MK-7 and Its Effects on Bone Quality and Strength

Nutrients. 2020 Mar 31;12(4):965. doi: 10.3390/nu12040965.

Abstract

Vitamin K acts as a cofactor and is required for post-translational γ-carboxylation of vitamin K-dependent proteins (VKDP). The current recommended daily intake (RDI) of vitamin K in most countries has been established based on normal coagulation requirements. Vitamin K1 and menaquinone (MK)-4 has been shown to decrease osteocalcin (OC) γ-carboxylation at RDI levels. Among the several vitamin K homologs, only MK-7 (vitamin K2) can promote γ-carboxylation of extrahepatic VKDPs, OC, and the matrix Gla protein at a nutritional dose around RDI. MK-7 has higher efficacy due to its higher bioavailability and longer half-life than other vitamin K homologs. As vitamin K1, MK-4, and MK-7 have distinct bioactivities, their RDIs should be established based on their relative activities. MK-7 increases bone mineral density and promotes bone quality and strength. Collagen production, and thus, bone quality may be affected by MK-7 or MK-4 converted from MK-7. In this review, we comprehensively discuss the various properties of MK-7.

Keywords: bone metabolism; bone quality; menaquinone-7; osteocalcin; vitamin K2.

Publication types

  • Review

MeSH terms

  • Biological Availability
  • Bone Density / drug effects*
  • Bone and Bones / metabolism*
  • Collagen / metabolism
  • Dietary Supplements*
  • Humans
  • Osteocalcin / metabolism*
  • Recommended Dietary Allowances*
  • Vitamin K 1 / pharmacokinetics
  • Vitamin K 1 / pharmacology
  • Vitamin K 2 / analogs & derivatives*
  • Vitamin K 2 / pharmacokinetics
  • Vitamin K 2 / pharmacology

Substances

  • Osteocalcin
  • Vitamin K 2
  • menatetrenone
  • Vitamin K 1
  • menaquinone 7
  • Collagen