The one randomised trial that combined an incretin with supervised exercise
One randomised trial has combined a GLP-1 receptor agonist with supervised exercise. Its result is the single most useful piece of evidence in this area.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Page 3 of 18 of this archive, newest first.
One randomised trial has combined a GLP-1 receptor agonist with supervised exercise. Its result is the single most useful piece of evidence in this area.
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 older-adult diet-and-exercise trials are the closest analogue to rapid pharmacological weight loss, and they are twenty years old.
What the Journal would want measured before treating this as settled in either direction.
Supply interruption is the commonest cause of unplanned re-titration in this market, and it is almost never framed that way.
A substantial proportion of the abnormal results generated during rapid weight loss are consequences of the weight loss rather than findings about the person.
Almost every practical recommendation in circulation was established in a population that does not resemble the people now following it.
The trials studied planned withdrawal. Almost nobody stops that way.
Nausea and gastric delay attenuate over weeks at an unchanged dose. That single physiological fact is the entire justification for holding.
The evidence base is one secondary analysis, several small studies and a large amount of extrapolation from bariatric surgery.
What the trials measured, which in the case of micronutrients is very little.
The dose-response curve in this class flattens near its top. That has direct consequences for whether the final rung is worth climbing.
Every major phase 3 protocol in this class allowed escalation to be delayed for tolerability. Almost no product label explains the mechanics of doing so.
Every additional analyte raises the probability of a flagged result and lowers the average information content of the panel.
Both the reassuring reading and the alarming reading are supportable from the same tables. This piece sets out which is which.
What the renal and hepatic outcome programmes actually measured, and over what duration.
What the regulatory dossiers actually contain on dose selection is remarkably thin, and worth knowing before treating the ladder as settled science.
The evidence base is one secondary analysis, several small studies and a large amount of extrapolation from bariatric surgery.
The receptor is expressed in more tissues than the popular account allows, and that is the whole story.
The assay is not the problem. The interpretation of a lagging integral as a current measurement is the problem.