Green Hannah, Tilston Peter, Fearnhill Esther, Pillay Deenan, Dunn David T
HIV Group, Medical Research Council Clinical Trials Unit, 222 Euston Road, London, United Kingdom.
J Acquir Immune Defic Syndr. 2008 Oct 1;49(2):196-204. doi: 10.1097/QAI.0b013e318185725f.
The use of different lists of resistance mutations has resulted in estimates of transmitted HIV drug resistance (THDR) that are often not comparable.
We estimated the rate of THDR based on the 3 definitions: > or =1 major mutation(s) listed on the International AIDS Society (IAS)-USA drug resistance mutation (DRM) 2006 list; > or =1 surveillance drug resistance mutation(s) (SDRM) on the published list by Shafer et al; and low-level/intermediate/high-level resistance to > or =1 drug(s) according to the Stanford HIVdb interpretation algorithm. Analyses were based on genotypic resistance tests conducted during 1997-2005 on antiretroviral therapy-naive patients and reported to the UK HIV Drug Resistance Database. The effect on THDR rates of revisions to the IAS-DRM list was also examined.
Overall, 10.0%, 9.2%, and 10.4% of the 8272 samples available for analysis were classified as having THDR by the IAS-DRM, SDRM, and Stanford definitions, respectively; however, there was discordance for 244 (3%) samples. Changes in the version of the IAS-DRM list over time resulted in 4%-7% differences in the estimated rate of THDR, which increased from 4%-5% during 1997-2000 to 5%-7% during 2001-2005.
The choice of genotypic definition had a minor influence on the estimated rate of THDR. The SDRM list is recommended for epidemiological estimates of THDR as it has been designed with such studies in mind.
使用不同的耐药突变列表导致对传播的HIV耐药性(THDR)的估计往往不可比。
我们基于以下3种定义估计了THDR率:国际艾滋病学会(IAS)-美国2006年耐药突变(DRM)列表上列出的≥1个主要突变;Shafer等人发表的列表上的≥1个监测耐药突变(SDRM);以及根据斯坦福HIVdb解释算法对≥1种药物的低水平/中等水平/高水平耐药。分析基于1997年至2005年期间对未接受抗逆转录病毒治疗的患者进行的基因型耐药性检测,并报告给英国HIV耐药数据库。还研究了IAS-DRM列表修订对THDR率的影响。
总体而言,在可用于分析的8272个样本中,分别有10.0%、9.2%和10.4%根据IAS-DRM、SDRM和斯坦福定义被分类为具有THDR;然而,有244个(3%)样本存在不一致。IAS-DRM列表版本随时间的变化导致THDR估计率有4%-7%的差异,该估计率从1997年至2000年期间的4%-5%增加到2001年至2005年期间的5%-7%。
基因型定义的选择对THDR估计率有较小影响。推荐使用SDRM列表进行THDR的流行病学估计,因为它在设计时就考虑到了此类研究。