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Atherosclerosis and Inflammation in HIV Disease

Atherosclerosis and Inflammation in HIV Disease
HIV 疾病中的动脉粥样硬化和炎症
批准号:
7914065
负责人:
Janet Lo
金额:
$14.16万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-02 至 2013-07-31
关键词:
Adipose tissueAgeAngiographyAnti-Retroviral AgentsArterial Fatty StreakAtherosclerosisAttenuatedBiologyBiometryC-reactive proteinCD4 Positive T LymphocytesCD8-Positive T-LymphocytesCD8B1 geneCardiacCardiologyCardiovascular DiseasesCardiovascular systemCategoriesCellsCholesterolChronicCoenzyme ACombined Modality TherapyCommunitiesCoronaryCoronary ArteriosclerosisCytotoxic T-LymphocytesDevelopmentDiabetes MellitusDisciplineDiseaseDrug or chemical Tissue DistributionDyslipidemiasEndocrinologyEnvironmentEventExcess MortalityFatty acid glycerol estersFutureGeneral PopulationGlucose Metabolism DisordersGoalsGrantHIVHIV InfectionsHealth Services AccessibilityHyperinsulinismImageImmune System DiseasesIndividualInfectionInflammationInflammatoryInsulin ResistanceInterferonsK-Series Research Career ProgramsLeadLinkMeasuresMedicineMentorsMentorshipMetabolicOxidoreductasePatientsPhysiologicalPlacebo ControlPlacebosPlayPopulationPravastatinPrevalencePreventionPrevention strategyProductionRandomizedRecruitment ActivityResearchResearch PersonnelRiskRisk FactorsRoleSliceSmokeT cell responseT-Cell ActivationT-LymphocyteT-Lymphocyte SubsetsTranslational ResearchVirus DiseasesVisceralX-Ray Computed Tomographyabstractingblood glucose regulationburden of illnesscardiovascular risk factorcareer developmentcohortdesigndetectorfluorodeoxyglucose positron emission tomographyimmune functionimprovedinhibitor/antagonistmonocytenovelpatient orientedpatient populationpreventprogramsresponseskillstranscription factortreatment strategy

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Survival of HIV-infected patients worldwide has remarkably improved with the use of anti-retroviral therapy. Metabolic and cardiovascular complications associated with HIV infection and its treatment are becoming more evident as this patient population ages with chronic viral infection. Metabolic and inflammatory changes in HIV-infected patients including dyslipidemia, insulin resistance, fat redistribution with abnormal adipocytokine secretion, alterations in monocyte subsets, and T-cell activation may increase the risk of atherosclerotic disease. The aims of the proposed grant are: 1) to determine the prevalence and degree of subclinical coronary atherosclerosis using CT angiography in patients with HIV compared to agematched control subjects without HIV infection, 2) to examine risk factors for coronary atherosclerosis in HIV patients, specifically evaluating the potential roles of adipocytokines, monocyte subsets, and T cell activation in atherosclerosis development, and 3) to perform a randomized, placebo-controlled, physiologic study in HIV patients with subclinical coronary atherosclerosis comparing the effects of statin therapy vs. placebo on plaque inflammation (as determined by 18F-fluorodeoxyglucose positron emission tomography), inhibition of plaque progression (as determined by coronary CT angiography), monocyte subsets and T cell response. Characterization of the atherosclerotic disease burden as well as identification of risk factors associated with atherosclerotic disease in HIV will be instrumental to guide the future design of appropriate prevention and treatment strategies for the HIV patient population. To achieve these aims, the candidate will be mentored by internationally recognized experts from several relevant disciplines in patient-oriented and translational research, endocrinology, cardiology, inflammation biology, HIV medicine, cardiac imaging, and biostatistics. Their mentorship and the strength of the candidate's institutional support will provide a well-suited academic environment to conduct this research and to nurture the candidate's career development. This K23 career development award will help the candidate to acquire the additional research skills to achieve her goal of becoming an independent patientoriented translational investigator. (End of Abstract)
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Reducing Arterial Inflammation and Improving Metabolic Health by Dual CCR2 and CCR5 Antagonism in People Living with HIV
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    $77.2万
  • 财政年份:
    2020
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    2020
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