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一项横断面单中心研究中与HIV相关脂肪代谢障碍综合征的危险因素

Risk factors for the HIV-associated lipodystrophy syndrome in a cross-sectional single-centre study.

作者信息

Schwenk A, Breuer J P, Kremer G, Römer K, Bethe U, Franzen C, Fätkenheuer G, Salzberger B

机构信息

Department of Infectious Diseases, St. George s Hospital Medical School, Cranmer Terrace, London SW17 0RE, UK.

出版信息

Eur J Med Res. 2000 Oct 30;5(10):443-8.

Abstract

OBJECTIVE

Risk factors for the HIV-associated lipodystrophy syndrome (HALS) were studied in a single-centre, cross-sectional study. -

PATIENTS AND METHODS

278 consecutive HIV-infected outpatients at a German tertiary care centre were enrolled. Changes in body shape were quantified using linear analogue scales. Cumulative treatment duration for each antiretroviral drug, CD4 cells, viral load and age were investigated as potential risk factors for a clinical diagnosis of lipodystrophy syndrome by logistic regression.

RESULTS

HALS was diagnosed in 88 patients. The risk of HALS increased significantly with longer protease inhibitor treatment (relative risk 1.61 (95% confidence interval, 1. 24 to 2.09, per year); older age and a history of low CD4 cell counts were cofactors in this multivariate model, but nucleoside analogues did not contribute significantly. Neither pattern nor severity of disease were predicted by these risk factors. Treatment durations and other risk factors were highly correlated with each other.

CONCLUSIONS

These findings support a pathogenetic role for protease inhibitor toxicity, advanced HIV disease, and ageing. No evidence for an additional effect of nucleoside analogues was found. The high correlation of potential risk factors indicates that this and other available studies may be too small to detect multiple risk factors without major confounding.

摘要

目的

在一项单中心横断面研究中对与HIV相关的脂肪代谢障碍综合征(HALS)的危险因素进行研究。

患者与方法

纳入德国一家三级护理中心的278例连续的HIV感染门诊患者。使用线性模拟量表对体型变化进行量化。通过逻辑回归分析,将每种抗逆转录病毒药物的累积治疗时长、CD4细胞、病毒载量及年龄作为脂肪代谢障碍综合征临床诊断的潜在危险因素进行研究。

结果

88例患者被诊断为HALS。随着蛋白酶抑制剂治疗时间延长,HALS风险显著增加(相对风险1.61(95%置信区间为1.24至2.09,每年));在该多变量模型中,年龄较大及既往CD4细胞计数低是辅助因素,但核苷类似物并无显著影响。这些危险因素无法预测疾病的类型及严重程度。治疗时长与其他危险因素之间高度相关。

结论

这些发现支持蛋白酶抑制剂毒性、晚期HIV疾病及衰老在发病机制中的作用。未发现核苷类似物有额外作用的证据。潜在危险因素之间的高度相关性表明,本研究及其他现有研究规模可能过小,无法在无重大混杂因素的情况下检测多种危险因素。

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