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Cholesterol synthesis is the trigger and isoprenoid dependent interleukin-6 mediated inflammation is the common causative factor and therapeutic target for atherosclerotic vascular disease and age-related disorders including osteoporosis and type 2 d

机译:胆固醇的合成是触发因素,类胡萝卜素依赖性白介素6介导的炎症是动脉粥样硬化性血管疾病和年龄相关疾病(包括骨质疏松症和2型糖尿病)的常见病因和治疗靶点

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摘要

This is a unifying theory that cholesterol metabolites (isoprenoids) are an integral component of the signaling pathway for interleukin-6 (IL-6) mediated inflammation. IL-6 inflammation is the common causative origin for atherosclerosis, peripheral vascular disease, coronary artery disease, and age-related disorders including osteoporosis, dementia, Alzheimer's disease and type 2 diabetes. Therapeutic effects of bisphosphonates and statins are mediated by isoprenoid depletion. Statins and bisphosphonates act in the cholesterol pathway to deplete isoprenoids. Anti-inflammatory properties of statins and bisphosphonates are due to isoprenoid depletion with subsequent inhibition of IL-6 mediated inflammation. Therapeutic targets for the prevention and control of all the above diseases should focus on cholesterol metabolites and IL-6 mediated inflammation. Prevention of atherosclerotic vascular disease and age-related disorders will be by utilization of cholesterol lowering agents or techniques and/or treatment with statins and/or bisphosphonates to inhibit IL-6 inflammation through regulation of cholesterol metabolism.
机译:这是一个统一的理论,即胆固醇代谢物(异戊二烯类)是白介素6(IL-6)介导的炎症信号传导途径的组成部分。 IL-6炎症是动脉粥样硬化,周围血管疾病,冠状动脉疾病以及与年龄相关的疾病(包括骨质疏松症,痴呆症,阿尔茨海默氏病和2型糖尿病)的常见病因。双膦酸盐和他汀类药物的治疗作用是由类异戊二烯消耗介导的。他汀类药物和双膦酸盐在胆固醇途径中起作用,以消耗类异戊二烯。他汀类药物和双膦酸盐类药物的抗炎特性是由于类异戊二烯的消耗,随后抑制了IL-6介导的炎症。预防和控制以上所有疾病的治疗目标应集中在胆固醇代谢物和IL-6介导的炎症。预防动脉粥样硬化性血管疾病和与年龄有关的疾病将通过利用胆固醇降低剂或技术和/或他汀类药物和/或双膦酸盐治疗来通过调节胆固醇代谢来抑制IL-6炎症。

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