent risk factor for vascular disease in patients with the metabolic syndrome. In patients without the metabolic syndrome, elevated SUA levels are associated with increased risk for vascular disease. (First Release August 1 2007; J Rheumatol 2007;334:1882-7) Key Indexing Terms:
SERUM URIC ACID From the Department of Internal Medicine, Vascular Medicine Section; Julius Centre for Health Sciences and Primary Care; Department of Neurology, Rudolph Magnus Institute of Neuroscience; and Department of Rheumatology and Clinical Immunology, University Medical Centre, Utrecht, The Netherlands. J. Hjortnaes, BSc; J. Olijhoek, MD; F. Visseren, MD, PhD, Department of Internal Medicine, Vascular Medicine Section; A. Algra, MD, PhD, Julius Centre for Health Sciences and Primary Care, Department of Neurology, Rudolph Magnus Institute of Neuroscience; M. Huisman, MD; J. Jacobs, MD, PhD, Department of Rheumatology and Clinical Immunology, University Medical Centre; Y. van der Graaf, MD, PhD, Julius Centre for Health Sciences and Primary Care. Address reprint requests to Dr. F.L.J. Visseren, Department of Internal Medicine, Section of Vascular Medicine, University Medical Centre Utrecht (UMCU), G02.402, Utrecht, The Netherlands. E-mail: F.L.J.Visseren@umcutrecht.nl Accepted for publication May 3, 2007. |