MenaQ7® (All-Trans Vitamin K2 MK-7)

Evidence Level
Moderate
3 Clinical Trials
5 Documented Benefits
3/5 Evidence Score

MenaQ7® (originally NattoPharma, now part of Gnosis/Lesaffre) is the original commercial all-trans menaquinone-7 (MK-7) ingredient, derived historically from a controlled natto fermentation process and now also available as a synthetically produced all-trans MK-7. Standardized for high all-trans isomer purity, MenaQ7® has been the test article in several long-running randomized controlled trials evaluating vitamin K2 effects on bone mineral density, arterial stiffness, and matrix Gla protein activation in postmenopausal women. The 3-year Knapen trial showed reduced age-related bone loss at the lumbar spine and femoral neck and parallel improvement in carotid–femoral pulse wave velocity, consistent with MK-7's role in carboxylating bone- and vascular-protective Gla proteins.

Studied Dose Bone density and arterial stiffness RCTs in postmenopausal women used MenaQ7® 180 mcg/day for 3 years. Maintenance and broader product positioning commonly use 45–180 mcg/day. EU and many national regulatory authorities recognize MK-7 within their vitamin K reference intakes.
Active Compound Menaquinone-7 (MK-7), all-trans isomer — MenaQ7® by Gnosis/Lesaffre (formerly NattoPharma); originally produced via controlled Bacillus subtilis natto fermentation, now also available as synthetic all-trans MK-7 with high isomeric purity

Benefits

Long-term bone density support

In a 3-year randomized controlled trial in healthy postmenopausal women, MenaQ7® (180 mcg/day) reduced the age-related decline in bone mineral content and bone mineral density at the lumbar spine and femoral neck vs placebo. Effects are modest compared with pharmaceutical osteoporosis therapy but reached statistical significance over the multi-year window.

Arterial stiffness and vascular elasticity

Three-year MenaQ7® supplementation was associated with improvements in carotid–femoral pulse wave velocity and stiffness index in healthy postmenopausal women, alongside reductions in inactive (uncarboxylated) matrix Gla protein — supporting the proposed vascular role of MK-7 in keeping MGP active.

Activation of vitamin-K-dependent Gla proteins

MenaQ7® reliably reduces circulating inactive osteocalcin and matrix Gla protein, indicating improved carboxylation status of these bone- and vascular-protective proteins — a mechanistic biomarker that underpins MK-7's clinical positioning.

Long half-life and once-daily dosing

MK-7 has a plasma half-life of roughly 3 days versus about 1 hour for MK-4. Once-daily MenaQ7® dosing can therefore maintain stable, biologically meaningful circulating levels — practical for both consumer and clinical formulations.

Original commercial all-trans MK-7

MenaQ7® was the first commercially established all-trans MK-7 ingredient and has supported the clinical trial base that underpins most other branded MK-7 products. It remains a benchmark reference for clinical evidence in the MK-7 category.

Mechanism of action

1

Gamma-carboxylation of Gla-domain proteins

MK-7 is an essential cofactor for gamma-glutamyl carboxylase, which converts glutamate residues in Gla-domain proteins (osteocalcin, matrix Gla protein, GAS6, Protein S) to gamma-carboxyglutamate, enabling these proteins to bind calcium and perform their physiological functions.

2

Osteocalcin activation and bone matrix formation

Carboxylated osteocalcin binds hydroxyapatite (bone mineral) and helps incorporate calcium into the bone matrix. Inadequate K2 leaves osteocalcin undercarboxylated and impairs this binding, contributing to age-related bone loss that MK-7 supplementation may help mitigate.

3

Matrix Gla protein activation and vascular protection

Carboxylated matrix Gla protein is the body's primary inhibitor of vascular calcification, binding calcium ions in vessel walls and limiting calcium phosphate deposition. K2 deficiency leaves MGP inactive and is associated with greater arterial calcification, which MK-7 supplementation may help reduce.

4

Long-chain menaquinone tissue distribution

Compared with shorter menaquinones, MK-7's longer isoprenoid side chain supports efficient incorporation into circulating lipoproteins and extra-hepatic tissue delivery — explaining its disproportionate effect on extra-hepatic Gla proteins like osteocalcin and MGP relative to MK-4.

Clinical trials

1
MenaQ7® (180 mcg/day) for Bone Mineral Density in Postmenopausal Women — 3-Year RCT

Randomized, double-blind, placebo-controlled trial of MenaQ7® MK-7 (180 mcg/day) vs placebo in 244 healthy postmenopausal women over 3 years. Outcomes: bone mineral density at lumbar spine and femoral neck, osteocalcin carboxylation status. Published in Osteoporosis International.

244 healthy postmenopausal women; 3-year intervention.

MenaQ7® MK-7 significantly improved osteocalcin carboxylation and reduced age-related decline in bone mineral content and bone mineral density at the lumbar spine and femoral neck vs placebo. Effects were modest in magnitude compared with pharmaceutical osteoporosis therapy but reached statistical significance over the 3-year window.

2
MenaQ7® (180 mcg/day) and Arterial Stiffness — 3-Year RCT

Randomized, double-blind, placebo-controlled trial of MenaQ7® MK-7 (180 mcg/day) vs placebo in 244 healthy postmenopausal women over 3 years. Outcomes: carotid–femoral pulse wave velocity, stiffness index, circulating inactive matrix Gla protein. Published in Thrombosis and Haemostasis.

244 healthy postmenopausal women; 3-year intervention.

Three-year MenaQ7® supplementation was associated with improvements in carotid–femoral pulse wave velocity and stiffness index vs placebo, alongside significant reductions in inactive matrix Gla protein, supporting MK-7's vascular health rationale.

3
MK-7 pharmacokinetics vs phylloquinone — Blood

Pharmacokinetic study comparing synthetic vitamin K1 (phylloquinone) and natto-derived MK-7 supplementation in healthy adults to characterize plasma kinetics, half-life, and accumulation. Published in Blood.

Healthy adult volunteers; pharmacokinetic study.

MK-7 demonstrated a very long plasma half-life and far more stable serum levels than phylloquinone, with 7- to 8-fold accumulation during prolonged intake. This pharmacokinetic profile supports once-daily dosing of MenaQ7® and explains its disproportionate effect on extra-hepatic vitamin K–dependent proteins.

Side effects and drug interactions

Common Potential side effects

Excellent safety profile at typical doses (45–180 mcg/day).
No clinically significant adverse events reported in multi-year MenaQ7® RCTs.
Mild GI discomfort possible with very high doses or in sensitive individuals.
Not extensively studied in pregnancy beyond dietary intake levels; consult clinician.
No tolerable upper intake limit established by most regulatory authorities for MK-7.

Important Drug interactions

Warfarin and other vitamin K antagonists — MK-7 directly opposes the drug's mechanism; coordinate carefully with anticoagulation clinic.
Direct oral anticoagulants (DOACs) — limited interaction data, but maintain consistent vitamin K intake.
Broad-spectrum antibiotics — may reduce intestinal K2 production; supplemental K2 may become more important.
Bile acid sequestrants and orlistat — may reduce absorption of fat-soluble vitamins including K2.

Frequently asked questions about MenaQ7® (All-Trans Vitamin K2 MK-7)

What is the recommended dosage of MenaQ7® (All-Trans Vitamin K2 MK-7)?

The clinically studied dose for MenaQ7® (All-Trans Vitamin K2 MK-7) is Bone density and arterial stiffness RCTs in postmenopausal women used MenaQ7® 180 mcg/day for 3 years. Maintenance and broader product positioning commonly use 45–180 mcg/day. EU and many national regulatory authorities recognize MK-7 within their vitamin K reference intakes.. Always follow product labeling and consult a healthcare provider for personalized dosing recommendations.

What is MenaQ7® (All-Trans Vitamin K2 MK-7) used for?

MenaQ7® (All-Trans Vitamin K2 MK-7) is studied for long-term bone density support, arterial stiffness and vascular elasticity, activation of vitamin-k-dependent gla proteins. In a 3-year randomized controlled trial in healthy postmenopausal women, MenaQ7® (180 mcg/day) reduced the age-related decline in bone mineral content and bone mineral density at the lumbar spine and femoral neck vs placebo.

Are there side effects from taking MenaQ7® (All-Trans Vitamin K2 MK-7)?

Reported potential side effects may include: Excellent safety profile at typical doses (45–180 mcg/day). No clinically significant adverse events reported in multi-year MenaQ7® RCTs. Always consult a healthcare provider before starting any new supplement, especially if you have underlying conditions or take medications.

Does MenaQ7® (All-Trans Vitamin K2 MK-7) interact with medications?

Known drug interactions may include: Warfarin and other vitamin K antagonists — MK-7 directly opposes the drug's mechanism; coordinate carefully with anticoagulation clinic. Direct oral anticoagulants (DOACs) — limited interaction data, but maintain consistent vitamin K intake. Consult a pharmacist or healthcare provider if you take prescription medications.

Is MenaQ7® (All-Trans Vitamin K2 MK-7) good for bone health?

Yes, MenaQ7® (All-Trans Vitamin K2 MK-7) is researched for Bone Health support. In a 3-year randomized controlled trial in healthy postmenopausal women, MenaQ7® (180 mcg/day) reduced the age-related decline in bone mineral content and bone mineral density at the lumbar spine and femoral neck vs placebo.

References(4 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Knapen MH, Drummen NE, Smit E, Vermeer C, Theuwissen E. Three-year low-dose menaquinone-7 supplementation helps decrease bone loss in healthy postmenopausal women. Osteoporos Int. 2013;24(9):2499-507. doi: 10.1007/s00198-013-2325-6.PubMedUsed to support: 3-year RCT in 244 healthy postmenopausal women — MenaQ7® MK-7 (180 mcg/day) significantly improved vitamin K status and decreased age-related decline in bone mineral content and bone mineral density at the lumbar spine and femoral neck vs placebo.
  2. Knapen MH, Braam LA, Drummen NE, Bekers O, Hoeks AP, Vermeer C. Menaquinone-7 supplementation improves arterial stiffness in healthy postmenopausal women. A double-blind randomised clinical trial. Thromb Haemost. 2015;113(5):1135-44. doi: 10.1160/TH14-08-0675.PubMedUsed to support: 3-year RCT in 244 healthy postmenopausal women — MenaQ7® MK-7 (180 mcg/day) significantly improved carotid–femoral pulse wave velocity and stiffness index and reduced inactive matrix Gla protein vs placebo, supporting MK-7's cardiovascular role.
  3. Schurgers LJ, Teunissen KJ, Hamulyak K, Knapen MH, Vik H, Vermeer C. Vitamin K-containing dietary supplements: comparison of synthetic vitamin K1 and natto-derived menaquinone-7. Blood. 2007;109(8):3279-83. doi: 10.1182/blood-2006-08-040709.PubMedUsed to support: Pharmacokinetic comparison showing MK-7 has a much longer plasma half-life than phylloquinone, with stable serum levels and 7–8-fold accumulation during prolonged intake — mechanistic basis for once-daily MenaQ7® dosing and extra-hepatic Gla-protein activation.
  4. Beulens JW, Booth SL, van den Heuvel EG, Stoecklin E, Baka A, Vermeer C. The role of menaquinones (vitamin K2) in human health. Br J Nutr. 2013;Review of vitamin K2 health effects.PubMedUsed to support: Comprehensive review of menaquinone (vitamin K2) biology and clinical evidence in bone and cardiovascular health, providing context for the MK-7 evidence base that underpins MenaQ7® positioning.