THE EFFECTS OF AGE AND HIGHLY ACTIVE ANTIRETROVIRAL THERAPY ON BRAIN FUNCTION
THE EFFECTS OF AGE AND HIGHLY ACTIVE ANTIRETROVIRAL THERAPY ON BRAIN FUNCTION
批准号:
8481587
负责人:
Beau M Ances
金额:
$35.66万
依托单位:
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:
2010-09-28 至 2015-06-30
关键词:
20 year oldAcuteAffectAgeAgingAlzheimer&aposs DiseaseAreaBiological MarkersBrainBrain MappingCaregiversChronicClinicalClinical Nurse SpecialistsClinical TrialsCommunitiesDevelopmentDiseaseEarly treatmentElderlyEventFaceFrequenciesFunctional disorderFutureGoalsGoldGray unit of radiation doseHIVHIV diagnosisHIV-2Highly Active Antiretroviral TherapyImageImpairmentInterventionKnowledgeLifeMeasuresMemoryMethodsNeurocognitiveNeurologicNeuronal DysfunctionNeuronsNeuropsychological TestsOutcomeParticipantPatientsPharmaceutical PreparationsPremature aging syndromePrevalenceRegimenResearchRestRiskSeriesSurrogate EndpointSymptomsTechniquesTestingTimeTranslatingViral load measurementVirusVisitage effectaging brainblood oxygen level dependentfollow-upnervous system disorderneuroimagingneurotoxicneurotoxicitynormal agingnovel strategiespreventpublic health relevance
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Human immunodeficiency virus (HIV) infected patients are now living longer due to highly active antiretroviral therapy (HAART). More than 50% of all HIV infected patients will be > 50 years old by 2015. However, HAART has not decreased the prevalence of neurological disorders in HIV infected patients. Older HIV infected patients are at greater risk for developing neurological disorders and are a significant burden to caregivers. In addition, debate also exists concerning the overall efficacy of HAART as better brain penetrating regimens (neuroHAART) may control the virus in the brain but cause neurotoxicity. Current assessment of neurocognitive disorders due to HIV entails lengthy neuropsychological testing which may not be sensitive to early signs of neuronal dysfunction. It is imperative that an early presymptomatic biomarker is identified to test interventions that prevent HIV infected patients from developing neurocognitive impairment. One promising new approach is non-invasive neuroimaging of resting state brain functional connections. This technique has identified the default mode network- a series of brain areas involved in organizing memories and preparing for the future events. Our preliminary results demonstrate that HIV diminishes the integrity of brain functional connections within this network by 40%. HIV also amplifies the effects of aging as older infected patients have brain network connections equivalent to seronegative subjects who are 15-20 years older. We hypothesize that HIV-induced decreases in neuronal connectivity within the default mode network will precede neuropsychological testing differences. The proposal will: 1) measure the effects of HIV on brain functional connections; 2) investigate if HIV accelerates aging of brain networks; 3) evaluate the effects of neuroHAART on brain connections. These results will assist nurses and clinicians in deciding when to initiate HAART and help them evaluate the efficacy of tailored adjunctive neuroprotective therapies.
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