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Saturday, 27 December 2025

There’s nothing boring about boron – why 3mg of boron should be in multivitamins and some could take 6-10mg

 


Contents of a common multivitamin for adults


I wrote this post a while back and, the more I think about it, the more I see boron as a potentially useful autism therapy. It is safe, OTC, very cheap and has several mechanisms that should be beneficial. Notably, it reduces inflammation (CRP can fall as much as 50% in 10 days) and it increases estrogen receptor beta signaling (relevant to the brain and bones); both these factors are very relevant in severe autism. It has no effect on estrogen receptor alpha, so avoids the side effects of phytoestrogens and estradiol. I started taking it myself.

Believe it or not, even with a strange subject like boron, there is an autism angle.

I originally stumbled upon boron while researching bone metabolism. I expected it to be relevant only for bones and joint pain. Instead, I was surprised by the sheer breadth of its biological effects: inflammation, hormones, detoxification, memory, immunity, even cancer risk.

Boron is one of those nutrients that no one thinks about because it has not yet been officially classified as essential for humans. That means:

·         No recommended daily intake

·         Almost no multivitamin includes it

·         Most people are taking in less than 1 mg/day through diet

And yet clinically meaningful benefits only begin at least 3 mg/day.

This is especially relevant to people with restricted diets. Many autistic individuals eat the infamous “beige diet” of pasta, bread, chips/crisps, and nuggets. Telling them that avocados contain boron or that leafy greens contain manganese goes nowhere.

Even Monty, now 22, who eats very well, does not reach 3 mg/day of boron from food. He would need to drink half a bottle of high-boron Pinot Noir a day to get close!  

This post has some of the science at the back as non-essential reading.

If you are male, make sure to read the part about male hormones. It looks like a potentially good way to avoid benign prostate enlargement as you age. Prostate size was reduced by about 35% in those with high boron in their drinking water. Not surprisingly, this potential therapy has not been seriously followed up.

If you are female take a note of the female hormone effects.

 

What Boron Actually Does

From the open-access paper Nothing Boring About Boron just click on it to read the full paper


Boron influences multiple systems simultaneously. Benefits documented at 3+ mg/day include:

1. Bone health

·  Essential for bone growth and mineralization

·  Improves calcium and magnesium use

·  Synergistic with vitamin D and estrogen

2. Collagen health (Joints, bone matrix, intervertebral discs, eyes etc)

Remarkably, studies show that adults with a high boron intake seem protected from getting osteoarthritis in later life. Boron is even therapeutic in people who already have this type of arthritis. 

·   Boron improves collagen cross-linking, making fibres stronger, more elastic, and more resistant to breakdown.

·   Enhances vitamin D and magnesium biochemistry, both required for hydroxylating proline/lysine — the two amino acids that give collagen structural strength.

·   Reduces collagen-degrading enzymes (MMP-2 and MMP-9), protecting connective tissue from inflammatory destruction.

·   Boosts bone collagen quality, improving bone strength independently of calcium intake.

·   Supports joint cartilage and reduces arthritis symptoms, likely via improved collagen structure and reduced inflammation.

·   May slow collagen degeneration in the vitreous, explaining why boron sometimes helps with eye floaters.

3. Hormone regulation

·  Increases free testosterone in men

·  Normalizes estrogen metabolism in women

·  Enhances vitamin D activation

·  Reduces SHBG (sex hormone–binding globulin)

4. Anti-inflammatory effects

·  Reduces CRP, TNF-α, IL-6

·  Lowers oxidative stress

·  Raises glutathione peroxidase, catalase, and SOD

5. Detoxification

·   Reduces toxicity of heavy metals

·    Mitigates pesticide-induced oxidative stress

·    Improves cell membrane stability

6. Brain health

·    Improves electrical activity in the brain

·    Enhances short-term memory

·    Supports NAD⁺ and SAM-e pathways

·    Has neuroprotective properties

7. Anti-cancer activity

·     Signals against prostate, breast, lung cancer

·     Reduces tumor growth in models

·     Enhances chemotherapy efficacy

·     Protects normal tissue from chemo damage

Across dozens of studies these effects do not appear at <3 mg/day.

Safety is extremely high, with an upper limit of 20 mg/day for adults.

Boron and Autism — Small Study, Big Signal

A 2024 study examined boron in a rat autism model induced by propionic acid (PPA). 

Effects of Boron on Learning and Behavioral Disorders in Rat Autism Model Induced by Intracerebroventricular Propionic Acid

This model replicates:

·   neuroinflammation

·   microglial activation

·   elevated cytokines

·   reduced Purkinje cells

·   learning/social behaviour deficits

·   increased BDNF (a maladaptive elevation)

What 4 mg/kg boron (boric acid) did:

  • improved learning and social interaction
  • significantly lowered TNF-α, IL-6, IL-1β
  • reduced microglial & astrocyte activation
  • restored Purkinje cell numbers
  • normalised BDNF
  • provided broad neuroprotection

This lines up with boron’s known biology:

  • anti-inflammatory
  • antioxidant
  • mitochondrial support
  • hormone modulation
  • detoxification
  • microglial regulation

This does not mean boron is a cure for autism, but it clearly has biological relevance.

Given the low cost, excellent safety, and widespread deficiency, 3+ mg/day makes sense for most people, especially those with restrictive diets or systemic inflammation.

Boron and Hormones — Very Interesting Male vs Female Effects

Boron’s effect on hormones is surprisingly strong and well documented. This is where things get very interesting because the effects differ between men and women.

In Men: Free Testosterone Booster

Studies show that 6 mg/day of boron for 1 week:

  • free testosterone by 25%
  • estradiol by 50%
  • SHBG (sex hormone-binding globulin)
  • inflammatory markers (CRP dropped by 60%)

Why does this matter?

Reduced SHBG means more biologically active testosterone. This is not like taking steroids; it is allowing your existing testosterone to circulate freely.

Results seen:

  • increased libido
  • improved mood
  • better energy
  • increased muscle response to training
  • reduced inflammation
  • possibly lower prostate cancer risk 

There was a Turkish observational study (from the 1990s, often cited in boron research summaries) looking at a village with very high natural boron levels in soil and drinking water.

Men in this village consumed boron intakes around 6–30 mg/day (far above typical Western intake of 1 mg/day).

Compared with men from nearby normal-boron areas, they had:

·         Significantly smaller prostate volumes

·         Lower PSA levels

·         Lower rates of prostate enlargement (BPH)

No increase in adverse effects was detected in these high-boron consumers.

Boron has several effects relevant to prostate size:

·         Lowers inflammation (↓ NF-κB, ↓ cytokines)

·         Improves androgen–estrogen balance

·         Mild increase in free testosterone

·         Mild decrease in estradiol

This combination tends to lead to smaller prostates and lower PSA, especially in older men.

Does This Apply to Supplement Use?

Probably, but not to the same magnitude unless the dosage is comparable.

BORON SUPPLEMENT EFFECTS:

3 mg/day → measurable anti-inflammatory and hormonal effects

6–10 mg/day → stronger hormonal shift

10–12 mg/day → studied in athletes for testosterone effects

Does this explain why boron helps older men?

Yes. Older men typically develop:

·         Low free testosterone

·         Higher estradiol

·         Chronic prostate inflammation

Boron improves those three issues at once.

 

In Women: Estrogen Metabolism & Menopause Support

Boron helps women balance estrogen in a very different way:

·         increases estrogen when estrogen is too low

·         reduces “bad” estrogen metabolites (16α-hydroxyestrone)

·         increases “good” metabolites (2-hydroxyestrone)

·         improves response to vitamin D

·         reduces menstrual pain

·         supports bone density after menopause

In post-menopausal women:

·         urine calcium loss drops dramatically

·         vitamin D activation improves

·         bone turnover markers improve

Women deficient in magnesium or vitamin D benefit especially.

Why the Sex Difference?

Boron seems to act primarily by:

·    lowering SHBG (men see a larger effect), Sex Hormone–Binding Globulin is a protein made in the liver that binds tightly to sex hormones, mainly Testosterone, Dihydrotestosterone (DHT) and Estradiol

·    shifting estrogen metabolites (women see a larger effect)

·    enhancing vitamin D activation (beneficial for all)

·    reducing inflammation (universally helpful)

This dual effect is rare—few minerals have male/female divergence.

Boron-Rich Foods and Typical Intake Levels

Food

Boron (mg per 100 g)

Notes

Avocado

2.1 mg

One of the richest natural sources

Raisins

2.5 mg

Dried fruit is consistently high

Prunes

1.9 mg

Very dense source

Almonds

2.8 mg

Nuts are excellent

Hazelnuts

2.7 mg

Similar to almonds

Peanuts

1.4 mg

Lower but common

Peanut butter

1.9 mg

Higher concentration

Beans (various)

0.5–1.5 mg

Good but variable

Chickpeas

0.7 mg

Decent source

Lentils

0.7 mg

Regular intake helps

Dates

1.1 mg

Very effective

Red wine

0.5–0.7 mg per glass

Grapes are boron-rich

Apples

0.3 mg

Everyday source

Pears

0.4 mg

Another fruit source

Vegetables (general)

0.1–0.6 mg

Depends on soil content

Typical Daily Intake From Diet

·         Developed countries average 0.8–1.4 mg/day

·         Mediterranean diet: 2–3 mg/day

·         Vegan diets: 3–6 mg/day (high fruit/nut consumption)

Nearly all Western omnivorous diets fall below the 3 mg/day threshold associated with documented benefits.

Conlusion

Boron is one of the few nutrients where:

·         the safety is high

·         the benefits are large

·         the deficiency is common

·         the cost is trivial

And because modern diets (and nearly all multivitamins) provide little to none, 3 mg/day is a simple, evidence-based upgrade for anyone—especially those with osteopenia, inflammation, hormonal imbalance, or restrictive diets such as those often seen in autism.

Higher doses like 10mg would seem appropriate for specific groups that are likely to benefit from the effects described in this post.

How much boron did they give the rats with autism?

One thing you very quickly learn when reading animal studies is that the dose used in rats is almost always huge. The same is true in the recent study looking at boron in a propionic-acid model of autism. On paper, the researchers used “2 mg/kg and 4 mg/kg of boric acid.” That sounds modest, rats are small.

In toxicology, a rat “mg/kg” is not the same as a human “mg/kg.” Rats have a much faster metabolism, and their surface-area-to-body-weight ratio is different. If you dose a human the same way you dose a rat, you will rapidly enter “please call poison control” territory.

To make sense of rodent studies, you have to convert the dose using the FDA’s body-surface-area formula. When you do that, the “4 mg/kg” rat dose becomes roughly the human equivalent of:

45 mg/day of boric acid

which equals 7–8 mg of elemental boron, a dose that’s above normal diet but within the range of commercially available supplements.

But, that is a conservative conversion. There are other conversion models that give an equivalent human dose much higher, in the 35-80 mg/day range.

In reality, nobody knows the human dose that would give the same benefits as found in the rat study. Those rats with autism were essentially on very high pharmacological boron, not the gentle nutritional 3 mg/day found in health-food circles.

No wonder the effects were dramatic:

·         inflammation markers (IL-6, IL-1β, TNF-α) crashed

·         microglia and astrocytes calmed down

·         Purkinje cell loss reversed

·         learning and social behaviours improved

All good news — just not at “one avocado per day” boron levels.This is the same situation as resveratrol, curcumin, sulforaphane, luteolin, quercetin, and a dozen other compounds: the rodent study shows us mechanism and potential, but not a directly usable human dose. Still, what is remarkable is that even at low human doses (3–10 mg/day), boron does show measurable changes in humans: reduced inflammation, altered SHBG, higher free testosterone, better vitamin D handling, and nicer bone and joint metabolism.

So the take-home message is that the autism rat study used a boron dose equivalent to well above what humans safely take as a supplement — but it confirms that boron is a potent anti-inflammatory and neuroprotective micronutrient, and that even low doses may be biologically meaningful.

Perfectly reasonable to include boron in a multivitamin. It would save people a lot of bother.

Not reasonable to copy rat dosing, unless you happen to be a rat!





24 comments:

  1. Hope you had a nice Christmas break and Happy New Year to you and your family.

    Thank you for this post.As a women going through Peri Menopause I am hoping this will help alleviate. Will add it to my list.

    For a 6 year old boy and women in 40s shall I take Solgar 3MG Boron?
    Can you recommend the one uou are taking?

    ReplyDelete
    Replies
    1. Gabbana, look for supplements that contain Calcium Fructoborate or
      Boron Glycinate, Citrate, or Aspartate.

      I think it is best to stay well clear of the upper safe limits that are stated at 20mg for you and 6mg for your son. But you want a dose high enough to actually do something good.

      I would try 3mg for your son and 6mg for you. I myself am taking 10mg with no negative effects of any kind. That is the dose my son will trial (he is 60kg).

      If you trial 6mg on yourself, you can always increase it later to 10mg. Many products contain 3mg, some 6mg and some 10mg.

      Delete
    2. Thank you for your reply.

      Delete
  2. Thank you very much Peter for this insightful post. Since boron increases free DHT, would this still be advisable for women with PCOS? The neuroprotective effects are tempting though. What benefits did you notice in Monty?

    ReplyDelete
    Replies
    1. There are different types of PCOS. If you have high free testosterone or high DHT then boron would not be wise.

      If you have inflammatory or insulin resistant PCOS a small dose might still be beneficial.

      I came across boron for myself and only very recently started giving it to Monty. I don't expect anything dramatic, since his autism is already well managed.

      Delete
    2. Thanks Peter!!

      Delete
  3. Offtopic but there are any trials done with Zonisamide for asd? We would like to know what the ideal dose for this medication would be, main target would be calcium T-cells, Verapamil made things worse after 3 days I had to drop it because hyperactivity became unbearable along with dissasociation and adhd like symptoms, maybe a different type of calcium channels is the problem.
    I saw a comment here saying Zonisamide below the epilepsy dosage made things better, that dose would mean 25mg or lower? And when to decide if its working or not? Thanks and Happy New Year Peter

    ReplyDelete
    Replies
    1. I can only give my personal experience with Zonisamide. We trialed it on my daughter years ago. We didn’t notice any effects personally but both her school and therapists pulled us aside to ask what we have been doing as she was noticeably more engaged. We told her pediatrician who said,”great let’s double the dose”, we did then completely lost the effect, and were never able to get it back after going down in dose again.
      On a somewhat related note, my mother in law started getting old age seizures, and was put on Zonisamide too. If anything it made her worse. The interesting thing was that the seizures were completely erasing any memories she had of that day, which makes me wonder if there’s a similar thing happening with some of our ASD kids. The good news is the doctors swapped the medication and Mother in law is now doing fine.
      So yes it comes down to different individual different results, and yes there should be more research in this area for kids with ASD.

      Delete
    2. For Zonisamide, epilepsy doses in children often start around 1–2 mg/kg/day and can go up to 8–12 mg/kg/day.

      A reduced, sub-epileptic dose, might be in the 12.5–25 mg/day range depending on weight.

      An alternative is Ethosuximide, It is a classic anti-epileptic, very selective for T-type calcium channels, mainly used for absence seizures. It has been tried in ASD in small studies or case reports, sometimes with benefit for hyperactivity or stereotypies. Here again it would be wise to start at a low dose. The issue reported here was how to make such a low dosage, due to how the product is sold. There actually is an oral syrup in some countries.

      Delete
    3. Hey Peter, for how long you should trial a medicine to see if there is a benefit or not? On chatgpt with Zonisamide I got told that minimum is 12-16 weeks, but that seems way to much.

      Delete
    4. Yes, way too much.

      When I trialed Verapamil for summertime raging, I could see the effect in 30 minutes.

      That said, many people report that certain supplements seem to be beneficial for a week or two and then the body reacts via feedback loops and the effect fades away.

      Delete
  4. Nice! Thank you for the article. I believe reducing crp is likely to help prevent migraines as well. Because of that, and the many other benefits, I will give Boron a try.

    ReplyDelete
  5. I came across this article/research about how KCC2 impacts reward learning and thought you might be interested:

    https://www.sciencedaily.com/releases/2025/12/251210223635.htm

    This is not autism research (not much of it these days unfortunately) but these insights drawn from the paper might be another vector in understanding one way that Bumetanide can have a direct effect on misfiring dopamine expressing neurons which has been an area of study for autism research about as long as there has been autism research.

    Also, I hope all is well Peter with you and your family this winter!

    ReplyDelete
    Replies
    1. Thanks Tyler!

      Nice to hear from you. All is well with us, in fact we are having heavy snow today and enjoying the view from the warmth inside.

      Thank you for sharing this article. it is a very interesting find.

      You are absolutely right that this is not autism research, but the mechanisms described are highly relevant. KCC2 is best known for its role in maintaining low intracellular chloride in neurons, which allows GABA to function as an inhibitory neurotransmitter. When KCC2 expression is reduced, intracellular chloride rises and GABA becomes less effective at restraining neural firing. This basic mechanism has been implicated for years in autism, epilepsy, and neuropathic pain.

      What this new study adds is insight into dopamine circuits and reward learning. The authors show that lowering KCC2 in specific neurons leads to heightened dopaminergic activity and stronger cue–reward associations. In effect, reduced KCC2 changes how these neurons encode and respond to signals, promoting more rigid or habit-like learning. While the study is not about autism, altered reward processing and dopamine signaling have long been areas of interest in autism research, making this a useful mechanistic contribution.

      Importantly, KCC2 is much more than a simple chloride pump. In addition to controlling intracellular chloride levels, KCC2 also plays structural and signaling roles at synapses. It influences dendritic spine stability, excitatory synapse strength, receptor trafficking, and the timing and coordination of neuronal firing. As a result, reduced KCC2 does not merely increase excitability, it alters how neural networks are wired, synchronized, and plastic over time. These effects can persist even if chloride levels are partially corrected with bumetanide.

      This distinction is relevant when considering bumetanide. Bumetanide does not increase KCC2 expression, but by inhibiting NKCC1 it lowers intracellular chloride and can partially restore inhibitory GABA signaling. This may help stabilize downstream circuits, including dopamine-expressing neurons. However, correcting chloride alone cannot fully reproduce normal KCC2 function, which likely explains why bumetanide’s effects are incomplete and variable across individuals.

      The importance of KCC2 is perhaps most clearly established in neuropathic pain, where loss of KCC2 converts normally inhibitory sensory signals into excitatory ones, leading to central sensitization and chronic pain. In that field, restoring KCC2 function — not merely lowering chloride — can reverse pain behaviors even in the presence of ongoing injury. This strongly supports the idea that KCC2 loss causes persistent network dysfunction, not just transient changes in excitability.

      Overall, this new research does not prove anything specific about autism, but it strengthens a unifying idea, that KCC2 is a key regulator of circuit stability across the brain, and when its function is reduced, different symptoms emerge depending on which circuits are affected — pain, seizures, altered reward learning, or neurodevelopmental features.

      Hopefully, there will be an effective drug to upregulate KCC2 one day. Until then we can only downregulate/block NKCC1.

      Delete
    2. Wasn't there a drug in development a few years back (maybe quite a few) that worked directly on KCC2 expression? In this research (on rats) they used two lab specific drugs which have likely never been tested on humans and may not be safe as KCC2 has effects all over the body. I think I remember one of the diuretic drugs both depressing NKCC1 and depressing KCC2 at the same time (kinda cancelling each other out). It has been a while since I looked into this much so maybe there is a KCC2 upregulator somewhere that is safe for humans for all I know.

      Delete
    3. Tyler, as far as I am aware there still is no approved drug to unregulate KCC2. The main interest is to treat neuropathic pain. I spoke to a drug researcher a while back who said that NKCC1 is much more "drugable" than KCC2, so not to expect much.

      Delete
    4. Ovid Therapeutics is developing a kcc2 activator OV-350. The drug is currently in phase 1 trial. At the moment, it is being developed and studied only as a treatment for epilepsy, but fingers crossed.

      For anyone interested, here is the link -
      https://ovidrx.com/our-science/programs/ov350/

      Delete
  6. This might come in handy for a disorder marked by bone anomalies. Thank you Peter!
    /L

    ReplyDelete
    Replies
    1. Indeed Ling, in fact many autisms are associated with a very high chance of osteoporosis.

      Boron, vitamin D, calcium and vitamin K plus exercise are wise steps to achieve a good peak bone density while young.

      Many drugs used in severe autism are not good for bones. Also if you avoid dairy you need another source of calcium.

      Delete
  7. Hello ! NAG is as effective as Clemastine for remyelination ? What would be the comparable dose of NAG to 1-2mg of clemastine?

    ReplyDelete
    Replies
    1. Yes — there are studies suggesting N-acetyl-glucosamine (NAG) can support myelination, mainly from animal models and early human research. The effect appears indirect, via glycosylation pathways and immune modulation, and is not the same mechanism as clemastine’s direct remyelination action.

      Because of this, there is no NAG dose equivalent to 1–2 mg of clemastine.

      Safe dosing for NAG (adults):
      500–1,000 mg/day (conservative)
      1,500–3,000 mg/day commonly used

      Up to 6 g/day used short-term in MS studies and reported as well tolerated
      NAG is generally safe for long-term use, while clemastine is limited by sedation and anticholinergic effects.
      They are not substitutes, but may be complementary.

      Delete
  8. Peter, Boric acid increase sirt1.

    Two boron-containing compounds affect the cellular viability of SH-SY5Y cells in an in vitro amyloid-beta toxicity model

    https://pmc.ncbi.nlm.nih.gov/articles/PMC7478136/

    ReplyDelete
    Replies
    1. Stephen, the research on boron all seems to come from Turkey, which is interesting. There seem to be numerous possible beneficial effects at dose from 3-10mg a day.

      At very high doses there are negative effects. The quoted upper safe limit for adults is 20mg.

      I think it is a good choice, so I take it myself.

      Delete

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