Vitamin K2 (MK‑7) Lowers Calcification Risk in Dialysis Patients
Quick Summary:
A short‑term study gave high‑dose vitamin K2 (menaquinone‑7, MK‑7) to people on chronic haemodialysis. The supplement cut a blood marker linked to artery hardening by up to 46 % – the higher the dose, the bigger the drop. Vitamin K1 (phylloquinone) intake didn’t affect this marker.
What The Research Found
- MK‑7 reduced the inactive form of MGP – a protein that protects blood vessels from calcium buildup.
- The reduction was dose‑dependent:
- 360 µg three times a week → 17 % drop
- 720 µg three times a week → 33 % drop
- 1,080 µg three times a week → 46 % drop
- People who ate more vitamin K2 from food already had lower levels of the “inactive” MGP marker.
- Vitamin K1 (the K‑type found in leafy greens) did not influence the marker.
- Some participants stopped early because the tablets smelled bad and caused mild stomach upset.
Study Details
- Who was studied: 200 adults receiving regular haemodialysis (a kidney‑replacement therapy).
- How long: 8 weeks (about two months).
- What they took: MK‑7 capsules, given three times a week at one of three doses – 360 µg, 720 µg, or 1,080 µg.
- How the effect was measured: Blood levels of “desphosphorylated‑uncarboxylated‑MGP” (dp‑uc‑MGP), a lab test that signals how well the body can stop calcium from depositing in arteries.
What This Means For You
- If you are on haemodialysis: High‑dose vitamin K2 might help keep your blood vessels softer and less prone to calcification, but the right dose isn’t settled yet.
- If you eat a lot of leafy greens (vitamin K1): This study suggests K1 alone may not protect against this specific calcification marker in dialysis patients.
- If you consider a supplement: Look for MK‑7 (not K1) and be aware that large doses can have an unpleasant smell or mild stomach upset. Talk to your kidney doctor before starting any new vitamin regimen.
- For the general public: Maintaining a balanced diet that includes both K1 (green veggies) and K2 (fermented foods like natto, cheese, and some meats) is still a good heart‑healthy habit, even though K2 showed the stronger effect in this patient group.
Study Limitations
- Short follow‑up: Only 8 weeks, so we don’t know if the benefits last or if any long‑term side effects appear.
- Surrogate marker only: The study measured a blood test, not actual hardening of arteries or heart events.
- Drop‑outs due to taste/smell: The unpleasant odor of the tablets may limit real‑world use.
- No comparison to a placebo: All participants received some dose of MK‑7, so we can’t tell how much of the change was due to the supplement versus other factors.
- Specific to dialysis patients: Results may not apply to people with normal kidney function.
Always discuss new supplements with your healthcare provider, especially if you have kidney disease or are on dialysis.
Technical Analysis Details
Key Findings
This study found that pharmacological doses of vitamin K2 (menaquinone-7, MK-7) significantly reduced levels of desphosphorylated-uncarboxylated matrix Gla protein (dp-uc-MGP), a biomarker for vascular calcification risk, in hemodialysis patients. Higher MK-7 doses (1080 µg thrice weekly) produced the greatest reduction (46%), while baseline dp-uc-MGP levels correlated inversely with dietary menaquinone intake but not phylloquinone (vitamin K1) intake. Gastrointestinal side effects, linked to the tablets' unpleasant smell, were a notable barrier to adherence.
Study Design
The study was an observational, randomized dose-finding trial involving 200 chronic hemodialysis patients. Participants were randomly assigned to receive 360, 720, or 1080 µg of MK-7 thrice weekly for 8 weeks. Dp-uc-MGP levels were measured pre- and post-intervention. Dietary vitamin K intake (K1 and K2) was assessed via a detailed questionnaire.
Dosage & Administration
Three MK-7 doses were tested:
- Low dose: 360 µg thrice weekly
- Medium dose: 720 µg thrice weekly
- High dose: 1080 µg thrice weekly
Supplements were administered as capsules. The study reported dropouts primarily due to gastrointestinal discomfort caused by the tablets’ odor.
Results & Efficacy
- Dp-uc-MGP levels decreased dose-dependently:
- 17% reduction in the 360 µg group
- 33% reduction in the 720 µg group
- 46% reduction in the 1080 µg group
- Baseline dp-uc-MGP was not associated with phylloquinone (K1) intake (P = 0.92) but showed a significant inverse correlation with menaquinone (K2) intake (P = 0.023).
- No clinical outcomes (e.g., calcification progression) were measured; results focused solely on dp-uc-MGP as a surrogate biomarker.
Limitations
- Short duration (8 weeks) limits conclusions on long-term efficacy or safety
Original Study Reference
Vitamin K2 supplementation in haemodialysis patients: a randomized dose-finding study.
Source: PubMed
Published: 2014
📄 Read Full Study (PMID: 24285428)