HIV Neuropathogenesis in a Cohort of Long-Term Surviving Young Adults in Romania
HIV Neuropathogenesis in a Cohort of Long-Term Surviving Young Adults in Romania
批准号:
7337134
负责人:
CRISTIAN L ACHIM
金额:
$13.64万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-01-01 至 2008-12-31
关键词:
Adverse effectsAgeAge DistributionAntiviral AgentsAntiviral TherapyBehavioralBiological MarkersBrazilCerebrospinal FluidChinaChronicClassificationClinicalComorbidityComplicationCountryDeveloped CountriesDeveloping CountriesDiagnosisDiseaseDisease MarkerDrug abuseEquilibriumEvaluationFutureGenderGeneticGeographic DistributionHIVHIV InfectionsHIV-1Hepatitis C virusHeterogeneityHighly Active Antiretroviral TherapyHospitalsImmunologic MarkersImpairmentIn VitroIndiaInfantInfectionInflammationInflammatoryInternationalLaboratoriesLengthLong-Term SurvivorsLongitudinal StudiesMacrophage ActivationMeasuresMediator of activation proteinMetabolicMetabolic ActivationMonitorNeuraxisNeurocognitiveNeurologicNeuropathogenesisNeuropsychological TestsNeuropsychologyNeurotropismOpportunistic InfectionsPathogenesisPathologyPatientsPilot ProjectsPlayPopulationPredispositionPrevalencePrevalence StudyQualifyingResearchResearch InfrastructureResearch PersonnelRiskRisk FactorsRoleRomaniaSerologicalTest ResultTestingTherapeuticThinkingTimeToxic effectTreatment ProtocolsViralViral Load resultViral ProteinsWorkantiretroviral therapybasechemokine receptorcohortdesigninsightneurobehavioralneuropsychiatryneuropsychologicalneurotoxicneurotoxicityprogramsrelating to nervous systemresponseyoung adult
中文摘要
描述(由申请人提供):慢性神经心理障碍(NPI)是接受抗病毒治疗(HAART)的HIV感染长期存活者的主要并发症。发病机制仍然未知,但可能的候选者是:神经毒性病毒蛋白;药理学副作用;行为风险因素(例如药物滥用);慢性炎症伴神经胶质细胞活化;患者遗传背景可能调节对感染的代谢和内分泌反应;年龄;性别;以及特定的机会性病理学。我们现在已经在布加勒斯特的维克托婴儿医院(VBH)确定了一个独特的患者队列,这可能有助于破译与长期HIV感染相关的一些特定NP风险因素。这些患者是唯一有资格进行纵向研究的:他们形成了一个高度同质的队列(平均18岁)。o.)对于相似的病毒株感染(进化枝F),HAART方案(约100 mg/kg),7年),以及遗传背景。我们将组建一个由75名受试者组成的队列(25名HIV+伴NPI,25名HIV+不伴NPI,25名HIV-),将通过定期神经医学和NP检查以及疾病的血清学和脑脊液(CSF)标志物的临床实验室评价进行为期2年的研究。为了测量NPI,我们将使用在加州大学圣地亚哥分校的HIV神经行为研究中心(HNRC)开发的测试电池。具体目标1:证明在罗马尼亚的一个全面的神经心理学(NP)测试电池,已被广泛验证用于检测和表征HIV-1感染的神经行为影响在美国的跨文化适用性具体目标#2:确定罗马尼亚年轻人与艾滋病毒的共病因素,并将其与NPI的程度进行比较。具体目标#3:表征罗马尼亚进化枝F HIV的神经毒性潜力及其对抗病毒治疗的敏感性。该项目将证明其可行性,并将帮助建立在罗马尼亚进行神经行为学和病毒学研究的基础设施,因为罗马尼亚尚未对HIV-1的神经认知表现进行系统研究。罗马尼亚队列可以提供一个独特的见解,在未来的艾滋病毒相关的NPI长期生存的HAART。
英文摘要
DESCRIPTION (provided by applicant): Chronic neuropsychologic impairment (NPI) is a major complication in HIV infected long-term survivors on antiviral therapy (HAART). The pathogenesis is still unknown but likely candidates are: neurotoxic viral proteins; pharmacologic side effects; behavioral risk factors (e.g. drug abuse); chronic inflammation accompanied by neuroglial activation; the patient genetic background potentially modulating the metabolic and endocrinologic response to infection; age; gender; and also specific opportunistic pathologies. We have now identified a unique patient cohort at the Victor Babes Hospital (VBH) in Bucharest that may help in deciphering some of the specific NP risk factors associated with long term HIV infection. These patients are uniquely qualified for a longitudinal study: they form a highly homogenous cohort (average 18 y. o.) with similar viral strain infection (clade F), HAART regimen (approx. 7 years), and genetic background. We will assemble a cohort of 75 subjects (25 HIV+ with NPI, 25 HIV+ without NPI, and 25 HIV-) that will be studied for 2 years through regular neuromedical and NP exams and clinical laboratory evaluations of serologic and cerebrospinal fluid (CSF) markers of disease. To measure NPI we will use a test battery developed at the HIV Neurobehavioral Research Center (HNRC) at UC San Diego. Specific Aim #1: Demonstrate the cross-cultural applicability in Romania of a comprehensive neuropsychological (NP) test battery that has been extensively validated for detecting and characterizing neurobehavioral effects of HIV-1 infection in the U.S. Specific Aim #2: Identify comorbid factors in the Romanian young adults with HIV and compare them to the degree of NPI. Specific Aim #3: Characterize the neurotoxic potential of the Romanian clade F HIV and its susceptibility to antiviral treatments. This project will demonstrate feasibility and will help develop an infrastructure to perform neurobehavioral and virological studies in Romania, where no systematic studies of the neurocognitive manifestations of HIV-1 have been performed. The Romanian cohort could provide a unique insight in the future of HIV- associated NPI in long term-survivors on HAART.
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