Improving Autonomic Function and Balance in Diabetic Neuropathy

改善糖尿病神经病变的自主功能和平衡

基本信息

  • 批准号:
    8990869
  • 负责人:
  • 金额:
    --
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2013
  • 资助国家:
    美国
  • 起止时间:
    2013-07-01 至 2017-06-30
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Objectives: Impaired glucose regulation (IGR) is associated with development of autonomic neuropathy and balance impairment that may be disabling for the patient. Diabetic Veterans suffer disproportionately from disability related to autonomic neuropathy and impaired balance control. Autonomic symptoms and defects in autonomic function are common in patients with impaired glucose regulation (IGR) even when the subject only has impaired glucose tolerance (IGT). In uncontrolled trials, improved diet and exercise can significantly improve and even reverse neuropathy associated with IGR, however blinded controlled trials are needed to establish the role of an intense tailored lifestyle modification program in slowing progression or reversing diabetic autonomic neuropathy and balance impairment. IGR includes patients with mild type 2 diabetes mellitus (DM2), IGT, and impaired fasting glucose (IFG) based on standardized ADA criteria for the diagnosis of DM2. We hypothesize that, compared to IGR participants advised to follow the current standard care recommendations on diet and exercise (Standard Care or "SC"), IGR participants undergoing a carefully monitored, tailored intensive diet, physical activity and balance enhancement program (DPAEP), will show greater improvement in autonomic function and balance control. Furthermore, we will test the hypothesis that improvement in autonomic function, balance control and mobility will correlate strongly with each other and with improvement in metabolic function, clinical measures of autonomic function and quality of life. At the end of the study we should be able to determine if an individually tailored 12 month DPAEP program can (1) reverse or delay the progression of autonomic neuropathy in subjects with IGR, (2) improve and sustain improvement in balance control, (3) evaluate factors that are associated with impaired autonomic function and balance and if improvement in these factors parallels improvement in the primary, secondary and other efficacy measures in the study. Research Plan: This is a single blinded, parallel group, intention-to-treat study comparing a carefully monitored, tailored intensive DPAEP intervention with an SC group. In the study, specific measures of autonomic neuropathy progression, balance, mobility, metabolic function, and quality of life will be compared between the two groups. Evidence for the feasibility of this proposal is provided by pilot data showing that a lifestyle intervention program that improves diet and increases mobility can also improve autonomic function and balance in patients with diabetic neuropathy. This new proposal will be highly relevant to the rehabilitation of diabetic veterans with autonomic and balance impairment that are at risk of increased falls. Methods: 80 participants with defined IGR and autonomic neuropathy, age 30-80 years, will be randomized into one of two groups (DPAEP and SC). Participants will be recruited over 32 and followed over 12 months. The DPAEP group will participate in an intense dietary, aerobic exercise and balance program. They will be assessed three times a week. SC participants will receive general dietary and exercise advice and will receive follow up. The primary efficacy measure is the expiration:inspiration (E:I) ratio at 12 months. The secondary efficacy measure is the trunk repositioning error (TRE) measured at 6 months. Other outcomes will assess sustained balance control, skin sweat gland innervation, metabolic parameters, clinical response, and quality of life. The Specific Aims are to determine in subjects with IGR and autonomic neuropathy over 12 months: (1) The effect of a DPAEP intervention on autonomic function; (2) The effect of a DPAEP intervention on balance control; (3) The relationships between autonomic function or balance control to (a) mobility, (b) changes in glucose, insulin, or lipid metabolism and weight loss, and (c) clinical outcomes and quality of life.
描述(由申请人提供): 目的:葡萄糖调节受损(IGR)与自主神经病变和平衡障碍的发展相关,可能导致患者残疾。糖尿病退伍军人患不成比例的残疾有关的自主神经病变和受损的平衡控制。自主神经症状和自主神经功能缺陷在葡萄糖调节受损(IGR)患者中是常见的,即使受试者仅具有葡萄糖耐量受损(IGT)。在非对照试验中,改善饮食和运动可以显着改善甚至逆转与IGR相关的神经病变,但是需要盲法对照试验来确定强烈定制的生活方式改变计划在减缓进展或逆转糖尿病自主神经病变和平衡障碍中的作用。IGR包括轻度2型糖尿病(DM 2)、IGT和空腹血糖受损(IFG)患者,基于诊断DM 2的标准化ADA标准。我们假设,与建议遵循当前关于饮食和运动的标准护理建议(标准护理或“SC”)的IGR参与者相比,接受仔细监测、定制的强化饮食、体力活动和平衡增强计划(DPAEP)的IGR参与者将显示出自主神经功能和平衡控制的更大改善。此外,我们将测试的假设,即自主神经功能,平衡控制和流动性的改善将密切相关,彼此之间的代谢功能,自主神经功能和生活质量的临床措施的改善。 在研究结束时,我们应该能够确定单独定制的12个月DPAEP程序是否可以(1)逆转或延迟IGR受试者的自主神经病变的进展,(2)改善和维持平衡控制的改善,(3)评估与受损的自主神经功能和平衡相关的因素,以及这些因素的改善是否与主要的改善平行,研究中的次要和其他疗效指标。 研究计划:这是一项单盲、平行组、意向治疗研究,比较了仔细监测、定制的强化DPAEP干预与SC组。在这项研究中,将比较两组之间自主神经病变进展、平衡、移动性、代谢功能和生活质量的具体指标。试点数据提供了这一建议的可行性证据,表明改善饮食和增加活动能力的生活方式干预计划也可以改善糖尿病神经病变患者的自主神经功能和平衡。这一新的建议将是高度相关的糖尿病退伍军人与自主神经和平衡障碍的康复是在增加福尔斯的风险。 方法:80名年龄30-80岁的IGR和自主神经病变患者随机分为两组(DPAEP组和SC组)。参与者将招募超过32名,并随访超过12个月。 DPAEP组将参加激烈的饮食,有氧运动和平衡计划。他们将每周接受三次评估。SC参与者将获得一般饮食和运动建议,并将接受随访。主要疗效指标为12个月时的呼气:吸气(E:I)比。次要疗效指标是6个月时测量的躯干复位误差(TRE)。其他结果将评估持续平衡控制,皮肤汗腺神经支配,代谢参数,临床反应和生活质量。 具体目的是在12个月以上的IGR和自主神经病变受试者中确定:(1)DPAEP干预对自主功能的影响;(2)DPAEP干预对平衡控制的影响;(3)自主功能或平衡控制与(a)活动性,(B)葡萄糖、胰岛素或脂质代谢的变化和体重减轻之间的关系,以及(c)临床结果和生活质量。

项目成果

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JAMES W RUSSELL其他文献

JAMES W RUSSELL的其他文献

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{{ truncateString('JAMES W RUSSELL', 18)}}的其他基金

ShEEP Request for Autonomic Nervous System Integrated Evaluation Laboratory
ShEEP 请求建立自主神经系统综合评价实验室
  • 批准号:
    9361301
  • 财政年份:
    2017
  • 资助金额:
    --
  • 项目类别:
NAD+ and SIRT1 Regulate Mitochondrial Function in Diabetic Neuropathy
NAD 和 SIRT1 调节糖尿病神经病变中的线粒体功能
  • 批准号:
    9174947
  • 财政年份:
    2016
  • 资助金额:
    --
  • 项目类别:
NAD+ and SIRT1 Regulate Mitochondrial Function in Diabetic Neuropathy
NAD 和 SIRT1 调节糖尿病神经病变中的线粒体功能
  • 批准号:
    10406480
  • 财政年份:
    2016
  • 资助金额:
    --
  • 项目类别:
Improving Autonomic Function and Balance in Diabetic Neuropathy
改善糖尿病神经病变的自主功能和平衡
  • 批准号:
    9108883
  • 财政年份:
    2013
  • 资助金额:
    --
  • 项目类别:
SIRT1 Overexpression in Cellular Mitochondrial Metabolism and Function
SIRT1 在细胞线粒体代谢和功能中的过表达
  • 批准号:
    7449824
  • 财政年份:
    2008
  • 资助金额:
    --
  • 项目类别:
IMPAIRED GLUCOSE TOLERANCE CAUSES NEUROPATHY
葡萄糖耐量受损导致神经病
  • 批准号:
    7603724
  • 财政年份:
    2007
  • 资助金额:
    --
  • 项目类别:
IMPAIRED GLUCOSE TOLERANCE CAUSES NEUROPATHY
葡萄糖耐量受损导致神经病
  • 批准号:
    7376534
  • 财政年份:
    2006
  • 资助金额:
    --
  • 项目类别:
IMPAIRED GLUCOSE TOLERANCE CAUSES NEUROPATHY
葡萄糖耐量受损导致神经病
  • 批准号:
    7199853
  • 财政年份:
    2005
  • 资助金额:
    --
  • 项目类别:
Oxidative Stress Induces Apoptosis in Diabetic Neurons
氧化应激诱导糖尿病神经元凋亡
  • 批准号:
    6365183
  • 财政年份:
    2002
  • 资助金额:
    --
  • 项目类别:
Oxidative Stress Induces Apoptosis in Diabetic Neurons
氧化应激诱导糖尿病神经元凋亡
  • 批准号:
    6821356
  • 财政年份:
    2002
  • 资助金额:
    --
  • 项目类别:

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激素治疗、绝经年龄、既往产次和 APOE 基因型会影响老年人的认知。
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