Answering the narrow version, because the broad one does not have a single answer. A defensible baseline is short: HbA1c and fasting glucose, a lipid panel with ApoB if you can get it, ALT and AST, creatinine with eGFR, TSH, ferritin and B12, and a full blood count. That set catches the things that change, the things that explain symptoms, and the things that alter the prescribing decision. Almost everything else on the long circulating lists is either invariant, uninterpretable without a specific question, or an incidental finding waiting to cause an unnecessary workup.
I got a full panel before starting and a repeat at three months, and the second one is more useful than the first purely because I now have something to compare against.
What I am after is how often to repeat it, because quarterly seems to be the convention and I cannot find the reasoning.
Not looking for reassurance. Looking for the part I have got wrong.
sarah.morrison said:A defensible baseline is short: HbA1c and fasting glucose, a lipid panel with ApoB if you can get it, ALT and AST, creatinine with eGFR, TSH, ferritin…
sarah.morrison has the substance of this right. The condition it depends on is worth stating. One addition: if the lab changes analytical platform between your draws, the comparison breaks and nobody tells you. It is worth asking when a value moves inexplicably.
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View ResultsLipidDoc_ATL said:I got a full panel before starting and a repeat at three months, and the second one is more useful than the first purely because I now have something…
This matches mine closely enough to be worth saying so. The single most useful discipline is bringing the whole panel to a clinician rather than one flagged value. One out-of-range result in isolation generates anxiety and unnecessary tests; the same result next to the trend and the rest of the panel usually generates a shrug.
Adding the clinical framing, because it changes how the question reads.
Blood work came back perfect. baseline bloodwork + this community = winning. 🏆