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As a result, it has been proposed that Arg2 could limit the bioavailability of Arg and consequently NO, thereby aiding in the control of oxidative stress and inflammatory processes [17, 77]

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Adult patients with type 2 diabetes at high risk for cardiovascular events (N=9340) were randomized to receive once-daily Victoza (0.6 mg-1.8 mg once daily with all patients being titrated to 1.8 mg once daily) or placebo