Revolutionizing dementia detection: Leveraging vision and Swin transformers for early diagnosis

IF 1.6 3区 医学 Q3 GENETICS & HEREDITY
Rini P L, Gayathri K S
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引用次数: 0

Abstract

Dementia, an increasingly prevalent neurological disorder with a projected threefold rise globally by 2050, necessitates early detection for effective management. The risk notably increases after age 65. Dementia leads to a progressive decline in cognitive functions, affecting memory, reasoning, and problem-solving abilities. This decline can impact the individual's ability to perform daily tasks and make decisions, underscoring the crucial importance of timely identification. With the advent of technologies like computer vision and deep learning, the prospect of early detection becomes even more promising. Employing sophisticated algorithms on imaging data, such as positron emission tomography scans, facilitates the recognition of subtle structural brain changes, enabling diagnosis at an earlier stage for potentially more effective interventions. In an experimental study, the Swin transformer algorithm demonstrated superior overall accuracy compared to the vision transformer and convolutional neural network, emphasizing its efficiency. Detecting dementia early is essential for proactive management, personalized care, and implementing preventive measures, ultimately enhancing outcomes for individuals and lessening the overall burden on healthcare systems.

痴呆症检测的革命性变革:利用视觉和 Swin 变压器进行早期诊断
痴呆症是一种日益普遍的神经系统疾病,预计到 2050 年全球发病率将增加三倍。65 岁以后患病风险明显增加。痴呆症会导致认知功能逐渐下降,影响记忆、推理和解决问题的能力。这种衰退会影响个人执行日常任务和做出决策的能力,因此及时发现至关重要。随着计算机视觉和深度学习等技术的出现,早期检测的前景变得更加广阔。在正电子发射断层扫描等成像数据上采用复杂的算法,有助于识别细微的大脑结构变化,从而在早期阶段进行诊断,采取更有效的干预措施。在一项实验研究中,与视觉变换器和卷积神经网络相比,斯温变换器算法显示出更高的整体准确性,突出了其效率。早期检测痴呆症对于主动管理、个性化护理和实施预防措施至关重要,最终可提高个人的治疗效果,减轻医疗保健系统的总体负担。
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来源期刊
CiteScore
5.90
自引率
7.10%
发文量
40
审稿时长
4-8 weeks
期刊介绍: Neuropsychiatric Genetics, Part B of the American Journal of Medical Genetics (AJMG) , provides a forum for experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. It is a resource for novel genetics studies of the heritable nature of psychiatric and other nervous system disorders, characterized at the molecular, cellular or behavior levels. Neuropsychiatric Genetics publishes eight times per year.
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