Co-Founder and CEO of Cryton Biosciences. Developing therapeutics to stabilize and restore mitochondrial function. https://nitter.cf/t.co/hQWBgkwwCZ

Minneapolis, MN
Joined May 2020
Excited to launch Cryton Biosciences with my friend and co-founder Dr. Vivek Verma @vermabio Every biotech company begins with a specific scientific question; and the answer defines the value it contributes towards human health. Ours is: Can we therapeutically stabilize or enhance mitochondrial function and deliver a clinical benefit? We believe we can. And we are starting with the greatest unmet need: Cancer. More details on specifics will be coming soon. Follow for more updates! crytonbio.com/
UMN startup company @CrytonBio, is advancing a breakthrough technology to enhance mitochondrial function to treat diseases like colorectal cancer. @steffingomes
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America is 250 years old. I've lived here for 17 years..which is about 7% of her entire existence. Wild to think just how young America is, in the context of time. Proud to be an American. HBD to the greatest nation in the world 🇺🇸
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This breakthrough needs to get more attention on this platform. U of M does fantastic research,
Researchers at the University of Minnesota have helped create the world's first synthetic cell that can feed, grow and reproduce. Built entirely from non-living chemical components, SpudCell marks a major breakthrough in biological engineering with the potential to transform medicine, manufacturing and more. twin-cities.umn.edu/news-eve…
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Anosh Steffin Gomes retweeted
In our experiments, ER-positive luminal MCF7 breast cancer cells relied more on mitochondrial ATP production and showed lower lactate production. In contrast, triple-negative MDA-MB-231 cells showed a much higher glycolytic ATP contribution and higher lactate production. This is a key metabolic characteristic because triple-negative breast cancer cells are more aggressive, grow faster, invade more easily and respond less predictably to therapy than ER-positive luminal cells. These data support a central idea: Aggressiveness in cancer is not only genetic as it is also metabolic and lactate production is related to aggressiveness. The more aggressive triple-negative phenotype appears strongly linked to glycolytic dependency and lactate production, while the less aggressive ER-positive luminal phenotype retains a more mitochondrial metabolic profile. pubmed.ncbi.nlm.nih.gov/3699…
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This push back is warranted. I'm all for people living healthy lives. But this fixation on longevity is making people less resilient. The human body is remarkably resilient, just do a few things right, stop worrying and you'll live a very long and healthy life.
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Here's why people can't defend Ivermectin or the "pharma doesn't want cures like Ivermectin, because they'd lose money on other chronic drugs", conspiracy once you understand pharma's business model: here are the facts: 1. Pharma can absolutely repurpose existing compounds, file new patents, get approval and sell (ex. Celgene repurposed Thalidomide into a multi billion $ cancer drug). If old drugs can make money, they will absolutely find a way. The fact that they haven't done so with Ivermectin, says everything you need to know about the drug. 2. Pharma LOVES cures (ex. Hep C drug made Gilead billions). Most diseases are so hard to cure, that's why we treat patients chronically. Pharma doesn't care about chronic vs cures, so long it makes billions. In fact, cures make more business sense because once you cure a patient, your competitors have little incentive to enter that market.
Replying to @ValerieAnne1970
Let's assume what you're claiming is true. Ivermectin, which is mfg by a pharma is really a wonder drug and can treat all diseases, why then has no pharma run RCTs and obtained FDA approval for any of these diseases you claim it treats? Surely it would make them billions?
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Another "mitochondrial health" advice that I can easily call bullshit (these charlatans don't even try hard enough). No, please don't use nicotine (in whatever form) to mitigate "Oxidative stress". You know what can boost your mitochondrial health? Exercise.
-Nicotine is a mitochondrial uncoupler -Increases testosterone and DHT Paired with aspirin and vitamin c cigarettes might actually be beneficial.
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Anosh Steffin Gomes retweeted
Heart disease is the #1 killer. If you’re going to focus on one thing, this is it. My bloodwork is below. ApoB is the North Star metric. Many docs say it’s the only thing that matters. There is 1 ApoB protein attached to each bunch of cholesterol (fat) as it travels through the blood. Know and control this number. My ApoB is in the top 1% of all humans. Under 50 is ideal. Over 70 is bad. Up near 90 or higher and you are on a fast track to heart disease. Average doctor will send you on your way at these numbers and tell you to come back when you have a heart attack. Most won’t even include it in bloodwork. The system is broken. My LDL is top 5%. Over 80 is bad. Over 100 is really bad. My triglycerides are optimal. Under 100 is good. Over 120 or so is bad. But I’m part of the 20% of humans with high Lipo(a). It’s genetic. 49 is very bad and there is nothing I can do about it with diet or lifestyle. This increases risk in all areas. And pharmacology cant impact it. It’s why my heart contrast scan showed plaque buildup already. So what do I do? Hyper focus on the others. Make sure ApoB is very low around 40. Work on LDL and triglycerides more. Workout. Get heart rate up above 120 for 120 minutes or more per week. Zone 2 is great for heart health. I’m fasting for 72 hours 1x a quarter. No calories. This lets my body enter a deep state of autophagy and my good cells eat my bad cells. My body consumes some of the soft plaque on the walls of my arteries. This also helps reduce my cancer risk because my healthy cells eat my B cells and unhealthy cells that are more likely to turn into cancer. I recently started Repatha - peptide that creates more receptors on the outside of my liver that pull these proteins out of my blood. It’s expensive at $550 a month because my insurance won’t cover it. Statins are great options for a lot of people. Cheap and effective. Some side effects. The bottom line: If you don’t know these numbers, you are foolish! Don’t wait until you have a heart problem.
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This is the way. Finally AHA revised guidelines for people to aggressively reduce cholesterol early with statins and other therapeutics. If you're south Asian/Indian descent, get Lp(a) checked ASAP. Anti-statin idiots to come out in 3..2..1.. nytimes.com/2026/03/13/healt…
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Sleep 7–8h Ex 4–5h/wk (strength + cardio) Diet: home-cooked (protein, carbs, veg, fruit) Avoid sugar, alc, smoking Hair: minox Skin: tretinoin + moisturize Sunlight Sauna: 20 min, 4×/wk (if available) Prioritize relationships Do work you love Saved you $1M.
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This is why now is the best time to start a biotech/deep tech co - as I did. High-capex costs are dropping fast. You can do more with less (people and capital). Pace of experiments remains limited by cells' doubling time, but everything else is getting much faster and cheaper.
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There's quite a bit of debate on the topic of statins. As someone on statin therapy, I do have a dog in this fight. Here's a quick account of my personal journey.
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Thanks Dr @LorickFoxPA. He's clearly engagement farming. Spreading misinformation under the guise of "nuance" as an MD is irresponsible. In his recent video, he claims to take 80mg atorva as an N=1 blinded RCT. When I pointed out how asanine it is, he blocked me 😂
Replying to @nicknorwitz
I was one of the investigators for the lovastatin dose ranging trial, so I have been prescribing statins since before they were FDA approved as an investigator. As an Associate of the American College Cardiology (with Certification in Cardiovascular Knowledge (CCK) by the ACC which is a newly offered examination which is as close to a board certification in Cardiology as is available for PA's and NP's) I have been prescribing statins to reduce the risk of heart attack stroke and cardiovascular death as well as progression of all vascular disease, reduce the risk of dementia, and in the case of atorvastatin, reduce the risk of kidney failure related to diabetes (PLANET and PLANET2 trials). The majority of your article is nonsense. At least it's important as any direct effect on cholesterol, the reduction in intra-arterial inflammation is likely the primary reason that statins reduce the risk of acute myocardial infarction because they reduce the risk of plaque rupture which is caused by that inflammation. (this is why the blood test CRP, which is a test for inflammation, is often done as part of cardiovascular risk assessment) There are only three classes of drugs that have been shown to reduce the risk of heart attack, stroke and cardiovascular death (MACE - Major Adverse Cardiovascular Events), as well as reduce the risk of progression of all vascular disease, and reducing the risk of dementia (dementia reduction is proven for the statins, still pending for the latter two below), that are traditionally thought of as "cholesterol reducing" drugs. 1. Statins 2. PSK9i 3. Bempedoic Acid No other drugs that change cholesterol values on lab testing have been shown to make any difference in health with the exception that Zetia, ONLY when added to max dose statin improves outcomes whereas Zetia alone does not Also, GLP-1 and SGLT2 drugs reduce cardiovascular risk regardless if the patient has diabetes. Of all of these, the statins are by far the safest with the least side effects. An anecdote about statins: We found my father dead of his third heart attack at age 52. He had his first at age 36. Paying absolutely no attention to my cholesterol, I started atorvastatin 80 mg a little more than 20 years ago. About seven years ago, I underwent cardiac catheterization for chest pain (turned out to be non-cardiac chest pain) it was essentially clean (had "lump and bumps" consistent with 65). Anecdote only, although I have seen similar results in numerous patients, atorvastatin let me beat genetics. Baychol, the only statin removed from the market (~2002) (numbers are from memory I can't find a reference) for roughly 15 deaths from rhabdomyolysis. Of those 15 deaths, roughly 9 were simultaneously on another drug that they either should not have been on, based on the prescribing literature, or for which day should have been having regular drug lab monitoring, which they weren't). That means that the "most dangerous" statin that had to be pulled from the market, was pulled for 6 deaths and there had been greater than 6 million prescriptions. (I apologize that I do not have hard numbers, but these are in the appropriate order of magnitude) The bottom line is that statins are safe, effective, have a few side effects (and I have never had a patient complain of weight gain with a statin by the way, although that's "only" in some number of thousands of patients in 39 years. ) BTW, The whole point of p values is to determine if something is statistically significant. If the p value says it isn't, then it isn't statistically significant no matter your opinion to the contrary.
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Update: He blocked me 😂so here's the YT link youtube.com/watch?v=s05mUXTc… Clickbait review with a ridiculous proposal to perform an N=1 "blinded randomized placebo-controlled trial" on himself with 80 mg atorvastatin 😂 (more on that below). Link to the mysterious study his "doc friend texted him about" that wasn't referenced anywhere in his video for some reason: tinyurl.com/5epj9tbm Here's the steelman: Per this study, statin users were observed to have a reduction in muscle mass even with high physical activity (PA). Here are the counterpoints: 1. It's NOT an RCT, as claimed in the video. It's a prospective observational study. 2. Major issue: In the statin cohort, the authors admit they don't know the statin type, dose, or duration of treatment prior to study start. 3. He claims even higher physical activity statin users had a steeper decline in muscle mass (true observation in this study) but conveniently omits that grip strength decline was actually lower in the group with high-quality diet or exercise. Finally, on his "proposed N=1" study. @nicknorwitz I'm no doctor, but I don't believe any doctor will prescribe a 20-something with the highest dose lipophilic statin unless they have a compelling reason to do so (severe FH etc). Nonetheless, I can't wait for your findings (sarcasm btw) 😂
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Based on his stupid rationale, here's everything else that's "almost significant" (and there's no such thing like that 😂): Hyperglycaemia Headache Dizziness Insomnia Vision blurred Cough And more. Now ask yourself, why did he pick weight gain? Cheap clicks.
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