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Imaging Techniques in Alzheimer’s Disease: A Review of Applications in Early Diagnosis and Longitudinal Monitoring

机译:阿尔茨海默病的影像学技术:早期诊断和纵向监测中的应用综述

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摘要

Background. Alzheimer’s disease (AD) is a progressive neurodegenerative disorder affecting many individuals worldwide with no effective treatment to date. AD is characterized by the formation of senile plaques and neurofibrillary tangles, followed by neurodegeneration, which leads to cognitive decline and eventually death. Introduction. In AD, pathological changes occur many years before disease onset. Since disease-modifying therapies may be the most beneficial in the early stages of AD, biomarkers for the early diagnosis and longitudinal monitoring of disease progression are essential. Multiple imaging techniques with associated biomarkers are used to identify and monitor AD. Aim. In this review, we discuss the contemporary early diagnosis and longitudinal monitoring of AD with imaging techniques regarding their diagnostic utility, benefits and limitations. Additionally, novel techniques, applications and biomarkers for AD research are assessed. Findings. Reduced hippocampal volume is a biomarker for neurodegeneration, but atrophy is not an AD-specific measure. Hypometabolism in temporoparietal regions is seen as a biomarker for AD. However, glucose uptake reflects astrocyte function rather than neuronal function. Amyloid-β (Aβ) is the earliest hallmark of AD and can be measured with positron emission tomography (PET), but Aβ accumulation stagnates as disease progresses. Therefore, Aβ may not be a suitable biomarker for monitoring disease progression. The measurement of tau accumulation with PET radiotracers exhibited promising results in both early diagnosis and longitudinal monitoring, but large-scale validation of these radiotracers is required. The implementation of new processing techniques, applications of other imaging techniques and novel biomarkers can contribute to understanding AD and finding a cure. Conclusions. Several biomarkers are proposed for the early diagnosis and longitudinal monitoring of AD with imaging techniques, but all these biomarkers have their limitations regarding specificity, reliability and sensitivity. Future perspectives. Future research should focus on expanding the employment of imaging techniques and identifying novel biomarkers that reflect AD pathology in the earliest stages.
机译:背景。阿尔茨海默病(AD)是一种对全世界许多人的进步神经退行性疾病,无效迄今为止。 AD的特征在于形成老年斑块和神经纤维斑,其次是神经变性,导致认知下降并最终死亡。介绍。在广告中,病理变化发生在疾病发作前多年。由于疾病改性疗法可能是AD早期阶段中最有益的,因此早期诊断和疾病进展的早期诊断和纵向监测的生物标志物是必不可少的。使用相关生物标志物的多种成像技术用于识别和监控广告。目的。在这篇综述中,我们讨论了对其诊断用途,益处和限制的成像技术的当代早期诊断和纵向监测。另外,评估了用于AD研究的新技术,应用和生物标志物。发现。降低海马体积是神经变性的生物标志物,但萎缩不是特异性的措施。临时区域中的低血压率为AD的生物标志物。然而,葡萄糖摄取反映了星形胶质细胞功能而不是神经元功能。淀粉样蛋白-β(Aβ)是AD的最早标志,可以用正电子发射断层扫描(PET)测量,但由于疾病的进展,Aβ积累停滞。因此,Aβ可能不是用于监测疾病进展的合适生物标志物。 Tau积累的测量与宠物放射体制物具有早期诊断和纵向监测的有希望的,但需要大规模验证这些放射性机构。实施新的加工技术,其他成像技术和新型生物标志物的应用可以有助于了解广告并找到治疗方法。结论。提出了几种生物标志物,用于提前诊断和具有成像技术的广告的早期诊断和纵向监测,但所有这些生物标志物都有关于特异性,可靠性和敏感性的局限性。未来的观点。未来的研究应该侧重于扩大成像技术的就业,并识别最早反映广告病理的新型生物标志物。

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