首页> 外文期刊>International journal of infectious diseases : >Late presentation and transmitted drug resistance mutations in new HIV-1 diagnoses in Detroit
【24h】

Late presentation and transmitted drug resistance mutations in new HIV-1 diagnoses in Detroit

机译:底特律新HIV-1诊断中的晚期呈报和传播的耐药性突变

获取原文
           

摘要

Objective: To characterize the epidemiology and transmitted drug resistance mutation (TDRM) patterns among individuals with newly diagnosed HIV-1 infection seen at Henry Ford Hospital in Detroit from 2006 to 2008. Methods: This was a retrospective analysis of medical records from individuals aged >=18 years with a new diagnosis of HIV-1 infection. Individuals who underwent genotypic resistance testing were included in the study. Results: One hundred thirty-three individuals were included; 99 (74%) were males, 104 (78%) were African-Americans, and 61 (46%) had a CD4+ count of @?200 cells/@ml. The prevalence of TDRM was 17% (23/133). Non-nucleoside reverse transcriptase mutations occurred in 11 (8%), nucleoside reverse transcriptase mutations in 13 (10%), and protease inhibitor mutations in 10 (8%). CD4+ count >350 cells/@ml and HIV viral load on presentation were associated with TDRM in the multivariate analysis (p=0.004 and p<0.001 respectively). Conclusions: Late diagnosis of HIV-1 and transmitted antiretroviral resistance are relatively common in Detroit. While most newly diagnosed persons were candidates for antiretroviral therapy on presentation, the high prevalence of TDRM has significant implications in the selection of first-line highly active antiretroviral therapy (HAART).
机译:目的:研究2006年至2008年在底特律亨利福特医院发现的HIV-1感染者的流行病学特征和传播耐药性突变(TDRM)特征。方法:本研究回顾性分析了年龄> = 18岁,具有新的HIV-1感染诊断。该研究包括接受基因型耐药性测试的个体。结果:包括133个人。男性中99人(74%),非裔美国人104人(78%)和61人(46%)的CD4 +计数为200细胞/ ml。 TDRM的患病率为17%(23/133)。非核苷逆转录酶突变发生在11(8%),核苷逆转录酶突变发生在13(10%),蛋白酶抑制剂突变发生在10(8%)。在多变量分析中,CD4 +计数> 350细胞/ ml和呈现的HIV病毒载量与TDRM相关(分别为p = 0.004和p <0.001)。结论:底特律相对较晚诊断HIV-1和传播抗逆转录病毒耐药性。虽然大多数新诊断的患者都可以作为抗逆转录病毒治疗的候选药物,但TDRM的高流行对选择一线高活性抗逆转录病毒治疗(HAART)具有重要意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号