Alcohol and dysfunctional skeletal muscle mass: implications in aging
酒精和骨骼肌质量功能障碍:对衰老的影响
基本信息
- 批准号:10811081
- 负责人:
- 金额:$ 18.25万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-09-20 至 2025-08-31
- 项目状态:未结题
- 来源:
- 关键词:Activities of Daily LivingAddressAgeAgingAlcohol consumptionAlcoholic Liver DiseasesAlcoholsAreaBioenergeticsBiological MarkersBiopsyCaringChronologyClinical ResearchCross-Sectional StudiesDataDiseaseElderlyElectron TransportEquilibriumHIVHIV InfectionsHealthHealth Care CostsHeavy DrinkingHigh PrevalenceHomeostasisImpairmentIndividualInfrastructureInterventionLife ExpectancyLife StyleLinkLiver diseasesLongevityMaintenanceMeasuresMediatingMitochondriaMitochondrial DNAMitochondrial ProteinsMuscleMuscle MitochondriaMuscle functionMyoblastsMyopathyNational Institute on Alcohol Abuse and AlcoholismOutcomePathologyPatient Self-ReportPersonsPhysical PerformancePhysiologicalPredispositionProductionQuality of lifeReportingRiskRisk FactorsRisk ReductionRoleSIVScienceSkeletal MuscleStrategic PlanningSyndromeTestingUnited Statesalcohol consequencesalcohol effectalcohol exposurealcohol researchbinge drinkingcohortcomorbidityfrailtyimprovedindexinginsightmitochondrial dysfunctionmortalitymuscle formmuscle strengthnervous system disorderpharmacologicpreventprotein expressionreduced alcohol usestressortherapeutic targetwalking speed
项目摘要
Abstract Alcohol and dysfunctional skeletal muscle mass: implications in aging
Alcohol use decreases skeletal muscle strength and function resulting in alcohol-related myopathy; one of the
earliest alcohol-associated pathologies. Alcohol use is disproportionately on the rise among older individuals,
with 25% engaging in heavy drinking and 11% reporting binge drinking. The increasing average life expectancy
in the United States leads us to predict that alcohol use will be an important factor exacerbating dysfunctional
SKM mass in chronological aging. Functional skeletal muscle mass is a critical contributor to overall physical
performance. Poor physical performance is closely linked to frailty syndrome that increases the risk of adverse
health outcomes, is a significant predictor of needing specialized care, and increases the risk for all-cause
mortality. Hence there is a critical need to understand the underlying mechanisms that can be targeted to reduce
risk, delay onset, or better manage frailty. One of the salient skeletal muscle-mediated mechanisms contributing
to physical performance and frailty is mitochondrial function. However, there is a gap in our understanding of the
interactions of alcohol use on physical performance and frailty in chronological aging, and on the role of
mitochondrial dyshomeostasis as a contributing factor. We propose a cross sectional study among people over
the age of 60 with or without alcohol use, with no overt underlying comorbidities, to test the overall hypothesis
that alcohol use decreases physical performance and increases frailty risk. We will investigate the mechanisms
involved in alcohol-associated dysregulation of SKM mitochondrial homeostasis to identify modifiable targets
amenable for lifestyle or pharmacological interventions. The results generated using these hypothesis-driven
studies will provide data that will inform translational targeted interventions to improve muscle mitochondrial
function. This application addresses one of the target areas of NIAAA's Strategic Plan to develop effective
strategies to prevent consequences of alcohol use in older individuals and is highly responsive to the NOSI:
“Alcohol and aging” and leverages the interdisciplinary translational team science approach within an outstanding
scientific infrastructure provided by the Comprehensive Alcohol Research Center at LSUHSC-NO.
摘要:酒精和骨骼肌质量功能障碍:对衰老的影响
饮酒会降低骨骼肌的力量和功能,导致酒精相关性肌病之一;
最早与酒精相关的病症在老年人中呈不成比例地增加,
25% 的人酗酒,11% 的人酗酒。 平均预期寿命不断延长。
在美国,我们预测饮酒将是加剧功能失调的一个重要因素
按时间顺序老化的 SKM 质量是整体身体状况的关键贡献者。
身体表现不佳与虚弱综合症密切相关,虚弱综合症会增加不良风险。
健康结果,是需要专门护理的重要预测因素,并增加全因风险
因此,迫切需要了解可降低死亡率的潜在机制。
风险、延迟发作或更好地控制虚弱是骨骼肌介导的显着机制之一。
然而,我们对线粒体功能的理解存在差距。
饮酒对身体机能和衰老过程中的虚弱的相互作用,以及对
我们建议对超过 10 岁的人进行一项横断面研究。
60 岁,无论是否饮酒,没有明显的潜在合并症,以检验总体假设
饮酒会降低身体机能并增加虚弱风险,我们将研究其机制。
参与酒精相关的 SKM 线粒体稳态失调以确定可修改的目标
使用这些假设驱动产生的结果适合生活方式或药物干预。
研究将提供数据,为转化针对性干预措施提供信息,以改善肌肉线粒体
该应用程序解决了 NIAAA 战略计划的目标领域之一,以开发有效的功能。
预防老年人饮酒后果的策略,并对 NOSI 高度敏感:
“酒精与衰老”,并在杰出的研究中利用跨学科转化团队科学方法
由 LSUHSC-NO 综合酒精研究中心提供的科学基础设施。
项目成果
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Liz Simon其他文献
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{{ truncateString('Liz Simon', 18)}}的其他基金
Alcohol-induced myomiR dysregulation: mechanisms of impaired skeletal muscle regeneration in SIV/HIV
酒精引起的 myomiR 失调:SIV/HIV 骨骼肌再生受损的机制
- 批准号:
9310227 - 财政年份:2016
- 资助金额:
$ 18.25万 - 项目类别:
Alcohol-induced myomiR dysregulation: mechanisms of impaired skeletal muscle regeneration in SIV/HIV
酒精引起的 myomiR 失调:SIV/HIV 骨骼肌再生受损的机制
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9976400 - 财政年份:2016
- 资助金额:
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8337160 - 财政年份:2012
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