Are the impairments of arginine metabolism as found in Alzheimer's disease also present in patients developing post-operative delirium and cognitive decline?
Are the impairments of arginine metabolism as found in Alzheimer's disease also present in patients developing post-operative delirium and cognitive decline?
批准号:
10810134
负责人:
Emma Louise Cunningham
金额:
$20.08万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
未结题
起止时间:
2020-05-15 至 2026-05-31
中文摘要
摘要:老年人在接受手术时需要特殊的护理,主要是因为周围的事件
英文摘要
Abstract: Older people require specific care when undergoing an operation, principally because events around
surgery and anesthesia can precipitate delirium. The prevalence of postoperative delirium depends on type of
surgery, but an overall postoperative incidence of 17% is a reasonable estimate. The pathophysiological
mechanisms that underpin postoperative delirium and its sequelae have yet to be systematically studied. Certain
pathways may account for the development of delirium itself, while others may drive longer-term cognitive
outcomes such as progression of dementia. The degree to which these interrelate, are separate or shared is
completely unknown. One approach to investigate the neural basis of delirium has been to use CSF samples
obtained through regional anesthesia. We propose investigating the neural basis of delirium by using CSF
samples obtained in the course of spinal anesthesia, combining biomarkers with clinical and demographic
information. Our preliminary data indicates arginine metabolism may be a predictor of delirium in CSF. In this
study we aim to extend on our previous work, and accurately quantify all arginine related metabolites and
complement this data set with protein expression levels for this metabolic cascade. Our goal is to develop a
comprehensive picture of arginine metabolism in CSF and correlate these results with current pathophysiological
biomarkers of Alzheimer’s disease. Further, having extended our biochemical coverage of arginine metabolism,
we will develop novel biomarkers capable of predicting those patients at greatest risk of developing delirium and
subsequent cognitive decline. Having defined the biochemical signature of delirium, it will be important to
determine which patients later developed dementia and/or significant neurodegeneration following surgery.
Therefore, we will complete a long term follow up of our original patients to determine who developed Alzheimer’s
disease or one of its related dementias and correlate those findings with our results. Moreover, and to ensure
the validity of our delirium biomarker panel, we will prospectively recruit participants undergoing planned joint
replacement surgery at Beaumont Health (>4,000 at Beaumont Royal Oak, 2018), perform pre-operative clinical
and cognitive assessments and postoperative delirium screening. Having access to such a large and diverse
patient population will provide the us with an optimal, independent validation set. In summary, our overarching
goals for this proposal are to: (i) develop an existing collaboration with the largest CSF-delirium repository to
date (n=358) in order to extend on current findings; (ii) develop new biomarker panels; (iii) perform a long term
follow up of our initial cohort and (iv) validate our findings in a large and diverse US based population.
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