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Ance Administration, Ministry of Wellness and Welfare, Taiwan, plus the National Overall health Research Institute, Taiwan, for kindly giving the study information for analysis. The interpretation and conclusions contained herein do not represent those of your aforementioned institutions. Author Contributions Conceived and developed the experiments: VCK JTH. Performed the experiments: VCK WSC. Analyzed the data: VCK JTH WSC YFH THC. Contributed reagents/materials/analysis tools: YFH THC. Wrote the paper: VCK. Obtained grants for investigation: JTH. Organized research meetings: JTH. References 1. Bhansing KJ, van Bon L, Janssen M, Radstake TR Gout: a clinical syndrome illustrated and discussed. Neth J Med 68: 352-359. 2. Zhu Y, Pandya 24195657 BJ, Choi HK Prevalence of gout and hyperuricemia in the US general population: the National Overall health and Nutrition Examination Survey 2007-2008. Arthritis Rheum 63: 31363141. three. Krishnan E, Pandya BJ, Chung L, Dabbous O Hyperuricemia and the danger for subclinical coronary atherosclerosis–data from a potential observational cohort study. Arthritis Res Ther 13: R66. 4. Kanbay M, Sanchez-Lozada LG, Franco M, Madero M, Solak Y, et al. Microvascular illness and its part inside the brain and cardiovascular technique: a potential role for uric acid as a cardiorenal toxin. Nephrol Dial Transplant 26: 430437. 5. Puddu P, Puddu GM, Cravero E, Vizioli L, Muscari A Relationships amongst hyperuricemia, endothelial dysfunction and cardiovascular disease: SPDB web molecular mechanisms and clinical implications. J Cardiol 59: 235242. 6. Feig DI, Kang DH, Johnson RJ Uric acid and cardiovascular danger. N Engl J Med 359: 18111821. 7. Ford ES Uric acid and mortality from all-causes and cardiovascular disease amongst adults with and with no diagnosed diabetes: findings in the National Overall health and Nutrition Examination Survey III Linked Mortality Study. Diabetes Res Clin Pract 93: e8486. eight. Kok VC, Horng JT, Lin HL, Chen YC, Chen YJ, et al. Gout and subsequent increased danger of cardiovascular mortality in non-diabetics aged 50 and above: a population-based cohort study in Taiwan. BMC Cardiovasc Disord 12: 108. 9. Erdogan D, Tayyar S, Uysal BA, Icli A, Karabacak M, et al. Effects of allopurinol on coronary microvascular and left ventricular function in individuals with idiopathic dilated cardiomyopathy. Can J Cardiol 28: 721727. ten. George J, Carr E, Davies J, Belch JJ, Struthers A High-dose allopurinol improves endothelial function by profoundly SIS-3 site minimizing vascular oxidative strain and not by lowering uric acid. Circulation 114: 25082516. 11. Muir SW, Harrow C, Dawson J, Lees KR, Weir CJ, et al. Allopurinol use yields potentially helpful effects on inflammatory indices in these with recent ischemic stroke: a randomized, double-blind, placebo-controlled trial. Stroke 39: 33033307. 12. Siu YP, Leung KT, Tong MK, Kwan TH Use of allopurinol in slowing the progression of renal disease by way of its capability to reduced serum uric acid level. Am J Kidney Dis 47: 5159. 13. Stone PH Allopurinol a new anti-ischemic role for an old drug. J Am Coll Cardiol 58: 829830. 14. Yiginer O, Ozcelik F, Inanc T, Aparci M, Ozmen N, et al. Allopurinol improves endothelial function and reduces oxidant-inflammatory enzyme of myeloperoxidase in metabolic syndrome. Clin Res Cardiol 97: 334340. 15. Rekhraj S, Gandy SJ, Szwejkowski BR, Nadir MA, Noman A, et al. High-dose allopurinol reduces left ventricular mass in patients with ischemic heart disease. J Am Coll Cardiol 61: 926932. 16. Goicoechea M, de.Ance Administration, Ministry of Wellness and Welfare, Taiwan, plus the National Well being Investigation Institute, Taiwan, for kindly delivering the analysis information for analysis. The interpretation and conclusions contained herein don’t represent these on the aforementioned institutions. Author Contributions Conceived and made the experiments: VCK JTH. Performed the experiments: VCK WSC. Analyzed the data: VCK JTH WSC YFH THC. Contributed reagents/materials/analysis tools: YFH THC. Wrote the paper: VCK. Obtained grants for research: JTH. Organized analysis meetings: JTH. References 1. Bhansing KJ, van Bon L, Janssen M, Radstake TR Gout: a clinical syndrome illustrated and discussed. Neth J Med 68: 352-359. two. Zhu Y, Pandya 24195657 BJ, Choi HK Prevalence of gout and hyperuricemia within the US basic population: the National Overall health and Nutrition Examination Survey 2007-2008. Arthritis Rheum 63: 31363141. 3. Krishnan E, Pandya BJ, Chung L, Dabbous O Hyperuricemia plus the danger for subclinical coronary atherosclerosis–data from a potential observational cohort study. Arthritis Res Ther 13: R66. four. Kanbay M, Sanchez-Lozada LG, Franco M, Madero M, Solak Y, et al. Microvascular illness and its part in the brain and cardiovascular method: a possible part for uric acid as a cardiorenal toxin. Nephrol Dial Transplant 26: 430437. 5. Puddu P, Puddu GM, Cravero E, Vizioli L, Muscari A Relationships among hyperuricemia, endothelial dysfunction and cardiovascular illness: molecular mechanisms and clinical implications. J Cardiol 59: 235242. six. Feig DI, Kang DH, Johnson RJ Uric acid and cardiovascular danger. N Engl J Med 359: 18111821. 7. Ford ES Uric acid and mortality from all-causes and cardiovascular disease amongst adults with and with out diagnosed diabetes: findings from the National Overall health and Nutrition Examination Survey III Linked Mortality Study. Diabetes Res Clin Pract 93: e8486. 8. Kok VC, Horng JT, Lin HL, Chen YC, Chen YJ, et al. Gout and subsequent improved threat of cardiovascular mortality in non-diabetics aged 50 and above: a population-based cohort study in Taiwan. BMC Cardiovasc Disord 12: 108. 9. Erdogan D, Tayyar S, Uysal BA, Icli A, Karabacak M, et al. Effects of allopurinol on coronary microvascular and left ventricular function in individuals with idiopathic dilated cardiomyopathy. Can J Cardiol 28: 721727. ten. George J, Carr E, Davies J, Belch JJ, Struthers A High-dose allopurinol improves endothelial function by profoundly minimizing vascular oxidative pressure and not by lowering uric acid. Circulation 114: 25082516. 11. Muir SW, Harrow C, Dawson J, Lees KR, Weir CJ, et al. Allopurinol use yields potentially helpful effects on inflammatory indices in these with recent ischemic stroke: a randomized, double-blind, placebo-controlled trial. Stroke 39: 33033307. 12. Siu YP, Leung KT, Tong MK, Kwan TH Use of allopurinol in slowing the progression of renal disease by means of its capability to lower serum uric acid level. Am J Kidney Dis 47: 5159. 13. Stone PH Allopurinol a brand new anti-ischemic role for an old drug. J Am Coll Cardiol 58: 829830. 14. Yiginer O, Ozcelik F, Inanc T, Aparci M, Ozmen N, et al. Allopurinol improves endothelial function and reduces oxidant-inflammatory enzyme of myeloperoxidase in metabolic syndrome. Clin Res Cardiol 97: 334340. 15. Rekhraj S, Gandy SJ, Szwejkowski BR, Nadir MA, Noman A, et al. High-dose allopurinol reduces left ventricular mass in individuals with ischemic heart disease. J Am Coll Cardiol 61: 926932. 16. Goicoechea M, de.

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