Tassiopoulos Katherine, Williams Paige L, Seage George R, Crain Marilyn, Oleske James, Farley John
Center for Biostatistics in AIDS Research, Harvard School of Public Health, Boston, MA 02115, USA.
J Acquir Immune Defic Syndr. 2008 Apr 15;47(5):607-14. doi: 10.1097/QAI.0b013e3181648e16.
Antiretroviral therapy has been associated with hypercholesterolemia in HIV-infected children. Few longitudinal studies have been conducted to examine this association, however.
To evaluate the incidence of and risk factors for development of hypercholesterolemia in a large pediatric study.
Prospective cohort study (Pediatric AIDS Clinical Trials Group 219C).
A total of 2122 perinatally HIV-infected children free of hypercholesterolemia at entry.
Development of hypercholesterolemia (total cholesterol >or=220 mg/dL at 2 consecutive visits). Cox proportional hazards models were used to evaluate risk factors.
Thirteen percent of children had hypercholesterolemia at entry, and an additional 13% developed hypercholesterolemia during follow-up for an incidence rate of 3.4 cases per 100 person-years (95% confidence interval [CI]: 3.0 to 3.9). After adjustment for age, boosted protease inhibitor (PI) use (hazard ratio [HR] = 13.9, 95% CI: 6.73 to 28.6), nonboosted PI use (HR = 8.65, 95% CI: 4.19 to 17.9), and nonnucleoside reverse transcriptase inhibitor use (HR = 1.33, 95% CI: 1.04 to 1.71) were associated with increased risk of hypercholesterolemia, and higher viral load was protective (>50,000 vs. <or=400 copies/mL; HR = 0.59, 95% CI: 0.39 to 0.90). Self-reported adherent subjects had higher risk.
PIs were significant risk factors for hypercholesterolemia. Higher viral load was protective and may reflect nonadherence. Further follow-up is critical to evaluate long-term consequences of chronic PI exposure and hypercholesterolemia.
抗逆转录病毒疗法与感染HIV的儿童出现高胆固醇血症有关。然而,很少有纵向研究来检验这种关联。
在一项大型儿科研究中评估高胆固醇血症的发生率及发病危险因素。
前瞻性队列研究(儿科艾滋病临床试验组219C)。
共有2122名出生时感染HIV且入组时无高胆固醇血症的儿童。
高胆固醇血症的发生(连续2次就诊时总胆固醇≥220mg/dL)。采用Cox比例风险模型评估危险因素。
13%的儿童在入组时患有高胆固醇血症,另有13%在随访期间出现高胆固醇血症,发病率为每100人年3.4例(95%置信区间[CI]:3.0至3.9)。在调整年龄后,使用增强型蛋白酶抑制剂(PI)(风险比[HR]=13.9,95%CI:6.73至28.6)、未增强型PI(HR=8.65,95%CI:4.19至17.9)和非核苷类逆转录酶抑制剂(HR=1.33,95%CI:1.04至1.71)与高胆固醇血症风险增加相关,而较高的病毒载量具有保护作用(>50,000拷贝/mL与≤400拷贝/mL相比;HR=0.59,95%CI:0.39至0.90)。自我报告依从性好的受试者风险更高。
PI是高胆固醇血症的重要危险因素。较高的病毒载量具有保护作用,可能反映了不依从性。进一步随访对于评估长期暴露于PI和高胆固醇血症的长期后果至关重要。