Skip to main content
. 2019 Feb 1;20(3):628. doi: 10.3390/ijms20030628

Table 3.

Overview of vitamin K effects on circulating levels of MGP forms.

Population, Age, Study, Design Study Groups Intervention Time End-Points Result
General Population
500 mg/day K1 3 years MGP (ng/mL) ↑ 3.5%
388 healthy men and postmenopausal women, 68 y, [140], randomized, double-blind, placebo-controlled placebo ↓ 4%
500 mg/day K1 + 10 μg vitamin D ↓ 80%
374 general population subjects, 60–80 y, [90], randomized, placebo-controlled Placebo + 10 μg vitamin D 3 years UcMGP (pmol/L) ↓ 4%
DpucMGP (pmol/L) ↓ 31%
DpcMGP (pmol/L) -
180 μg/day MK-7 UcMGP (nmol/L) -
DpucMGP (pmol/L) ↓ 46%
DpcMGP (pmol/L) -
360 μg/day MK-7 UcMGP (nmol/L) -
DpucMGP (pmol/L) -
60 general population subjects, 40–65 y, [137], DpcMGP (pmol/L) -
randomized, double-blind, placebo-controlled placebo 12 weeks UcMGP (nmol/L) -
10 μg/day MK-7 ↓ 12.1%
20 μg/day MK-7 ↓ 10.9%
45 μg/day MK-7 ↓ 12.3%
90 μg/day MK-7 ↓ 33.6%
180 μg/day MK-7 ↓ 39.7%
360 μg/day MK-7 ↓ 56%
44 general population subjects, 18–45 y, [138], randomized, double-blind, placebo-controlled placebo 3 months DpucMGP (pmol/L) ↑ 16.8%
10 μg/day MK-7 -
20 μg/day MK-7 6 weeks DpucMGP (pmol/L) -
18 healthy subjects treated with VKA for 4 weeks, 29 y, [141], observational 45 μg/day MK-7 -
45 μg/day MK-7 ↓ 38%
42 healthy children, 6–10 y, [139], randomized, placebo-controlled placebo 2 months DpucMGP (pmol/L) -
90 μg/day MK-7 ↓ 36%
69 healthy subjects, 20–40 y, [139], randomized, placebo-controlled placebo 7 weeks DpucMGP (pmol/L) -
244 healthy, postmenopausal women, 59.5 y, [92], randomized, double-blind, placebo-controlled 180 μg/day MK-7 ↓ 32%
placebo 3 years DpucMGP (pmol/L) ↑ 22%
CKD and HD patients
DpucMGP (pmol/L) ↓ 27%
17 HD patients, 59 y, [68], non- placebo controlled 135 μg/day MK-7 6 weeks DpcMGP (pmol/L) -
45 μg/day MK-7 ↓ 17.9%
135 μg/day MK-7 ↓ 36.7%
53 HD patients, 64.6 y, [66], randomized, non- placebo controlled 360 μg/day MK-7 6 weeks DpucMGP (pmol/L) ↓ 61.1%
360 μg, thrice weekly MK-7 ↓ 17%
720 μg, thrice weekly MK-7 ↓ 33%
200 HD patients, 70.8 y, [62], randomized, prospective, single-blind 1080 μg, thrice weekly MK-7 8 weeks DpucMGP (pmol/L) ↓ 46%
7 HD patients, 75 y, [142], observational Stop VKA 5 days DpucMGP (pmol/L) ↓ 40%
90 μg/day MK-7 DpucMGP (pmol/L) ↓ 19%
+10 μg/day MGP (pg/mL)
vitamin D
10 μg/day vitamin D DpucMGP (pmol/L)
42 CKD patients, stages 3–5, 58y, [143], Randomized, non-placebo controlled 9 months MGP (pg/mL)
90 μg/day MK-7 ↓ 10.7%
+10 μg/day
vitamin D
42 CKD patients, stages 4–5, 58 y, [72], randomized, double-blind 10 μg/day vitamin D 270 days DpucMGP (pmol/L)
50 HD patients, 64.6 y, [94], pre–post intervention 360 μg/day MK-7 4 weeks DpucMGP (pmol/L) ↓ 86%
High CVD risk and HF patients
DpMGP (nmol/L)
PMGP (nmol/L)
UcMGP (pmol/L)
1 Keutel syndrome patient, 21 y, [108], case-report, observational 10 mg/day K1 3 months CMGP (pmol/L) -
↓ 45%
2 mg/day K1
72 AVC patients, 69.1 y, [144], single-center, open-label placebo 12 months DpucMGP (pmol/L)

MGP: matrix Gla protein; ucMGP: uncarboxylated MGP; dpucMGP: dephosphorylated, uncarboxylated MGP; dpcMGP: dephosphorylated, carboxylated MGP; dpMGP: dephosphorylated MGP; pMGP: phosphorylated MGP; cMGP: carboxylated MGP; MK-7: menaquinone-7; VKA: vitamin K antagonist; CKD: chronic kidney disease; HD: hemodialysis; CVD: cardiovascular disease; HF: heart failure; AVC: aortic valve calcification. The percentages reflect change of circulating MGP forms from baseline. - = no statistically significant difference, ↑ = statistically significant positive association, ↓ = statistically significant negative association.