Heterogeneity in neurocognitive change trajectories among people with HIV starting antiretroviral therapy in Rakai, Uganda

被引:15
|
作者
Rubin, Leah H. [1 ,2 ,3 ]
Saylor, Deanna [1 ]
Nakigozi, Gertrude [4 ]
Nakasujja, Noeline [5 ]
Robertson, Kevin [6 ]
Kisakye, Alice [4 ]
Batte, James [4 ]
Mayanja, Richard [4 ]
Anok, Aggrey [4 ]
Lofgren, Sarah M. [7 ]
Boulware, David R. [7 ]
Dastgheyb, Raha [1 ]
Reynolds, Steven J. [8 ,9 ]
Quinn, Thomas C. [8 ,9 ]
Gray, Ronald H. [3 ]
Wawer, Maria J. [3 ]
Sacktor, Ned [1 ]
机构
[1] Johns Hopkins Univ, Dept Neurol, Sch Med, 600 N Wolfe St Meyer 6-113, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD 21205 USA
[3] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidmiol, Baltimore, MD 21205 USA
[4] Rakai Hlth Sci Program, Kalisizo, Uganda
[5] Makerere Univ, Dept Psychiat, Kampala, Uganda
[6] Univ North Carolina Chapel Hill, Dept Neurol, Chapel Hill, NC USA
[7] Univ Minnesota, Minneapolis, MN USA
[8] NIAID, Div Intramural Res, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[9] Johns Hopkins Univ, Sch Med, Med, Baltimore, MD USA
关键词
HIV; Global health; Cognitive impairment; PREFRONTAL-HIPPOCAMPAL INTERACTIONS; NEUROPSYCHOLOGICAL TEST-PERFORMANCE; INTIMATE PARTNER VIOLENCE; DOMAIN CRITERIA RDOC; INFECTED PATIENTS; RURAL UGANDA; HIV-1-ASSOCIATED DEMENTIA; COGNITIVE PERFORMANCE; CONSTRUCT-VALIDITY; SEXUAL COERCION;
D O I
10.1007/s13365-019-00768-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Considerable heterogeneity exists in patterns of neurocognitive change in people with HIV (PWH). We examined heterogeneity in neurocognitive change trajectories from HIV diagnosis to 1-2 years post-antiretroviral therapy (ART). In an observational cohort study in Rakai, Uganda, 312 PWH completed a neuropsychological (NP) test battery at two-time points (ART-naive, 1-2 years post-ART initiation). All NP outcomes were used in a latent profile analysis to identify subgroups of PWH with similar ART-related neurocognitive change profiles. In a subset, we examined subgroup differences pre-ART on cytokine and neurodegenerative biomarkers CSF levels. We identified four ART-related change subgroups: (1) decline-only (learning, memory, fluency, processing speed, and attention measures), (2) mixed (improvements in learning and memory but declines in attention and executive function measures), (3) no-change, or (4) improvement-only (learning, memory, and attention measures). ART-related NP outcomes that are most likely to change included learning, memory, and attention. Motor function measures were unchanged. Subgroups differed on eight of 34 pre-ART biomarker levels including interleukin (IL)-1 beta, IL-6, IL-13, interferon-gamma, macrophage inflammatory protein-1 beta, matrix metalloproteinase (MMP)-3, MMP-10, and platelet-derived growth factor-AA. The improvement-only and mixed subgroups showed lower levels on these markers versus the no-change subgroup. These findings provide support for the need to disentangle heterogeneity in ART-related neurocognitive changes, to focus on higher-order cognitive processes (learning, memory, attention) as they were most malleable to change, and to better understand why motor function remained unchanged despite ART treatment. Group differences in pre-ART CSF levels provide preliminary evidence of biological plausibility of neurocognitive phenotyping.
引用
收藏
页码:800 / 813
页数:14
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