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This also supports the finding that the cardiovascular benefits are not restricted to those agents structurally similar to human GLP-1 but are more likely a class effect that is seen in all GLP-1RAs

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Participants were randomly assigned to receive either semaglutide or a placebo

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Further analysis of the proposed D-malate pathway intermediate was hampered by the possible involvement of a cellular malate racemase and the unavailability of a msadh mutant strain