Peps for Gout

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brelynn0330 49732

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My husband gets the absolute worst gout flare ups. Like absolutely crippling. He works with doctors...does the best he cab with diet control but it still happens and puts him out of commission. We have been dabbling in peptide land for a bit now but haven't expanded beyond weight management. Curious if anyone has experience with gout and has found any peptides to help with a gout flare ups.
 
I don't have gout. But here are the peps that I know of that are supposed to help with inflammation:

BPC-157 - aids tissue healing

TB-500 - aids in repair and reduces inflammation

KPV- works to suppress inflammation without suppressing the immune system

GHK-cu - suppresses inflammation signalling

MOTS-c - helps with metabolic dysfunction and systemic inflammation

I'll add that I haven't tried these yet. They're all on my to-do list, though. I'm working through several persistent injuries myself.
 
Is he on Allopurinol or Febuxostat? Either of those is mandatory and life-long drugs for Gout Management.

I have not found a specific peptide to help, but then I have been taking Allo for years, so my flares are very limited anyway.
 
Try one of the GLP-1's in general for inflammation, may be a good place to start. I have read where Gout got better or more manageable for some people (Reddit) but for others it got worse.
 
brelynn0330 said:
My husband gets the absolute worst gout flare ups. Like absolutely crippling. He works with doctors...does the best he cab with diet control but it still happens and puts him out of commission. We have been dabbling in peptide land for a bit now but haven't expanded beyond weight management. Curious if anyone has experience with gout and has found any peptides to help with a gout flare ups.
Is he on Colchicine? Diet makes a big difference. Foods high in quercitin help.

My husband has a condition that is very similar. The flare ups are exactly like gout but can occur anywhere in the body.. I too am interested if any peps might help.
 
brelynn0330 said:
My husband gets the absolute worst gout flare ups. Like absolutely crippling. He works with doctors...does the best he cab with diet control but it still happens and puts him out of commission. We have been dabbling in peptide land for a bit now but haven't expanded beyond weight management. Curious if anyone has experience with gout and has found any peptides to help with a gout flare ups.
I was like your husband for years and they put me on Febuxostat (Uloric). That helped. Allopurinol and Colchicine didn't work for me. I started Reta nine months ago, went off the Febuxostat after a few weeks, and have only had a couple twinges since, easily treated by ibuprofen. Recent research has shown that gout is 90% hereditary and 10% diet. I can thank my father's side of the family. I've also cycled KPV and that helps put out the fire as well.
 
Chili777 said:
I was like your husband for years and they put me on Febuxostat (Uloric). That helped. Allopurinol and Colchicine didn't work for me. I started Reta nine months ago, went off the Febuxostat after a few weeks, and have only had a couple twinges since, easily treated by ibuprofen. Recent research has shown that gout is 90% hereditary and 10% diet. I can thank my father's side of the family. I've also cycled KPV and that helps put out the fire as well.
So Reta really helped, and KPV? Thank you for the information. My husband has been running 2-3 times a week. That has seemed to help him.
 
desinr-gal said:
So Reta really helped, and KPV? Thank you for the information. My husband has been running 2-3 times a week. That has seemed to help him.
Yes, I'm convinced it did. My flares were debilitating and recurring. Not just the big toes, but ankles, wrists and elbows. I was on allopurinol for 20 years and finally started getting hives and welts, so I had to stop. It's only efficacious in 40% of cases, as I found out. Febuxostat stopped most flares, but it was still a 3-4 times a year thing and only Prednisone helped at that point.

When I started Reta, I thought I was flaring for the first 2 weeks but stayed with it, and my joints calmed down again. I started skipping doses to see how I responded and no flares. I finally stopped Febuxostat after a month on Reta and have had next to no occurrences since, and the couple times I did, they were minor and completely stopped by ibuprofen. The deposits (tophi) in my elbows and wrists have shrunk to nothing. I still keep Febuxostat in my cabinet, but it's been untouched since the end of September. Hope this helps.
 
QueenMuntha said:
Is he on Allopurinol or Febuxostat? Either of those is mandatory and life-long drugs for Gout Management.

I have not found a specific peptide to help, but then I have been taking Allo for years, so my flares are very limited anyway.
Yep allopurinol hes been on it a few years now and unfortunately still gets brutal flare ups
 
brelynn0330 said:
Yep allopurinol hes been on it a few years now and unfortunately still gets brutal flare ups
Allopurinol either works or it doesn't. Febuxostat worked for me until Reta, but some people don't tolerate it and it does little during attacks. Prednisone does, but it's nasty stuff. It makes me hangry.
 
Chili777 said:
Yes, I'm convinced it did. My flares were debilitating and recurring. Not just the big toes, but ankles, wrists and elbows. I was on allopurinol for 20 years and finally started getting hives and welts, so I had to stop. It's only efficacious in 40% of cases, as I found out. Febuxostat stopped most flares, but it was still a 3-4 times a year thing and only Prednisone helped at that point.

When I started Reta, I thought I was flaring for the first 2 weeks but stayed with it, and my joints calmed down again. I started skipping doses to see how I responded and no flares. I finally stopped Febuxostat after a month on Reta and have had next to no occurrences since, and the couple times I did, they were minor and completely stopped by ibuprofen. The deposits (tophi) in my elbows and wrists have shrunk to nothing. I still keep Febuxostat in my cabinet, but it's been untouched since the end of September. Hope this helps.
That is fantastic! I am so happy for you! And thank you for sharing this information 💗 💗
 
His Dr may need to adjust dose up. I’m taking 300mg daily and haven’t had a flair up in 20+ years. I hope he finds a solution because that shit hurts baaaad
 
It sounds like the dose of allopurinol is not high enough to decrease uric acid to safe levels, if gout flare ups are still happening. Gout does permanent damage to joints so it is important to stop attacks and high uric acid levels are also a cardiovascular disease risk. The standard approach is to increase dose until uric acid levels are ok.
 
brelynn0330 said:
My husband gets the absolute worst gout flare ups. Like absolutely crippling. He works with doctors...does the best he cab with diet control but it still happens and puts him out of commission. We have been dabbling in peptide land for a bit now but haven't expanded beyond weight management. Curious if anyone has experience with gout and has found any peptides to help with a gout flare ups.
For FUN , A few research peptides (like certain rice-derived or other experimental ones) have shown anti-gout effects in mouse studies, but those aren’t really available for practical use right now. RDP1, RDP2, and RDP3 (Rice-Derived Peptides) isolated from regular white rice ( Oryza sativa ).

These short peptides (around 8-9 amino acids long) have shown strong effects in mouse/rat studies: lowering uric acid by inhibiting xanthine oxidase (like allopurinol does), reducing kidney damage, and calming inflammation from urate crystals.

RDP2 and RDP3 in particular worked on all stages of gout in the studies — both hyperuricemia prevention and acute flare reduction.

R14 — from wild rice ( Oryza minuta ) leaves. It mainly targets the inflammatory response (NLRP3 inflammasome and IL-1β) triggered by gout crystals.

These come from Chinese research groups (published in journals like Journal of Agricultural and Food Chemistry and Food & Function ). They're very promising in animal models but are not available as commercial peptides for human use. They're still in the lab/experimental stage.

Other Experimental Ones:

Some spider venom-derived peptides (like NCTX14 or NCTX15 ).

Certain tuna-derived or other food protein hydrolysate peptides.

Synthetic ones like optimized short versions of the rice peptides (e.g., hexapeptide RDP1-M3).

These are cool science but not practical options in the current peptide gray market. Stick with BPC-157 (and maybe TB-500) if you're exploring peptides for your husband those are what people actually use and report on for gout flare help. The rice ones aren't realistic to source or dose safely right now.

Always loop in his doctor before trying anything.
 
lessthanhalf said:
It sounds like the dose of allopurinol is not high enough to decrease uric acid to safe levels, if gout flare ups are still happening. Gout does permanent damage to joints so it is important to stop attacks and high uric acid levels are also a cardiovascular disease risk. The standard approach is to increase dose until uric acid levels are ok.
At the peak, I was taking as much as 500-800 mg of Allopurinol a day, in a split dose. It was just not effective for me and it's not effective for many people, despite it being the front line medication. It also does nothing for active flares and can actually make a flare worse. My uric acid levels never got above 6.5 and yet I suffered regular attacks. I think Febuxostat is much more effective, but brings its own set of potential side effects. Reta is what finally put an end to it, and it started working before I really started losing weight. I don't think it was just a coincidence.

I do think people should increase their dosage to ensure they are not a non-responder to allopurinol, as high as 500 mg. But if there is no relief, don't waste time on it like I did. Move to Febuxostat to gain some stability, and then consider Reta, especially if weight is a contributing factor. Just my experience.
 
I would still get an occasional flair up even when taking allopurinol and colchine daily. I haven’t had a flair up since starting tirz, even though rapid weight loss can cause flair ups... I can’t say Tirz was the resolution but it certainly helped me start eating better and I have focused on staying hydrated. Hydration is a huge factor.
 
I’m on 300mg Allopurinol daily and I haven’t had a flare up since I went up from 100mg. I never want to feel that again. I couldn’t even go to the bathroom during one flare. I had to pee in a bucket on the side of my bed; literally couldn’t even gently set my foot on the floor; it was terrible.
 
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