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Clinical Trial of CNS Penetrating ART to Prevent NeuroAIDS in China

Clinical Trial of CNS Penetrating ART to Prevent NeuroAIDS in China
中枢神经系统穿透性ART预防神经艾滋病在中国的临床试验
批准号:
8644912
负责人:
Scott L Letendre
金额:
$52.34万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-07-15 至 2015-03-31
关键词:
ABCB1 geneAIDS clinical trial groupAIDS neuropathyAIDS preventionAIDS/HIV problemAccountingAddressAdherenceAnti-Retroviral AgentsAreaBiological AssayBiological MarkersBiological PreservationBlood - brain barrier anatomyBone DiseasesBrainBrain InjuriesCD14 geneCD4 Positive T LymphocytesCYP2B6 geneCardiovascular DiseasesCaucasiansCaucasoid RaceCellsCharacteristicsChinaChinese PeopleChronicChronic DiseaseClinicalClinical TrialsCommunitiesComorbidityComplexComplicationDataDevelopmentDisadvantagedDiseaseDisease ProgressionDoseDrug IndustryEffectivenessEncephalopathiesEnrollmentEnvironmentEuropeFrequenciesFundingGenesGeneticGenetic MarkersGenetic PolymorphismGoalsGovernmentGuidelinesHIVHLA-DR4 AntigenHepaticHepatitisHepatitis B VirusHepatitis CHepatitis C virusHepatitis VirusesHigh PrevalenceHospitalsHuman GeneticsImpaired cognitionImpairmentIndividualInfectionInflammationInterleukin-6Kidney DiseasesLamivudineLeadLifeLinkLiver diseasesLow PrevalenceMedicalMental disordersMetabolic DiseasesMetabolismMonocyte Chemoattractant Protein-1MoodsNational Institute of Mental HealthNervous system structureNeuraxisNeurocognitiveNeurogliaNevirapineNorth AmericaOutcome StudyParticipantPatientsPenetrationPerceptionPerformancePermeabilityPharmaceutical PreparationsPharmacologyPhasePopulationPopulation StudyPrevalencePreventionProceduresProvincePublic HealthRandomizedRandomized Controlled Clinical TrialsRecoveryRegimenReportingResearchResearch InfrastructureResearch Project GrantsResourcesRiskRisk FactorsSafetySample SizeSingle Nucleotide PolymorphismTenofovirTherapeuticTimeUnited StatesVariantViral Load resultViral hepatitisVirus DiseasesWorkZidovudineantiretroviral therapyarmbasecohortcostcost effectivedesigndrug metabolismefavirenzexperiencefollow-uphigh riskimmune activationinjection drug useinjuredmicrobialmolecular markernervous system disorderneuropsychologicalpathogenpreventprimary outcomeprogramspublic health relevancepublic-private partnershiprandomized trialresearch studyresponsevolunteer

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Advances in treatment have transformed HIV disease to a chronic illness in most individuals in the U.S. The most common central nervous system (CNS) complication of chronic HIV disease is HIV-associated neurocognitive disorder (HAND). In the U.S., HAND prevalence estimates range up to 55% of treated individuals. HAND is also common outside the U.S. For example, our current project in China identified that more than a third of nearly 150 treated HIV (+) individuals in Anhui and Yunnan provinces had HAND. Data such as these support that the benefits of antiretroviral therapy (ART) can be incomplete, with many patients not returning to normal neurocognitive performance or, worse, developing new neurocognitive impairment while taking ART. One explanation for this is the limited penetration of some antiretrovirals into the nervous system. Recent reports have identified that worse antiretroviral penetration characteristics are associated with worse control of HIV replication and worse neurocognitive performance. Most reports, however, have focused on treatment - rather than prevention - of HAND. Like many other medical conditions, prevention of HAND may be a more cost-effective public health goal than treating disease that has already occurred. We propose to build on our prior work in China by performing a phase IV, randomized, controlled clinical trial of the safety and effectiveness of ART that differs in its penetration characteristics in 250 ART-naive individuals who have normal neurocognitive performance. The primary objective will be to determine the effects of better penetrating (BP) ART (zidovudine-lamivudine-nevirapine) compared with worse penetrating (WP) ART (tenofovir-lamivudine-efavirenz) on the prevention of HAND. We hypothesize that volunteers who are randomized to BP-ART will be less likely to neurocognitively decline over 96 weeks of observation than those who are randomized to WP-ART. The secondary objective will be to assess the influence on study outcomes of two conditions: persistent immune activation and viral hepatitis. In an exploratory aim, the project will also assess the influence on study outcomes of a concise panel of drug disposition-associated genetic polymorphisms. Demonstrating that HAND can be prevented by using BP-ART should influence HIV treatment guidelines in the U.S., China, and elsewhere and ultimately lead to preservation of normal neurocognitive functioning in people afflicted with HIV/AIDS.
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会议论文
Aging, Polypharmacy and Neurotoxicity in Adults Living with HIV
Aging, Polypharmacy and Neurotoxicity in Adults Living with HIV
Aging, Polypharmacy and Neurotoxicity in Adults Living with HIV
Measurement of ART Drug Concentrations in Brain by 19F-MRS as an Indicator of Neurotoxicity
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