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Prolonged-release nicotinic acid: a review of its use in the treatment of dyslipidaemia.

机译:烟酸缓释剂:其在血脂异常治疗中的应用综述。

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摘要

Prolonged-release (PR) nicotinic acid (niacin) [Niaspan] is an oral, once-daily formulation of the lipid-modifying drug designed to produce less vasodilatory flushing than crystalline immediate-release (IR) nicotinic acid and less hepatotoxicity than previous sustained-release formulations of nicotinic acid.PR nicotinic acid appears to retain the same level of efficacy as crystalline IR nicotinic acid and be better tolerated than older nicotinic acid formulations. Nicotinic acid has beneficial effects on all traditional blood lipid and lipoprotein fractions and is the most effective agent for increasing high-density lipoprotein (HDL)-cholesterol (HDL-C) and reducing lipoprotein(a). The effects of PR nicotinic acid are often additive when used in combination with HMG-CoA reductase inhibitors (statins), making it a useful addition when lipid goals are not achieved with the usual statin monotherapy or when additional correction of a specific lipid abnormality is required. PR nicotinic acid also slows atherosclerotic progression and even appears to produce regression of atherosclerosis in patients on stable statin therapy. PR nicotinic acid is a logical drug choice for treating atherogenic dyslipidaemia commonly associated with type 2 diabetes mellitus and the metabolic syndrome, and has been shown to be effective in patients with diabetes without adversely affecting glycaemic control in the majority of patients. The incidence of vasodilatory flushing with PR nicotinic acid is lower than with IR nicotinic acid and it decreases substantially over time as tolerance develops. To date, there has been no clinically significant hepatotoxicity observed with PR nicotinic acid. Therefore, once-daily PR nicotinic acid appears to maximise the potential benefits of nicotinic acid, while minimising any historical tolerability or safety concerns.
机译:烟酸缓释(PR)烟酸(Niaspan)是一种脂质修饰药物的口服口服制剂,每日一次,与以前的持续烟毒相比,结晶性速释(IR)烟酸产生的血管扩张性潮红少,肝毒性小烟酸释放制剂。PR烟酸似乎保持与结晶IR烟酸相同的功效,并且比较早的烟酸制剂具有更好的耐受性。烟酸对所有传统的血脂和脂蛋白组分都有有益作用,并且是增加高密度脂蛋白(HDL)-胆固醇(HDL-C)和减少脂蛋白的最有效药物。当与HMG-CoA还原酶抑制剂(他汀类药物)联合使用时,PR烟酸的作用通常是加和的,当常规的他汀类单一疗法无法达到脂质目标或需要对特定脂质异常进行进一步校正时,PR烟酸的作用是有用的。 。 PR烟酸还可以减缓动脉粥样硬化的发展,甚至在稳定他汀类药物治疗的患者中似乎会产生动脉粥样硬化的消退。 PR烟酸是用于治疗通常与2型糖尿病和代谢综合征相关的动脉粥样硬化性血脂异常的合乎逻辑的药物选择,并且已显示在大多数糖尿病患者中对糖尿病患者有效且不会对血糖控制产生不利影响。 PR烟酸的血管舒张冲洗的发生率低于IR烟酸,随着耐受性的发展,其随时间的推移而显着降低。迄今为止,用PR烟酸还没有观察到临床上明显的肝毒性。因此,每天一次的PR烟酸似乎可以最大程度地提高烟酸的潜在益处,同时将历史耐受性或安全性问题降至最低。

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