Related Experiment Video
Updated: Oct 4, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Vitamin K Supplementation in Chronic Kidney Disease Patients: Where is the Evidence?
Stefanos Roumeliotis1, Vassilios Liakopoulos1, Leon J Schurgers2
1Division of Nephrology and Hypertension, 1st Department of Internal Medicine, AHEPA Hospital, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Insights
Vitamin K supplementation may help reduce vascular calcification in chronic kidney disease (CKD) patients. This intervention could improve cardiovascular outcomes by activating Matrix Gla Protein, a key inhibitor of vascular calcification.
Area of Science:
- Nephrology
- Cardiology
- Nutritional Science
Background:
- Vascular calcification (VC) is common in chronic kidney disease (CKD), predicting cardiovascular (CV) mortality.
- Matrix Gla Protein (MGP), a VC inhibitor, needs vitamin K for activation.
- CKD patients often have poor vitamin K status and significant CV calcification.
Purpose of the Study:
- To review human studies on vitamin K supplementation in CKD patients.
- To explore vitamin K's role in mitigating VC progression and CV risk in CKD.
- To suggest future research directions in this field.
Main Methods:
- Focus on interventional human studies.
- Analysis of vitamin K supplementation effects on VC and MGP activity.
- Review of epidemiological data linking vitamin K status to VC and CV outcomes.
Main Results:
- Epidemiological data link vitamin K depletion to VC progression and adverse CV outcomes.
- Vitamin K supplementation (especially menaquinone 7) may reduce inactive MGP.
- Potential for retarding or reversing VC in early and advanced CKD.
Conclusions:
- Vitamin K supplementation is a promising strategy for managing VC in CKD patients.
- Further interventional studies are needed to confirm efficacy and optimal protocols.
- Addressing vitamin K deficiency is crucial for cardiovascular health in CKD.
Abstract:
Vascular calcification (VC) is highly prevalent in Chronic Kidney Disease (CKD) patients, progresses gradually with deterioration of kidney function and is a strong, independent predictor of cardiovascular (CV) mortality. Matrix Gla Protein (MGP), the most potent inhibitor of VC, requires vitamin K as a co-factor to become biologically active. Accumulating epidemiological data have associated vitamin K depletion with VC progression and CV outcomes. CKD patients are characterized by poor vitamin K status and at the same time, pronounced CV calcification. In early and advanced CKD, including end-stage kidney disease, exogenous supplementation of vitamin K (especially with menaquinone 7, its most bioavailable form) might decrease the inactive form of MGP (dephosphorylated, uncarboxylated MGP) and probably retard the progression or even reverse VC. Here, we focus and discuss the interventional human studies of vitamin K supplementation in CKD patients and suggest future directions in this area of interest.
Related Concept Videos
Chronic Kidney Disease III: Interprofessional Care
Chronic Kidney Disease II: Clinical Manifestations
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Chronic Kidney Disease I: Introduction
Chronic Kidney Disease IV: Nursing Management

