Departments of Medicine, University of Tokyo, Tokyo, Japan.
Clin Infect Dis. 2010 Feb 15;50(4):597-604. doi: 10.1086/650003.
Stavudine-containing antiretroviral regimens are widely used in developing countries. Stavudine-associated lipodystrophy commonly occurs, without a clear predictable pattern owing to the unknown interaction between stavudine and the host, among patients who received this regimen. The aim of this study was to determine the clinical risk factors and human leukocyte antigen (HLA) alleles associated with stavudine-associated lipodystrophy.
A case-control, cross-sectional study was conducted for HIV-infected patients receiving stavudine-containing antiretroviral regimens. Clinical assessments for lipodystrophy by physical examination, anthropometry, and dual-energy X-ray absorptiometry were obtained. On the basis of their clinical assessment, the patients were classified into 2 groups: the case group (moderated to severe lipodystrophy) and the control group (absent to mild lipodystrophy). The clinical characteristics and allelic distribution of HLA-A, HLA-B, HLA-C, HLA-DRB1, HLA-DQB1, and HLA-DPB1 were compared between the case group and the control group, to determine the possible association with stavudine-associated lipodystrophy.
There were 103 patients; 55 patients were in the case group, and 48 patients were in the control group. By use of forward stepwise logistic regression, the presence of HLA-B4001 (odds ratio [OR], 14.05; 95% confidence interval [CI], 2.57-76.59; P=.002) and a longer duration of stavudine treatment (OR, 1.02; 95% CI, 1.00-1.04; P=.02) were significantly associated with stavudine-associated lipodystrophy, whereas a higher body mass index during treatment (OR, 0.73; 95% CI, 0.61-0.86; P<.001) was associated with a lower risk for lipodystrophy. HLA-B4001 has a high specificity (95.8%) and a positive predictive value (88.9%) for lipodystrophy.
HLA-B4001 is a strong genetic risk factor for stavudine-associated lipodystrophy in HIV-infected patients in Thailand. HLA-B4001 may be used as a genetic marker to predict which patients will develop stavudine-associated lipodystrophy, to avoid or shorten the duration of stavudine use. This finding needs to be confirmed in further replication studies.
在发展中国家,含司他夫定的抗逆转录病毒方案被广泛应用。由于司他夫定与宿主之间未知的相互作用,接受该方案的患者中常出现脂肪营养不良,但无明确的可预测模式。本研究旨在确定与司他夫定相关的脂肪营养不良相关的临床危险因素和人类白细胞抗原(HLA)等位基因。
对接受含司他夫定的抗逆转录病毒方案的 HIV 感染者进行病例对照、横断面研究。通过体格检查、人体测量和双能 X 射线吸收法对脂肪营养不良进行临床评估。根据临床评估,将患者分为两组:病例组(中重度脂肪营养不良)和对照组(无或轻度脂肪营养不良)。比较病例组和对照组的 HLA-A、HLA-B、HLA-C、HLA-DRB1、HLA-DQB1 和 HLA-DPB1 的临床特征和等位基因分布,以确定与司他夫定相关的脂肪营养不良的可能关联。
共纳入 103 例患者;55 例患者为病例组,48 例患者为对照组。采用逐步向前逻辑回归,HLA-B4001 存在(比值比[OR],14.05;95%置信区间[CI],2.57-76.59;P=.002)和更长的司他夫定治疗时间(OR,1.02;95%CI,1.00-1.04;P=.02)与司他夫定相关脂肪营养不良显著相关,而治疗期间较高的体重指数(OR,0.73;95%CI,0.61-0.86;P<.001)与脂肪营养不良风险较低相关。HLA-B4001 对脂肪营养不良具有高特异性(95.8%)和阳性预测值(88.9%)。
在泰国感染 HIV 的患者中,HLA-B4001 是司他夫定相关脂肪营养不良的一个强烈遗传危险因素。HLA-B4001 可作为一种遗传标志物,预测哪些患者会出现司他夫定相关的脂肪营养不良,以避免或缩短司他夫定的使用时间。这一发现需要在进一步的复制研究中得到证实。