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Over a median follow-up of 3.3 years, semaglutide 2.4 mg reduced the risk of major adverse cardiovascular eventscardiovascular death, non-fatal heart attack, or non-fatal strokeby approximately 20% compared with placebo

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The observed difference between the individuals with type 1 diabetes and UFMs (Table 1) was in contrast to the cross-sectional serum proteomics study of Zhang et al, in which the authors reported downregulation of GPX3 in type 1 diabetes and type 2 diabetes [4]