Four obesity stereotypes [some are GLP resistant]

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"The cheek-swab genetic test groups people into four basic obesity phenotypes (meaning observable traits): Hungry Gut, Hungry Brain, Emotional Hunger, and Slow Burn. (A person might belong to more than one of these groups.)"

Hungry Brain - Individuals who feel persistently hungry despite eating enough calories.

Hungry Gut - Those who feel full but experience quick returns of hunger due to faster gastric emptying.

Emotional Hunger - People who eat in response to emotional triggers rather than physical hunger.

Slow Burn - Individuals with a lower metabolic rate, making weight maintenance challenging.

Tag yourself, I'm Emotional Hunger all the way to the moon and back.
 
Mr.Tired said:
"The cheek-swab genetic test groups people into four basic obesity phenotypes (meaning observable traits): Hungry Gut, Hungry Brain, Emotional Hunger, and Slow Burn. (A person might belong to more than one of these groups.)"

Hungry Brain - Individuals who feel persistently hungry despite eating enough calories.

Hungry Gut - Those who feel full but experience quick returns of hunger due to faster gastric emptying.

Emotional Hunger - People who eat in response to emotional triggers rather than physical hunger.

Slow Burn - Individuals with a lower metabolic rate, making weight maintenance challenging.

Tag yourself, I'm Emotional Hunger all the way to the moon and back.
Have you tried any of the Glp-1 and if so, did they work?
 
AI Overview GLP-1 receptor agonists (GLP-1RAs) show potential for treating diabetic peripheral neuropathy (DPN) by

improving nerve structure, function, and alleviating pain, potentially through neuroprotective and anti-inflammatory mechanisms. Studies suggest they may improve nerve size and axonal function, with some evidence showing reversal of nerve damage.

Key Aspects of GLP-1 for DPN:

Positive Effects: Research indicates that GLP-1RAs can lead to improvements in nerve conduction studies, clinical neuropathy scores, and nerve fiber structure, with one study showing 93% of patients had improved nerve size at 3 months.

Mechanisms: These medications may work independently of weight loss, possibly by enhancing

Na+/K+cap N a raised to the positive power / cap K raised to the positive power

-ATPase pump function, reducing inflammation, and protecting nerve cells.

Pain Reduction: Preliminary evidence suggests a significant reduction in peripheral neuropathy pain, according to PubMed.

Current Status: While findings are promising, they are based on smaller studies and preclinical models. Larger, long-term trials are necessary to confirm efficacy and establish optimal usage.

Potential Risks: Some, though not all, studies have raised questions about a potential association between GLP-1RA use and an increased risk of a rare eye condition called nonarteritic anterior ischemic optic neuropathy (NAION).

Combination Treatment: Research indicates that combinations, such as the experimental drug CagriSema, are being investigated for stronger effects, notes diaTribe.

It is essential for patients to consult healthcare providers regarding the management of DPN and the use of these medications.

Glucagon-like peptide-1 receptor agonists reverse nerve morphological abnormalities in diabetic peripheral neuropathy - PubMed

Mar 15, 2024 — According to a study, glucagon-like peptide-1 receptor agonists (GLP-1 RAs) can improve nerve structure in patients with diabetic ...

National Institutes of Health (NIH) | (.gov)

Impact of glucagon-like peptide-1 receptor agonists on axonal ...

Dec 23, 2024 — GLP-1RA therapy improves clinical and neurophysiological outcomes in DPN. Treatment with GLP-1RA may reverse axonal dysfunction by...

View attachment 15000

American Physiological Society Journal

View attachment 15002

Therapeutic Effects of GLP-1 Receptor Agonists and DPP-4 ...

Apr 26, 2025 — Furthermore, GLP-1RAs may facilitate the regeneration of peripheral nerves, providing a dual therapeutic effect of pain relief and...

National Institutes of Health (NIH) | (.gov)

Glucagon-like peptide-1 receptor agonists in neuropathic pain

Jul 1, 2025 — Despite promising preclinical findings, clinical evidence supporting the use of GLP-1RAs for neuropathic pain remains limited [5,6...

View attachment 15001

The Korean Journal of Pain

View attachment 15003

Glucagon-like peptide-1 receptor agonists for the management of diabetic peripheral neuropathy

Jan 18, 2024 — Glucagon-like peptide-1 receptor (GLP-1R) agonists may have neuroprotective effects in diabetic peripheral neuropathy (DPN). DPN i...

Frontiers

GLP-1 agonists: a game changer in pain treatment and addiction

Jul 28, 2025 — These medications act on various parts of the body, including the brain and nervous system. They may reduce inflammation, protect ...

View attachment 15004

National Institutes of Health (NIH) | (.gov)

Trial Testing New GLP-1 Drug To Reduce Pain of Peripheral ...

Nov 17, 2025 — At the moment, there is no cure or disease-modifying treatment for painful diabetes-related peripheral neuropathy, but people can ...

diaTribe

GLP-1 RA Weight Loss Drugs May Carry Untold Ocular Burden

Jul 3, 2025 — 11. Similarly, a systematic review and meta-analysis of 60 randomized controlled trials with 60,077 patients showed that the incid...

View attachment 15006
 
toologic said:
Have you tried any of the Glp-1 and if so, did they work?
I've been taking 2mg of reta for a little over a month and it is definitely working.
 
Good-Heart6425 said:
AI Overview GLP-1 receptor agonists (GLP-1RAs) show potential for treating diabetic peripheral neuropathy (DPN) by

improving nerve structure, function, and alleviating pain, potentially through neuroprotective and anti-inflammatory mechanisms. Studies suggest they may improve nerve size and axonal function, with some evidence showing reversal of nerve damage.

Key Aspects of GLP-1 for DPN:

Positive Effects: Research indicates that GLP-1RAs can lead to improvements in nerve conduction studies, clinical neuropathy scores, and nerve fiber structure, with one study showing 93% of patients had improved nerve size at 3 months.

Mechanisms: These medications may work independently of weight loss, possibly by enhancing

Na+/K+cap N a raised to the positive power / cap K raised to the positive power

-ATPase pump function, reducing inflammation, and protecting nerve cells.

Pain Reduction: Preliminary evidence suggests a significant reduction in peripheral neuropathy pain, according to PubMed .

Current Status: While findings are promising, they are based on smaller studies and preclinical models. Larger, long-term trials are necessary to confirm efficacy and establish optimal usage.

Potential Risks: Some, though not all, studies have raised questions about a potential association between GLP-1RA use and an increased risk of a rare eye condition called nonarteritic anterior ischemic optic neuropathy (NAION).

Combination Treatment: Research indicates that combinations, such as the experimental drug CagriSema, are being investigated for stronger effects, notes diaTribe .

It is essential for patients to consult healthcare providers regarding the management of DPN and the use of these medications.

Glucagon-like peptide-1 receptor agonists reverse nerve morphological abnormalities in diabetic peripheral neuropathy - PubMed

Mar 15, 2024 — According to a study, glucagon-like peptide-1 receptor agonists (GLP-1 RAs) can improve nerve structure in patients with diabetic ...

National Institutes of Health (NIH) | (.gov)

Impact of glucagon-like peptide-1 receptor agonists on axonal ...

Dec 23, 2024 — GLP-1RA therapy improves clinical and neurophysiological outcomes in DPN. Treatment with GLP-1RA may reverse axonal dysfunction by...

View attachment 15000

American Physiological Society Journal

View attachment 15002

Therapeutic Effects of GLP-1 Receptor Agonists and DPP-4 ...

Apr 26, 2025 — Furthermore, GLP-1RAs may facilitate the regeneration of peripheral nerves, providing a dual therapeutic effect of pain relief and...

National Institutes of Health (NIH) | (.gov)

Glucagon-like peptide-1 receptor agonists in neuropathic pain

Jul 1, 2025 — Despite promising preclinical findings, clinical evidence supporting the use of GLP-1RAs for neuropathic pain remains limited [5,6...

View attachment 15001

The Korean Journal of Pain

View attachment 15003

Glucagon-like peptide-1 receptor agonists for the management of diabetic peripheral neuropathy

Jan 18, 2024 — Glucagon-like peptide-1 receptor (GLP-1R) agonists may have neuroprotective effects in diabetic peripheral neuropathy (DPN). DPN i...

Frontiers

GLP-1 agonists: a game changer in pain treatment and addiction

Jul 28, 2025 — These medications act on various parts of the body, including the brain and nervous system. They may reduce inflammation, protect ...

View attachment 15004

National Institutes of Health (NIH) | (.gov)

Trial Testing New GLP-1 Drug To Reduce Pain of Peripheral ...

Nov 17, 2025 — At the moment, there is no cure or disease-modifying treatment for painful diabetes-related peripheral neuropathy, but people can ...

diaTribe

GLP-1 RA Weight Loss Drugs May Carry Untold Ocular Burden

Jul 3, 2025 — 11. Similarly, a systematic review and meta-analysis of 60 randomized controlled trials with 60,077 patients showed that the incid...

View attachment 15006
Please try not to copy and paste walls of text from Ai. Try to summarize what you find out.
 
Good-Heart6425 said:
Humbly apologize for copy/paste above.

It's not just you. It's becoming common, and irritating. I have snarled more than once this week at work "Stop puking AI slop at me. If the solution was something the lying machine had enough understanding of nuance and accuracy to do well, I wouldn't have needed to bother asking you in the first place." It's going to get common enough in time to annoy EVERYBODY, and then we'll all stop doing it, but for now, it's a thing.
 
Regarding the appreciated info on GLPs for peripheral neuropathy, the higher the dose the better it seems, like 8 mg for reta and 10 mg for tirz. Above that, may be diminishing returns (on average) for weight loss, metabolic bloodwork, and other benefits.

As alluded to, cagri may also help, including in different ways for nerve issues, since amylin receptors are throughout the nervous system. ARA-290 is promising for nerve repair based on human studies but requires cycling to prevent unknown long-term effects.

Good-Heart6425 said:
Humbly apologize for copy/paste above.

You can always put in quotes:

Code:

YADA YADA YADA

Chat GPT said:
YADA YADA YADA

which will make any long text just a few lines.
 
Mr.Tired said:
"The cheek-swab genetic test groups people into four basic obesity phenotypes (meaning observable traits): Hungry Gut, Hungry Brain, Emotional Hunger, and Slow Burn. (A person might belong to more than one of these groups.)"

Hungry Brain - Individuals who feel persistently hungry despite eating enough calories.

Hungry Gut - Those who feel full but experience quick returns of hunger due to faster gastric emptying.

Emotional Hunger - People who eat in response to emotional triggers rather than physical hunger.

Slow Burn - Individuals with a lower metabolic rate, making weight maintenance challenging.

Tag yourself, I'm Emotional Hunger all the way to the moon and back.
I think I would be "slow burn" because I don't really eat a lot. I also have a problem with sugar .. even when I don't have a large portion sugar still causes issues.
 
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