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本文引用的文献

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Screening for lipid disorders in children: US Preventive Services Task Force recommendation statement.儿童脂质紊乱筛查:美国预防服务工作组建议声明
Pediatrics. 2007 Jul;120(1):e215-9. doi: 10.1542/peds.2006-1812.
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Drug therapy of high-risk lipid abnormalities in children and adolescents: a scientific statement from the American Heart Association Atherosclerosis, Hypertension, and Obesity in Youth Committee, Council of Cardiovascular Disease in the Young, with the Council on Cardiovascular Nursing.儿童和青少年高危脂质异常的药物治疗:美国心脏协会青少年动脉粥样硬化、高血压和肥胖委员会、青年心血管疾病理事会以及心血管护理理事会的科学声明
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Cardiovascular risk reduction in high-risk pediatric populations.
Pediatrics. 2007 Mar;119(3):618-21. doi: 10.1542/peds.2006-3557.
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Change to a once-daily combination including boosted atazanavir in HIV-1-infected children.改为每日一次的联合用药方案,其中包括在感染HIV-1的儿童中使用增强型阿扎那韦。
Pediatr Infect Dis J. 2006 Sep;25(9):809-14. doi: 10.1097/01.inf.0000234069.37972.94.
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Incidence of opportunistic and other infections in HIV-infected children in the HAART era.高效抗逆转录病毒治疗(HAART)时代HIV感染儿童中机会性感染及其他感染的发病率
JAMA. 2006 Jul 19;296(3):292-300. doi: 10.1001/jama.296.3.292.
6
Dyslipidemia among perinatally HIV-infected children enrolled in the PACTS-HOPE cohort, 1999-2004: a longitudinal analysis.1999 - 2004年参加PACTS - HOPE队列研究的围产期感染艾滋病毒儿童的血脂异常:一项纵向分析
J Acquir Immune Defic Syndr. 2006 Apr 1;41(4):453-60. doi: 10.1097/01.qai.0000218344.88304.db.
7
96-week comparison of once-daily atazanavir/ritonavir and twice-daily lopinavir/ritonavir in patients with multiple virologic failures.多次病毒学失败患者中阿扎那韦/利托那韦每日一次与洛匹那韦/利托那韦每日两次的96周比较。
AIDS. 2006 Mar 21;20(5):711-8. doi: 10.1097/01.aids.0000216371.76689.63.
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Quality of life for children and adolescents: impact of HIV infection and antiretroviral treatment.儿童和青少年的生活质量:艾滋病毒感染及抗逆转录病毒治疗的影响
Pediatrics. 2006 Feb;117(2):273-83. doi: 10.1542/peds.2005-0323.
9
Improvement in dyslipidaemia after switching stavudine to tenofovir and replacing protease inhibitors with efavirenz in HIV-infected children.在感染HIV的儿童中,将司他夫定换为替诺福韦并将蛋白酶抑制剂替换为依非韦伦后血脂异常的改善情况。
Antivir Ther. 2005;10(8):917-24.
10
Hypertriglyceridemia and hypercholesterolemia in human immunodeficiency virus-1-infected children treated with protease inhibitors.接受蛋白酶抑制剂治疗的人类免疫缺陷病毒1型感染儿童的高甘油三酯血症和高胆固醇血症
Arch Med Res. 2006 Jan;37(1):129-32. doi: 10.1016/j.arcmed.2005.05.013.

围产期感染艾滋病毒儿童中高胆固醇血症发病率与抗逆转录病毒治疗(包括蛋白酶抑制剂)的关联。

Association of hypercholesterolemia incidence with antiretroviral treatment, including protease inhibitors, among perinatally HIV-infected children.

作者信息

Tassiopoulos Katherine, Williams Paige L, Seage George R, Crain Marilyn, Oleske James, Farley John

机构信息

Center for Biostatistics in AIDS Research, Harvard School of Public Health, Boston, MA 02115, USA.

出版信息

J Acquir Immune Defic Syndr. 2008 Apr 15;47(5):607-14. doi: 10.1097/QAI.0b013e3181648e16.

DOI:10.1097/QAI.0b013e3181648e16
PMID:18209684
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3089963/
Abstract

CONTEXT

Antiretroviral therapy has been associated with hypercholesterolemia in HIV-infected children. Few longitudinal studies have been conducted to examine this association, however.

OBJECTIVE

To evaluate the incidence of and risk factors for development of hypercholesterolemia in a large pediatric study.

DESIGN

Prospective cohort study (Pediatric AIDS Clinical Trials Group 219C).

PARTICIPANTS

A total of 2122 perinatally HIV-infected children free of hypercholesterolemia at entry.

OUTCOME

Development of hypercholesterolemia (total cholesterol >or=220 mg/dL at 2 consecutive visits). Cox proportional hazards models were used to evaluate risk factors.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

目的

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。

设计

前瞻性队列研究(儿科艾滋病临床试验组219C)。

参与者

共有2122名出生时感染HIV且入组时无高胆固醇血症的儿童。

观察指标

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。

结果

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。

结论

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。