首页> 外文期刊>JAIDS: Journal of acquired immune deficiency syndromes >Does genetic diversity of HIV-1 non-B subtypes differentially impact disease progression in treatment-naive HIV-1-infected individuals? A systematic review of evidence: 1996-2010.
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Does genetic diversity of HIV-1 non-B subtypes differentially impact disease progression in treatment-naive HIV-1-infected individuals? A systematic review of evidence: 1996-2010.

机译:HIV-1非B型亚型的遗传多样性是否会影响未接受过HIV-1感染的个体的疾病进展?对证据的系统评价:1996-2010年。

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摘要

With 88% of HIV-1-infected individuals living in areas of high prevalence of non-B subtypes and with expanded global access to antiretroviral treatment (ART), studying disease progression amongst non-B subtypes gains relevance. Optimized clinical management is a possibility with knowledge of non-B subtype profiles at baseline, which is currently not possible due to lack of subtype-specific point-of-care assays. In a systematic review, we synthesized global evidence on differential disease progression amongst non-B subtypes in ART-naive individuals. Due to lack of consistent effect measures, we avoided pooling data and inferred patterns with respect to disease progression outcomes (ie, AIDS, Death, CD4, viral load changes). Subtypes C and D were more aggressive, followed by G, AE, and AG, and A being the least aggressive of all HIV-1 subtypes. Evidence of greater rates of disease progression in globally prevalent C and D subtypes highlight the importance of expanding early HIV detection, and determining subtype profile at baseline with CD4 staging to optimize the quality of ART delivery and care in global settings.
机译:88%的HIV-1感染者生活在非B型亚型的高流行地区,并且在全球范围内广泛获得抗逆转录病毒治疗(ART),因此研究非B型亚型之间的疾病进展具有相关性。知道基线时的非B亚型概况,有可能实现优化的临床管理,由于缺乏亚型特异性的即时检测,目前尚无法实现。在系统的综述中,我们综合了天真的ART患者非B亚型之间疾病进展差异的全球证据。由于缺乏一致的疗效指标,我们避免了就疾病进展结果(即艾滋病,死亡,CD4,病毒载量变化)汇总数据和推断模式。 C和D型亚型更具攻击性,其次是G,AE和AG,A是所有HIV-1亚型中攻击性最低的。在全球普遍存在的C和D亚型中,疾病进展速度加快的证据凸显了扩大早期HIV检测和通过CD4分期确定基线基线亚型分布的重要性,以优化ART递送和在全球环境中的护理质量。

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