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The weight-loss drug led to favorable changes in lipoproteins, glycoproteins and inflammation biomarkers in people with fatty liver disease.
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At 50% uptake, and assuming a 15.5% discontinuation rate as observed in the SOUL trial, an estimated 59,332 MACE, 14,215 cardiovascular deaths, 41,744 nonfatal myocardial infarctions, and 12,260 nonfatal strokes could be prevented
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