Detection Of Alzheimer's Disease Research Articles

Utilizing Profound Learning Methods for Alzheimer's Infection Discovery: An Exhaustive Survey

Alzheimer’s disease (AD) is a major public health issue around the world. It is a progressive disease that causes memory loss and cognitive decline. Early detection is essential for early intervention and treatment of AD. In recent years, there has been a surge in the use of deep learning techniques to analyze complex medical data. This includes neuroimaging data as well as genetic data. This has led to promising advances in the detection of AD. In this paper, we will review the application of various deep learning methods in the field of Alzheimer’s Disease. We will look at the challenges that traditional diagnostic methods face and how these challenges can be overcome by using deep learning approaches. We will also look at different deep learning architectures and data modalities and techniques used in the field of AD detection. Finally, we will look at limitations and future direction of the field to help researchers and practitioners to develop more accurate and effective AD detection methods. Keywords: Alzheimer's Disease, deep learning, neuroimaging, biomarkers, early detection, diagnosis.

Predicting Alzheimer’s progression in MCI: a DTI-based white matter network model

ObjectiveThis study aimed to identify features of white matter network attributes based on diffusion tensor imaging (DTI) that might lead to progression from mild cognitive impairment (MCI) and construct a comprehensive model based on these features for predicting the population at high risk of progression to Alzheimer’s disease (AD) in MCI patients.MethodsThis study enrolled 121 MCI patients from the Alzheimer’s Disease Neuroimaging Initiative (ADNI). Among them, 36 progressed to AD after four years of follow-up. A brain network was constructed for each patient based on white matter fiber tracts, and network attribute features were extracted. White matter network features were downscaled, and white matter markers were constructed using an integrated downscaling approach, followed by forming an integrated model with clinical features and performance evaluation.ResultsAPOE4 and ADAS scores were used as independent predictors and combined with white matter network markers to construct a comprehensive model. The diagnostic efficacy of the comprehensive model was 0.924 and 0.919, sensitivity was 0.864 and 0.900, and specificity was 0.871 and 0.815 in the training and test groups, respectively. The Delong test showed significant differences (P < 0.05) in the diagnostic efficacy of the combined model and APOE4 and ADAS scores, while there was no significant difference (P > 0.05) between the combined model and white matter network biomarkers.ConclusionsA comprehensive model constructed based on white matter network markers can identify MCI patients at high risk of progression to AD and provide an adjunct biomarker helpful in early AD detection.

A LeViT–EfficientNet-Based Feature Fusion Technique for Alzheimer’s Disease Diagnosis

Alzheimer’s disease (AD) is a progressive neurodegenerative condition. It causes cognitive impairment and memory loss in individuals. Healthcare professionals face challenges in detecting AD in its initial stages. In this study, the author proposed a novel integrated approach, combining LeViT, EfficientNet B7, and Dartbooster XGBoost (DXB) models to detect AD using magnetic resonance imaging (MRI). The proposed model leverages the strength of improved LeViT and EfficientNet B7 models in extracting high-level features capturing complex patterns associated with AD. A feature fusion technique was employed to select crucial features. The author fine-tuned the DXB using the Bayesian optimization hyperband (BOHB) algorithm to predict AD using the extracted features. Two public datasets were used in this study. The proposed model was trained using the Open Access Series of Imaging Studies (OASIS) Alzheimer’s dataset containing 86,390 MRI images. The Alzheimer’s dataset was used to evaluate the generalization capability of the proposed model. The proposed model obtained an average generalization accuracy of 99.8% with limited computational power. The findings highlighted the exceptional performance of the proposed model in predicting the multiple types of AD. The recommended integrated feature extraction approach has supported the proposed model to outperform the state-of-the-art AD detection models. The proposed model can assist healthcare professionals in offering customized treatment for individuals with AD. The effectiveness of the proposed model can be improved by generalizing it to diverse datasets.

Early Detection of Alzheimers Disease using Deep Learning

Alzheimer’s disease (AD) poses a significant challenge to global healthcare systems due to its progressive nature and impact on patient’s lives. Accurate and early detection of AD is crucial for timely intervention and management. In this paper, we propose the use of deep learning models, including Convolutional Neural Networks (CNNs), MobileNet, and VGG16 for the classification of Magnetic Resonance Imaging (MRI) scans into different AD stages. Index Terms—Alzheimer’s disease , Deep Learning , Convolu- tional Neural Networks(CNN) , MobileNet , VGG16 , MRI scans

Intelligence model for Alzheimer’s disease detection with optimal trained deep hybrid model

Alzheimer’s disease (AD), a neurodegenerative disorder, is the most common cause of dementia and continuing cognitive deficits. Since there are more cases each year, AD has grown to be a serious social and public health issue. Early detection of the diagnosis of Alzheimer’s and dementia disease is crucial, as is giving them the right care. The importance of early AD diagnosis has recently received a lot of attention. The patient cannot receive a timely diagnosis since the present methods of diagnosing AD take so long and are so expensive. That’s why we created a brand-new AD detection method that has four steps of operation: pre-processing, feature extraction, feature selection, and AD detection. During the pre-processing stage, the input data is pre-processed using an improved data normalization method. Following the pre-processing, these pre-processed data will go through a feature extraction procedure where features including statistical, enhanced entropy-based and mutual information-based features will be extracted. The appropriate features will be chosen from these extracted characteristics using the enhanced Chi-square technique. Based on the selected features, a hybrid model will be used in this study to detect AD. This hybrid model combines classifiers like Long Short Term Memory (LSTM) and Deep Maxout neural networks, and the weight parameters of LSTM and Deep Maxout will be optimized by the Self Updated Shuffled Shepherd Optimization Algorithm (SUSSOA). Our Proposed SUSSOA-based method’s statistical analysis of best values such as 57%, 53%, 28%, 25%, and 21% is higher than the other models like SSO, BMO, HGS, BRO, BES, and ISSO respectively.

Precise prediction of cerebrospinal fluid amyloid beta protein for early Alzheimer's disease detection using multimodal data.

Alzheimer's disease (AD) constitutes a neurodegenerative disorder marked by a progressive decline in cognitive function and memory capacity. The accurate diagnosis of this condition predominantly relies on cerebrospinal fluid (CSF) markers, notwithstanding the associated burdens of pain and substantial financial costs endured by patients. This study encompasses subjects exhibiting varying degrees of cognitive impairment, encompassing individuals with subjective cognitive decline, mild cognitive impairment, and dementia, constituting a total sample size of 82 participants. The primary objective of this investigation is to explore the relationships among brain atrophy measurements derived from magnetic resonance imaging, atypical electroencephalography (EEG) patterns, behavioral assessment scales, and amyloid β-protein (Aβ) indicators. The findings of this research reveal that individuals displaying reduced Aβ1-42/Aβ-40 levels exhibit significant atrophy in the frontotemporal lobe, alongside irregularities in various parameters related to EEG frequency characteristics, signal complexity, inter-regional information exchange, and microstates. The study additionally endeavors to estimate Aβ1-42/Aβ-40 content through the application of a random forest algorithm, amalgamating structural data, electrophysiological features, and clinical scales, achieving a remarkable predictive precision of 91.6%. In summary, this study proposes a cost-effective methodology for acquiring CSF markers, thereby offering a valuable tool for the early detection of AD.

Alzheimer’s disease classification algorithm based on fusion of channel attention and densely connected networks

Mild cognitive impairment (MCI) is a syndrome that occurs in the preclinical stage of Alzheimer’s disease (AD) and is also an early signal of the onset of AD. Early detection and accurate differentiation between MCI and AD populations, and providing them with effective intervention and treatment, are of great significance for preventing or delaying the onset of AD. In this paper, we propose a deep learning model, SE-DenseNet, that combines channel attention and dense connectivity networks and apply it to the field of magnetic resonance imaging (MRI) data recognition for the diagnosis of AD and MCI. First, to extract MRI features with high quality, a slicing algorithm based on two-dimensional image information entropy is proposed to obtain AD brain lesion features with stronger representation ability. Second, in terms of model structure, SENet is introduced as a channel attention module and redistribute the weight of image features in the channel dimension; use DenseNet as the main architecture to maximize information flow, and each layer is directly interconnected with subsequent layers. It enables the network to learn and extract relevant features from the input data and improve the classification ability of the network. Finally, our proposed model is validated on the Alzheimer’s Disease Neuroimaging Initiative (ADNI) dataset, the results have shown that the accuracy for the four classification tasks of AD-NC, AD-MCI, NC-MCI, and AD-NC-MCI can reach 98.12%, 97.42%, 97.42%, and 95.24%, respectively. At the same time, the sensitivity and specificity have also achieved satisfactory results, exhibited a high performance in comparison with the classic machine learning algorithm and several existing state-of-the-art deep learning methods, demonstrating the proposed method is a powerful tool for the early diagnosis and detection of AD.

A Comprehensive Review of Advancement in Speech-Based Approach for Alzheimer Disease Detection in India

Alzheimer’s Disease (AD), accounting for 60%-70% of dementia cases, is poised to afflict India as the second-largest country by mid-century, as indicated by a recent World Health Organization (WHO) study. The socio-economic landscape in India presents unique challenges, with a population that may not be adequately educated on allocating resources for healthcare beyond the age of 60, especially for conditions like Alzheimer's, which currently lacks a definitive cure. Addressing this impending health crisis necessitates innovative, early diagnosis and cost-effective solutions. This comprehensive review paper explores the potential of utilizing speech data analysis for the early detection of Alzheimer’s Disease (AD), offering a pragmatic approach to mitigate the severity of cases. By harnessing speech data, the aim is to diagnose the condition in its early stages, minimizing costs and enabling timely interventions to impede its progression. Early diagnosis is paramount, as it opens doors to effective treatments and preventative measures. The paper systematically reviews various processes involved in developing a mathematical model for the early detection of Alzheimer’s Disease (AD). It delves into key aspects such as data collection methodologies, pre-processing techniques, feature extraction methods, and diverse classifiers. The intention is to provide a thorough understanding of the intricacies involved in creating an accurate and reliable model for early Alzheimer's detection. In light of Alzheimer’s Disease (AD) representing a substantial majority of dementia cases, this review paper serves as a valuable resource for researchers, healthcare professionals, and policymakers. It fosters a deeper comprehension of potential avenues for leveraging speech data specifically in the context of Alzheimer's. As we confront the impending surge in Alzheimer's cases in India, this comprehensive review work contributes to the foundation of knowledge needed to develop scalable and accessible solutions, making a substantial impact on public health.

Analysis of EEG characteristics in Alzheimer’s disease

Alzheimer’s disease (AD) brings a heavy burden to society and families because of the high misdiagnosis rate, prevalence rate, and disability rate. At present, the treatment of AD still faces great challenges. Early intervention can effectively delay the disease progression and improve the burden of symptom care. However, the key to early intervention is accurately identifying and assessing the disease. The examination is difficult to be widely used because of its high invasive cost. There is an urgent need for a simple, convenient, and non-invasive diagnosis of AD. Studies have shown that the brain number of AD patients is slower than that of healthy people, and the complexity of EEG is disturbed. Clinical practice has proved that the specificity and sensitivity of α, β, δ, θ absolute power and α/θ absolute power ratio, especially θ absolute power and α/θ absolute power ratio in the model, are important electrophysiological indexes for AD diagnosis EEG. Non-invasive and economical electrophysiological techniques can characterize and identify the EEG characteristics of AD patients from different angles. They are relatively simple to implement, and patients have a high degree of cooperation. Therefore, EEG, as a diagnostic method of AD, can improve the accuracy of differential diagnosis and early detection of AD and quantify the severity of the disease. It has the advantage of non-invasive convenience and price, which is of great significance for early diagnosis of AD.

Pathophysiology characterization of Alzheimer's disease in South China's aging population: for the Greater-Bay-Area Healthy Aging Brain Study (GHABS).

The Guangdong-Hong Kong-Macao Greater-Bay-Area of South China has an 86million population and faces a significant challenge of Alzheimer's disease (AD). However, the characteristics and prevalence of AD in this area are still unclear due to the rarely available community-based neuroimaging AD cohort. Following the standard protocols of the Alzheimer's Disease Neuroimaging Initiative, the Greater-Bay-Area Healthy Aging Brain Study (GHABS) was initiated in 2021. GHABS participants completed clinical assessments, plasma biomarkers, genotyping, magnetic resonance imaging (MRI), β-amyloid (Aβ) positron emission tomography (PET) imaging, and tau PET imaging. The GHABS cohort focuses on pathophysiology characterization and early AD detection in the Guangdong-Hong Kong-Macao Greater Bay Area. In this study, we analyzed plasma Aβ42/Aβ40 (A), p-Tau181 (T), neurofilament light, and GFAP by Simoa in 470 Chinese older adults, and 301, 195, and 70 had MRI, Aβ PET, and tau PET, respectively. Plasma biomarkers, Aβ PET, tau PET, hippocampal volume, and temporal-metaROI cortical thickness were compared between normal control (NC), subjective cognitive decline (SCD), mild cognitive impairment (MCI), and dementia groups, controlling for age, sex, and APOE-ε4. The prevalence of plasma A/T profiles and Aβ PET positivity were also determined in different diagnostic groups. The aims, study design, data collection, and potential applications of GHABS are summarized. SCD individuals had significantly higher plasma p-Tau181 and plasma GFAP than the NC individuals. MCI and dementia patients showed more abnormal changes in all the plasma and neuroimaging biomarkers than NC and SCD individuals. The frequencies of plasma A+/T+ (NC; 5.9%, SCD: 8.2%, MCI: 25.3%, dementia: 64.9%) and Aβ PET positivity (NC: 25.6%, SCD: 22.5%, MCI: 47.7%, dementia: 89.3%) were reported. The GHABS cohort may provide helpful guidance toward designing standard AD community cohorts in South China. This study, for the first time, reported the pathophysiology characterization of plasma biomarkers, Aβ PET, tau PET, hippocampal atrophy, and AD-signature cortical thinning, as well as the prevalence of Aβ PET positivity in the Guangdong-Hong Kong-Macao Greater Bay Area of China. These findings provide novel insights into understanding the characteristics of abnormal AD pathological changes in South China's older population.

Cognitive impairment, neurodegenerative disorders, and olfactory impairment: A literature review.

&lt;br&gt;&lt;b&gt;Introduction:&lt;/b&gt; The early detection and diagnosis of dementia are of key importance in treatment, slowing disease progression, or suppressing symptoms. The possible role of changes in the sense of smell is considered with regard to potential markers for early detection of Alzheimer's disease (AD).&lt;/br&gt; &lt;br&gt;&lt;b&gt;Materials and methods:&lt;/b&gt; A literature search was conducted using the electronic databases PubMed, Scopus, and Web of Science between May 30, 2022 and August 2, 2022. The term "dementia" was searched with keyword combinations related to olfaction.&lt;/br&gt; &lt;br&gt;&lt;b&gt;Results:&lt;/b&gt; A total of 1,288 records were identified through the database search. Of these articles, 49 were ultimately included in the analysis. The results showed the potential role of changes in the sense of smell as potential biomarkers for early detection of AD. Multiple studies have shown that olfactory impairment may be observed in patients with AD, PD, MCI, or other types of dementia. Even though smell tests are able to detect olfactory loss caused by neurodegenerative diseases, they cannot reliably distinguish between certain diseases.&lt;/br&gt; &lt;br&gt;&lt;b&gt;Conclusions:&lt;/b&gt; In individuals with cognitive impairment or neurodegenerative diseases, olfactory assessment has repeatedly been reported to be used for early diagnosis, but not for differential diagnosis.&lt;/br&gt.

Neuro-cogniguard: a Deep Learning Approach for Early Alzheimer's Detection

Neuro-cogniguard: a Deep Learning Approach for Early Alzheimer's Detection

Performance of SOBA-AD blood test in discriminating Alzheimer’s disease patients from cognitively unimpaired controls in two independent cohorts

Amyloid-beta (Aβ) toxic oligomers are critical early players in the molecular pathology of Alzheimer’s disease (AD). We have developed a Soluble Oligomer Binding Assay (SOBA-AD) for detection of these Aβ oligomers that contain α-sheet secondary structure that discriminates plasma samples from patients on the AD continuum from non-AD controls. We tested 265 plasma samples from two independent cohorts to investigate the performance of SOBA-AD. Testing was performed at two different sites, with different personnel, reagents, and instrumentation. Across two cohorts, SOBA-AD discriminated AD patients from cognitively unimpaired (CU) subjects with 100% sensitivity, > 95% specificity, and > 98% area under the curve (AUC) (95% CI 0.95–1.00). A SOBA-AD positive readout, reflecting α-sheet toxic oligomer burden, was found in AD patients, and not in controls, providing separation of the two populations, aside from 5 SOBA-AD positive controls. Based on an earlier SOBA-AD study, the Aβ oligomers detected in these CU subjects may represent preclinical cases of AD. The results presented here support the value of SOBA-AD as a promising blood-based tool for the detection and confirmation of AD.

Application of Convolutional Neural Networks for Early Detection and Classification of Alzheimer's disease from MRI Images

This study investigates the application of convolutional neural networks (CNNs) and traditional machine learning algorithms for the early detection and classification of Alzheimer's disease (AD) using brain Magnetic Resonance Imaging (MRI) data. We compare the performance of CNNs with Support Vector Machines (SVM), Random Forest (RF), and Gradient Boosting Machines (GBM) on a dataset comprising MRI images from AD patients and healthy controls. Results show that CNNs achieved the highest accuracy (90.2%) and area under the receiver operating characteristic curve (AUC-ROC) of 0.95, outperforming SVM, RF, and GBM. The CNN model also exhibited high sensitivity (87.5%) and specificity (92.6%) in distinguishing between AD patients and healthy controls. These findings highlight the effectiveness of CNN-based approaches in leveraging raw MRI images for accurate and early detection of AD.

Evaluating p-tau217 and p-tau231 as Biomarkers for Early Diagnosis and Differentiation of Alzheimer's Disease: A Narrative Review.

The escalating prevalence of Alzheimer's disease (AD) highlights the urgent need to develop reliable biomarkers for early diagnosis and intervention. AD is characterized by the pathological accumulation of amyloid-beta plaques and tau neurofibrillary tangles. Phosphorylated tau (p-tau) proteins, particularly p-tau217 and p-tau231, have been identified as promising biomarker candidates to differentiate the disease progression from preclinical stages. This narrative review is devoted to a critical evaluation of the diagnostic accuracy, sensitivity, and specificity of p-tau217 and p-tau231 levels in the detection of AD, measured in plasma, serum, and cerebrospinal fluid, compared to established biomarkers. Additionally, the efficacy of these markers in distinguishing AD from other neurodegenerative disorders is examined. The significant advances offered by p-tau217 and p-tau231 in AD diagnostics are highlighted, demonstrating their unique utility in early detection and differential diagnosis. This comprehensive analysis not only confirms the excellent diagnostic capabilities of these markers, but also deepens the understanding of the molecular dynamics of AD, contributing to the broader scientific discourse on neurodegenerative diseases. This review is aimed to provide key information for researchers and clinicians across disciplines, filling interdisciplinary gaps and highlighting the role of p-tau proteins in revolutionizing AD research and clinical practice.

Ubi-AD : Towards Ubiquitous, Passive Alzheimer Detection using the Smartwatch

Alzheimer’s disease (AD) is a insidious and progressive neurodegenerative disease, the annual relevant social cost for AD patients can reach about $1 trillion in the world. Therefore, early diagnosis and treatment of AD play a vital role in slowing disease progression. However, existing detection methods for cognitive impairment can not consistently screen the stage of AD. To tackle this challenge, we propose an AD detection system, Ubi-AD, which combines the features of multiple biomarkers to realize passive and accurate AD detection. Unlike existing work, Ubi-AD can passively recognize the AD digital biomarkers during daily smartwatch usage without interfering with the user. At the user end, Ubi-AD first extracts the non-speech sounds (pause words, such as em, ah), which contain no privacy-sensitive content. Then, Ubi-AD recognizes the user’s walking activity, dining activity, and sleep activity from daily activities. Ubi-AD analyzes these data from smartwatch and predicts the AD stages using a multi-modal fusion neural network at the cloud end. We evaluate our model on a collected dataset from 45 volunteers. As a result, Ubi-AD can reach a detection accuracy of \(93.4\% \) , which means that Ubi-AD can provide multiple effective biomarkers for ubiquitous and passive detection in daily life.

Alzheimer Disease Using Machine Learning

The successful development of amyloid-based biomarkers and tests for Alzheimer’s disease (AD) represents an important milestone in AD diagnosis. However, two major limitations remain. Amyloid-based diagnostic biomarkers and tests provide limited information about the disease process and they are unable to identify individuals with the disease before significant amyloid-beta accumulation in the brain develops. The objective in this study is to develop a method to identify potential blood-based non-amyloid biomarkers for early AD detection. The use of blood is attractive because it is accessible and relatively inexpensive. Our method is mainly based on machine learning (ML) techniques (support vector machines in particular) because of their ability to create multivariable models by learning patterns from complex data. Using novel feature selection and evaluation modalities we identified 5 novel panels of non-amyloid proteins with the potential to serve as biomarkers of early AD. In particular, we found that the combination of A2M, ApoE, BNP, Eot3, RAGE and SGOT may be a key biomarker profile of early disease. Disease detection models based on the identified panels achieved sensitivity (SN) &gt; 80%, specificity (SP) &gt; 70%, and area under receiver operating curve (AUC) of at least 0.80 at prodromal stage (with higher performance at later stages) of the disease. Existing ML models performed poorly in comparison at this stage of the disease suggesting that the underlying protein panels may not be suitable for early disease detection. Our results demonstrate the feasibility of early detection of AD using non-amyloid based biomarkers.

Multiomics analysis to explore blood metabolite biomarkers in an Alzheimer’s Disease Neuroimaging Initiative cohort

Alzheimer's disease (AD) is a neurodegenerative disease that commonly causes dementia. Identifying biomarkers for the early detection of AD is an emerging need, as brain dysfunction begins two decades before the onset of clinical symptoms. To this end, we reanalyzed untargeted metabolomic mass spectrometry data from 905 patients enrolled in the AD Neuroimaging Initiative (ADNI) cohort using MS-DIAL, with 1,304,633 spectra of 39,108 unique biomolecules. Metabolic profiles of 93 hydrophilic metabolites were determined. Additionally, we integrated targeted lipidomic data (4873 samples from 1524 patients) to explore candidate biomarkers for predicting progressive mild cognitive impairment (pMCI) in patients diagnosed with AD within two years using the baseline metabolome. Patients with lower ergothioneine levels had a 12% higher rate of AD progression with the significance of P = 0.012 (Wald test). Furthermore, an increase in ganglioside (GM3) and decrease in plasmalogen lipids, many of which are associated with apolipoprotein E polymorphism, were confirmed in AD patients, and the higher levels of lysophosphatidylcholine (18:1) and GM3 d18:1/20:0 showed 19% and 17% higher rates of AD progression, respectively (Wald test: P = 3.9 × 10–8 and 4.3 × 10–7). Palmitoleamide, oleamide, diacylglycerols, and ether lipids were also identified as significantly altered metabolites at baseline in patients with pMCI. The integrated analysis of metabolites and genomics data showed that combining information on metabolites and genotypes enhances the predictive performance of AD progression, suggesting that metabolomics is essential to complement genomic data. In conclusion, the reanalysis of multiomics data provides new insights to detect early development of AD pathology and to partially understand metabolic changes in age-related onset of AD.

Neuron-level explainable AI for Alzheimer’s Disease assessment from fundus images

Alzheimer’s Disease (AD) is a progressive neurodegenerative disease and the leading cause of dementia. Early diagnosis is critical for patients to benefit from potential intervention and treatment. The retina has emerged as a plausible diagnostic site for AD detection owing to its anatomical connection with the brain. However, existing AI models for this purpose have yet to provide a rational explanation behind their decisions and have not been able to infer the stage of the disease’s progression. Along this direction, we propose a novel model-agnostic explainable-AI framework, called Granula̲\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\underline{la}$$\\end{document}r Neuron-lev̲\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\underline{v}$$\\end{document}el Expla̲\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\underline{a}$$\\end{document}iner (LAVA), an interpretation prototype that probes into intermediate layers of the Convolutional Neural Network (CNN) models to directly assess the continuum of AD from the retinal imaging without the need for longitudinal or clinical evaluations. This innovative approach aims to validate retinal vasculature as a biomarker and diagnostic modality for evaluating Alzheimer’s Disease. Leveraged UK Biobank cognitive tests and vascular morphological features demonstrate significant promise and effectiveness of LAVA in identifying AD stages across the progression continuum.

On the road to biological blood diagnosis of Alzheimer's disease?

The growing number of people suffering from Alzheimer's disease (AD) represents a major public health problem. The diagnosis of AD is multidisciplinary and involves the use of amyloid and tau biomarkers measured in cerebrospinal fluid. Recent advances in analytical techniques now allow us to measure these biomarkers in blood. Blood biomarkers offer particularly promising potential for early, minimally invasive detection of AD, as well as for differential diagnosis of dementia and patient follow-up. The aim of this review is to provide an overview of current and candidate blood biomarkers for AD, their informative value, and their potential to be integrated into clinical practice in the near future.