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Vitamin K2 / MK-4 / MK-7

Also known as menaquinone, mk4, mk7, menatetrenone, vitamin k-2.

Vitamin K2 (menaquinones, including MK-4 and MK-7) is a fat-soluble vitamin involved in blood clotting and in proteins that regulate calcium in bone and blood vessels.

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Last reviewed September 20, 2026 · Jump to references

Educational information only. This page does not provide medical advice or determine whether a supplement is appropriate for you. Review supplements with a qualified healthcare professional, especially if you take medication, are pregnant, have surgery scheduled, or have a chronic medical condition.

Important cautions

  • Interferes with warfarin-type anticoagulantshigh concern

    Vitamin K opposes warfarin and similar drugs. Starting, stopping or changing a vitamin K supplement can destabilise INR and change bleeding or clotting risk. Discuss with the prescribing clinician first.

  • Disclose before proceduresmoderate concern

    Tell surgical and anaesthetic teams about vitamin K supplements, particularly if you take an anticoagulant or have a clotting disorder.

  • Hidden in combination productsmoderate concern

    Many vitamin D and bone formulas include K2. Check labels to avoid unintended intake.

Discuss with a clinician if any of these apply

  • Bleeding disorders or anticoagulants

Evidence by use

Each use is rated on its own. There is no single overall effectiveness score.

  • Preventing vitamin K deficiency bleeding

    Established for a defined use

    Vitamin K's role in clotting is established; newborn prophylaxis uses vitamin K1 and is a medical intervention.

  • Bone mineral density and fracture reduction

    Limited or mixed

    Human trials are mixed; some show effects on bone markers or density without consistent fracture reduction.

    Populations studied: Postmenopausal adults in most trials.

  • Arterial calcification and cardiovascular outcomes

    Limited or mixed

    Studied but not established; several randomised trials have not shown meaningful benefit.

  • Counteracting calcium supplement risks

    Insufficient evidence

    A popular marketing claim without adequate human evidence.

Interactions to review

  • Warfarin and other vitamin K antagonists

    medication · high severity · strong evidence

    Direct pharmacological opposition; changes in intake alter INR.

  • Orlistat, cholestyramine, mineral oil

    medication · moderate severity · moderate evidence

    Reduce absorption of fat-soluble vitamins including vitamin K.

  • Long-term broad-spectrum antibiotics

    medication · low severity · limited evidence

    May reduce vitamin K status in people with poor intake.

  • INR testing

    laboratory · high severity · strong evidence

    Vitamin K intake changes INR results in people on vitamin K antagonists.

Complete Research Guide

Open each section for the available evidence. Gaps are stated rather than inferred.

Overview

Vitamin K allows the body to activate proteins needed for blood clotting and for directing calcium into bone rather than soft tissue. K1 comes mainly from leafy greens, K2 from fermented foods and animal products. Most interest in K2 supplements comes from bone and artery claims that remain under study.

Technical detail

Fat-soluble vitamin family. MK-4 and MK-7 differ in half-life: MK-7 persists longer in circulation, MK-4 is cleared quickly, so equal label amounts are not equivalent.

Section last reviewed Sep 20, 2026

Structure & Properties

K1 (phylloquinone) and K2 (menaquinones) share a common ring structure with different side chains. MK-7 is usually produced by bacterial fermentation, MK-4 is typically synthetic.

Technical detail

All forms are fat-soluble and require dietary fat for absorption; light and oxidation degrade them. Trans-MK-7 is the biologically relevant isomer, and products vary in isomer purity. Do not assume interchangeability between K1, MK-4 and MK-7.

Section last reviewed Sep 20, 2026

How It Works

Vitamin K is the cofactor that switches on certain proteins, including clotting factors in the liver and matrix Gla protein and osteocalcin outside the liver.

Technical detail

Acts as cofactor for gamma-glutamyl carboxylase. Warfarin and related drugs inhibit vitamin K epoxide reductase, so vitamin K intake directly opposes their anticoagulant effect — the mechanistic basis of the most important interaction.

Section last reviewed Sep 20, 2026

Human Research

Vitamin K's clotting role is beyond dispute. For bone, trials report changes in biochemical markers and some density findings, but fracture evidence is inconsistent and much of the strongest early data came from single-country studies with high-dose MK-4. Trials of K2 for arterial calcification and cardiovascular events have largely not shown clinically meaningful benefit.

Technical detail

Evidence is assessed separately by form, dose, population and outcome. Marker changes such as undercarboxylated osteocalcin are not established surrogates for fractures.

Section last reviewed Sep 20, 2026

Laboratory Research

Animal and cell studies show that vitamin K-dependent matrix Gla protein limits vascular calcification and that deficiency promotes it.

Evidence gap: Non-human evidence. It explains why the cardiovascular hypothesis was tested and does not itself demonstrate benefit in people.

Section last reviewed Sep 20, 2026

Processing & Interactions

Absorption needs dietary fat, and fat malabsorption or bile problems reduce it. The critical interaction is with warfarin and similar anticoagulants, where changes in vitamin K intake shift INR and bleeding risk.

Technical detail

Anyone taking warfarin, acenocoumarol or phenprocoumon should keep vitamin K intake consistent and discuss supplements before starting or stopping them; abrupt changes destabilise INR. Direct oral anticoagulants (apixaban, rivaroxaban, dabigatran) do not work through vitamin K and are not affected the same way. Orlistat, cholestyramine and long-term broad-spectrum antibiotics can reduce vitamin K status.

Section last reviewed Sep 20, 2026

Safety & Precautions

Vitamin K has low direct toxicity and no established upper intake level, but it is not risk-free in context: it can make vitamin K antagonist anticoagulation less effective or unstable, which is a serious clinical problem. People with bleeding or clotting disorders, liver disease affecting clotting factors, or planned surgery should review supplements with their clinician. Combined vitamin D and K products mean people sometimes take K2 without realising it.

Section last reviewed Sep 20, 2026

Administration & Studied Formulations

Softgels, capsules, tablets and combination vitamin D + K2 products are common. Trials have used MK-4 in high daily amounts and MK-7 in much smaller daily amounts.

Technical detail

Adequate intake values are published for vitamin K overall; no tolerable upper intake level is set, which does not imply unlimited safety with anticoagulants. Study amounts were selected for the population and outcome tested and are not personal recommendations.

Section last reviewed Sep 20, 2026

Applications & Related Therapies

Adequate vitamin K is part of nutrient adequacy, met through leafy greens, fermented foods and dairy. For bone health, the better-supported approach remains adequate calcium, vitamin D and protein, resistance exercise, fall prevention and, where indicated, prescription osteoporosis treatment. K2 is not a substitute for those.

Section last reviewed Sep 20, 2026

Cases, Considerations & Ethics

Educational example: a person on warfarin starts a bone supplement containing MK-7 and their INR drifts below range at the next check. The decision factors are which anticoagulant is involved, whether intake is consistent, and whether the monitoring clinician knows about the supplement. Questions to ask: does this product contain vitamin K, does it affect my anticoagulant, and should my INR be checked sooner? Claims that K2 makes calcium supplements safe or reverses artery calcification go well beyond current human evidence.

Section last reviewed Sep 20, 2026

References

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