AIDS and Aging Research Platform (AARP)
艾滋病和老龄化研究平台 (AARP)
基本信息
- 批准号:10683071
- 负责人:
- 金额:$ 76.99万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2020
- 资助国家:美国
- 起止时间:2020-08-15 至 2025-04-30
- 项目状态:未结题
- 来源:
- 关键词:AccelerationAcquired Immunodeficiency SyndromeAddressAgeAge-associated memory impairmentAgingAmericanAreaBehavioral ResearchBiology of AgingBrainCapsicumCardiovascular DiseasesCaringCessation of lifeChronic DiseaseClinicClinicalDataDevelopmentDiabetes MellitusEducationElderlyEquipment and supply inventoriesFutureGeriatricsGerontologyGeroscienceGoalsHIVHearingHospitalizationImpaired cognitionIndividualInfrastructureInterventionInvestigationKidney DiseasesLinkLiver diseasesLongevityMalignant NeoplasmsMentorsMetabolic syndromeModelingMolecularNeurocognitionOutcomes ResearchPersonsPhenotypePhysical FunctionPilot ProjectsPreventionR24ResearchResearch PersonnelResourcesScienceSensoryShockSiteStrokeSyndromeSystemTestingTimeTrainingUnited States National Institutes of HealthVisionWorkantiretroviral therapyclinical careclinical phenotypeclinical research sitecognitive testingcomorbiditydata integrationdisabilityexercise programexperiencefallsfrailtyfunctional declinefunctional disabilityhealthspanhuman old age (65+)improvedinsightinterdisciplinary collaborationmeetingsmiddle agemortalitymultiple chronic conditionsprogramsresponsesmall moleculesocialsuccesstool
项目摘要
ABSTRACT
Effective antiretroviral therapy (ART) for people living with HIV (PLWH) has dramatically reduced mortality
resulting in many surviving into middle and old age. Despite this success, PLWH experience high rates of
comorbidities, multimorbidity (>1 major chronic illness), and functional decline at ages 10-15 years younger
than uninfected controls. Geriatric syndromes, such as frailty and falls, are becoming more prevalent in PLWH.
Thus, there is an urgent need to focus on the healthspan of PLWH rather than just mortality. Healthspan, in
contrast to lifespan, is defined as the time someone is healthy not just alive. The Claude D. Pepper Older
American Independence Centers (OAlCs) were established to help define aging phenotypes and advance
research into the causes, prevention and treatment of functional decline with age. OAlCs have developed and
validated functional assessments in aging, but lack depth and breadth of HIV expertise. In contrast, Centers for
AIDS Research (CFARs) have unparalleled expertise in HIV-related basic, clinical and social/behavioral
research, but lack robust resources and expertise in aging biology, geriatric clinical phenotypes and functional
assessments. Our R24 project, “Developing Research At The Interface Of HIV And Aging” was in response to
PA-12-064 "Network and Infrastructure Support for Development of Interdisciplinary Aging Research." Through
this R24 we successfully linked CFARs and OAICs to support pilot projects in high-priority focus areas and
mentor researchers at the interface of HIV and Aging. Our vision for this proposal is to build on this success
deepening the ongoing linkage of CFARs and OAICs and expanding the network to include Nathan Shock
Centers of Excellence in the Basic Biology of Aging (NSCs) and the McKnight Brain Institutes (MBIs). By
bringing together OAICs expertise on functional decline in aging, with NSC expertise in aging biology and the
mechanisms underlying function decline, with MBI expertise on age-related cognitive decline, and CFAR
expertise on HIV, we create an integrated approach to advancing and accelerating investigation at the
interface of HIV and aging via the following Aims:
Aim 1. Provide specific training models and a brief inventory of tools to efficiently collect data to improve HIV
clinical care and outcomes research. Aim 2. Using a geroscience approach, provide a platform for pilot studies
to determine the links between molecular hallmarks of aging with functional decline, and the development of
common comorbidities among aging PLWH. Aim 3. Develop infrastructure for evaluating interventional
approaches and their application to HIV care. Aim 4. Provide educational support, implementation advice and
mentoring for emerging investigators to establish/advance research programs in HIV and aging.
These synergistic aims leverage and expand the infrastructure and close ties built in the R24 of HIV expertise
from CFARs with the gerontology and functional assessment expertise within the OAlCs and expand them with
inclusion of NSCs and MBIs to enhance and accelerate investigation at the interface of HIV and aging.
摘要
对艾滋病毒感染者(PLWH)进行有效的抗逆转录病毒疗法(ART)已大大降低了死亡率
导致许多人活到了中年和老年。尽管取得了这一成功,但艾滋病毒携带者的感染率很高,
年龄小于10-15岁的合并症、多发病(>1种主要慢性疾病)和功能下降
比未受感染的对照组多。老年综合征,如虚弱和福尔斯,在PLWH中越来越普遍。
因此,迫切需要关注艾滋病毒/艾滋病感染者的健康寿命,而不仅仅是死亡率。健康,在
与寿命不同,它被定义为一个人健康而不仅仅是活着的时间。克劳德D。胡椒老
美国独立中心(OAlCs)的建立是为了帮助定义衰老表型,
研究功能随年龄下降的原因、预防和治疗。OAlCs已经开发并
在老龄化方面的功能评估得到验证,但缺乏艾滋病毒专门知识的深度和广度。相比之下,
艾滋病研究(CFARs)在艾滋病毒相关的基础,临床和社会/行为方面拥有无与伦比的专业知识
研究,但缺乏强大的资源和专业知识,在老化生物学,老年临床表型和功能
评估。我们的R24项目,“在艾滋病毒和老龄化的界面发展研究”是为了回应
PA-12-064“跨学科老龄化研究发展的网络和基础设施支持。“通过
在这一R24中,我们成功地将CFAR和OAIC联系起来,以支持高优先重点领域的试点项目,
指导艾滋病毒和老龄化接口的研究人员。我们对这一提案的设想是在这一成功的基础上
深化CFAR和OAIC之间的现有联系,并将网络扩展到包括内森·肖克
卓越中心在衰老的基础生物学(NSC)和麦克奈特脑研究所(MBIs)。通过
将OAIC在衰老功能衰退方面的专业知识与NSC在衰老生物学方面的专业知识结合起来,
功能下降的潜在机制,MBI对年龄相关的认知下降和CFAR的专业知识
我们在艾滋病毒方面的专业知识,我们创造了一种综合方法来推进和加快调查,
艾滋病毒和老龄化的接口,通过以下目的:
目标1.提供具体的培训模式和工具的简要清单,以有效收集数据,改善艾滋病毒
临床护理和结果研究。目标2.采用老年科学方法,为试点研究提供平台
以确定衰老的分子标志与功能衰退之间的联系,以及
老年PLWH中常见的合并症。目标3.开发用于评价干预的基础设施
方法及其在艾滋病毒护理中的应用。目标4。提供教育支持、实施建议和
指导新兴的研究人员建立/推进艾滋病毒和老龄化的研究计划。
这些协同目标利用和扩大了R24中建立的艾滋病毒专门知识的基础设施和密切联系
从老年医学和功能评估专业知识的CFAR OAlCs,并扩大他们与
纳入NSC和MBIs,以加强和加速艾滋病毒和老龄化界面的调查。
项目成果
期刊论文数量(5)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Evaluating the Sick Quitting Hypothesis for Frailty Status and Reducing Alcohol Use Among People With HIV in a Longitudinal Clinical Cohort Study.
在一项纵向临床队列研究中评估艾滋病毒感染者虚弱状态的病戒假说和减少饮酒。
- DOI:10.1097/jnc.0000000000000445
- 发表时间:2024
- 期刊:
- 影响因子:0
- 作者:Ruderman,StephanieA;Drumright,LydiaN;Delaney,JosephAC;Webel,AllisonR;Fitzpatrick,AnnetteL;Whitney,BridgetM;Nance,RobinM;Hahn,AndrewW;Ma,Jimmy;Mixson,L.Sarah;Eltonsy,Sherif;Willig,AmandaL;Mayer,KennethH;Napravnik,Sonia
- 通讯作者:Napravnik,Sonia
Validity Properties of a Self-reported Modified Frailty Phenotype Among People With HIV in Clinical Care in the United States.
- DOI:10.1097/jnc.0000000000000389
- 发表时间:2023-03-01
- 期刊:
- 影响因子:2
- 作者:Ruderman, Stephanie A.;Webel, Allison R.;Willig, Amanda L.;Drumright, Lydia N.;Fitzpatrick, Annette L.;Odden, Michelle C.;Cleveland, John D.;Burkholder, Greer;Davey, Christine H.;Fleming, Julia;Buford, Thomas W.;Jones, Raymond;Nance, Robin M.;Whitney, Bridget M.;Mixson, L. Sarah;Hahn, Andrew W.;Mayer, Kenneth H.;Greene, Meredith;Saag, Michael S.;Kamen, Charles;Pandya, Chintan;Lober, William B.;Kitahata, Mari M.;Crane, Paul K.;Crane, Heidi M.;Delaney, Joseph A. C.
- 通讯作者:Delaney, Joseph A. C.
Tobacco Smoking and Pack-Years Are Associated With Frailty Among People With HIV.
吸烟和吸烟年数与艾滋病毒感染者的虚弱有关。
- DOI:10.1097/qai.0000000000003242
- 发表时间:2023
- 期刊:
- 影响因子:0
- 作者:Ruderman,StephanieA;Odden,MichelleC;Webel,AllisonR;Fitzpatrick,AnnetteL;Crane,PaulK;Nance,RobinM;Drumright,LydiaN;Whitney,BridgetM;Mixson,LyndseySarah;Ma,Jimmy;Willig,AmandaL;Haidar,Lara;Eltonsy,Sherif;Mayer,KennethH;
- 通讯作者:
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STEVEN N. AUSTAD其他文献
STEVEN N. AUSTAD的其他文献
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{{ truncateString('STEVEN N. AUSTAD', 18)}}的其他基金
A New Translational Rat Model for Evaluating Anti-Aging Interventions
用于评估抗衰老干预措施的新转化大鼠模型
- 批准号:
10665539 - 财政年份:2022
- 资助金额:
$ 76.99万 - 项目类别:
A New Translational Rat Model for Evaluating Anti-Aging Interventions
用于评估抗衰老干预措施的新转化大鼠模型
- 批准号:
10369517 - 财政年份:2022
- 资助金额:
$ 76.99万 - 项目类别:
A Four Core Genotype (FCG) Approach to Investigating Sex Differences in Health and Longevity
研究健康和长寿性别差异的四核心基因型 (FCG) 方法
- 批准号:
9504206 - 财政年份:2018
- 资助金额:
$ 76.99万 - 项目类别:
A sex difference approach to evaluating resilience as a predictor of healthspan in mice
评估弹性作为小鼠健康寿命预测因子的性别差异方法
- 批准号:
10166754 - 财政年份:2017
- 资助金额:
$ 76.99万 - 项目类别:
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