Vitamin
Vitamin K2
Also known as: Menaquinone-7, MK-7, Vitamin K2 (MK-7), natto-derived K2
Vitamin K2 (MK-7) is a long-chain menaquinone that activates bone and vascular proteins involved in calcium regulation, supporting bone mineralization and cardiovascular health. MK-7 from plant sources like chickpea offers improved bioavailability and longer tissue half-life compared to K1.
Primary uses
- Bone density
- Cardiovascular health
- Calcium metabolism
- Dental health
- Bone health
- Brain health
- Hormone support
- Bone health and mineralization
- Arterial calcification prevention
- Osteocalcin activation
- Vascular calcification prevention
- Arterial elasticity support
How it works
- Activates osteocalcin (bone mineralization protein)
- Activates matrix Gla protein (vascular health)
- γ-carboxylation of vitamin K-dependent proteins
- Directs calcium to bone, away from soft tissues
Dosage
- Typical range
- 45–180 mcg daily
- Timing
- With meals containing dietary fat
- With food
- Essential—fat-soluble vitamin; absorption enhanced with dietary lipids
- Duration
- Bone mineralization benefits may require 6–12 months of consistent use; vascular benefits similarly require long-term intake
- Special populations
- Pregnant and breastfeeding women should maintain adequate K2 intake (safe at typical supplemental doses). Caution in those on warfarin or other vitamin K antagonists—consult physician before supplementing.
Forms
- Softgel
- Combined D3+K2
- Capsule
- Menaquinone-7 (MK-7)· 70/100
- Natto-derived K2· 70/100
- Menaquinone-7 (chickpea-derived fermentation)· 70/100
- Oil-based suspension· 70/100
- MK-4 (menaquinone-4)· 70/100
- Menatetrenone· 70/100
Safety
Contraindications
- Warfarin and other vitamin K antagonists—high-dose supplementation may reduce drug efficacy; consistent intake is preferred over variable intake
Known interactions
Evidence notes
Strong RCT and observational evidence, particularly for bone density and fracture risk reduction; good evidence for vascular calcification prevention. MK-7 form shows superior bioavailability and half-life (2.5 days) compared to MK-4 or vitamin K1. EPIC-Norfolk and other large cohort studies support cardiovascular benefits.
Grade A: Multiple well-designed human trials support the main claims.
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