首页> 外文期刊>Brazilian Journal of Infectious Diseases >Prevalence and factors associated with darunavir resistance mutations in multi-experienced HIV-1-infected patients failing other protease inhibitors in a referral teaching center in Brazil
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Prevalence and factors associated with darunavir resistance mutations in multi-experienced HIV-1-infected patients failing other protease inhibitors in a referral teaching center in Brazil

机译:在巴西的转诊教学中心中,患有其他蛋白酶抑制剂失败且经历过多次HIV-1感染的多经验HIV-1感染患者中,与darunavir耐药突变相关的患病率和相关因素

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Information about resistance profile of darunavir (DRV) is scarce in Brazil. Our objectives were to estimate the prevalence of DRV resistance mutations in patients failing protease inhibitors (PI) and to identify factors associated with having more DRV resistance mutations. All HIV-infected patients failing PI-based regimens with genotyping performed between 2007 and 2008 in a referral teaching center in S?o Paulo, Brazil, were included. DRV-specific resistance mutations listed by December 2008 IAS-USA panel update were considered. Two Poisson regression models were constructed to assess factors related to the presence of more DRV resistance mutations. A total of 171 HIV-infected patients with available genotyping were included. The number of patients with lopinavir, saquinavir, and amprenavir used in previous regimen were 130 (76%), 83 (49%), and 35 (20%), respectively. The prevalence of major DRV resistance mutations was 50V: 5%; 54M: 1%; 76V: 4%; 84V: 15%. For minor mutations, the rates were 11I: 3%; 32I: 7%; 33F: 23%; 47V: 6%; 54L: 6%; 74P: 3%; 89V: 6%. Only 11 (6%) of the genotypes had > 3 DRV resistance mutations. In the clinical model, time of HIV infection of > 10 years and use of amprenavir were independently associated with having more DRV resistance mutations. In the genotyping-based model, only total number of PI resistance mutations was associated with our outcome. In conclusion, the prevalence of DRV mutations was low. Time of HIV infection, use of amprenavir and total number of PI resistance mutations were associated with having more DRV mutations.
机译:在巴西,有关地那那韦(DRV)耐药性的信息很少。我们的目标是评估蛋白酶抑制剂(PI)失败的患者中DRV耐药性突变的患病率,并确定与更多DRV耐药性突变相关的因素。纳入了2007年至2008年之间在巴西圣保罗的转诊教学中心进行的基于PI的基因分型失败的所有HIV感染患者。考虑了2008年12月IAS-USA小组更新中列出的DRV特异性抗药性突变。构建了两个Poisson回归模型来评估与更多DRV抗性突变的存在相关的因素。共有171名HIV感染患者进行了基因分型。先前方案中使用的洛匹那韦,沙奎那韦和氨普那韦的患者人数分别为130(76%),83(49%)和35(20%)。主要的DRV耐药性突变的患病率为50V:5%; 54M:1%; 76V:4%; 84V:15%。对于微小突变,比率为11I:3%; 32I:7%; 33F:23%; 47V:6%; 54升:6%; 74P:3%; 89V:6%。仅11个(6%)基因型具有> 3个DRV抗性突变。在临床模型中,HIV感染时间> 10年和使用氨普那韦与更多的DRV耐药性突变独立相关。在基于基因分型的模型中,只有PI耐药性突变的总数与我们的结果相关。总之,DRV突变的患病率较低。 HIV感染时间,氨普那韦的使用以及PI抗药性突变的总数与更多的DRV突变有关。

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