| 主权项 |
1. A method for using a pharmaceutical composition comprising
administering to a subject a subtherapeutic dose of the pharmaceutical composition by a treatment regime comprising at least one intervention-cycle, wherein one intervention-cycle comprises a treatment period of 1 week to 9 months of treatment and a rest period of 1 to 12 months of discontinuation of treatment, wherein the intervention-cycle is repeated, wherein the (a) functional and morphological properties of an arterial wall in the subject are maintained or improved, (b) arterial aging in the subject is prevented, reduced, or reversed, (c) worsening or occurrence of cardiovascular disorders in the subject are decreased, or a combination thereof, wherein the subject comprises at least one cardiovascular disorder or at least one risk factor for a cardiovascular disorder or a risk for a coronary heart disease (10-year risk) according to the Framingham Risk Score of more than 10% wherein the cardiovascular disorder is selected from the group consisting of ischemic heart disease, carotid and intracerebral artery disease, peripheral arterial disease, aortic aneurism, and any combinations thereof, or wherein the risk factor for a cardiovascular disorder is a disorder selected from the group consisting of diabetes, metabolic syndrome, hypercholesterolemia, hypertension, chronic inflammatory disorder, psoriasis, and any combinations thereof, or wherein the risk factor for a cardiovascular disorder is a risky life style selected from the group consisting of smoking, obesity, and a combination thereof, and wherein the pharmaceutical composition comprises: at least one renin-angiotensin-aldosterone system inhibitor in a subtherapeutic daily dose, wherein the subtherapeutic daily dose of the at least one renin-angiotensin-aldosterone system inhibitor does not change the systolic and/or diastolic blood pressure by more than 15%, wherein the at least one renin-angiotensin-aldosterone system inhibitor is an angiotensin II receptor antagonist selected from the group consisting of azilsartan, losartan, eprosartan, irbesartan, olmesartan, candesartan, valsartan, telmisartan and any pharmaceutically acceptable salt or ester thereof and combinations thereof, and at least one HMG-CoA reductase inhibitor in a subtherapeutic daily dose, wherein the subtherapeutic daily dose of the at least one HMG-CoA reductase inhibitor does not change the LDL cholesterol level in a subject by more than 15%, wherein the at least one HMG-CoA reductase inhibitor is selected from the group consisting of mevastatin, pitavastatin, lovastatin, simvastatin, pravastatin, fluvastatin, atorvastatin, cerivastatin, rosuvastatin, and any pharmaceutically acceptable salt or ester thereof, and combinations thereof. |
