Neuropsychopharmacology Research Group, Sunnybrook Research Institute, Toronto, Ontario, Canada.
Neuropsychopharmacology Research Group, Sunnybrook Research Institute, Toronto, Ontario, Canada; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.
Neurochem Int. 2022 Jan;152:105250. doi: 10.1016/j.neuint.2021.105250. Epub 2021 Dec 2.
Agitation is a common neuropsychiatric symptom that becomes more prevalent as Alzheimer's disease (AD) increases in severity. The treatment of agitation is an urgent and unmet need due to the poor outcomes associated with it, its disruptive impact on patients and caregivers, and the lack of efficacious and safe treatments. Recent research on agitation in AD with blood-based biomarkers has advanced the search for its biomarkers beyond the brain and provides new insights to understand its mechanisms and improve treatments. Here, we reviewed studies of blood-based biomarkers of agitation in AD, which show that inflammatory biomarkers are increased in patients with agitation, may predict the development of agitation, and are associated with symptom severity. In addition, they may also track symptom severity and response to treatment. Other biomarkers associated with agitation include markers of oxidative stress, brain cholesterol metabolism, motor activity, and clusterin, a chaperone protein. These results are promising and need to be replicated. Preliminary evidence suggests a role for these biomarkers in interventional studies for agitation to predict and monitor treatment response, which may eventually help enrich study samples and deliver therapy likely to benefit individual patients. Advances in blood-based biomarkers of AD including those identified in "-omic" studies and high sensitivity assays provide opportunities to identify new biomarkers of agitation. Future studies of agitation and its treatment should investigate blood-based biomarkers to yield novel insights into the neurobiological mechanisms of agitation, monitoring symptoms and response to treatment, and to identify patients likely to respond to treatments.
激越症是一种常见的神经精神症状,随着阿尔茨海默病(AD)的严重程度增加而变得更加普遍。由于与激越症相关的不良后果、其对患者和护理人员的破坏性影响以及缺乏有效和安全的治疗方法,激越症的治疗是一个紧迫的未满足的需求。最近,关于 AD 伴血液生物标志物激越症的研究,已经超越了大脑,为寻找其生物标志物提供了新的视角,并为理解其机制和改善治疗方法提供了新的思路。在这里,我们回顾了 AD 伴激越症的血液生物标志物研究,这些研究表明,炎症生物标志物在激越症患者中增加,可能预测激越症的发生,并与症状严重程度相关。此外,它们还可能跟踪症状的严重程度和治疗反应。与激越症相关的其他生物标志物包括氧化应激标志物、脑胆固醇代谢标志物、运动活性标志物和载脂蛋白,一种伴侣蛋白。这些结果很有前景,但需要进一步验证。初步证据表明,这些生物标志物在干预激越症的研究中具有预测和监测治疗反应的作用,这可能最终有助于丰富研究样本,并为可能受益于个体患者的治疗提供疗法。AD 的血液生物标志物的进展,包括“组学”研究和高灵敏度检测中确定的标志物,为识别新的激越症生物标志物提供了机会。未来对激越症及其治疗的研究应调查血液生物标志物,以深入了解激越症的神经生物学机制,监测症状和治疗反应,并识别可能对治疗有反应的患者。