#54

I don’t know if Nilotinib is potentially helpful, but… Nilotinib is inexpensive (in many parts of the world… 120 rupees to the US$):

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#55

Thanks, I didn’t know. 50 mg/kg in rats: Quercetin administration abrogates the Parkinson’s disease (PD)-like motor and non-motor symptoms and attenuates the behavioral, neurochemical and biochemical deficits induced by rotenone toxicity in rats - MDS Abstracts

Unclear benefits per this poll though: Nutrients | Free Full-Text | Parkinson Symptom Severity and Use of Nutraceuticals

(but probably low risk as well, so good bet?)

I haven’t read everything yet, but: “Their re-examination points towards some results suggesting positive effects, but these findings will require further investigation. A parallel clinical trial of nilotinib (supported by Cure Parkinson’s and Van Andel Institute) did not find the same results and indicated that the drug was insufficiently accessing the brain. […] It is important to understand that these studies involve re-analysing data in a biased fashion – searching results for any interesting correlations or effects, and as such, these investigations should be considered as ‘hypothesis generating’ exercises. Researchers use these sorts of analyses to find new ideas for experiments that can then be tested, and further research will be required before isradipine or nilotinib can be re-examined in people with Parkinson’s.” ( Post-hoc analyses of the isradipine and nilotinib trial results - Cure Parkinson's ).

What’s the relationship between quercetin and nilotinib/dasatinib btw?

If you’re already taking lithium, then you may need to change your dosage if you start an SGLT2i (see: Starting empagliflozin or dapagliflozin in patients on lithium? Monitor lithium levels )

What’s your current lithium dose? This trial suggests 30-45mg/day, “slowly titrated in each patient up to the maximum tolerated dosage in this range”: CTG Labs - NCBI

Regarding Nilotinib, I guess we’ll soon get the results of this trial, which may help you to make a decision: CTG Labs - NCBI

Also: have you checked your blood pressure? (see thread: Pressão arterial ideal que devemos atingir? Sistólica abaixo de 110 ou 100? ) I wonder whether lowering mean BP AND BP variability can decrease PD risk (for instance with an ARB/sartan or a dihydropyridine calcium channel blockers like isradipine).

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#56

Quercitin and nilotinib (plus like a million other things I guess) are senolytics, and somewhere I read about “synergistic cytotoxicity” which maybe was meant to be good but sounded a bit scary to me. I’m a little protective of my brain cells. But really, I don’t know. These articles quickly soar over my head.

I DO take lithium, although my doctor for some reason is terrified of it (actually, he is convinced it causes tremor) so I only take 5mg a day. I wouldn’t mind titrating up–think I’ll look up signs of maxing out. Thx!

Yes, I eagerly follow all the trials, particularly the repurposed drug trials. Wish results came faster!

Parkies tend to run low blood pressure, and I am no exception, generally running like 110/65 or so. Maybe it’s one bright spot in an otherwise grim landscape :o)

#57

Your doctor is right, but as far as I can determine it’s only at prescribed therapeutic levels.

Does your doctor know that the doses of lithium we are taking in the form of lithium orotate are much much lower than commonly prescribed?

I have been taking lithium orotate for over two decades at doses from 5 - 15 mg of elemental lithium.

As I reported previously, I had started to develop what I believed were age-related "essential tremors. I did not associate the tremors with the lithium supplement. But, who knows?
A few weeks after I started rapamycin my tremors went away and I have been free of them since. I was not aware that lithium was a probable cause as I developed tremors when I was about 78 yrs. old.

“The available evidence suggests higher lithium doses and plasma levels are associated with an increased risk of developing lithium tremor, implying a dose-response relationship”

“Tremor was related to higher doses, to higher concentrations, and to higher gradients of lithium in plasma”

“Lithium tremor revisited: pathophysiology and treatment”
https://sci-hub.se/10.1111/acps.12171

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#58

I take 1 mg of lithium orotate daily. It seems to be a good microdose. Lithium is also synergistic with Rapamycin. Supposedly it cancels Rapa’s lipid effects. Maybe I need to dose higher?

http://www.pnas.org/doi/10.1073/pnas.1913212116

However, the study is done in flies, which is never 100% translatable. So, here’s hoping.

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#59

Yes it’s frustrating how slow trial results come out. You can often get them faster by contacting the authors. For instance the results of this trial are not yet out ( Risk Reduction for Alzheimer's Disease - Full Text View - ClinicalTrials.gov ) but the author told me that it failed: 2y of intensive BP control with losartan and amlodipine + physical exercise did not improve cognitive performance.

Yes I’m aware of the hypotension risk in PD but I’d still look at BP, especially continuously over a day or week (for instance with a device like Aktiia) because:

  1. Hypertension in mid-life may be a risk factor for PD later in life: Hypertension and Diagnosis of Parkinson’s Disease: A Meta-Analysis of Cohort Studies - PMC
  2. Some antihypertensive drugs are considered as potential repurposed treatments for PD (namely CCBs like isradipine and ARBs like candesartan/telmisartan)
  3. Blood pressure variability (BPV, aka the variations during the day and week) seem to matter more than the mean for neurological diseases. Maybe you spend a lot of time during the day in hypotension and/or hypertension and don’t know it. And it seems that CBBs and ARBs can “smooth” the BP (without reducing it too much at low doses). See: Blood pressure variability: methodological aspects, clinical relevance and practical indications for management - a European Society of Hypertension position paper 2023
  4. Knowledge is power.
  5. It may be useful to detect and manage orthostatic hypotension: Smartwatch May Help Parkinson’s Patients Manage Blood Pressure Drops

Regarding telmisartan/candesartan, see as well: The Endotoxin Hypothesis of Parkinson’s Disease 2023:

If LPS contributes to PD, then a number of possible therapeutic strategies could be considered for further evaluation in clinical trials as outlined below. However, if LPS is elevated in only a subset of PD, patient stratification would be essential for targeting the most appropriate patients. Monitoring of blood LPS levels in such trials would provide important validation of the mechanistic principle, alongside clinical efficacy measures. […] (4) Blocking LPS receptors. Candesartan, an existing drug licensed for the treatment of hypertension, has been shown to reduce TLR4 expression and activity, is expected to cross the BBB, and has a good safety profile, making it an attractive candidate for repurposing in Parkinson’s disease.

Does anyone know how to test for serum LPS?

I’m also curious:

  • Are there things that you tried but stopped because they did not seem to work or had bad side effects?
  • Among all your interventions, if you had to keep only one, which one would it be?
  • Have you considered selegiline/deprenyl at a low dose? (it may protect the BBB from LPS, see: Anyone taking Selegiline / Deprenyl For Longevity? - #55 by Vulcan )
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#60

Also, what about your LDL levels and have you considered statins? @Joseph_Lavelle wrote recently:

ldl picks up the LPS which is then cleared from the body when the ldl is picked up by the liver. Statins make the liver produce more ldl receptors to remove ldl from the bloodstream. This is why ldl measurements decrease and how the lps gets taken out. So, statins help with removal of lps, according to Krause.

I don’t know if the above is correct but the use of cholesterol-lowering drugs is associated with decreased risk for PD:

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However, “other observations suggest that statin therapy may increase PD risk by diverse mechanisms including reduction of CoQ10. In conclusion, there are strong controversies regarding the protective role of statins in PD neuropathology.”

There was one successful clinical trial of lovastatin: A Double-Blind, Randomized, Controlled Trial of Lovastatin in Early-Stage Parkinson’s Disease 2021

Lovastatin 80 mg/day or placebo with 1:1 randomization was administered for 48 weeks. […] Lovastatin treatment in patients with early-stage PD was associated with a trend of less motor symptom worsening and was well tolerated.

And one failed of simvastatin: Evaluation of Simvastatin as a Disease-Modifying Treatment for Patients With Parkinson Disease: A Randomized Clinical Trial 2022

1-month phase of simvastatin, 40 mg daily, followed by 23 months of simvastatin, 80 mg daily, before a 2-month washout period […] In this randomized clinical trial, simvastatin was futile as a disease-modifying therapy in patients with PD of moderate severity, providing no evidence to support proceeding to a phase 3 trial.

So maybe statins are only symptomatic and not DMT.

There’s an ongoing study to see if statins can prevent Levodopa Induced Dyskinesia: Preventing Levodopa Induced Dyskinesia in Parkinson’s Disease With HMG-CoA Reductase Inhibitors (STAT-PD)

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#61

Sorry for the 3rd post in a row but wow… I’ve just checked the supplemental material of the just published Association of cardiovascular disease management drugs with Lewy body dementia: a case–control study and table S5 shows that the 4th best-performing drug to prevent Lewy body dementia is… the immunosuppressant Tacrolimus! With a 1y OR of 0.46 [0.32-0.59]. Tacrolimus is not in their 3y model, but the 9th most performing in the 3y model is another immunosuppressant currently tested in the ITP: Methotrexate. This is surprisingly not mentioned in the paper itself.

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#62

I know, lithium causes tremors, but I think you’re right–more at the doses used to treat bipolar disorder, which is grams a day. The dose makes the poison, eh?

The problem is, my doctor thinks I’m nuts (you’re taking rapamycin!? That’s a dangerous cancer drug! You’re using exenatide!? It has side effects! ) so I have trouble getting him to listen to anything.

You know, having Parkinson’s has side effects. Growing old has side effects. We choose which ones WE want to risk.

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#63

Ooof. You ask hard questions.

Let’s see–I did try the whole NAC NMN thing, and I’m ashamed to say part of the reason I leapt on the Peter-Attia-It-Doesn’t-Cross-The-BBB-anyway conclusion was because I didn’t like the pills: they were big and smelled terrible.

Metformin. Also read along the way there wasn’t a lot of point. Also read some stuff about metformin vs. exercise…and I exercise like a crazy person.

Mannitol. There were some iffy, non-placebo controlled positive-ish results that I ultimately decided I didn’t buy.

Tryptophan–because I listened to a far-out theory by Dr. Jonathan Sackner-Bernstein and I’ll try anything. In a nutshell, he believes PD is lack of dopamine transport, not lack of dopamine. Since dopamine is toxic (thus killing their overstuffed neurons) he thinks the fix is to block synthesis. Ha. I felt awful pretty quickly.

Just FYI: Venglustat. I was in the Sanofi/Genzyme study, NOT on placebo, for nearly the full three years, before the study was stopped.

I take Azilect, which was all the neuroprotective rage when I was diagnosed. I know it’s kind of fallen out of favor. I’ve debated switching to seligiline.

Here’s what I think in general though: any treatment for the cause of PD (as opposed to the symptoms) isn’t gonna make you feel miraculously better. It’s going to keep neurons from dying, or maybe nurture baby ones, and I’m not convinced that’ll be detectable on a day-to-day basis.

If something makes you feel different overnight, to me it screams placebo.

I am musing on what I wouldn’t give up. I didn’t even MENTION my keto diet, or hot tub/cold pool, or exercise, or non-negotiable sleep routine. You see?

BTW I’ve had PD for 10 years.

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#64

Thanks for your detailed answer! What about non-motor symptoms like sleep and depression? (besides diet, hot/cold tub, exercise and sleep hygiene) (for the context: I’m interested in PD because I have a high polygenic PD & DLB risk…)

I agree. I’m getting more and more optimistic though. For instance, when I see the cognitive and gait improvement in this study with empagliflozin: Canagliflozin - Another Top Anti-aging Drug - #363 by adssx

I asked Cure Parkinson’s UK whether they were considering empagliflozin and they’ve just answered:

Empagliflozin came in 3rd place at last summer’s iLCT meeting. The committee are very keen to see it progress to clinical trial in PD and suggested that a small Phase 1b biomarker study exploring target engagement and confirming brain penetrance in a PD cohort would be useful. But there were concerns around what target engagement looks like in PD. So there were suggestions that more preclinical work required on potential mechanisms of action. Empagliflozin has only been preclinically tested in neurotoxin models of PD, so the committee felt that there was a need for testing in a synuclein model. In terms of costings, the preclinical work is probably £200K, while Phase 1b would be ~£500K.

If anyone wants to contribute, here’s how to donate (there are tax-efficient ways to donate for US and UK taxpayers) :hugs: (feel free to DM me as well, I can put you in touch with the Cure PD team)

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#65

Well, I think you might have snuck into my house and gone through my cabinets.

Yes, I take Simvastatin. My cholesterol levels were pretty high, probably because I eat keto, and I have been eating keto since my diagnosis. (The statin works though–my levels are good now.) And, because of the statin I also take coQ10.

And thinking on it, you asked about the one thing I would not give up and I would probably say that: my diet. Also, before rapamycin I used to do four-day fasts. I still practice time-restricted eating, sometimes OMAD. And now I take Acarbose, which allows me to cheat a little…berries and such. I wear a CGM, not all the time, but enough to have a sense of what I can eat.

For whatever reason, I have been VERY lucky: I sleep well, and I am not particularly depressed. My right arm is stiff, and when I am nervous, my right hand shakes. Of course I get instantly nervous whenever I want to show someone how unaffected I am.

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#66

Interesting that you have a “pure” motor PD subtype. I wonder whether it’s different to treat.

If you’re on a keto diet and often fast then SGLT2 might be counter indicated because of the DKA risk.

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#67

I don’t understand how ambroxol may work in PD. It looks like ambroxol inhibits autophagy :thinking: Effects of ambroxol on the autophagy-lysosome pathway and mitochondria in primary cortical neurons 2018:

This was not expected as ambroxol has been shown to increase macroautophagy in human neuronal cells containing GBA1 mutations. The lower dose or different type of neuron might account for the discrepancy. […] The mechanism by which TFEB is activated following ambroxol treatment in mouse cortical neurons requires further investigation. For example, is it a compensatory mechanism due to the inhibition of macroautophagy following ambroxol treatment?

This 2023 study also showed a HIGHER risk of Parkinson’s following ambroxol use at the normal dose of 90 mg/day (vs. about 10x more in the PD trials): Association Between Ambroxol at the Usual Dose and the Risk of Parkinson’s Disease in Chronic Lung Disease

Any idea @momgotshocked?

High-dose NR looks interesting, higher doses may be needed if it does not cross the BBB well?

  • Vitamin B3 supplement shows early promise for Parkinson’s 2022: “1000mg of nicotinamide riboside daily for 30 days […] The supplement also showed promising signs that it may improve metabolism and reduce inflammation in the brain, which could have protective effects in the brain. And the participants who showed the greatest increase in NAD levels also showed some mild improvements in their Parkinson’s symptoms.”
  • NR-SAFE: a randomized, double-blind safety trial of high dose nicotinamide riboside in Parkinson’s disease 2023: “NR 1500 mg twice daily […] The trial met all prespecified outcomes. NR therapy was well tolerated with no moderate or severe adverse events, and no significant difference in mild adverse events. NR therapy was associated with clinical improvement of total MDS-UPDRS scores. However, this change was also associated with a shorter interval since the last levodopa dose. NR greatly augmented the blood NAD metabolome with up to 5-fold increase in blood NAD+ levels.”

It also ranked near the top in Mischley’s survey: Parkinson Symptom Severity and Use of Nutraceuticals (“NAD+ or its precursors”)

There are two ongoing trials, ending in December 2024, so results expected next year:

Nicotinamide riboside failed in the ITP in 2016 (1000 ppm, started at 8 mo, 1000 ppm for mice means about 1,400 mg for a 60 kg human if I’m not wrong). However, interestingly, the ITP still decided to test NR again in 2022, this time in a higher dose of 2400 ppm (so about 3,333 mg for a 60 kg human) and combined with metformin. I don’t know what their reasoning was, but there might be something here for PD in glycemic control (with low-dose metformin, GLP1RA, or SGLT2, probably to protect the neurons?) + NR (to promote neurogenesis?).

@TomParkinson: I think you’ve been testing high-dose NR for a few weeks, how is it going?

I wonder what else could promote neurogenesis, some ideas:

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#68

The initial theory about ambroxol (as far as I know) was that it only acted as a chaperone for missing/improperly-folded glucocerebrosidase. Glucocerebrosidase helps to digest particular sugars in the lysosomal membrane when it inverts and forms little vesicles of cellular garbage for digestion. If the vesicles aren’t digested, the lysosomes eventually fill up with their own membrane bits–no room left for anything else. It sure sounds like ambroxol would improve macroautophagy, doesn’t it?

And there seemed to be some evidence that many people with PD have low G-Case levels, whether or not they have a GBA mutation. I’m not sure I would bother if I didn’t, though.

BUT, just recently I read that ambroxol does something else, at the mitochondrial level. I think Simon Stott wrote an article on it in Science of Parkinson’s. I need to dig that paper up. And yes, if it’s a dose thing, I take over a gram a day.

I wish I knew…

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#69

Indeed, thanks for mentioning it, I hadn’t read it: Just a lysosomal enzyme… – The Science of Parkinson's

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#70

New seminal paper reporting immunological shifts during early-stage PD: Immunological shifts during early-stage Parkinson’s disease identified with DNA methylation data on longitudinally collected blood samples 2024

Additionally, we noted previously unrecognized decreases in the naive B cell compartment in the defined PD and Prod patient group. Over time, we observed the proportion of innate immune cells in PD blood increased, but the proportion of adaptive immune cells decreased. We identified decreases in T and B cell subsets associated with REM sleep disturbances and early cognitive decline. […] Neutrophils can increase the permeability of the blood-brain barrier (BBB), giving all immune cells increased access to the CNS […] Comparing PD to HC, we found an increase in neutrophils and a decrease in monocytes and eosinophils. In PD patients, there is an increase in neutrophils and monocytes over time, with a consistent trend in the Prod group as well. We observed a slight decrease in monocytes in more symptomatic PD patients. […] We identified a strong decrease in CD4+ memory T cells and naive B cells in clinically defined and prodromal PD. In PD patients, we see a significant decrease in many adaptive immune cell populations over time, including all naive lymphocytes and memory T cells. In the prodromal group, there is a significant decrease in the naïve lymphocytes but not a significant trend in the memory compartments.

How can rapamycin impact the above? I checked a bit on the forum and most users report no changes in blood measures of neutrophils, lymphocytes, monocytes, eosinophils & basophils. (e.g., Concerns about immune suppression - #9 by RapAdmin ).

However, the most important finding in this paper seems to be the “strong decrease in CD4+ memory T cells and naive B cells” and these are hard to find according to @RapAdmin: Using HBA1C and LDL to Determine Ideal Rapamycin Dosage - #84 by RapAdmin

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#71

Another study found a similar result: Association Between Use of Any of the Drugs Prescribed in Norway and the Subsequent Risk of Parkinson Disease 2023

Of the 10 classes related to a lower risk of PD, there were 2 classes associated with a reduced PD risk of 30% or more, which were other nervous system drugs (N07) and antineoplastic drugs (L01). […] Similarly, the lower previous use of antineoplastic drugs (L01) among PD cases might also be related to a lower risk of smoking-related cancers in this group.

The L01 category features the usual suspects: ATC code L01 - Wikipedia

  • L01BA Folic acid analogues such as methotrexate (currently tested in the ITP)
  • L01EA BCR-ABL tyrosine kinase inhibitors such as dasatinib, nilotinib, and bosutinib
  • L01EG Mammalian target of rapamycin (mTOR) kinase inhibitors (temsirolimus, everolimus, ridaforolimus, and sirolimus)
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#72

I’ve recently looked in the forum for data re: neutrophils because mine are elevated (not the absolute count but the %). In my case that’s because of a near chronic bladder infection I’ve been dealing with and only recently identified as such (the symptoms were UTI after UTI after UTI which basically means it never went away). In any case I looked specifically for that metric as I’m thinking more in terms of forensic clues for myself.

And rapa users are reporting DECREASED neutrophils while on rapa. This is anecdotal but I did hunt out pretty extensively on the forum and it seemed to be clearly a trend.

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#73

Continuation of lipophilic statins like atorvastatin is associated with decreased risk of Parkinson’s:

Results: Among the 43,810 statin initiators, the incidence rate for PD was 1.68 and 3.52 per 1,000,000 person-days for lipophilic and hydrophilic statins, respectively. Continuation of lipophilic statins was associated with a decreased risk of PD (hazard ratio [HR] 0.42 [95% confidence interval 0.27–0.64]) as compared with statin discontinuation, which was not modified by comorbidities or medications. There was no association between hydrophilic statins and occurrence of PD. Among lipophilic statins, a significant association was observed for simvastatin (HR 0.23 [0.07–0.73]) and atorvastatin (HR 0.33 [0.17–0.65]), especially in female users (HR 0.11 [0.02–0.80] for simvastatin; HR 0.24 [0.09–0.64] for atorvastatin). As for atorvastatin users, the beneficial effect was seen in the elderly subgroup (HR 0.42 [0.21–0.87]). However, long-term use of statins, either lipophilic or hydrophilic, was not significantly associated with PD in a dose/duration-response relation.

lee2013.pdf (268.2 KB)

Our study provides evidence that statins, especially atorvastatin, can reduce the risk of PD.

Possible prevention but not treatment?

This study suggests that statin use may have a detrimental effect on baseline nigrostriatal dopamine degeneration and long-term outcomes in patients with Parkinson’s disease.

Yeah, probably doesn’t work for treatment…

Findings In this randomized clinical trial, a double-blind, parallel-group, placebo-controlled futility trial involving 235 participants from 23 sites within the UK, participants in the simvastatin group had an additional deterioration in Movement Disorder Society Unified Parkinson Disease Rating Scale part III scores while not taking medication at 24 months compared with those in the placebo group (−1.52 points).

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