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Wilson's disease, an autosomal recessive disorder caused by mutations in the ATP7B gene leading to copper accumulation, and alpha-1 antitrypsin (A1AT) deficiency, linked to mutations in the SERPINA1 gene, are significant contributors to hepatic steatosis [3,9]

Providers evaluate cardiovascular history, renal function, thyroid concerns, and medication interactions before initiation

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Similarly, alternative treatments should be explored by individuals with a history of pancreatitis or severe gastrointestinal disorders

This combination effectively targets the two primary components of body composition: fat reduction and muscle maintenance

For patients on fully insured plans, TDI enforces federal MHPAEA requirements