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Do HIV-1 non-B subtypes differentially impact resistance mutations and clinical disease progression in treated populations? Evidence from a systematic review

机译:HIV-1非B型亚型是否会影响治疗人群的耐药突变和临床疾病进展?系统审查的证据

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There are 31 million adults living with HIV-1 non-B subtypes globally, and about 10 million are on antiretroviral therapy (ART). Global evidence to guide clinical practice on ART response in HIV-1 non-B subtypes remains limited. We systematically searched 11 databases for the period 1996 to 2013 for evidence. Outcomes documented included time to development of AIDS and/or death, resistance mutations, opportunistic infections, and changes in CD4 cell counts and viral load. A lack of consistent reporting of all clinical end points precluded a meta-analysis. In sum, genetic diversity that precipitated differences in disease progression in ART-na?ve populations was minimized in ART-experienced populations, although variability in resistance mutations persisted across non-B subtypes. To improve the quality of patient care in global settings, recording HIV genotypes at baseline and at virologic failure with targeted non-B subtype-based point-of-care resistance assays and timely phasing out of resistance-inducing ART regimens is recommended.Keywords: HIV-1, non-B subtypes, disease progression, resistance mutation, differential impact, systematic review, evidence
机译:全球有3100万成年人患有HIV-1非B型亚型,约有1000万正在接受抗逆转录病毒疗法(ART)。指导临床实践的HIV-1非B亚型ART反应的全球证据仍然有限。我们系统地搜索了1996年至2013年期间的11个数据库以作为证据。记录的结果包括艾滋病和/或死亡的发展时间,耐药性突变,机会性感染以及CD4细胞计数和病毒载量的变化。由于缺乏对所有临床终点的一致报告,因此无法进行荟萃分析。总而言之,尽管在非B亚型中抵抗力突变的变异性仍然存在,但在未接受过ART治疗的人群中促成疾病进展差异的遗传多样性已降至最低。为了提高在全球范围内的患者护理质量,建议使用针对性的非B亚型基于即时护理的耐药性检测方法记录基线和病毒学失败时的HIV基因型,并及时淘汰诱导耐药性的ART方案。 HIV-1,非B亚型,疾病进展,耐药突变,差异影响,系统评价,证据

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