How bad is my kidney function? Ok to continue cycle?

Been on a cycle of test + primo + tren at 600, 200, 200 respectively for the past 2 months.

Bloodwork looks good overall but have some borderline kidney markers:

Creatinine 1.35 (slightly elevated)
BUN 14
EGFR 70
Cystatin C 1.1 (slightly elevated)


Was hoping to run the cycle another month -- think it's safe to do? Or should I stop, or at least stop the tren?
 
Did you rest at least 48h before taking the bloodwork? Were you hydrated? Are you taking ancillaries or other supplements?

If it was me, I'd take tren out, and increase test and/or primo. Use a supplement to help with kidney function. And likely drink more water over 5L. Also if you didn't rest at least 48h before bloodwork it can skew those markers
 
Did you rest at least 48h before taking the bloodwork? Were you hydrated? Are you taking ancillaries or other supplements?

If it was me, I'd take tren out, and increase test and/or primo. Use a supplement to help with kidney function. And likely drink more water over 5L. Also if you didn't rest at least 48h before bloodwork it can skew those markers
No I worked out the day prior. I had a little water before the bloodwork but not much because it was a fasted draw very early in the morning (7am)


Ancillaries Im taking are pitavastatin, ezetemibe, telmisartan, fish oil, NAC+ TUDCA
 
Being rehydrated may play a part. Weigh yourself before you go to bed then again in the morning after you take a pee and you will see how much water you lost overnight. My weight can change 2-4 pounds depending on all the factors. So that is 1-2 quarts/liters i need to be rehydrated. How much water do you normally drink? Training does not effect my blood work much but it can for some people. When in doubt take out the tren.
 
Being rehydrated may play a part. Weigh yourself before you go to bed then again in the morning after you take a pee and you will see how much water you lost overnight. My weight can change 2-4 pounds depending on all the factors. So that is 1-2 quarts/liters i need to be rehydrated. How much water do you normally drink? Training does not effect my blood work much but it can for some people. When in doubt take out the tren.


random but brother i’m sorry for calling you a troll weeks ago, you turned out to be right. you were voicing your concern and skepticism of targeting LDL alone, i ignored it and took bempedoic acid + ezetimbe + pitavastatin from 100+ ldl and instantly felt like shit within 1-2 weeks. come to find out the statin blocks production in the brain, and the brain gets most of its cholestrol locally, coq10, vitamin d, etc. cholestrol gets blamed cause it would be giving away power to us if they admitted that it’s several different things, so they just tell us it is this one thing. chatgpt helped me a lot. God bless.
 
random but brother i’m sorry for calling you a troll weeks ago, you turned out to be right. you were voicing your concern and skepticism of targeting LDL alone, i ignored it and took bempedoic acid + ezetimbe + pitavastatin from 100+ ldl and instantly felt like shit within 1-2 weeks. come to find out the statin blocks production in the brain, and the brain gets most of its cholestrol locally, coq10, vitamin d, etc. cholestrol gets blamed cause it would be giving away power to us if they admitted that it’s several different things, so they just tell us it is this one thing. chatgpt helped me a lot. God bless.
I know we're getting off topic but this is interesting-- so you no longer take pita or eze? Because I take both. I'd like to hear @Ghoul thoughts because I think he's the one that got a lot of us on the pita+ eze train haha
 
I know we're getting off topic but this is interesting-- so you no longer take pita or eze? Because I take both. I'd like to hear @Ghoul thoughts because I think he's the one that got a lot of us on the pita+ eze train haha
The other brother didn't specify dosages or timeline. But usually you start with 1 compound, low dose, and start from there. From his post it sounds like he did the 3 at the same time and not low-dosage.
 
random but brother i’m sorry for calling you a troll weeks ago, you turned out to be right. you were voicing your concern and skepticism of targeting LDL alone, i ignored it and took bempedoic acid + ezetimbe + pitavastatin from 100+ ldl and instantly felt like shit within 1-2 weeks. come to find out the statin blocks production in the brain, and the brain gets most of its cholestrol locally, coq10, vitamin d, etc. cholestrol gets blamed cause it would be giving away power to us if they admitted that it’s several different things, so they just tell us it is this one thing. chatgpt helped me a lot. God bless.
That you for the kind words.
The brain makes all is't own cholesterol as the cholesterol molecule is to big to pass the blood brain barrier. But many statins can get through.
Brain shrinkage is associated with with dementia etc.
I am not against statins especially the newer generation ones. I just ask how it affects longevity and all systems in the body and not just the heart. People should self educate in my opinion to make the best choice for them selves.
 
It isn't completely wrong
It is.

It has nothing to do with Pitavastatin like he claimed it did.

Even in those old gen 1 statins where it could happen, less than 1% of people reported brain fog or cognitive issues.



He did not take pita and start "feeling like shit" from his brain being affected. That's idiotic.


> Since there are 32 million Americans on statins the risk of cognitive impairment can be extrapolated to be between 0.1–1% for the entire population taking a statin.
 
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I know we're getting off topic but this is interesting-- so you no longer take pita or eze? Because I take both. I'd like to hear @Ghoul thoughts because I think he's the one that got a lot of us on the pita+ eze train haha
Ghouls apprentice here:
"There are two types of statins either lipophilic like atorvastatin and simvastatin or hydrophilic like rosuvastatin.24 Hydrophilic statins are less cross‐plasma membrane so they have less pleiotropic effects compared to lipophilic statins.24 Of note, statins are also classified according to their nature, either natural like simvastatin and lovastatin, or synthetic like rosuvastatin.24 Natural and synthetic statins have different pharmacokinetic properties but they have similar lipid‐lowering effects. Remarkably, statins lead to a dose‐dependent effect in reducing cholesterol and LDL.25"

Source: Pros and cons for statins use and risk of Parkinson's disease: An updated perspective - PMC

Newever statins don't generally cross the blood brain barrier, and have been shown to reduce Parkinson's Disease by lowering inflammation.

Conclusion of above study:
"PD is the second most common NBD consequent to AD. Statins are the most common lipid‐lowering agents used in the management of dyslipidemia and the prevention of primary and secondary CVD events. Statins are not used in the management of PD, but they are frequently used in the cardiovascular disorders commonly associated with PD in the elderly population. Therefore, the use of statins in that population may affect PD outcomes. Statins have many pleiotropic effects like antioxidant and anti‐inflammatory effects. The possible effects of statins on PD neuropathology are conflicting either protective or harmful on PD neuropathology. As well, there is a controversial point regarding the role of serum lipids in the pathogenesis of PD. In this bargain, as statins reduce serum cholesterol, they may affect the PD neuropathology in bidirectional ways either protective or harmful. The protective role of statins against PD risk is through modulation of inflammatory, lysosomal signaling pathways, and microglia activation. However, long‐term statins therapy for primary or secondary prevention of CVDs may increase PD risk by different mechanisms including reduction of CoQ10. Taken together, according to the recent and updated studies, controversial points still present regarding the short‐ and long‐term effects of statins on PD neuropathology. Therefore, large‐scale prospective and retrospective studies are warranted in this regard to confirm the mechanistic role of statins in PD neuropathology."

 
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