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Vitamin K2

Menaquinone / MK-7 / MK-4 · Foundation

LimitedLittle human data, early, small, or narrow.

Directs calcium toward bone and away from arteries in theory; the human outcome data is thinner than the pairing with D3 implies.

250-fold
Nominal daily mass gap between the 45 mg MK-4 bone trials and a typical 180 mcg MK-7 supplement (different vitamers, not a potency equivalence)

What it is

The vitamin that tells calcium where to go, into bone rather than arteries. It is the quiet counterpart to vitamin D, and the reason "D3+K2" became a standard pairing, though the pairing rests more on mechanism than on outcome trials.

How it works

K2 activates two proteins: osteocalcin, which binds calcium into bone, and matrix Gla protein, which stops calcium depositing in artery walls. Vitamin D increases calcium absorption; K2 is proposed to direct where it lands. Elegant, plausible, and only partly tested in humans.

Which form to buy

MK-7 (menaquinone-7)Daily supplementation

Long half-life means once-daily dosing holds levels; the form in most modern trials, typically 90-180 mcg.

The practical default.

MK-4 (menaquinone-4)The Japanese trial base

Short half-life; the osteoporosis trials used a pharmacological 45 mg PER DAY total (typically 15 mg three times daily), not what supplements provide.

Do not assume supplement doses replicate those trials.

K1 (phylloquinone)Clotting, from greens

The leafy-green form, mostly used by the liver for clotting factors.

Different job; a normal diet covers it.

NattoThe food source

Fermented soybeans, by far the richest MK-7 source, and an acquired taste.

The original, if you can stomach it.

What it actually does, graded

Improves bone mineral density markersLimited

Mixed: some trials show benefit, others none, and the strongest osteoporosis data used pharmacological MK-4 doses far above supplements.

Reduces arterial calcification progressionLimited

Mixed: dialysis trials improved inactive-MGP markers WITHOUT slowing calcification, and postmenopausal work measured arterial stiffness instead. A 2026 RCT did find modestly slowed coronary calcium progression at 360 mcg MK-7 in symptomatic coronary disease, clinical significance unknown.

Reduces fracture riskLimited

Not consistently demonstrated in Western populations at supplement doses.

Required alongside vitamin D to prevent harmNone shown

A very common marketing claim. No trial shows vitamin D supplementation causes arterial calcification that K2 then prevents.

Pros and cons

Pros
  • A genuinely elegant mechanism with real biology behind it
  • Safe at supplement doses with a long usage history
  • Cheap when bought as MK-7
Cons
  • The D3+K2 pairing is sold as necessary; the evidence for necessity is not there
  • The impressive bone trials used doses 250x higher than typical supplements
  • A genuine, serious interaction with warfarin

What to expect

  • Nothing perceptible, the studied outcomes are bone density and arterial scans over years.

Interactions

AvoidWarfarin and other vitamin-K antagonistsVitamin K directly opposes how these drugs work. This is the interaction that actually matters, consistency of intake is what anticoagulation clinics manage, and adding a supplement without telling them is genuinely risky.
CompatibleVitamin DThe intended pairing, though "necessary" overstates the evidence.

Is it for you?

Probably worth it if
  • You already supplement vitamin D and want the mechanistically sensible companion, with expectations set low
  • Bone-density concerns you are managing with a clinician
Probably skip it if
  • You eat plenty of greens and fermented foods and take no vitamin D

Who should avoid it

  • Anyone on warfarin or another vitamin-K antagonist, without their anticoagulation clinic explicitly agreeing

Research on this supplement

Papers about this supplement, not proof of the claims above. A title says what was studied, which is sometimes a negative result or a different question entirely.

  • The effect of vitamin K2 supplementation on bone turnover biochemical markers in postmenopausal osteoporosis patients: a systematic review and meta-analysis
  • The effect of vitamin K supplementation on cardiovascular risk factors: a systematic review and meta-analysis
  • Efficacy of vitamin K2 in the prevention and treatment of postmenopausal osteoporosis: A systematic review and meta-analysis of randomized controlled trials

What the evidence says

The mechanism is real. K2 activates proteins that regulate where calcium is deposited. Human outcome evidence is where it thins: a few bone-density and arterial-stiffness trials with modest or mixed results, and nothing establishing that adding K2 to D3 changes fracture or cardiovascular outcomes. The routine D3+K2 pairing is mechanistic reasoning sold as an established requirement.

What studies used

MK-7 trials commonly used 90-180 mcg/day. Fat-soluble; studies dosed it with meals.

Reported from published studies and product labelling — a record of what was used in research, not a recommendation. What is right for you is a conversation with a clinician.

Watch out for

  • Vitamin K directly opposes warfarin, anyone anticoagulated needs their prescriber involved before starting or stopping it, and consistency matters more than amount

Evidence base

A8,926 research papers
established literature

Strong human evidence: either a phase 3 or 4 trial report alongside review-level evidence, or ten or more randomised controlled trial reports.

This letter measures how much human research exists, not whether it works for you — the tier above (Limited) is the read on quality.

Research (12)

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