US20060166948A1

US20060166948A1 - Compositions comprising vitamin k for treating or preventing age-related stiffening of arteries

Info

Publication number: US20060166948A1
Application number: US10/525,591
Authority: US
Inventors: Cees Vermeer
Original assignee: VITAK BV
Current assignee: Nattopharma ASA
Priority date: 2002-08-30
Filing date: 2003-09-01
Publication date: 2006-07-27
Also published as: US20160250160A1; EP1556025B1; SI1556025T1; US9364447B2; DK1556025T3; US12144785B2; EP1556025A1; WO2004019923A1; US20050261257A1; AU2003264150A1; ES2361740T3; DE60336161D1; ATE499094T1; PT1556025E; GB0220182D0

Abstract

Vitamin K is effective in counteracting the reduction in arterial elasticity normally associated with the aging process. A pharmaceutical composition or nutritional formulation comprising vitamin K can be used to combat age-related stiffening of the arteries, and the consequences thereof, namely pulmonary congestion, hypertension, left ventricular hypertrophy, congestive (right sided) heart failure, left sided or left ventricular failure, chronic cardiac failure, angina pectoris, myocardial infarction, Mönckeberg's sclerosis and stroke.

Description

FIELD OF THE INVENTION

The present invention concerns the use of vitamin K and derivatives thereof to prevent or treat a reduction in elasticity and distensibility of the vasculature, and thereby to lower blood pressure and prevent cardiovascular disease.

BACKGROUND

The process of aging is associated with irreversible physiological changes to the circulatory system, leading to an increased risk of blood pressure disorders, Coronary Heart Disease (CHD), and stroke. For women, this risk rises dramatically after the onset of menopause. These conditions have a significant impact on quality of life for the middle-aged and elderly and account for a large proportion of deaths and chronic illnesses in modern societies.
Patients suffering from cardiovascular disorders are frequently prescribed anticoagulants, antihypertensives, cholesterol-lowering medications, and the like. These medications usually present harmful side-effects or health risks, and moreover, the chronic effects of taking such medication regularly over the course of years or decades are not well studied. As life expectancies increase, it would be desirable to find long-term, safe and reliable natural therapies to prevent, treat or even reverse the consequences of aging on the vasculature.
Changes in mechanical properties of the main arteries have major implications for the development of vascular disease. Arteries, especially the larger elastic arteries such as the common carotid artery, become stiffer with age. Peak elasticities are achieved at about age 14-15, after which they deteriorate gradually. Measures of large artery stiffening include compliance and distensibility. Compliance reflects the buffering capacity of the vascular vessel wall, and distensibility refers to the intrinsic vascular wall elasticity. In cross-sectional studies it has been shown that the distensibility and compliance of the elastic common carotid artery decrease linearly with age. The increase in arterial stiffness with increasing age is suggested to occur more rapidly in women aged between 45 and 60 years than in men of the same age group due to the lack of oestrogen after menopause.
Reductions in complicance and distensibility result in an impairment of the arterial system to cushion pulsatile pressure. Arterial stiffening results in a higher pulse wave velocity and earlier wave reflections. This increases systolic and pulse pressure and consequently cardiac workload. To compensate, the arterial diameter increases with age. Over time, arterial stiffening can contribute to the development of inter alia left ventricular hypertrophy, congestive heart failure and coronary heart disease.
It has long been recognized that vitamin K is an essential component of the diet. It was first identified as an element needed to prevent haemorrhaging by activating blood-clotting factors. Natural K-vitamers are menadione-derivatives differing from each other in the polyisoprenoid side chain attached to the 3-position of the ring structure. Vitamin K can be provided in the diet by dark green, leafy vegetables (K₁or phylloquinone), and by fermented foods such as cheese and curd (K₂or menaquinone). K₂vitamins are also synthesized in the small intestine by resident symbiotic bacteria. Vitamin K is also needed for carboxylation of two bone matrix proteins necessary for normal bone metabolism.
In EP-A-0 679 394 and likewise in Jpn. J. Pharmacol. (1997) 75:135-143 it is disclosed that a high dietary intake of vitamin K and related molecules can reduce arterial calcification, from which it is concluded that arteriosclerosis can be treated using vitamin K. Arteriosclerosis is a disease of the arteries characterized by inflammation, macrophage invasion, foam cell formation, intima thickening, accretion of cholesterol, and formation of an atherosclerotic plaque. The onset of atherosclerosis is invariably in the large arteries such aorta and coronary arteries. In more advanced stages one may see plaque rupture leading to sudden vascular occlusion, myocardial infarction and cerebrovascular accident (infarction of the brain).
A completely different process is that of vascular stiffening due to loss of elasticity of the arteries. Vascular stiffening is associated with ageing, diabetes mellitus and renal dysfunction; it is the result of degradation of the elastic lamellae in the tunica media resulting in loss of elasticity. The onset of vascular stiffening is generally seen in the smaller vessels, from extends to the larger arteries. This will lead to increased blood pressure, vascular widening, and in later stages to rupture of (mainly the small) arteries and capillaries. The present patent application relates to the effect of vitamin K on vascular stiffening. Studies have shown that also on a molecular level age-related stiffening of the arteries can be distinguished from arteriosclerotic/atherosclerotic calcification. Whereas atherosclerosis is invariably associated with inflammation and starts with destruction of the endothelial cell layer at the luminal side of the tunica intima, age-related stiffening is a process which originates in the tunica media, and is not associated with inflammation. It is believed that age-related stiffening occurs as a result of deposition of minerals around the elastic fibres of the tunica media, followed by degradation of the elastin structure. After deterioration of the elastin, the elastic properties of the artery depend on collagen, which is much less flexible.
For the first time, it has now been shown that arterial compliance and distensibility can be improved long-term by administering vitamin K, relative to subjects receiving no nutritional supplementation (placebo). Thus, administration of vitamin K is a useful therapeutic measure to prevent the development of cardiovascular disease conditions including hypertension, left ventricular hypertrophy, congestive heart failure, myocardial infarction, stroke, Mönckeberg's sclerosis and coronary heart disease.

SUMMARY OF THE INVENTION

In a first aspect, the invention provides use of a composition comprising vitamin K or a derivative thereof, optionally together with vitamin D or a derivative thereof, in the manufacture of a medicament or nutritional formulation for treating or preventing age-related stiffening of arteries.
In a second aspect, the invention provides use of a composition comprising vitamin K or a derivative thereof, optionally together with vitamin D or a derivative thereof, in the manufacture of a medicament or nutritional formulation for treating or preventing an age-related decrease in compliance and/or distensibility of arteries and/or an age-related increase in pulse pressure.
In another aspect, the invention provides use of a composition comprising vitamin K or a derivative thereof, optionally together with vitamin D or a derivative thereof, in the manufacture of a medicament or nutritional formulation for treating or preventing any of: hypertension, left ventricular hypertrophy, congestive heart failure, myocardial infarction, stroke, Mönckeberg's sclerosis, and coronary heart disease.
In a further aspect, the invention provides a composition for promoting healthy arteries, comprising vitamin K or a derivative thereof, and optionally vitamin D or a derivative thereof, and one or more additional components selected from: polyphenols, vitamin C, vitamin E (tocopherols and/or tocotrienols), L-Arginine, phytosterols, antihypertensive peptides, soluble fibers (e.g. guar, pectin), omega-3, omega-6 and/or omega-9 fatty acids, carnitine, taurine, coenzyme Q10, creatine, folic acid, folates, magnesium, potassium, vitamin B6, and vitamin B12.
In another aspect of the invention there is provided a composition for promoting healthy arteries which comprises: 0.5-1.5 mg vitamin K; 5-10 μg vitamin D; 450-550 mg Calcium; 7-12 mg Zinc; and 100-200 mg Magnesium.
In yet another aspect of the invention there is provided a kit comprising Vitamin K or a derivative thereof, and optionally vitamin D or a derivative thereof and a medicament, for simultaneous, separate or sequential administration, wherein said medicament is selected from the group consisting of: anticoagulants, antithrombotics, fibrinolytics, antihypertensives, diuretics, antianginals, hypolipidaemic agents, beta-blockers, ACE inhibitors, cardiac glycosides, phosphodiesterase inhibitors, anti-arrhythmics, and calcium antagonists.

DESCRIPTION OF THE FIGURES

FIG. 1 shows how the Distensibility Coefficient (DC) varies over a 3 year study period when placebo, Vitamin D (MD) and Vitamins K plus D (MDK) are administered to a group of postmenopausal women.
FIG. 2 shows how the Compliance Coefficient (CC) varies over a 3 year study period when placebo, Vitamin D (MD) and Vitamins K plus D (MDK) are administered to a group of postmenopausal women.
In each case the black bar represents the baseline measurement (100%), and the shaded bars are the % change relative to baseline after 3 years.

DETAILED DESCRIPTION OF THE INVENTION

This invention provides the first form of directed therapy for reducing age-related arterial stiffening (as distinct from stiffening due to atherosclerosis). Arterial elastic properties (compliance and distensibility) deteriorate with age. However, the severity of this downward trend was found to be significantly reduced in a group of menopausal women who regularly consumed a supplement of vitamin K (plus Vitamin D) over the course of 3 years. These women were selected for the study on the basis of criteria which included a lack of evidence of atherosclerotic disease and low risk factors for the disease.
Preferably vitamin K and derivatives refers to one or more compounds of Formula 1′, and/or their pharmaceutically or nutritionally acceptable salts,

here R may be any covalently linked organic group including polyisoprenoid residues, esters, ethers, thiol adducts, etc.
and especially the compounds thereof of Formula 2:

in which n is an integer from 1 to 12; and in which the broken lines indicate the optional presence of a double bond.
Vitamin K and derivatives thereof, as used herein, refers in particular to phylloquinone (also known as vitamin K₁), dihydrophylloquinone; menaquinone-4 (MK-4) and the long chain menaquinones. It is generally accepted that the naphthoquinone is the functional group, so that the mechanism of action is similar for all K vitamins. Differences may be expected, however, with respect to intestinal absorption, transport, tissue distribution, and bioavailability. For use in the present invention, phylloquinone and MK-4 are preferred, and phylloquinone is particularly preferred.
Sources of vitamin K which can be used according to the present invention include the following: phylloquinone from natural sources such as vegetable extracts, fats and oils, synthetic phylloquinone, synthetic vitamin K₃(menadione), different forms of vitamin K₂: synthetic MK-4, MK-5, MK-6, MK-7, MK-8, MK-9, MK-10, MK-11, MK-12 and MK-13, natto (food prepared from fermented soy-bean, rich in MK-7), and other fermented foods or dairy products.
The dose of vitamin K useful in performing the invention is not restricted but varies depending on, for example, the age of the subject and the degree of risk of developing arterial stiffening. Current AI values or Adequate Intakes (as determined by the Institute of Medicine) are 120 μg for men and 90 μg for women. Benefits may be derived by selecting dosages higher than the AI values, particularly in population groups where vitamin K deficiencies are common, for instance among postmenopausal women. For example, suitable dosages may lie in the range 10 to 1000 μg, more preferably 50 to 500 μg, and most preferably 100 to 200 μg vitamin K/day. Where national legislation permits, it may be advisable to provide dosage ranges as high as from 1 to 200 mg/day, preferably from 5 to 150 mg/day, and more preferably from 10 to 100 mg/day. No upper limit (UL) has been defined for vitamin K, since it is not known to have any adverse effects on the body.
In terms of body weight, daily dosage may vary between 0.5 to 50 μg/kg body weight/day, preferably 0.75 to 25 μg/kg body weight/day, more preferred 1 to 15 μg/kg body weight/day.
Vitamin D is included together with vitamin K in the composition used in the clinical study, and may play a role in supporting the function of vitamin K in preventing arterial stiffening. Any form of natural or synthetic vitamin D may be employed, including vitamin D₁, vitamin D₂(calciferol), vitamin D₃(cholecalciferol) and vitamin D analogues (e.g. alfacalcidol, dihydrotachysterol, calcitriol). Natural sources of vitamin D include saltwater fish, organ meats, fish-liver oils and egg yolk. Suitable dosages of vitamin D are 2 to 50 μg/day, preferably 5 to 20 μg/day, and most preferably about 7 to 10 μg/day.
In the clinical study described in the Examples arterial wall property measurements were taken at t=0 and t=3 years. This is good support for concluding that ingestion of vitamin K over long periods is an effective way of limiting an increase in arterial stiffness. The preferred treatment period is a minimum of 6 months, more preferably at least 18 months, and ideally at least 36 months. In fact, as there are no adverse side-effects associated with dietary vitamin K supplementation, it should be regarded as an essential component of a healthy lifestyle over the course of a lifetime, and especially throughout middle age and old age.
The preferred route of administration of vitamin K is enterally, especially orally, but the parenteral or topical routes are viable alternatives. Vitamin K is conventionally provided in the form of tablets or capsules, i.e. in a pharmaceutical or dietary supplement format. For pharmaceutical preparations or dietary supplements the vitamin K may be compounded with pharmaceutically acceptable carriers, excipients or diluents in the forms of pills, tablets (coated or uncoated), hard or soft capsules, dragées, lozenges, oral solutions, suspensions and dispersions, syrups or sterile parenteral preparations. Suitable excipients include inert diluents such as calcium carbonate, sodium carbonate, lactose, calcium phosphate, sodium phosphate; granulating and disintegrating agents such as cornstarch or alginic acid; binding agents such as starch gelatin or acacia; effervescents; and lubricating agents such as magnesium stearate, stearic acid or talc.
It is also possible to deliver Vitamin K (optionally together with vitamin D) in a fortified food or beverage product. Preferred nutritional product formats include: juice drinks, dairy drinks, powdered drinks, sports drinks, mineral water, soy beverages, hot chocolate, malt drinks, biscuits, bread, crackers, confectioneries, chocolate, chewing-gum, margarines, spreads, yoghurts, breakfast cereals, snack bars, meal replacements, protein powders, desserts, and medical nutrition tube feeds and nutritional supplements.
Conventional additives may be included in the compositions of the invention, including any of those selected from preservatives, chelating agents, effervescing agents, natural or artificial sweeteners, flavoring agents, coloring agents, taste masking agents, acidulants, emulsifiers, thickening agents, suspending agents, dispersing or wetting agents, antioxidants, and the like.
As consumers who are at risk from stiffening arteries are also inclined to develop other ageing-related disorders, it may be of benefit to combine vitamin K (and optionally vitamin D) with other healthy or pharmaceutically active components in a single composition, or in the form of a kit for simultaneous, sequential or separate administration. For instance, it is envisaged that vitamin K could be provided in conjunction with medicaments selected from anticoagulants such as aspirin or COX-2 inhibitors, antithrombotics, fibrinolytics, antihypertensives, diuretics, antianginals, hypolipidaemic agents including statins, bile acid sequestrants, nicotinic acid derivatives, and fibrates, beta-blockers, ACE inhibitors, cardiac glycosides, phosphodiesterase inhibitors, antiarrhythmics, and calcium antagonists. Other bioactive substances for co-administration include: polyphenols, vitamin C, vitamin E (tocopherols and/or tocotrienols), L-Arginine, phytosterols, antihypertensive peptides, soluble fibers (e.g. guar, pectin), omega-3, omega-6 and/or omega-9 fatty acids, carnitine, taurine, coenzyme Q10, creatine, folic acid, folates, magnesium, potassium, vitamin B6, and vitamin B12.
Anyone perceived to be at risk from cardiovascular disorders or already suffering from conditions such as angina pectoris, hypertension, a history of stroke, and other cerebrovascular disorders can benefit from ingesting vitamin K in order to counteract age-related stiffening of the arteries. Particular target population groups are: postmenopausal women, diabetics, obese individuals, smokers, alcoholics, sedentary and inactive people, the elderly, hemodialysis patients, men over 40 years of age, people suffering from chronic stress, and those consuming an unhealthy diet prone to causing cardiovascular diseases.
Although it is believed that vitamin K is effective at limiting age-related stiffness throughout the network of arteries in the body, its therapeutic effect on the body is probably most significant with respect to its influence on the larger elastic arteries of the body, especially the common carotid arteries supplying blood to the neck and head, the aorta, and the renal arteries.
By reducing arterial stiffening, vitamin K also has the effects of counteracting the sequelae of arterial stiffening, namely hypertension, left ventricular hypertrophy, congestive heart failure, myocardial infarction, stroke and coronary heart disease. “Elevated blood pressure” or “hypertension” as used herein refers to a blood pressure persistently exceeding 140/90 mmHg (systolic/diastolic).

EXAMPLES

Clinical Study to Compare Effects of Supplementation of Vitamin D and Vitamin D+Vitamin K on a Group of Healthy Postmenopausal Women

Subjects
The participants were enrolled in a 3-year double-blind placebo-controlled clinical trial in which the effects of minerals, vitamin D- and vitamin K-containing supplements were investigated on bone mineral density and vessel wall characteristics. Inclusion criteria were: apparently healthy women, Caucasian, between 50 and 60 years old, and at least 2 years postmenopausal. Exclusion criteria were: use of oral anticoagulants, corticosteroids, hormone replacement therapy, vitamin concentrates or food supplements, and high alcohol consumption (>6 glasses/day). In total 181 women met the criteria for participation and were randomized into the study. Information on cardiovascular risk factors, current health status, medical history, drug use and smoking behaviour was collected before the start of the study. Within this trial participants underwent clinical examinations at 0, 3, 12, 18, 24 and 36 months. The vascular examinations took place at baseline and at the end of the study after 3 years.
All participants gave written informed consent and the trial was approved by the Maastricht University Hospital Medical Ethics Committee.
Study Design
The subjects were randomized into three groups. In the first group (n=60) participants received a placebo (maltodextrin), in the second group (n=58) participants received a supplement containing 500 mg calcium (natural calcium complex derived from milk), 10 mg zinc, 150 mg magnesium and 8 μg vitamin D₃(minerals+vitamin D=MD-group), and in the third group (n=63) participants received a supplement containing the same constituents as the MD group but with an additional 1 mg of vitamin K₁(minerals+vitamins D+K=MDK-group). The three different types of supplements were similar in appearance and taste, and participants were allowed to choose between a supplement in the form of a tasteless powder (to be mixed with water before intake) or in the form of chocolate-coated tablets with a crunchy malt core. Participants were instructed to take one sachet with powder or three tablets per day during evening hours, preferably after the meal. Also, they were advised to maintain their usual diets and to avoid taking supplements containing either calcium, vitamin D, or vitamin K for two months before and throughout the study. Novartis Consumer Health SA (Nyon, Switzerland) prepared and provided all supplements.
The right common carotid artery of each patient was investigated. The same investigator performed all examinations at the start and the end of the study and for each participant several repeated measurements (5-7) are made during one session. Reproducibility was evaluated for assessment of common carotid artery distension and diameter.
Before the vascular examination, height and weight were measured with standardized equipment to estimate the body mass index (weight/height²).
Measurements
The primary outcome measures for the purposes of this study were the vessel wall characteristics of the common carotid artery measured with ultrasound (ATL Mark V).
The ultrasonic vessel wall tracking system (WTS) to determine arterial wall properties has been described in detail before (Hoeks A P et al., Ultrasound Med Biol 1990; 16:121-8, and Kool M J F et al., Cardiovascular Research 1994;28:610-614). This ultrasound system provides estimates of the arterial end-diastolic diameter (d) and the change in diameter from diastole to systole (Δd) normalized for the end-diastolic diameter (Δd/d) for each captured heart beat. In parallel with diameter change measurement, arterial blood pressure was recorded at the level of the brachial artery by means of a semiautomated oscillometric device (DINAMAP). Pulse pressure (Δp), defined as systolic minus diastolic blood pressure, was determined by averaging the three measurements nearest to the distension measurements. From d, Δd and Δp, vascular distensibility (DC) and compliance (CC) were calculated according to the following equations:
DC=(2dΔd+Δd ²)/(d ² /Δp)(Distensibility Coefficient)
CC=π(2dΔd+Δd ²)/4Δp(Compliance Coefficient)
The intima-media thickness (IMT) of the posterior wall was measured simultaneously at the same location (2-3 cm proximal to the bifurcation) of the common carotid artery where the diameter and diameter changes were measured. At the end of the session, recorded IMT-files are processed employing the wall thickness program. The threshold for the derivative was maintained at 0.025. Each heart-beat within a recording resulted in an estimate of wall thickness; the median of the estimates per recording was used for further evaluation.
Statistical Analysis
Statistical analysis was performed using the Statistical Package SPSS(SPSS Corp, Chicago, Ill.). Results are presented as means±standard deviation (SD), unless indicated otherwise. Only participants who had completed the study were included in the analysis. Furthermore, participants who during the study had started to use medications which are known to have a direct effect on the vessel wall, were excluded from analysis. Also, participants with atherosclerotic plaques in the common carotid artery and a high variability in the results (arterial translation of >2 mm and beat-to-beat variation in distension of >20%) were excluded.
A paired t-test was used to evaluate the change in the vessel wall characteristics over the three years within each group. We considered a level of p<0.05 to be statistically significant. For every participant, the percentage change from baseline in all parameters was calculated and the mean change from baseline was calculated per group. Primary outcome analysis consisted of comparison of the change in DC, CC, PP and IMT between the MD-group and placebo and between the MDK-group and placebo. Linear regression analysis was used with the change in vascular parameters relative to baseline as dependent variable and the treatment groups and several covariates as explanatory variables. Baseline values of age, BMI, smoking (yes or no), heart rate and mean arterial pressure were chosen as covariates, because their influence on the change in vascular properties or response to the supplementation could not be excluded.
Vascular Parameters of Elasticity
Table 1 details the baseline measurements of each study group. Table 2 summarizes per group the differences between the mean values at baseline and at the end of the study for all vascular parameters with their paired-levels of significance. As was to be expected, the DC and CC in the placebo group decreased significantly (by 10% and 6%, respectively). The PP, on the other hand, increased by 7%, but the increase did not reach the level of significance. In the MD-group, DC decreased significantly (by 7%) and CC decreased by 4%, while the PP increased by 6%; however these latter two changes did not reach the level of significance. In the MDK-group, however, the DC and CC remained approximately constant over the three year period, the CC even showing a tendency to increase (+3%). The PP remained unchanged throughout the entire study period.
FIGS. 1 and 2 (see also Table 3 and Table 3a) illustrate the percentage change in DC and CC respectively of the three groups. After adjustment for baseline heart rate, mean arterial pressure, age, weight and smoking, the changes in the placebo-relative to the MDK-group remained statistically significant and were: 8.8% decrease of DC (95% Cl: 1.9 to 21.4), 8.6% decrease of CC (95% Cl: 1.8 to 20.3), and 6.3% increase of PP (95% Cl: −17.1 to −0.7). In the same analysis no differences were found between the changes in the placebo- and the MD-group: 2.5% decrease of DC (95% Cl: −14.8 to 6.3), 2.2% decrease of CC (95% Cl: −13.8 to 6.3), and 0.11% increase of PP (95% Cl: −5.6 to 12.1).
Discussion of Results
The deleterious effects on the arteries of aging over a period of 3 years are clearly evident from the control (placebo) group, and underline how rapidly the vasculature can go into decline. The medical practitioner, being aware of the link between a decrease in elasticity of the arteries and diverse cardiovascular conditions, would recognise from these data that there is an urgent need to find a treatment method capable of combating the rapid decline in arterial elasticity, particularly in postmenopausal women.
The MD group, who received a vitamin D supplement, failed to show any improvement in measures of vascular wall aging relative to the placebo group. It can be concluded that provision of vitamin D alone is not capable of delivering cardiovascular benefits to postmenopausal women fulfilling the criteria applied in the present study.

In stark contrast to the placebo and MD groups, the MDK group showed significant relative improvements in distensibility, compliance and pulse pressure over the 3 year period of the study. These results demonstrate that regular consumption of vitamin K, or of the combination of vitamin K and vitamin D, can slow and maybe even reverse the process of stiffening of the arteries. As a consequence of slowing down the process of arterial stiffening, vitamin K supplementation inevitably impacts on the incidence of cardiovascular disorders linked to arterial stiffening, including those related to increased strain on the heart and reduced responsiveness of the circulatory system to changes in demand.

TABLE 1


Baseline characteristics (mean ± standard deviation)
in the three treatment groups

	Placebo	MD-group	MDK-group
	(n = 40)	(n = 30)	(n = 38)
Baseline-characteristics	Mean ± SD	Mean ± SD	Mean ± SD

Age (yr)	54.1 ± 3.0	55.9 ± 2.8*	55.4 ± 2.8
Weight (kg)	69.5 ± 11.9	70.6 ± 11.1	66.3 ± 9.5
Height (m)	1.65 ± 0.05	1.65 ± 0.07	1.63 ± 0.06
BMI (kg/m²)	25.6 ± 4.3	26.0 ± 4.4	25.1 ± 3.1
Postmenopausal age (yr)	4.6 ± 3.7	7.6 ± 5.1**	5.1 ± 4.3
Non-smokers (%)	75.0	73.9	85.0
Diameter (μm)	7162 ± 562	7314 ± 582	7173 ± 411
Distension (μm)	372 ± 118	353 ± 83	332 ± 83
Pulse Pressure (mm Hg)	51.9 ± 11.1	52.9 ± 10.1	53.7 ± 14.3
Heart Rate (beats/min)	60.8 ± 9.2	63.1 ± 8.9	60.6 ± 6.6
CC (mm²/kPa)	0.64 ± 0.23	0.61 ± 0.20	0.56 ± 0.17
DC (MPa⁻¹)	15.8 ± 5.2	14.5 ± 4.0	14.0 ± 4.0
IMT (mm)	0.63 ± 0.11	0.64 ± 0.10	0.61 ± 0.05

*significant different from placebo (p < 0.05)
**significant different from placebo and MDK-group (p < 0.05)

TABLE 2


Change in vessel wall characteristics (mean ± SD) in study population after 3 years

	Placebo (n = 40)	MD-group (n = 30)	MDK-group (n = 38)
	Difference between	Difference between	Difference between
Vessel wall	T = 0 and T = 3 years	T = 0 and T = 3 years	T = 0 and T = 3 years
characteristics	(paired t-test)	(paired t-test)	(paired t-test)

Diameter (μm)	196 ± 295 (p = 0.00)	154 ± 179 (p = 0.00)	131 ± 226 (p = 0.00)
Distension (μm)	−21 ± 61 (p = 0.03)	−12.6 ± 47 (p = 0.15)	−3.9 ± 49 (p = 0.63)
Pulse Pressure	2.7 ± 9.9 (p = 0.09)	2.8 ± 10.1 (p = 0.14)	−0.18 ± 7.6 (p = 0.89)
(mm Hg)
DC (MPa⁻¹)	−1.8 ± 3.4 (p = 0.00)	−1.4 ± 3.0 (p = 0.02)	−0.39 ± 3.0 (p = 0.43)
CC (mm²/kPa)	−0.05 ± 0.1 (p = 0.01)	−0.04 ± 0.11 (p = 0.10)	0.01 ± 0.11 (p = 0.75)
IMT (mm)	0.05 ± 0.08 (p = 0.00)	0.02 ± 0.09 (p = 0.32)	0.06 ± 0.06 (p = 0.00)
Heart rate (beats/min)	3.0 ± 7.0 (p = 0.01)

TABLE 3


Mean % change from baseline in vessel wall characteristics.
(for each subject the % change from baseline is calculated
for each variable and then the mean of these
individual changes is calculated per group)

	Placebo	MD-group	MDK-group
	(n = 40) Mean	(n = 30) Mean	(n = 38) Mean
Vessel wall	% change from	% change from	% change from
characteristics	baseline	baseline	baseline

Diameter (μm)	2.8% ± 4.1	2.2% ± 2.5	1.8% ± 3.1
Distension (μm)	−4.3% ± 15.9	−2.4% ± 13.0	0.3% ± 15.9
Pulse Pressure	6.5% ± 19.7	6.3% ± 20.0	0.2% ± 13.4*
(mm Hg)
DC (MPa⁻¹)	−9.6% ± 21.4	−7.1% ± 18.3	−0.8% ± 21.9*
CC (mm²kPa)	−5.9% ± 19.5	−3.7% ± 18.6	2.7% ± 20.4*
MT (mm)	8.6% ± 13.5	4.0% ± 13.9	9.8% ± 9.8*

*significant difference with placebo after adjustment for age, weight, smoking, mean arterial pressure and heart rate (linear regression analysis table 3a)

TABLE 3a


Multivariate regression analysis of the effects of the MDK-group
and the MD-group compared to placebo on the change in vessel
wall characteristics after three years with the following covariables:
baseline age, weight, smoking, heart rate and mean arterial pressure.

Variables	Coefficient ± SEM	P	95% Cl

Y = change in DC
(% relative to baseline)
X = MDK	11.7 ± 4.9	0.020	1.9 to 21.4
X = MD	4.2 ± 5.3	0.430	−6.3 to 14.8
Y = change in CC
(% relative to baseline)
X = MDK	11.1 ± 4.7	0.019	1.8 to 20.3
X = MD	3.8 ± 5.0	0.459	−6.3 to 13.8
Y = change in PP
(% relative to baseline)
X = MDK	−8.9 ± 4.1	0.034	−17.1 to −0.70
X = MD	−3.3 ± 4.5	0.465	−12.1 to 5.6
Y change in IMT
(% relative to baseline)
X = MDK	3.0 ± 3.1	0.345	−3.23 to 9.15
X = MD	−2.4 ± 3.3	0.476	−8.9 to 4.2

Claims

1. Use of a composition comprising vitamin K or a derivative thereof, optionally together with vitamin D or a derivative thereof, in the manufacture of a medicament or nutritional formulation for treating or preventing age-related stiffening of arteries, not associated with arteriosclerosis.

2. Use of a composition according to claim 1, wherein said vitamin K is vitamin K₁(phylloquinone) or vitamin K₂(menaquinone).

3. Use of a composition according to claim 2 wherein said vitamin K is vitamin K₁(phylloquinone).

4. Use of a composition according to claim 1 wherein the daily dosage of vitamin K or a derivative thereof is in the range 50 μg-1000 μg.

5. Use of a composition according to claim 1 wherein the medicament or nutritional composition comprises vitamin D or a derivative thereof.

6. Use of a composition according to claim 5 wherein said vitamin D is vitamin D₃(cholecalciferol).

7. Use of a composition according to claim 1 wherein the medicament or nutritional formulation is for administration to a postmenopausal woman.

8. Use of a composition according to claim 1 wherein the medicament or nutritional formulation is to be administered over a period of at least 12 months, preferably at least 36 months.

9. Use of a composition according to claim 1 wherein said arteries are the common carotid arteries.

10. Use of a composition according to claim 1 for promoting healthy arteries, comprising vitamin K or a derivative thereof, optionally together with vitamin D or a derivative thereof, further comprising one or more additional components selected from: polyphenols, vitamin C, vitamin E (tocopherols and/or tocotrienols), L-arginine, phytosterols, antihypertensive peptides, soluble fibers (e.g. guar, pectin), omega-3, omega-6 and/or omega-9 fatty acids, carnitine, taurine, coenzyme Q10, creatine, folic acid, folates, magnesium, potassium, vitamin B6, and vitamin B12.

11. Use of a composition according to claim 10 which comprises in a single dose: 0.5-1 mg vitamin K and 5-10 μg vitamin D.

12. Use of a composition according to claim 10 which comprises: 0.5-1.5 mg vitamin K; 5-10 μg vitamin D; 450-550 mg Calcium; 7-12 mg Zinc; and 100-200 mg Magnesium.

13. Use of a composition according to claim 12 which comprises about 1 mg Vitamin K₁; 8 μg vitamin D₃, 500 mg Calcium, 10 mg Zinc; and 150 mg Magnesium.

14. Use of a composition according to claim 10 which is a food or beverage product or a dietary supplement.

15. A method of preventing or treating age-related arterial stiffening, not associated with arteriosclerosis, comprising administering to a person in need of such treatment an effective amount of vitamin K or a derivative thereof and optionally vitamin D or a derivative thereof.