Dubé Michael P, Parker Robert A, Tebas Pablo, Grinspoon Steven K, Zackin Robert A, Robbins Gregory K, Roubenoff Ronenn, Shafer Robert W, Wininger David A, Meyer William A, Snyder Sally W, Mulligan Kathleen
Division of Infectious Diseases, Indiana University, Indianapolis, Indiana, USA.
AIDS. 2005 Nov 4;19(16):1807-18. doi: 10.1097/01.aids.0000183629.20041.bb.
To determine if particular components of antiretroviral drug regimens are associated with greater insulin resistance, dyslipidemia, and peripheral lipoatrophy.
Metabolic and body composition variables were measured prospectively over 64 weeks in 334 antiretroviral-naive, HIV-infected subjects who were randomized to receive nelfinavir, efavirenz, or both, combined with zidovudine/lamivudine or didanosine/stavudine in a factorial design, multicenter trial. Subjects assigned to efavirenz (n = 110) were compared with those assigned to nelfinavir (n = 99); subjects assigned to zidovudine/lamivudine (n = 154) were compared with those assigned to didanosine/stavudine (n = 180). A subset of 157 subjects had serial dual-energy X-ray absorptiometry (DEXA) scans.
Lipid measures increased in all groups. Greater increases in high density lipoprotein (HDL) cholesterol occurred with efavirenz than with nelfinavir. Greater increases in total cholesterol, non-HDL cholesterol and HDL cholesterol occurred with stavudine and didanosine than with zidovudine/lamivudine. There were no differences in insulin resistance in the comparisons. After initial increases in the first 16 weeks, median limb fat decreased. Greater changes in percentage changes in limb fat occurred with didanosine/stavudine (-16.8%) than with zidovudine/lamivudine (+4.0%; P < 0.001 for overall change from baseline) and with nelfinavir (-13.1%) compared with efavirenz (+1.8%; P = 0.003).
Over 64 weeks, all regimens were associated with increases in lipids but insulin resistance did not differ between groups. Regimens containing didanosine/stavudine and regimens containing nelfinavir were associated with greater loss of limb fat.
确定抗逆转录病毒药物治疗方案的特定成分是否与更高的胰岛素抵抗、血脂异常和外周脂肪萎缩相关。
在一项多中心、析因设计试验中,对334例未接受过抗逆转录病毒治疗的HIV感染受试者进行了为期64周的前瞻性代谢和身体成分变量测量。这些受试者被随机分配接受奈非那韦、依非韦伦或两者,同时联合齐多夫定/拉米夫定或去羟肌苷/司他夫定。将分配接受依非韦伦的受试者(n = 110)与分配接受奈非那韦的受试者(n = 99)进行比较;将分配接受齐多夫定/拉米夫定的受试者(n = 154)与分配接受去羟肌苷/司他夫定的受试者(n = 180)进行比较。157名受试者的子集进行了系列双能X线吸收法(DEXA)扫描。
所有组的血脂指标均升高。依非韦伦组高密度脂蛋白(HDL)胆固醇的升高幅度大于奈非那韦组。司他夫定和去羟肌苷组总胆固醇、非HDL胆固醇和HDL胆固醇的升高幅度大于齐多夫定/拉米夫定组。比较中胰岛素抵抗无差异。在最初的16周增加后,肢体脂肪中位数下降。去羟肌苷/司他夫定组肢体脂肪百分比变化幅度(-16.8%)大于齐多夫定/拉米夫定组(+4.0%;从基线的总体变化P < 0.001),奈非那韦组(-13.1%)大于依非韦伦组(+1.8%;P = 0.003)。
在64周内,所有治疗方案均与血脂升高相关,但各组间胰岛素抵抗无差异。含去羟肌苷/司他夫定的治疗方案和含奈非那韦的治疗方案与更大程度的肢体脂肪减少相关。