by gumby on 8/23/24, 4:18 AM with 118 comments
by reissbaker on 8/23/24, 5:55 AM
1: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC419497/
by hi-v-rocknroll on 8/23/24, 5:06 AM
There are many GLP-1 agonists approved now. Some are approved for type-2 diabetes as one trade name, and may also be approved under another trade name at a higher dosage. For example, Lixisenatide came off-patent for diabetes in 2020 but it doesn't have an obesity formulation in the US. The various GLP-1 agonists have slightly different risk profiles of causing pancreatitis and/or thyroid cancers.
I don't know though maybe the freezing method (cryolipolysis) could potentially be useful for some people, but it's probably still too soon to characterize its long-term risks and other benefits.
Also, CagriSema (cagrilintide (long-acting amylin analogue) & semaglutide) is promising for obesity.
by notepad0x90 on 8/23/24, 6:56 AM
If there is a legitimate hormonal imbalance or genetic defect, I get it. But short of that, are there not only two root causes left? Which in my opinion would be:
1) Poor diet, which includes poor quality in food supply
2) Poor choices being made, or made for people. This includes car-centric cities, sedentary lifestyle and similar well known ailments of modern life.
The root cause isn't being solved, only the adverse effects are temporarily inhibited so long as people continue to afford dependency on the pharmaceutical industry. How can any medical professional support this?
It is already so hard to trust American medicine; doctors having intimate financial relationships with pharma is already a public secret. This certainly doesn't help. They already ruined generations by blaming weight gain on fats instead of sugar because of these corrupt relationships with pharma and other corporate types. I don't doubt the efficacy of the medicine, but the disease is not fatness, it is the reason we get fat that needs to be solved. Rarely do shortcuts result in long term solutions. Why is this different? How do I know this won't expose us to higher cancer risks, new types of diseases like nutrition absorption disorders or becoming over dependent on these medicines and developing malnutrition?
I just don't get the lack of skepticism.
by whitten on 8/23/24, 4:50 AM
It works in mice and probably works in humans but was not the main focus of the study so they didn't have a good control group to be able to prove it.
by avree on 8/23/24, 4:58 AM
by Hnrobert42 on 8/23/24, 4:41 AM
by tedunangst on 8/23/24, 5:13 AM
by sk11001 on 8/23/24, 4:53 AM
> Here, we present data from a proof-of-concept study on 30 individuals with obstructive sleep apnea and obesity who were randomized to a GLP-1 therapy-based weight loss regimen, continuous positive airway pressure, or a combination of both for 24 weeks.
They compared weight loss medication to a sleep apnea treatment and the weight loss medication group lost fat... which happens when your appetite is suppressed and you eat less - you lose some muscle and some fat, some of the fat you lose is visceral, some isn't.
by glp1guide on 8/23/24, 10:30 AM
I've been on the lookout personally for more negative side effects (it's almost suspicious how little there are, though it varies by person to person), but also excited to hear of benefits.
Some of the benefits recently led 23andMe to get into GLP1s:
https://glp1.guide/content/23andme-gets-into-glp1/
They even a paper on some possible benefits with Alzheimers, though I think the research is in it's infancy. I think the plastic story is a bit more compelling though.
by morgengold on 8/23/24, 2:02 PM
A caloric deficit leads to a loss of visceral fat. It wouldn't suprise me, if we see the same VAT activity if we had a control group with the same caloric deficit. Only then we could calculate the direct effect of GLP-1 to the VAT acitivity.
by deafpolygon on 8/23/24, 5:39 AM
by hiddencost on 8/23/24, 4:41 AM
by roschdal on 8/23/24, 5:01 AM