GLP-1 Agonists: A Promising Approach to Reduce Alcohol Consumption and Hospitalizations in Disorder Patients

Effective treatments for alcohol dependence are available; however, they are often underutilized and may not be suitable for every individual struggling with alcohol or substance dependency. Previous preliminary research involving both animal models and human subjects has indicated that GLP-1 agonists could play a pivotal role in significantly lowering the intake of alcohol and various other substances.

The use of GLP-1-agonists has demonstrated a marked decrease in the likelihood of hospitalisation due to alcohol use disorder. Notably, the medication semaglutide correlates with a 36% reduction in hospitalisation risk, while liraglutide shows a 28% reduction. Additionally, both medications have been linked to a significant decline in hospitalisation rates for any substance use disorder: semaglutide with a 32% lower risk, and liraglutide with a 22% lower risk.

The administration of semaglutide, liraglutide, and drugs for alcohol use disorder was linked to fewer hospitalisations resulting from physical illnesses. Specifically, semaglutide was associated with a 22% decrease in hospitalisations, and liraglutide with a 21% decrease, whereas AUD medications resulted in a 15% reduction in the same category. However, no significant correlation was found between the use of GLP-1 agonists and hospitalisations due to suicide attempts.

“The research idea stems from patient observations reporting less alcohol consumption since initiating a semaglutide drug. Similar observations have also been highlighted by scientists in international conferences, so we decided to examine this in more detail.”

Markku Lähteenvuo, Docent of Forensic Psychiatry, University of Eastern Finland and the Niuvanniemi Hospital

“Our study indicates that in addition to their benefits for obesity and diabetes management, GLP-1 agonists could offer promising assistance in addressing alcohol and substance use disorders; however, these results warrant further validation through rigorous randomised controlled trials,” Lähteenvuo emphasized.

Source:

Journal reference:

Lähteenvuo, M., et al. (2024). Repurposing Semaglutide and Liraglutide for Alcohol Use Disorder. JAMA Psychiatry. doi.org/10.1001/jamapsychiatry.2024.3599.

Are GLP-1 Agonists the New Heroes in the Battle Against Alcohol Dependence?

Ah, the age-old battle with alcohol dependence. A little drink here and there can lead to a sort of jolly downturn into a bottomless pit of regret, yes? But wait, what’s this? We’ve got some science on our hands that might just turn the tide! It appears ‘GLP-1 agonists’ — the substances often associated with those slightly bitter and very trendy weight-loss drugs — are stepping into the limelight as potential allies in curbing alcohol consumption!

The GLP-1 Revelation

As our delightful friends in the medical community inform us, while there are effective treatments available for alcohol dependence, they often gather dust on the shelf. But hold your horses! New preliminary studies suggest that these GLP-1 agonists might just be the magical elixirs we’ve been searching for. Think of them as potions from a wizard’s lab that can reduce one’s desire for both alcohol and other substances. You know, like finding out your favorite pub now offers kale smoothies – good riddance to the lager, eh?

Risk Reduction: A Statistical Delight!

Drinks in moderation? More like drinks on the verge of eviction! Research shows that GLP-1 agonists are associated with a noteworthy decline in hospitalizations due to alcohol use disorder. Semaglutide, the marvellous marvel, boasts a 36% reduced risk of hospitalization – yes, that’s not just a percentage! And liraglutide isn’t far behind with a robust 28%. Talk about a healthy dose of “cheers!”

The Lighter Side of Substance Use Disorders

But wait, there’s more! These savvy little agonists also chip away at hospital visits for other substance use issues. Semaglutide again takes the lead with a 32% reduction, while liraglutide steps in with a fine 22%. It’s almost like a competition! Who knew fighting substance abuse could look like a game show? “And the winner is …!”

Less Physical Illness? Yes Please!

As if that wasn’t enough, they also seem to trim down hospital visits due to physical ailments. We’re talking 22% fewer for semaglutide, 21% for liraglutide, and a respectable 15% for other alcohol use disorder (AUD) drugs. It’s a win-win situation — fewer visits for drinking and less time spent with hospitals blinking fluorescent lights at you. I mean, who actually enjoys those? Not me, that’s for sure.

“Our study suggests that besides obesity and diabetes, GLP-1-agonists may also help in the treatment of alcohol and substance use disorders; however, these findings need to be further validated in randomized controlled trials.”

— Markku Lähteenvuo, Docent of Forensic Psychiatry, University of Eastern Finland

The Future: More Studies to Come

Markku Lähteenvuo has struck a note of caution though. While the evidence is tantalizing, he insists we hold our applause until more randomized controlled trials confirm these findings. Let’s not throw the confetti just yet, people! Remember the time we thought that wearing socks with sandals was a good idea? Exactly!

The Bottom Line

If you’re one of the many who find themselves in a cycle of drinking a bit too much, this could be very promising news. While we await more robust studies, it seems there’s a flicker of hope in pushing back against alcohol dependence. And if GLP-1 agonists can help, perhaps we should be raising our glasses (filled with water, of course) to these little champions!

So there you have it – medical science weaving together diets and drinks into something that can actually safeguard our health. I can’t help but think how much fun it’d be to attend a medical convention where the doctors discuss diets and cocktails together. Wouldn’t that be a sight?

Source: University of Eastern Finland.

Journal reference: Lähteenvuo, M., et al. (2024). Repurposing Semaglutide and Liraglutide for Alcohol Use Disorder. JAMA Psychiatry. doi.org/10.1001/jamapsychiatry.2024.3599.

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