Lee Grace A, Seneviratne Tara, Noor Mustafa A, Lo Joan C, Schwarz Jean-Marc, Aweeka Francesca T, Mulligan Kathleen, Schambelan Morris, Grunfeld Carl
Metabolism Section (111F), San Francisco Department of Veterans Affairs Medical Center, San Francisco, CA 94121, USA.
AIDS. 2004 Mar 5;18(4):641-9. doi: 10.1097/00002030-200403050-00008.
Therapy with HIV protease inhibitors (PI) has been shown to worsen glucose and lipid metabolism, but whether these changes are caused by direct drug effects, changes in disease status, or body composition is unclear. Therefore, we tested the effects of the PI combination lopinavir and ritonavir on glucose and lipid metabolism in HIV-negative subjects.
A dose of 400 mg lopinavir/100 mg ritonavir was given twice a day to 10 HIV-negative men. Fasting glucose and insulin, lipid and lipoprotein profiles, oral glucose tolerance, insulin sensitivity by euglycemic hyperinsulinemic clamp, and body composition were determined before and after lopinavir/ritonavir treatment for 4 weeks.
On lopinavir/ritonavir, there was an increase in fasting triglyceride (0.89 +/- 0.15 versus 1.63 +/- 0.36 mmol/l; P = 0.007), free fatty acid (FFA; 0.33 +/- 0.04 versus 0.43 +/- 0.06 mmol/l; P = 0.001), and VLDL cholesterol (15.1 +/- 2.6 versus 20 +/- 3.3 mg/dl; P = 0.05) levels. There were no changes in fasting LDL, HDL, IDL, lipoprotein (a), or total cholesterol levels. Fasting glucose, insulin, and insulin-mediated glucose disposal were unchanged, but on a 2 h oral glucose tolerance test glucose and insulin increased. There were no changes in weight, body fat, or abdominal adipose tissue by computed tomography.
Treatment with 4 weeks of lopinavir/ritonavir in HIV-negative men causes an increase in triglyceride levels, VLDL cholesterol, and FFA levels. Lopinavir/ritonavir leads to a deterioration in glucose tolerance at 2 h, but there is no significant change in insulin-mediated glucose disposal rate by euglycemic hyperinsulinemic clamp.
有研究表明,使用HIV蛋白酶抑制剂(PI)进行治疗会使葡萄糖和脂质代谢恶化,但这些变化是由药物直接作用、疾病状态改变还是身体成分变化引起的尚不清楚。因此,我们测试了PI组合洛匹那韦和利托那韦对HIV阴性受试者葡萄糖和脂质代谢的影响。
给10名HIV阴性男性每天两次服用400mg洛匹那韦/100mg利托那韦。在洛匹那韦/利托那韦治疗4周前后,测定空腹血糖和胰岛素、脂质和脂蛋白谱、口服葡萄糖耐量、通过正常血糖高胰岛素钳夹技术测定的胰岛素敏感性以及身体成分。
服用洛匹那韦/利托那韦后,空腹甘油三酯(0.89±0.15对1.63±0.36mmol/L;P = 0.007)、游离脂肪酸(FFA;0.33±0.04对0.43±0.06mmol/L;P = 0.001)和极低密度脂蛋白胆固醇(15.1±2.6对20±3.3mg/dl;P = 0.05)水平升高。空腹低密度脂蛋白、高密度脂蛋白、中间密度脂蛋白、脂蛋白(a)或总胆固醇水平无变化。空腹血糖、胰岛素和胰岛素介导的葡萄糖处置未改变,但在2小时口服葡萄糖耐量试验中血糖和胰岛素升高。通过计算机断层扫描测量,体重、体脂或腹部脂肪组织无变化。
HIV阴性男性服用4周洛匹那韦/利托那韦会导致甘油三酯水平、极低密度脂蛋白胆固醇和游离脂肪酸水平升高。洛匹那韦/利托那韦会导致2小时时葡萄糖耐量恶化,但通过正常血糖高胰岛素钳夹技术测定的胰岛素介导的葡萄糖处置率无显著变化。