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and Braly, J

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Metals removed in these human studies included mercury, lead, gold, and arsenic

3.2 Iron dysregulation in modulating ferroptosis susceptibility Iron overload, as a key inducer of ferroptosis, disrupts cellular iron homeostasis by interfering with critical components of iron metabolism at both transcriptional and post-transcriptional levels, thereby significantly increasing cellular susceptibility to ferroptosis (59)

This is an important distinction between both peptides because Ghrelin is responsible for initiating the breakdown of fat for use as energy as well as preventing the breakdown of muscles

[#3] Adjustments based on phenytoin level : Whenever possible, correct for albumin