A reference interval is not a target, and a result outside one is not a diagnosis
Two sources of noise sit under every number: how reproducible the assay is, and how much the analyte varies within the same person on the same day.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Glycated haemoglobin as an endpoint, its lag, and its failure modes.
Two sources of noise sit under every number: how reproducible the assay is, and how much the analyte varies within the same person on the same day.
The argument for a baseline panel is that it makes every subsequent result interpretable. The argument against frequent monitoring is that noise accumulates faster than…
The alternatives with shorter windows, what they measure, and why they are rarely ordered.
What the trials measured, which in the case of micronutrients is very little.
The assay is not the problem. The interpretation of a lagging integral as a current measurement is the problem.
Every additional analyte raises the probability of a flagged result and lowers the average information content of the panel.
A twelve-analyte panel in a perfectly healthy person has roughly even odds of producing at least one flagged result.
Almost every misreading of a laboratory panel is a misunderstanding of what a reference interval is and how much a result has to move before the movement means anything.
The arithmetic of the reference change value, worked for the analytes that matter here.
A flag is a probability statement about a population. It is not a statement about the person holding the printout.
A substantial proportion of the abnormal results generated during rapid weight loss are consequences of the weight loss rather than findings about the person.
HbA1c integrates roughly three months of glycaemia with the most recent weeks weighted most heavily. Almost every misreading of it is a misreading of that weighting.
A flag is a probability statement about a population. It is not a statement about the person holding the printout.
The reference interval for alanine aminotransferase in most laboratories is derived from a population that included people with undiagnosed fatty liver.
A twelve-analyte panel in a perfectly healthy person has roughly even odds of producing at least one flagged result.
A substantial proportion of the abnormal results generated during rapid weight loss are consequences of the weight loss rather than findings about the person.
Which markers are informative, which are confounded, and which move for reasons unrelated to nutrition.
Timing is the whole of the post-cessation panel: draw it too early and it measures the treatment period.
What the pivotal programmes measured and how often, which is a more defensible template than most published monitoring schedules.
The panel drawn during a week of vomiting is measuring the vomiting.