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Biomarkers of Homestatic Dysregulation in Aging and Chronic Disease

Biomarkers of Homestatic Dysregulation in Aging and Chronic Disease
衰老和慢性病中稳态失调的生物标志物
批准号:
8156805
负责人:
Luigi Ferrucci
金额:
$32.32万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至

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中文摘要
翻译
该项目测试了这样一种假设,即导致老年人疾病易感性、残疾和虚弱的过程主要与进行性失调和生物机制网络中的储备减少有关,这些机制相互作用以维持稳定的能量稳态,或在稳态受到压力事件的严重挑战时重新获得一些平衡。这些网络的要素没有完全定义,但肯定包括:1。摄入身体产生能量所需的基本元素,包括营养物质和氧气;2. 影响不同形式能量利用的活动,包括静息代谢率、身体活动、认知活动和营养;3)能量流的神经控制,主要受交感神经系统和副交感神经系统的相互作用影响。这是一种处于快速调整变化中的调节系统,例如发生在温度快速变化或出血后的调节系统;4)内分泌系统,它也负责调节能量流的局部区域分布,但比ANS慢;5. 氧自由基(ROS)在有氧代谢过程中产生具有重要的信号特性,但也会对各种大分子产生较大的损伤。因此,生物对活性氧的清除和毒性的降低有着不同的机制。当能量流动减少或加速时,ROS的产生有增加的趋势,如果不能被抗氧化系统完全缓冲,会造成严重的损伤;6. 最终,任何类型的损伤都会引发炎症反应,这反过来又会导致生物体将能量利用分离到应该对抗对宿主的“侵略”的功能上。
英文摘要
This project tests the hypothesis that the process that leads to disease susceptibility, disability and frailty in older persons is mostly connected with a progressive dysregulation and reduced researve in the network of biological mechanisms that interact to amintain a stable energetic homeostasis, or to regain some equilibrium when the homestasis is critically challenged by a stressful event. The elements of these network are not completely defined but certainly include: 1. Intake of the essential elements that the body requires to create energy, including both the nutrients and oxygen; 2. Activities that affect the different forms of energy utilization, including resting metabolic rate, physical activity, cognitive activity and nutrition; 3) Neurological control of the energy flow, mostly affected by the interplay between the sympathetic and the parasympathetic nervous system. THis is the regulatory system that is in change of rapid adjustments, such as those that occur with rapid changes in temperature, or after bleeding; 4) The endocrine system , which is also in charge of modulating the locoregional distribution of energy flow, but acts more slowly than the ANS; 5. The production of Oxygen Free Radicals (ROS) during the aerobic metabolism has important signaling properties but can also produce large damage to all sort of macromolecules. Therefore, organism have elaborated different mechanism to scavenge ROS and reduce their toxicity. When the flow of energy is reduced or accelerated, the production of ROS tend to increase and if not completely buffered by antioxidant system, can cause severe damage; 6. Ultimately, any type of damage triggers an inflammatory response, which is turn causes the organism to segregate the energy utilization to the function that are supposed to fight the "aggression" to the host. Biomarkers for these 6 systems have been developed over the last few years and some of them use high throughput assays that allow their utilization in epidemiological studies. However, no current study has the broad range of information required to address the multysistem dysregulation hypothesis in an epidemiological setting. Therefore, we have identified a number of studies that have some of these information available and that can be used to test one or more partial components of our general hypothesis. By creating a network of collaboration with the research groups that are conducting those studies, we have gained access to data that complement those that we are already collecting in the BLSA. In particular, in the context of this project, we intend to use data from: a. The Baltimore Longitudinal STudy of Aging b. The InChianti Study c. The SardiNIA study d. The Women's Health and Aging Study e. The Health ABC Study f. The ICare/Dicomano Study g. The ASSI italian Initiative h. The ILSA Study i. The Il Sirente Study l. The AGES study. Collaborations between the LSS and the investigators of these studies have been already established. Other studies could be included in this initiative, based on opportiniries and needs of the research group. In the intial period of this project, we will test univariate hypothesis of an indepdent correlation between the different homeostatic domain and their association with geriatric-relevant outcomes, such as morbidity, frailty, disabilitya nd mortality. In thes econd phase of this project, we will attempt to study the effect on outcome of multiple biomarkers and physiological measures, within a specific domain and across different domains. The second part of this project requires some metodological and statistical development. This methodological component is considered an essential component of the project and will be conducted in collaboration with multiple academic institutions.
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Temporary CARD Facility
  • 批准号:
    10291099
  • 项目类别:
  • 资助金额:
    $3029.09万
  • 财政年份:
    --
  • 负责人:
    Luigi Ferrucci
  • 依托单位:
THE INCHIANTI FOLLOW-UP STUDY-260012111
  • 批准号:
    6828820
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    --
  • 负责人:
    Luigi Ferrucci
  • 依托单位:
Characterization Of TGF-b Signaling In a B-cell Lymphoma Cell Line
  • 批准号:
    8335774
  • 项目类别:
  • 资助金额:
    $30.19万
  • 财政年份:
    --
  • 负责人:
    Luigi Ferrucci
  • 依托单位:
The VALIDATE study
  • 批准号:
    8335795
  • 项目类别:
  • 资助金额:
    $10.68万
  • 财政年份:
    --
  • 负责人:
    Luigi Ferrucci
  • 依托单位:
海外基金