Monograph No. 005 / Vitamins
Vitamins
Vitamin K: Benefits, Dosage, and Safety
Vitamin K is a fat-soluble vitamin that acts as a coenzyme for the synthesis of proteins involved in blood clotting and bone metabolism.
Vitamin K is a fat-soluble vitamin that acts as a coenzyme for the synthesis of proteins involved in blood clotting and bone metabolism.
What vitamin k is
Vitamin K is the generic name for a family of fat-soluble compounds sharing a 2-methyl-1,4-naphthoquinone structure. The two natural groups are phylloquinone (vitamin K1), the main dietary form found mostly in green leafy vegetables, and the menaquinones (vitamin K2, designated MK-4 through MK-13), which are largely of bacterial origin and present in some animal-based and fermented foods. Phytonadione is a synthetic form of K1, and menadione (K3) is a synthetic form no longer used in supplements or fortified foods because laboratory studies in the 1980s and 1990s showed it can damage hepatic cells. Almost all long-chain menaquinones are also produced by bacteria in the human gut, and MK-4 is produced by the body from phylloquinone.
What it does
- Acts as a coenzyme for vitamin K-dependent carboxylase, the enzyme required to synthesize proteins involved in hemostasis (blood clotting)
- Supports synthesis of prothrombin (clotting factor II), a vitamin K-dependent plasma protein directly involved in blood clotting
- Supports carboxylation of osteocalcin, a vitamin K-dependent protein in bone that may be involved in bone mineralization or turnover
- Supports matrix Gla-protein (MGP), a vitamin K-dependent protein in vascular smooth muscle, bone, and cartilage that is under study for a possible role in reducing abnormal calcification
How much vitamin k per day
These are population reference values from the NIH and the Dietary Reference Intakes. They are targets for healthy people, not personal prescriptions. The last column is the Tolerable Upper Intake Level, the most you should get from all sources combined.
| Life stage | Daily target | Type | Upper limit |
|---|---|---|---|
| Infants 0-6 months | 2.0 mcg | AI | not established |
| Infants 7-12 months | 2.5 mcg | AI | not established |
| Children 1-3 years | 30 mcg | AI | not established |
| Children 4-8 years | 55 mcg | AI | not established |
| Children 9-13 years | 60 mcg | AI | not established |
| Adolescents 14-18 years (male and female) | 75 mcg | AI | not established |
| Adult men 19+ years | 120 mcg | AI | not established |
| Adult women 19+ years | 90 mcg | AI | not established |
| Pregnancy 14-18 years | 75 mcg | AI | not established |
| Pregnancy 19+ years | 90 mcg | AI | not established |
| Lactation 14-18 years | 75 mcg | AI | not established |
| Lactation 19+ years | 90 mcg | AI | not established |
Deficiency and who is at risk
Vitamin K deficiency is only considered clinically relevant when prothrombin time increases significantly due to a decrease in the prothrombin activity of blood. Bleeding and hemorrhage are the classic signs and occur only in severe cases. In newborns, deficiency can cause vitamin K deficiency bleeding (VKDB), with bleeding in the umbilicus, gastrointestinal tract, skin, nose, or other sites, and in some cases sudden intracranial bleeding with a high mortality rate. Because vitamin K is required for carboxylation of osteocalcin, deficiency could also reduce bone mineralization. Clinically significant deficiency in adults is very rare.
Groups more likely to fall short
- Newborns not treated with vitamin K at birth (poor placental transfer, low clotting factor levels, low vitamin K content of breast milk), at risk of vitamin K deficiency bleeding
- Exclusively breastfed infants (low vitamin K content of breast milk), at risk of late VKDB at age 2-12 weeks
- People with malabsorption disorders such as cystic fibrosis, celiac disease, ulcerative colitis, and short bowel syndrome
- People who have undergone bariatric surgery
Who may need more
- Newborns, who are recommended to receive a single intramuscular dose of 0.5 to 1 mg vitamin K1 at birth to prevent vitamin K deficiency bleeding
- Exclusively breastfed infants, given the low vitamin K content of breast milk
- People with malabsorption syndromes and gastrointestinal disorders (cystic fibrosis, celiac disease, ulcerative colitis, short bowel syndrome) who may need monitoring and, in some cases, supplementation
- People who have had bariatric surgery
Food sources
Green leafy vegetables and vegetable oils are the richest sources of phylloquinone. Examples per serving: natto 850 mcg (3 oz, as MK-7), frozen boiled collards 530 mcg (1/2 cup), frozen boiled turnip greens 426 mcg (1/2 cup), raw spinach 145 mcg (1 cup), raw kale 113 mcg (1 cup), boiled broccoli 110 mcg (1/2 cup), roasted soybeans 43 mcg (1/2 cup), carrot juice 28 mcg (3/4 cup), soybean oil 25 mcg (1 tbsp), edamame 21 mcg (1/2 cup), canola oil 10 mcg (1 tbsp). Meat, dairy, and eggs contain low phylloquinone but modest menaquinones (MK-4). The most common U.S. dietary sources are spinach, broccoli, iceberg lettuce, and soybean and canola oils.
Forms and absorption
Supplement forms include vitamin K1 as phylloquinone or phytonadione (synthetic K1) and vitamin K2 as MK-4 or MK-7. Few data are available on the relative bioavailability of the different forms; one study found both phytonadione and MK-7 are well absorbed, but MK-7 has a longer half-life. Free-form phylloquinone is absorbed at roughly 80%, but absorption from foods is significantly lower because plant phylloquinone is tightly bound to chloroplasts (the body absorbs only about 4% to 17% as much phylloquinone from spinach as from a tablet). Consuming vegetables with some fat improves absorption. Menadione (K3) is no longer used in supplements or fortified foods. Some single-nutrient vitamin K supplements provide very high amounts, such as 4,050 mcg (5,063% of the DV).
Safety, excess and interactions
Vitamin K has a low potential for toxicity and no Tolerable Upper Intake Level was set. The most important safety consideration is drug interaction: vitamin K can have a serious and potentially dangerous interaction with warfarin (Coumadin) and similar anticoagulants. People taking these drugs must keep their vitamin K intake from food and supplements consistent, because sudden changes can increase or decrease the anticoagulant effect. Anyone on anticoagulants should discuss vitamin K intake with their health care provider before using supplements. This information is educational and is not medical advice.
Too much
The Food and Nutrition Board did not establish a Tolerable Upper Intake Level for vitamin K because of its low potential for toxicity. The FNB reported that no adverse effects associated with vitamin K consumption from food or supplements have been reported in humans or animals. Note that this low-toxicity statement applies to phylloquinone and menaquinones, not to menadione (K3), the synthetic form that was shown to damage hepatic cells and is no longer used.
Interactions to know
- Warfarin (Coumadin) and similar vitamin K antagonists (phenprocoumon, acenocoumarol, tioclomarol): these anticoagulants antagonize vitamin K activity and deplete vitamin K-dependent clotting factors. Sudden changes in vitamin K intake can increase or decrease the anticoagulant effect, so intake must be kept consistent.
- Antibiotics: can destroy vitamin K-producing gut bacteria and may decrease vitamin K status; cephalosporins such as cefoperazone (Cefobid) may also inhibit vitamin K action. Supplements are usually needed only with prolonged use (beyond several weeks) plus poor intake.
- Bile acid sequestrants (cholestyramine/Questran, colestipol/Colestid): can reduce absorption of vitamin K and other fat-soluble vitamins; status should be monitored with long-term use.
- Orlistat (Alli, Xenical): reduces dietary fat absorption and can lower absorption of fat-soluble vitamins including vitamin K; combined with warfarin it may significantly increase prothrombin time.
How status is measured
Vitamin K status is not routinely assessed except in people who take anticoagulants or have bleeding disorders. The only clinically significant indicator is prothrombin time (the time it takes for blood to clot). Fasting plasma phylloquinone has been reported to range from 0.29 to 2.64 nmol/L in healthy people, but it is unclear whether this can quantitatively assess status, and no normal ranges for menaquinones are available.
What the evidence supports
We grade the strength of evidence behind each common reason people take vitamin k, mirroring how the NIH describes it.
Well-established physiological role described by ODS and the NASEM DRI report; vitamin K is essential for normal hemostasis.
ODS states vitamin K is a cofactor for gamma-carboxylation of osteocalcin, a role in normal bone physiology; the European Food Safety Authority approved a claim linking vitamin K to maintenance of normal bone.
ODS says it is unclear whether supplementation with any form reduces osteoporosis risk. A 2006 meta-analysis (mostly Japanese trials of MK-4 at 15 or 45 mg/day) showed benefit, but later randomized trials found no effect on bone mineral density; results are inconsistent and confounded by co-administered vitamin D and calcium.
Based mainly on observational Netherlands cohort data; ODS notes few supplementation trials exist and the role of vitamin K forms in arterial calcification and heart disease remains unclear and under active research. Association does not establish cause.
ODS notes substantial long-chain menaquinones are present in the large bowel and experts believe they satisfy at least some requirement, but the exact amount absorbed is unclear.
Sources
- S1.gov verifiedNIH Office of Dietary SupplementsVitamin K - Health Professional Fact Sheetods.od.nih.gov/factsheets/VitaminK-HealthProfessiona
- S2.gov verifiedNIH Office of Dietary SupplementsVitamin K - Consumer Fact Sheetods.od.nih.gov/factsheets/VitaminK-Consumer/
- S3.gov verifiedInstitute of Medicine (now NASEM), Food and Nutrition BoardDietary Reference Intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc (2001)nap.nationalacademies.org/catalog/10026/dietary-refe
Every figure on this page is quoted from the sources above. Science changes; we re-check and re-date pages as authorities update their guidance.