Ilowite N T, Samuel P, Ginzler E, Jacobson M S
University of New York, Stony Brook.
Arthritis Rheum. 1988 Jul;31(7):859-63. doi: 10.1002/art.1780310706.
Patients with systemic lupus erythematosus are at increased risk for premature atherosclerosis. We examined one possible etiologic factor, dyslipoproteinemia, both before and after corticosteroid therapy. We identified 2 distinct patterns of dyslipoproteinemia. One is attributable to active disease; the other is attributable, in part, to corticosteroid therapy. The dyslipoproteinemia of active disease consists of depressed high density lipoprotein cholesterol and apoprotein A-I with elevated very low density lipoprotein cholesterol and triglyceride, while the dyslipoproteinemia after corticosteroid therapy consists of increased total cholesterol, very low density lipoprotein cholesterol, and triglyceride. The possible pathophysiologic mechanisms responsible for these patterns, as well as the possible roles in premature atherosclerosis seen in systemic lupus erythematosus patients, are discussed.
系统性红斑狼疮患者发生过早动脉粥样硬化的风险增加。我们在皮质类固醇治疗前后研究了一个可能的病因因素,即血脂蛋白异常。我们识别出两种不同的血脂蛋白异常模式。一种归因于活动性疾病;另一种部分归因于皮质类固醇治疗。活动性疾病导致的血脂蛋白异常表现为高密度脂蛋白胆固醇和载脂蛋白A-I降低,极低密度脂蛋白胆固醇和甘油三酯升高,而皮质类固醇治疗后的血脂蛋白异常则表现为总胆固醇、极低密度脂蛋白胆固醇和甘油三酯增加。本文讨论了导致这些模式的可能病理生理机制,以及在系统性红斑狼疮患者过早动脉粥样硬化中可能发挥的作用。