Selenium

Selenium is an essential trace mineral the body uses to build the 25 known selenoproteins — including enzymes that protect cells from oxidative stress, recycle thyroid hormone, and support immune function. UK NHS reference intakes are 75 µg/day for men and 60 µg/day for women. The UK is historically a low-selenium country: average dietary intake fell after bread-flour sourcing shifted from selenium-rich North American wheat in the 1970s.

Camden Medicals editorial · Last reviewed 12 June 2026 · Next review June 2027

  • Cross-checked against
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  • NICE
  • BNF
  • EFSA
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Verifera Evidence ReviewCamden evidence review · independently appraised — graded, not guessed.

Camden's editorial team independently graded each health claim below on the strength of the published evidence — see the grade beside every condition.

Class
Mineral
Typical daily dose
50-200 µg/day in supplemental form
Top use evidence
Moderate
On this page
  1. What it is
  2. How it works

What it is

Selenium is element 34 on the periodic table — a non-metal that the body incorporates into proteins as the unusual amino acid selenocysteine. There are 25 known human selenoproteins, including the glutathione peroxidases (antioxidant defence inside cells), the iodothyronine deiodinases (which convert thyroid hormone T4 to active T3), and the thioredoxin reductases (redox balance, DNA synthesis).

UK food sources include Brazil nuts, fish, shellfish, meat, eggs, and cereal products. Brazil nuts are an extreme outlier: a single nut grown in selenium-rich Brazilian soil can supply 70-90 µg of selenium, but the content varies enormously batch to batch — making them an unreliable way to hit any specific daily amount.

Common supplemental forms in the UK are selenomethionine (organic, well absorbed, accumulates in tissues), sodium selenite and sodium selenate (inorganic salts, lower tissue retention than selenomethionine but cheaper), and selenium-enriched yeast (mostly selenomethionine with smaller fractions of selenocysteine and methylselenocysteine — total selenium content varies by manufacturer and the proportion of each form is rarely declared).

The UK is historically a low-selenium country. Soils across much of Britain are low in plant-available selenium, and average adult dietary intake declined after UK bread-flour sourcing shifted in the 1970s from selenium-rich North American wheat to lower-selenium European wheat. SACN reviewed the position in 2013 — see the regulatory references below — and concluded that average UK intakes had fallen but did not find evidence of widespread frank deficiency across the UK population.

At a glance

  • UK NHS reference intake: 75 µg/day (men), 60 µg/day (women).
  • Average UK adult intake has declined since the 1970s; SACN reviewed the issue in 2013 but did not find evidence of widespread deficiency.
  • Common supplemental forms: selenomethionine (organic, well absorbed), sodium selenite or selenate (inorganic), selenium-enriched yeast (mostly selenomethionine, content varies between manufacturers).
  • More is not better — chronic intake above 400 µg/day risks selenosis (hair loss, brittle nails, garlic-smelling breath, neuropathy). EFSA set the adult upper intake level at 255 µg/day in 2023.

What people use it for

  • UK adults whose dietary intake of selenium is low

    Topping up dietary selenium toward the NHS RNI of 75 µg/day (men) or 60 µg/day (women). Average UK adult intake has declined since the 1970s and many adults sit below the RNI in dietary surveys. [3,1]

    Some evidenceModerate
  • Adults with autoimmune (Hashimoto's) thyroiditis

    Some randomised trials and a 2010 meta-analysis report that selenium 200 µg/day lowers thyroid peroxidase (TPO) antibody titres over 3 months. Whether this changes the long-term progression of the autoimmune process or the need for levothyroxine is uncertain. UK NHS, the British Thyroid Association, and NICE do not currently recommend selenium as routine care for Hashimoto's — discuss with your GP or endocrinologist. [7,8]

    Popular, not provenMixed
  • Couples investigating male subfertility

    Limited evidence: small randomised trials in subfertile men report modest improvements in sperm motility with selenium 100-200 µg/day over ~90 days, sometimes combined with other antioxidants. Selenium is not a replacement for a urology workup. Discuss with your GP if you are trying to conceive. [5]

    Some evidenceLimited
  • Older adults with mild low-selenium status

    Older adults with low baseline selenium are commonly considered for adequacy. Above adequacy, supplementation has not been shown to improve hard outcomes in this group. The aim is to meet the RNI, not to push intake higher. [3]

    Some evidenceLimited
  • Adults already eating Brazil nuts, fish, eggs and meat regularly

    Routine supplementation may be unnecessary — dietary intake is likely already at or near the RNI. NHS guidance is that those who eat meat, fish, or nuts should obtain enough selenium from a varied diet. [1]

    Some evidenceModerate

How it works

Selenium is the active centre of the selenoenzymes that recycle cellular antioxidants, activate thyroid hormone, and support normal immune function — which is why early signs of low selenium status often show up as poorer thyroid hormone conversion and weaker antioxidant defence rather than as a single named symptom.

Common myths

Myth"Selenium boosts immunity"

RealityThe authorised UK health claim is that selenium "contributes to the normal function of the immune system" — a claim about adequacy supporting normal function, not about supplementation producing an above-normal effect. The two are commonly conflated by marketing. Selenium is required for normal immune function; people who are deficient benefit from correction. Above adequacy, immune-function gains have not been established. [2]

Myth"Selenium reduces cancer risk"

RealityThe Selenium and Vitamin E Cancer Prevention Trial (Lippman 2009 JAMA, 35,533 healthy US men) found no anti-cancer effect of selenium 200 µg/day. The earlier Nutritional Prevention of Cancer trial (Clark 1996) had reported reduced total cancer incidence in a smaller baseline-low-selenium population, but that finding did not replicate. In an adequately-nourished adult population, selenium supplementation does not lower cancer risk. [9,10]

Myth"More selenium is better for the thyroid"

RealityThe dose-response for selenium is U-shaped — both very low and chronically high intakes carry risks. Excess selenium has been associated with worse glucose metabolism (Stranges 2007) and, at sustained high intakes, selenosis (hair loss, brittle nails, garlic breath, neuropathy). For thyroid antibodies in Hashimoto''s, the trial dose is 200 µg/day for 3 months; more is not better, and routine selenium is not currently recommended by UK NHS or NICE for autoimmune thyroid disease. [11]

Myth"Brazil nuts are a reliable selenium supplement"

RealitySelenium content in Brazil nuts varies roughly tenfold between batches and origins — a single nut may supply anywhere from a few µg to ~90 µg. They are a good food source on average, but they are not a controlled way to deliver a specific daily amount. People who eat large handfuls daily for years have presented with selenosis. If a defined dose matters for a clinical reason, a labelled supplement is the more reliable route. [5]

Myth"Selenium is an anti-cancer / anti-ageing megadose"

RealitySustained intake above the EFSA upper limit (255 µg/day) does not provide additional benefit and increases the risk of adverse effects — most clearly the U-shaped diabetes signal seen in the SELECT and Stranges 2007 follow-up data. For nutritional purposes the goal is the RNI (75 µg men / 60 µg women). Megadose selenium positioning is marketing, not evidence. [12,11]

Common online questions

Synthesised from the questions UK shoppers most often ask online about Selenium. Each answer is editorial and links to its evidence in the Sources list below.

Should everyone in the UK take a selenium supplement?

No. The 2013 SACN review of selenium and health considered the evidence on UK intakes and did not find that the population needed routine supplementation. Average adult intake has declined since the 1970s and many adults sit below the RNI in dietary surveys, but most are not deficient. NHS guidance is that adults eating meat, fish, eggs, or nuts will generally obtain enough selenium from a varied diet. People most likely to benefit are those with consistently low intake or specific clinical reasons to consider it — discuss with your GP or pharmacist. [3,1]

Are Brazil nuts a reliable source of selenium?

On average yes, but they are not a reliable way to hit a specific daily amount. Selenium content in a single Brazil nut ranges roughly 70-90 µg in nuts grown in selenium-rich Brazilian soil — but the variation between batches and origins is around tenfold. Eating a couple every day is a reasonable dietary approach if you tolerate them; eating a large handful daily for years risks selenosis. If you need a defined dose for a clinical reason, a labelled supplement is the more controllable route. [5]

I have Hashimoto's thyroiditis — should I take 200 µg of selenium?

This is a discussion to have with your GP or endocrinologist. Trials (Gärtner 2002) and the Toulis 2010 meta-analysis show that selenium 200 µg/day reduces TPO antibody titres in autoimmune thyroiditis over 3 months — but whether this slows the underlying disease, reduces the need for levothyroxine, or prevents progression is not established. UK NHS, the British Thyroid Association, and NICE do not currently recommend routine selenium for Hashimoto''s. If you decide to try it, your clinician can help avoid stacking with other selenium sources and watch for the U-shaped diabetes-risk signal at long-term high intake. [7,8]

Selenomethionine, sodium selenite, or selenium yeast — which form should I pick?

At the doses used in supplements, the practical clinical differences between these forms are modest. Selenomethionine is well absorbed and accumulates in tissues over weeks because it goes into the body''s general protein pool; sodium selenite and selenate are inorganic, less retained, but functionally adequate. Selenium-enriched yeast is mostly selenomethionine with smaller fractions of selenocysteine and methylselenocysteine, but the proportions vary by manufacturer and are rarely declared on the label. The labelled µg of elemental selenium is what matters most; chase that number and the named form, not branded positioning.

How much selenium is too much?

EFSA''s 2023 review set the tolerable upper intake level for adults at 255 µg/day (alopecia is the early adverse effect). WHO and historical UK guidance reference 400 µg/day as the upper safe level. Sustained intakes above ~800 µg/day risk selenosis: the classic features are garlic-smelling breath (the body exhales dimethylselenide), hair loss, brittle white-flecked nails, GI symptoms, and peripheral neuropathy. NHS guidance is that supplementation up to 350 µg/day is unlikely to cause harm — but this is an upper safety bound, not a target. The right target is the RNI, not the ceiling. [1]

Does selenium "boost" the immune system?

The GB-authorised health claim is that selenium "contributes to the normal function of the immune system". That is a claim about adequacy supporting normal function — i.e. selenium is required for normal immune function — not about supplementation producing an above-normal effect in adults who are already replete. People who are deficient gain by correction; above adequacy, immune-function gains have not been demonstrated. [2]

I read that selenium reduces cancer risk — is that right?

The original signal came from the 1996 Nutritional Prevention of Cancer trial in adults with low baseline selenium. The much larger SELECT trial (Lippman 2009 JAMA, 35,533 men) did not replicate any anti-cancer effect of selenium in adults with adequate baseline status. Long-term high-dose selenium in already-replete adults has also been linked to a higher rate of new-onset type 2 diabetes (Stranges 2007). The fair summary is that selenium does not reduce cancer risk in the general adult population. [9,11]

⚖️ The official position

What may lawfully be claimed about Selenium in Great Britain. This is a regulatory position, not an evidence grade.

A health claim is authorised in Great Britain.

“Selenium contributes to the maintenance of normal hair”

“Selenium contributes to the maintenance of normal nails”

“Selenium contributes to the normal function of the immune system”

“Selenium contributes to the normal thyroid function”

“Selenium contributes to the protection of cells from oxidative stress”

“Selenium contributes to normal spermatogenesis”

This claim is authorised for use in Great Britain under the GB Nutrition and Health Claims regulation. A product may carry it when it provides at least 15% of the UK NRV per recommended daily portion.

Authorised UK health claims

Verbatim from the GB Nutrition and Health Claims Register (Reg 432/2012 as assimilated in GB). A product can carry these claims when it provides at least 15% of the UK NRV per recommended daily portion.

6 authorised claims — show / hide
  • "Selenium contributes to the maintenance of normal hair"
  • "Selenium contributes to the maintenance of normal nails"
  • "Selenium contributes to the normal function of the immune system"
  • "Selenium contributes to the normal thyroid function"
  • "Selenium contributes to the protection of cells from oxidative stress"
  • "Selenium contributes to normal spermatogenesis"

🔬 Camden’s evidence review

The research Camden reviewed, graded on its strength. This is our own appraisal — it sits beneath the official guidance above, never above it.

  1. Cancer prevention (general population)

    InsufficientEvidenceinsufficient

    The Selenium and Vitamin E Cancer Prevention Trial (SELECT, Lippman 2009 JAMA — 35,533 men) found no protective effect of selenium 200 µg/day, vitamin E, or the combination on prostate cancer or other cancers in relatively healthy US men with adequate baseline selenium. The earlier Nutritional Prevention of Cancer trial (Clark 1996 JAMA) showed reduced total cancer incidence in a smaller, baseline-low-selenium population, but the finding did not replicate. Bottom line: in a generally replete population, selenium does not lower cancer risk. [9,10]

  2. Hashimoto's thyroiditis — TPO antibody titres

    MixedEvidencemixed

    Several randomised trials (e.g. Gärtner 2002) and the Toulis 2010 systematic review report that selenium 200 µg/day reduces TPO antibody titres over 3 months in patients with autoimmune thyroiditis. Whether this antibody change alters long-term thyroid function, levothyroxine requirement, or progression to overt hypothyroidism is not established. UK NHS, BTA, and NICE do not currently advise routine selenium for Hashimoto''s. [7,8]

  3. Type 2 diabetes — possible adverse signal

    LimitedEvidencelimited

    Long-term selenium supplementation in already-replete adults has been linked to higher rates of new-onset type 2 diabetes (Stranges 2007, Annals of Internal Medicine — secondary analysis of the Nutritional Prevention of Cancer trial; signal echoed in SELECT). The dose-response across baseline selenium appears U-shaped: very low and chronically high intakes both carry risk. This is one of the strongest reasons to avoid supplementing above the RNI without a specific reason. [11]

  4. Prostate cancer — vitamin E + selenium combination harm signal

    ModerateEvidencemoderate

    SELECT extended follow-up (Klein 2011 JAMA) reported that vitamin E 400 IU/day was associated with an increased rate of prostate cancer in healthy men (hazard ratio ~1.17). Selenium alone did not show benefit. This is the most directly cited reason that combination "anti-cancer" antioxidant stacks marketed to men over 50 are no longer supported by the evidence. [12,9]

  5. Male subfertility — sperm motility

    LimitedEvidencelimited

    Small randomised trials in subfertile men have reported modest improvements in sperm motility with selenium 100-200 µg/day, sometimes combined with other antioxidants. Trial quality is variable and selenium is not standard fertility care in the UK. A urology referral is the right next step before supplementing. [5]

  6. Keshan disease — historical selenium-deficiency cardiomyopathy

    StrongEvidencestrong

    Keshan disease is a juvenile cardiomyopathy first described in selenium-deficient regions of rural China and largely resolved by population-level selenium supplementation. It is the clearest historical demonstration that selenium is an essential nutrient. Keshan is not a UK clinical issue and is not relevant to UK adult supplementation decisions; it is the reason selenium has the RNI it does. [5]

Safety

Selenium at intakes near the UK Reference Nutrient Intake (75 µg men / 60 µg women) is generally safe. Risks come from chronically high intake — selenosis features hair loss, brittle nails, and garlic-smelling breath — and from a U-shaped link with type 2 diabetes risk at sustained high doses.

Talk to your pharmacist or GP first if you:

  • You have a history of selenosis or chronically high selenium exposure.
  • You take lithium (theoretical interaction; clinical data are limited).
  • You are considering a high-dose protocol (e.g. 200 µg/day) for autoimmune thyroid disease — discuss with your GP or endocrinologist before starting.
  • You take an anticoagulant or antiplatelet — high-dose selenium has theoretical bleeding-risk concerns; data are limited.
  • You are pregnant or breastfeeding (do not exceed the adult RNI without professional advice).
  • You eat a large handful of Brazil nuts daily on top of a multivitamin (combined intake can exceed the EFSA upper level).

Common side effects: At intakes near the RNI: side effects are uncommon. With sustained high intakes (chronic >400 µg/day): garlic-smelling breath, hair loss, brittle white-flecked nails, GI symptoms, and peripheral neuropathy (selenosis).

Pregnancy and breastfeeding

The UK adult RNI for selenium is not raised in pregnancy (60 µg/day). Adequate selenium intake from a varied diet is generally regarded as appropriate in pregnancy. High-dose selenium supplementation during pregnancy is not recommended. As with any supplement, talk to your pharmacist, GP, or midwife before starting.

The adult RNI rises to 75 µg/day during breastfeeding. High-dose supplementation is not recommended; if you are considering anything above the RNI, discuss with your GP or pharmacist.

Talk to your GP, midwife, or pharmacist before starting any supplement during pregnancy or breastfeeding.

More clinical detail (for clinicians and informed readers)

Contraindications

  • History of selenosis or known chronically high selenium status — discuss with your pharmacist or GP before supplementing.
  • Pregnancy and breastfeeding — do not exceed the adult RNI without professional advice.

Drug interactions

  • Anticoagulants and antiplatelets — theoretical bleeding-risk concern at high selenium doses; clinical data are limited. Tell your prescriber about all supplements.
  • Lithium — theoretical interaction reported; clinical relevance is unclear. Discuss with your prescriber.
  • Niacin / statin combinations for cholesterol — antioxidant cocktails containing selenium have been reported to blunt the HDL-raising effect of niacin; relevance to modern lipid management is limited.
  • High-dose iron, zinc, and copper supplements — competitive mineral absorption may matter for combination products. Take separate single-mineral doses where precise dosing is needed.

This is not an exhaustive list. Always tell your prescriber and pharmacist about every supplement you take.

Common side effects

  • At intakes near the RNI, side effects are uncommon.

Rare side effects

  • Chronic high intake (selenosis): garlic-smelling breath (exhaled dimethylselenide), hair loss, brittle white-flecked nails, GI symptoms, peripheral neuropathy.
  • Long-term high-dose use has been linked to a higher rate of new-onset type 2 diabetes in baseline-replete adults (Stranges 2007).

How to take it

UK Reference Nutrient Intake
Typical supplemental range
50-200 µg/day in supplemental form
Timing
Anytime, with food.

How to spot quality

Look for

  • A named, specified form: selenomethionine, sodium selenite, sodium selenate, or selenium-enriched yeast.
  • µg of elemental selenium per serving stated explicitly, alongside % NRV (NRV = 55 µg).
  • For selenium-enriched yeast, the proportion that is selenomethionine declared on the label or technical data sheet.
  • Daily dose at or near the RNI for general supplementation (50-100 µg). Higher doses (e.g. 200 µg/day) reserved for specific clinical reasons.
  • GMP-certified manufacture; ideally third-party testing for total selenium content.

Red flags

  • Daily doses above 200 µg/day marketed for general use without a specific clinical rationale.
  • "Selenium boost" / "anti-cancer selenium" / megadose-for-everyone marketing positioning — not supported by the SELECT or Stranges 2007 evidence.
  • Brazil-nut-as-supplement products that do not declare a verified per-serving µg of selenium (content varies up to tenfold batch to batch).
  • Combination minerals stacking selenium with iron, zinc, and copper without considering competitive absorption interactions.
  • Selenium-enriched yeast products that do not declare the proportion of selenomethionine in the yeast.

Where Camden lands · gap declared

Camden's dedicated standalone selenium product is NB-550 (Purifera™ Selenium 200µg L-Selenomethionine, 120 capsules) — a single-active capsule supplying 200µg of selenium as L-selenomethionine, the well-absorbed organic form, at one capsule daily. The form is named, the elemental µg and %NRV are stated, and the dose carries the authorised thyroid, immune-function, and cell-protection claims. 200µg is a deliberately higher single-active dose — within the EFSA 2023 tolerable upper intake level of 255µg/day, but anyone already taking a multivitamin or eating Brazil nuts regularly should count their total selenium intake. Selenium also appears as a co-ingredient in NB-1284 (Collagen Complex Gummies, 55µg as sodium selenite, 100% NRV). For most UK adults selenium does not need supplementing on top of a varied diet — NB-550 is positioned for people with an identified reason to top up.

Reformulation or supplier clarification is in progress.

Commonly combined with

Other ingredients that share a biological pathway, cofactor relationship, or evidence-backed protocol with this one. Mechanisms below cite primary physiology — not folk pairing. Doses are literature ranges, not recommendations. Talk to your pharmacist or GP before changing your stack, especially if you take prescription medication.

Iodine (I)

Moderate evidence

Thyroid-cluster pairing — selenium deiodinase cofactor + iodine substrate.

Selenium cofactor for the deiodinase enzymes (DIO1, DIO2, DIO3) that convert T4 to T3. Iodine substrate for thyroid hormone synthesis. Mechanism complementary on thyroid axis. UK Article 13.1 thyroid claim for both.

Evidence: Camden iodine covers cluster. [2]

Doses studied: 100-200 µg selenium + 150 µg iodine (potassium iodide) daily.

Found in Camden: Purifera™ Selenium 200µg L-Selenomethionine 120 Capsules

Zinc

Moderate evidence

Antioxidant + immune cluster — selenium glutathione peroxidase + zinc SOD complementary.

Different metalloenzyme cofactor roles; UK Article 13.1 immune claims for both.

Evidence: UK Article 13.1 claims authorised. [2,2]

Doses studied: 100-200 µg selenium + 10-15 mg zinc daily.

Found in Camden: Purifera™ Selenium 200µg L-Selenomethionine 120 Capsules

Vitamin E (alpha-tocopherol)

Moderate evidence

Antioxidant cluster — selenium glutathione peroxidase + vitamin E lipid-membrane antioxidant.

GPX uses selenocysteine to detoxify lipid hydroperoxides; vitamin E scavenges peroxyl radicals in lipid membranes. Mechanism complementary on lipid-membrane antioxidant axis. UK Article 13.1 cell-protection claims for both.

Evidence: Mechanism well-established. [2,2]

Doses studied: 100-200 µg selenium + 12 mg vitamin E daily.

Found in Camden: Purifera™ Selenium 200µg L-Selenomethionine 120 Capsules

Biotin

Moderate evidence

Hair / nails cluster — biotin + selenium UK Article 13.1 hair / nails maintenance claims.

Both UK Article 13.1 hair / nails maintenance authorised. Different mechanisms; complementary.

Evidence: UK Article 13.1 hair / nails claims for both. [2,2]

Doses studied: 50-200 µg biotin + 100-200 µg selenium daily.

Kelp (brown seaweed)

Moderate evidence

Thyroid-cluster — selenium + iodine + zinc trio; kelp variability undermines clean iodine delivery.

Selenium deiodinase cofactor; iodine substrate (kelp variable). Mechanism complementary on thyroid axis if iodine delivery is controlled.

Evidence: UK Article 13.1 selenium thyroid claim. [2]

Doses studied: Controlled iodine via potassium iodide + 100-200 µg selenium — avoid kelp as iodine source.

Thyroid considerations apply

Saw Palmetto

Limited evidence

Men's-health cluster — selenium supports normal spermatogenesis (UK Article 13.1) alongside saw palmetto BPH-symptom support.

Selenium is a cofactor for selenoprotein P + glutathione peroxidase in seminiferous epithelium. UK Article 13.1 spermatogenesis claim. Saw palmetto modulates 5-α-reductase. Mechanism complementary.

Evidence: UK Article 13.1 selenium claim authorised. [2]

Doses studied: 320 mg saw palmetto + 100-200 µg L-selenomethionine daily.

Verifera™ is published by Camden Medicals — a UK supplement retailer. We have a commercial interest in some of the ingredients described here; we declare it on every page and our editorial process forbids adjusting copy to favour our own products. Read our editorial policy.

This page is information, not medical advice. Talk to your pharmacist or GP before starting any supplement, especially if you take prescribed medicines, are pregnant or breastfeeding, or have an existing condition.

Suspected side effects can be reported to the MHRA via the Yellow Card scheme: yellowcard.mhra.gov.uk