Sacktor Ned, Nakasujja Noeline, Skolasky Richard L, Rezapour Mona, Robertson Kevin, Musisi Seggane, Katabira Elly, Ronald Allan, Clifford David B, Laeyendecker Oliver, Quinn Thomas C
Departments of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Clin Infect Dis. 2009 Sep 1;49(5):780-6. doi: 10.1086/605284.
In the United States, clade B is the predominant human immunodeficiency virus (HIV) subtype, whereas in sub-Saharan Africa, clades A, C, and D are the predominant subtypes. HIV subtype may have an impact on HIV disease progression. The effect of HIV subtype on the risk of dementia has, to our knowledge, not been examined. The objective of this study was to examine the relationship between HIV subtype and the severity of HIV-associated cognitive impairment among individuals initiating antiretroviral therapy in Uganda.
Sixty antiretroviral-naive HIV-infected individuals with advanced immunosuppression who were at risk of HIV-associated cognitive impairment underwent neurological, neuropsychological, and functional assessments, and gag and gp41 regions were subtyped. Subtype assignments were generated by sequence analysis using a portion of the gag and gp41 regions.
Thirty-three HIV-infected individuals were infected with subtype A, 2 with subtype C, 9 with subtype D, and 16 with A/D recombinants. Eight (89%) of 9 HIV-infected individuals with subtype D had dementia, compared with 7 (24%) of 33 HIV-infected individuals with subtype A (P = .004).
These results suggest that, in untreated HIV-infected individuals with advanced immunosuppression who are at risk of developing HIV-associated cognitive impairment, HIV dementia may be more common among patients infected with subtype D virus than among those infected with subtype A virus. These findings provide the first evidence, to our knowledge, to demonstrate that HIV subtypes may have a pathogenetic factor with respect to their capacity to cause cognitive impairment. Additional studies are needed to confirm this observation and to define the mechanism by which subtype D leads to an increased risk of neuropathogenesis.
在美国,B亚型是主要的人类免疫缺陷病毒(HIV)亚型,而在撒哈拉以南非洲,A、C和D亚型是主要亚型。HIV亚型可能会影响HIV疾病的进展。据我们所知,尚未研究过HIV亚型对痴呆风险的影响。本研究的目的是探讨乌干达开始抗逆转录病毒治疗的个体中HIV亚型与HIV相关认知障碍严重程度之间的关系。
60名未接受过抗逆转录病毒治疗、有HIV相关认知障碍风险且免疫抑制严重的HIV感染者接受了神经学、神经心理学和功能评估,并对gag和gp41区域进行了亚型分析。通过对gag和gp41区域的一部分进行序列分析来确定亚型。
33名HIV感染者感染了A亚型,2名感染了C亚型,9名感染了D亚型,16名感染了A/D重组体。9名感染D亚型的HIV感染者中有8名(89%)患有痴呆,而33名感染A亚型的HIV感染者中有7名(24%)患有痴呆(P = .004)。
这些结果表明,在未治疗的、有HIV相关认知障碍风险且免疫抑制严重的HIV感染者中,感染D亚型病毒的患者比感染A亚型病毒的患者患HIV痴呆的情况可能更常见。据我们所知,这些发现首次证明了HIV亚型在导致认知障碍的能力方面可能具有致病因素。需要进一步的研究来证实这一观察结果,并确定D亚型导致神经发病风险增加的机制。