Vitamin D3 + K2New
Synergistic combination ensuring proper calcium metabolism—D3 increases calcium absorption while K2 directs it to bones instead of arteries.
Mechanism of Action
D3 acts as a hormone precursor regulating 1000+ genes. K2 activates osteocalcin (bone) and matrix GLA protein (arterial protection).
Latest Research
Reviewed Sep 30, 2026
As of September 2026, the vitamin D3 + K2 pairing is backed by two of the most rigorous recent trials in the field. In the VITAL Telomere study — a sub-study of the 25,871-person VITamin D and OmegA-3 TriaL (VITAL) — 1,031 adults had leukocyte telomere length measured at baseline, year 2 and year 4. Compared with placebo, 2,000 IU/day of vitamin D3 significantly reduced telomere attrition by 0.14 kilobases (about 140 base pairs) over four years (p = 0.039), keeping telomeres roughly 0.035 kb/year longer than placebo (p = 0.037) — a difference the investigators described as comparable to about three years of cellular aging. Marine omega-3 (1 g/day) showed no significant effect on telomere length. Telomere shortening is a hallmark of biological aging, though it is one biomarker among many and these are findings from a single trial. Separately, the DO-HEALTH trial (777 older adults, DNA-methylation aging clocks over 3 years) found omega-3 modestly slowed several epigenetic-aging clocks, while vitamin D and exercise showed no significant individual effect and a small additive signal appeared when all three were combined.
The K2 (menaquinone-7) component addresses where calcium ends up. In the 2026 VitaK-CAC randomized trial, 180 patients with symptomatic coronary artery disease (baseline calcium score 50–400 Agatston units) received MK-7 360 µg/day or placebo for two years. Coronary artery calcium rose from a median 145 to 214 units on placebo versus 135 to 184 units on MK-7 — a statistically significant between-group difference (p = 0.02) driven by slower calcification of previously non-calcified plaque, with no significant adverse effects. This fits the long-standing rationale for pairing the two: vitamin D3 improves calcium absorption while K2 activates matrix GLA protein to help direct that calcium into bone rather than arterial walls. These are population-level results from specific study groups and do not guarantee individual outcomes. Vitamin D3 + K2 is a dietary supplement, not a drug, and is not intended to diagnose, treat, cure or prevent any disease. Because K2 can interact with warfarin and other vitamin-K-antagonist blood thinners, and because higher-dose vitamin D calls for monitoring blood calcium and 25(OH)D levels, discuss dosing with your physician.
Latest Evidence · Randomized Controlled Trial
Vitamin K2 (MK-7) Slows Coronary Calcium Progression
Median coronary artery calcium score (Agatston units) over 2 years in patients with symptomatic coronary artery disease (baseline CAC 50–400 AU). Menaquinone-7 (MK-7) 360 µg/day vs placebo; between-group difference P = .02. Vossen et al., JAMA Cardiology, 2026.
Latest research
- Zhu H, Manson JE, et al. Vitamin D and marine ω-3 fatty acids supplementation and leukocyte telomere length: 4-year findings from the VITAL randomized controlled trial. Am J Clin Nutr, 2025.
- Vossen LM, et al. Two years of menaquinone-7 supplementation and coronary artery calcification: a randomized clinical trial (VitaK-CAC). JAMA Cardiology, 2026.
- Bischoff-Ferrari HA, et al. Individual and additive effects of vitamin D, omega-3 and exercise on DNA methylation clocks of biological aging (DO-HEALTH). Nature Aging, 2025.
Related on Peak Human
Dosing Protocol
5000 IU D3 / 200mcg K2-MK7IU/mcg
Standard starting dose based on research
Therapeutic Range
2000/100
Minimum
10000/300
Maximum
Morning with fat-containing meal
Dosages are general guidelines. Individual requirements vary based on body weight, health status, and specific goals. Start with lower doses and adjust based on response.
Benefits
Primary Benefits
- Bone health
- Immune function
- Cardiovascular protection
- Mood support
Secondary Benefits
Safety Information
Contraindications
Do not use if any of the following apply:
- •Hypercalcemia
- •Warfarin (K2 component)
- •Granulomatous disease
Potential Side Effects
Some users may experience:
This is not a complete list of interactions or side effects. Individual responses vary. Always start with the lowest effective dose and monitor your response. Report any adverse effects to your healthcare provider.
Quality Markers
Look for these specific quality indicators when sourcing this compound:
- D3 cholecalciferol form
- K2 as MK-7
- Third-party verified
Trusted Certifications
Note: Supplement quality varies dramatically between brands. Cheap supplements often contain fillers, incorrect doses, or contaminants. Investing in quality products from reputable manufacturers is essential for safety and efficacy.
Evidence Profile
Evidence Score
9/10
Strong Evidence
Multiple high-quality RCTs, meta-analyses, or consistent mechanistic data
Evidence Scale
8-10
Strong
5-7
Moderate
1-4
Emerging
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