Personalised neurostimulation for Parkinson's inspired by neurophysiological improvements observed after physical exercise
Personalised neurostimulation for Parkinson's inspired by neurophysiological improvements observed after physical exercise
批准号:
MR/Y014863/1
负责人:
Petra Fischer
金额:
$72.23万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2024
资助国家:
英国
项目状态:
未结题
起止时间:
2024 至 --
中文摘要
帕金森氏症引起的症状范围很广,不同的人有很大的不同。患者有不同的症状组合,包括震颤、迟缓、肌肉痉挛、行走困难和冲动,因此将受益于个性化的治疗方法。目前领先的两种治疗方法是多巴胺能药物和脑深部刺激(DBS),这两种方法在疾病的早期和中期非常有效。然而,后期大剂量的药物会导致副作用,包括幻觉、冲动和过度无法控制的运动。星展银行可以提供个性化的治疗方法,并将副作用降至最低,因为理论上它可以被编程为根据症状波动进行调整。然而,它需要侵入性手术,也会对认知,特别是记忆产生负面影响,因此只有少数患者(~10%)可以使用。非侵入性神经刺激也可以是个性化的,可能比DBS更具成本效益和更容易获得,因此将是更可取的--前提是能够开发出同样有效的方案或能够改善未得到满足的需求。我的目标是为帕金森氏症开发新的个性化非侵入性神经刺激方案,以改善运动和认知控制能力,超越现有疗法所能达到的效果。我将通过详细描述当大脑区域对运动控制进行优化时如何相互沟通来实现这一点。我们如何才能获得“最佳调谐”?据报道,帕金森氏症患者在进行高强度体育锻炼后的2-4个小时内感觉最好。一些人甚至表示,他们短暂地感觉自己根本没有帕金森氏症。我将利用锻炼的显著好处来确定哪些大脑活动模式应该恢复。然后,我将编写非侵入性神经刺激工具,以恢复已识别的模式,并测试它对个别症状的改善程度。我们将获得什么?我们将在锻炼后观察到的大脑活动变化将为为每个患者设计个性化神经刺激方案提供信息。从基本上盲目地向所有参与者提供同样的刺激来看,这是向前迈出的一大步。我们的目标是具体支持与每个人的症状改善相关的大脑活动模式,以解释患者之间症状的巨大差异。为了做到这一点,我将使用刺激工具的组合,包括电刺激和使用振动的感觉刺激。我们还将使用计算模型来寻找最有效的刺激参数。我的方法是及时的,因为新设备现在能够精确地协调多个部位的刺激,同时还可以测量大脑活动。组合工具和协调刺激多个大脑区域在临床上可能比单独与一个目标区域互动更有效。此外,我的工作有可能激励改进当前评估治疗成功的做法(例如,在调整药物或DBS参数时)。总而言之,摆脱基于大脑活动的一刀切的方法,在这种情况下,也是受锻炼启发的个性化神经刺激可能会彻底改变我们治疗帕金森氏症和其他运动障碍的方式。
英文摘要
Parkinson's causes a wide range of symptoms that vary strongly between individuals. Patients are burdened with different combinations of symptoms, including tremor, slowness, muscle cramps, walking difficulties and impulsivity, and would thus benefit from a personalized therapeutic approach.The two currently leading therapies are dopaminergic medication and deep brain stimulation (DBS), which can be highly effective in the early and middle stages of the disease. However, high medication doses in later stages can cause side effects including hallucinations, impulsivity, and excessive uncontrollable movements. DBS could deliver personalized therapies and minimize side effects as it can theoretically be programmed to adjust to symptom fluctuations. However, it requires invasive surgery, can also negatively affect cognition, in particular memory, and is thus available to only few patients (~10%). Non-invasive neurostimulation can also be personalized and could be more cost-effective and more accessible than DBS and would thus be preferrable - if protocols could be developed to be similarly effective or were able to improve unmet needs. My aim is to develop novel personalized non-invasive neurostimulation protocols for Parkinson's to improve both motor and cognitive control abilities beyond what existing therapies achieve. I will achieve this by characterizing in detail how brain areas communicate with each other when optimally tuned for movement control. How can we access "optimal tuning"?People with Parkinson's reportedly feel at their best within 2-4 hours after engaging in intense physical exercise. Some even report they briefly feel they do not have Parkinson's at all. I will capitalize on the striking acute benefits of exercise to identify which brain activity patterns should be restored. I will then program non-invasive neurostimulation tools to restore the identified patterns and test how well it improves individual symptoms.What will we gain?The changes in brain activity that we will observe following exercise will inform the design of a personalized neurostimulation protocol for each patient. This is a big step forwards from delivering the same stimulation essentially blindly to all participants. We aim to support specifically the brain activity patterns that are associated with symptom improvements in each individual to account for the large variability of symptoms across patients. To do this I will employ a combination of stimulation tools, including electrical stimulation and sensory stimulation using vibration. We will also use computational modelling to find the maximally effective stimulation parameters. My approach is timely as new devices now have the capability to precisely coordinate stimulation of multiple sites while also measuring brain activity. Combining tools and orchestrating stimulation of multiple brain areas likely will be clinically more effective than interacting with one target area alone. Additionally, my work has the potential to inspire improvements in current practises of assessing treatment success (e.g. when adjusting medication or DBS parameters). In summary, stepping away from a one-fits-all approach towards brain-activity based, and in this case also exercise-inspired, personalization of neurostimulation could revolutionize the way we treat Parkinson's and other movement disorders.
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