Yuen Tracy, Brouillette Marie-Josée, Fellows Lesley K, Ellis Ronald J, Letendre Scott, Heaton Robert, Mayo Nancy
*Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Québec, Canada;†Division of Clinical Epidemiology, McGill University Health Center, Montreal, Québec, Canada;‡Chronic Viral Illness Service, McGill University Health Centre and Department of Psychiatry, McGill University, Montreal, Québec, Canada;§Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Québec, Canada;Departments of ‖Neurosciences; and¶Psychiatry, University of California San Diego, San Diego, CA; and#HIV Neurobehavioural Research Centre, University of California San Diego, San Diego, CA.
J Acquir Immune Defic Syndr. 2017 Sep 1;76(1):48-54. doi: 10.1097/QAI.0000000000001466.
Little is known about the predictors of neurocognitive decline in HIV+ individuals with good virological control. Identification of modifiable risk factors would allow targeted interventions to reduce the risk of decline in higher risk individuals. The objective of this study was to develop a risk index to predict neurocognitive decline over 3 years in aviremic HIV+ individuals.
As part of the CNS HIV Anti-Retroviral Therapy Effects Research (CHARTER) study, HIV+ adults completed clinical evaluation and neuropsychological tests every 6 months. Group-based trajectory analysis was used to detect patterns of neurocognitive change; individuals who deteriorated ≥ 0.5 SD on at least one neuropsychological test were considered decliners. Multiple logistic regression was used to identify baseline sociodemographic, clinical, biological, and lifestyle factors associated with decline in the subgroup that was consistently aviremic during the first 3 years. A risk index was developed using the beta-coefficients from the final regression model.
Neurocognitive decline occurred in 23 of 191 (12%) participants followed longitudinally. The baseline factors that predicted decline were glomerular filtration rate ≤50 mL/min, known duration of HIV infection ≥15 years, education ≤12 years, and cerebrospinal fluid protein >45 mg/dL.
Using this analytic approach, neurocognitive decline was uncommon in this sample of aviremic HIV+ individuals. The 3-year risk of decline ranged from 2% in those with no risk factors to 95% in those with all 4. The strongest predictor was glomerular filtration rate, also a predictor of cardiovascular disease. This raises the possibility that controlling vascular risk factors could reduce the risk of neurocognitive decline.
对于病毒学控制良好的HIV感染者神经认知功能衰退的预测因素知之甚少。识别可改变的风险因素将有助于进行有针对性的干预,以降低高危个体功能衰退的风险。本研究的目的是建立一个风险指数,以预测病毒血症阴性的HIV感染者3年内的神经认知功能衰退情况。
作为中枢神经系统HIV抗逆转录病毒治疗效果研究(CHARTER)的一部分,HIV阳性成年人每6个月完成一次临床评估和神经心理学测试。基于组的轨迹分析用于检测神经认知变化模式;在至少一项神经心理学测试中恶化≥0.5标准差的个体被视为衰退者。多因素逻辑回归用于识别与前3年持续病毒血症阴性亚组中衰退相关的基线社会人口学、临床、生物学和生活方式因素。使用最终回归模型的β系数建立风险指数。
191名纵向随访参与者中有23名(12%)发生神经认知功能衰退。预测衰退的基线因素为肾小球滤过率≤50 mL/分钟、已知HIV感染持续时间≥15年、教育程度≤12年和脑脊液蛋白>45 mg/dL。
采用这种分析方法,在这个病毒血症阴性的HIV感染者样本中,神经认知功能衰退并不常见。3年衰退风险从无风险因素者的2%到具备所有4项风险因素者的95%不等。最强的预测因素是肾小球滤过率,它也是心血管疾病的一个预测因素。这增加了控制血管危险因素可能降低神经认知功能衰退风险的可能性。