So @AlexKChen 1 mg will be homeopathic for most individuals ā 2.5 to 3.75 mg weekly is a bit more likely to have a clinical effect. Iām still really torn in regard to neurocognitive decline whether GLPs/GIPs that cross the BBB are necessary. On a practical level, the compounders are not making the ones that cross the BBB as they arenāt that effective for weight loss - and this is where the $$$ are at.
My costs on Tirzepatide with Empower are ~$330 for 34 mg or $575 for 68 mg. However, this is in a vial at 17 mg/mL so really easy to titrate.
Tirzepatide is significantly GIP and weaker GLP-1 - and there is evidence that GIP is neuroprotective. I however think Semaglutide is probably the most potent on GLP-1 alone - but also doesnāt cross the BBB.
If you look at effects on the brain with GLP1ās- indirect effects through the vagus nerve seem very powerful, so the issue becomes do you need an actual brain level of the drug? If so, then Trulicity (Dulaglutide) is likely drug of choice, but then we have more expense with that.
Iāll address this issue in an upcoming blog on neurocognitive decline- I just went through the SGLT2-i on this series, but this is a particularly interesting area.
Do we go for lower GLP-1 potency, and a level in the brain, or do we go for a more potent GLP/GIP and think the effect is through vagus nerve signaling? There is a cost effect of this, which is $1100-1200/month vs. $100/month as I have no compounders doing dulaglutide.
My approach has been to go with the cost effective GLP, BUT not have all my āeggs in one basketā and make sure we have additional strategies in play.
The other complicating factor can be patients who really canāt afford to lose weight (yes this is a real factor in some patients ā a rarity - but common in my patients) - so there we need to go with a less potent GLP and then look at Rx of Trulicity, but then dose splitting to keep costs down, and still give a decent brain level.
I suspect it will be some time before we get a trial with semaglutide or Tirzepatide to really understand whether a direct brain level is needed.
Iād love others thoughts on this, as it continues to be an area that I would love better certainty on.
@Neo - thanks for this study. Interestingly, TruDiagnostic even 18 months ago had indicated the GLP-1 drugs were tracking very well as compared to almost everything else on being predictive of a lower epigentic age vs. chronology. So this study isnāt surprising. I have a lot of patients on GLP-1ās for longevity and neurocognitive decline risk. With all the bad media reports on these agents, it is important to understand they generally have an excellent safety profile, and the main issue is cost. Most people have some weight to lose, and it helps optimize this also. There are individuals who have a āguiltā around taking a drug to lose weight, as they consider this a personal failure. I find it therapeutic as physician to completely dismiss this, and let them know these a amazing longevity drugs, and that Iām thrilled to be able to Rx it, as it would be a problem if they had no weight to lose. The same issue comes up with Telmisartan - I love it when my patient has a bit of hypertension - as this gives me the opportunity to Rx a drug with great data for longevity, whereas my patients who are ideal body weight and have a SBP of 105 ā I canāt recommend these therapies.