Maher Bridget, Alfirevic Ana, Vilar F Javier, Wilkins Edmund G L, Park B Kevin, Pirmohamed Munir
Department of Pharmacology, The University of Liverpool, Ashton Street, Liverpool, UK.
AIDS. 2002 Oct 18;16(15):2013-8. doi: 10.1097/00002030-200210180-00005.
The pathogenic mechanisms underlying lipodystrophy in HIV-positive patients are largely unknown. TNF-alpha has many actions that are consistent with the features of lipodystrophy; therefore, an analysis was carried out to determine whether functionally active polymorphisms in the promoter region of the TNF-alpha gene are associated with the development of lipodystrophy.
Genetic case-control association study.
Individuals were genotyped for the -238 and -308 polymorphisms in the TNF-alpha gene using polymerase chain reaction-restriction fragment length polymorphism analysis. The genotype and allele frequencies for 61 HIV-positive patients with lipodystrophy were compared with (a) 35 HIV-positive patients with no evidence of lipodystrophy and (b) 239 healthy HIV-negative individuals.
The frequency of the variant rare -238 allele was significantly different (P = 0.01) in HIV-positive patients with lipodystrophy than in those without lipodystrophy. At the genotype level, a trend towards a difference between patients with and without lipodystrophy was observed (chi2 for linear trend 5.2, P = 0.02). For the -308 polymorphism, no difference was found in genotype and allele frequencies between HIV patients with and without lipodystrophy.
The data suggest that the -238 (but not the -308) promoter region TNF-alpha gene polymorphism is a determinant in the development of HIV-related lipodystrophy. However, the results need to be confirmed in larger numbers of patients as well as in an ethnically diverse population.
HIV阳性患者脂肪代谢障碍的致病机制在很大程度上尚不清楚。肿瘤坏死因子-α(TNF-α)的许多作用与脂肪代谢障碍的特征相符;因此,开展了一项分析以确定TNF-α基因启动子区域的功能活性多态性是否与脂肪代谢障碍的发生有关。
基因病例对照关联研究。
采用聚合酶链反应-限制性片段长度多态性分析对个体的TNF-α基因-238和-308多态性进行基因分型。将61例患有脂肪代谢障碍的HIV阳性患者的基因型和等位基因频率与(a)35例无脂肪代谢障碍证据的HIV阳性患者以及(b)239例健康的HIV阴性个体进行比较。
患有脂肪代谢障碍的HIV阳性患者中变异的罕见-238等位基因频率与未患脂肪代谢障碍的患者相比有显著差异(P = 0.01)。在基因型水平上,观察到患与未患脂肪代谢障碍的患者之间存在差异趋势(线性趋势的卡方值为5.2,P = 0.02)。对于-308多态性,患与未患脂肪代谢障碍的HIV患者在基因型和等位基因频率上未发现差异。
数据表明TNF-α基因-238(而非-308)启动子区域多态性是HIV相关脂肪代谢障碍发生的一个决定因素。然而,结果需要在更多患者以及不同种族人群中得到证实。