Causal relationship between Alzheimer’s disease and unstable angina: a bidirectional Mendelian randomization analysis DOI Creative Commons
Yuhang Chen,

Cong-ying Ren,

Cao Yu

и другие.

Frontiers in Psychiatry, Год журнала: 2024, Номер 15

Опубликована: Июль 9, 2024

Background Research from observational studies has demonstrated a link between Alzheimer’s disease (AD) and higher risk of cardiovascular (CVD). Uncertainty surrounds the exact genetic cause AD coronary heart disease, particularly unstable angina (UA). Mendelian randomization (MR) analysis was used to examine causal UA evaluate impact on UA. Methods The purpose bidirectional MR investigate exposure illness causation. Genetic instrumental variables for were obtained European populations using genome-wide association (GWAS). primary conclusions inverse variance weighted approach (IVW), other sensitivity techniques employed. Sensitivity analyses carried out heterogeneity horizontal pleiotropy guarantee accurate results. Results An elevated linked genetically predicted (IVW: OR=3.439, 95% CI: 1.565-7.555, P=0.002). A substantial relationship not supported by any evidence in reverse study OR=0.998, 0.995-1.001, P=0.190). Various produced consistent revealed no discernible or pleiotropy. Conclusions One factor that we found our trial AD. This highlights necessity researching underlying molecular mechanisms as well possibility creating individualized treatment plans based data.

Язык: Английский

Comparative efficacy, tolerability and acceptability of donanemab, lecanemab, aducanumab and lithium on cognitive function in mild cognitive impairment and Alzheimer's disease: A systematic review and network meta-analysis DOI
Itsuki Terao, Wakako Kodama

Ageing Research Reviews, Год журнала: 2024, Номер 94, С. 102203 - 102203

Опубликована: Янв. 20, 2024

Язык: Английский

Процитировано

53

Virtual brain twins: from basic neuroscience to clinical use DOI Creative Commons
Huifang Wang, Paul Triebkorn, Martin Breyton

и другие.

National Science Review, Год журнала: 2024, Номер 11(5)

Опубликована: Фев. 27, 2024

ABSTRACT Virtual brain twins are personalized, generative and adaptive models based on data from an individual’s for scientific clinical use. After a description of the key elements virtual twins, we present standard model personalized whole-brain network models. The personalization is accomplished using subject’s imaging by three means: (1) assemble cortical subcortical areas in subject-specific space; (2) directly map connectivity into models, which can be generalized to other parameters; (3) estimate relevant parameters through inversion, typically probabilistic machine learning. We use healthy ageing five diseases: epilepsy, Alzheimer’s disease, multiple sclerosis, Parkinson’s disease psychiatric disorders. Specifically, introduce spatial masks demonstrate their physiological pathophysiological hypotheses. Finally, pinpoint challenges future directions.

Язык: Английский

Процитировано

35

Anti‐amyloid antibody treatments for Alzheimer's disease DOI Creative Commons
Robert Perneczky, Geert Dom, Andrew Chan

и другие.

European Journal of Neurology, Год журнала: 2023, Номер 31(2)

Опубликована: Сен. 11, 2023

Abstract Our aim is to review the most recent evidence on novel antibody therapies for Alzheimer's disease directed against amyloid‐β. This a joint statement of European Association Neurology and Psychiatric Association. After numerous unsuccessful endeavors create disease‐modifying therapy disease, substantial consistent supporting clinical effectiveness monoclonal antibodies aimed at amyloid‐β finally emerging. The latest trials not only achieved their primary objective slowing progression over several months but also demonstrated positive secondary outcomes decrease in levels as observed through positron emission tomography scans. Taken whole, these findings mark significant breakthrough by substantiating that reducing yields tangible benefits, beyond mere changes biomarkers. Concurrently, regular utilization new generation drugs will determine whether statistical efficacy translates into clinically meaningful improvements. may well signify dawning era development disease.

Язык: Английский

Процитировано

40

Broadening Horizons: Exploring the Cathepsin Family as Therapeutic Targets for Alzheimer's Disease DOI Creative Commons
Xiaohui Liu, Xiaotong Liu,

Yue Wu

и другие.

Aging and Disease, Год журнала: 2024, Номер unknown, С. 0 - 0

Опубликована: Янв. 1, 2024

Alzheimer's disease (AD) is an intricate neurodegenerative disorder characterized by the accumulation of misfolded proteins, including beta-amyloid (Aβ) and tau, leading to cognitive decline. Despite decades research, precise mechanisms underlying its onset progression remain elusive. Cathepsins are a family lysosomal enzymes that play vital roles in cellular processes, protein degradation regulation immune responses. Emerging evidence suggests cathepsins may be involved AD pathogenesis. can influence activation microglia astrocytes, resident cells brain. However, cathepsin dysfunction lead notably Aβ tau. In addition, dysregulated activity induce exaggerated response, promoting chronic inflammation neuronal patients with AD. By unraveling classification, functions, AD's pathogenesis, this review sheds light on their involvement devastating disease. Targeting could promising novel approach for mitigating pathological processes contribute AD, providing new avenues treatment prevention.

Язык: Английский

Процитировано

5

Current therapeutics for Alzheimer’s disease and clinical trials DOI Creative Commons
Danqing Xiao, Chen Zhang

Exploration of neuroscience, Год журнала: 2024, Номер 3(3), С. 255 - 271

Опубликована: Июнь 27, 2024

Alzheimer’s disease (AD) is a major type of dementia and neurodegenerative disease, characterized by memory loss cognitive decline. Over decades, significant efforts have been dedicated to finding its cause, pathogenic mechanisms, biomarkers for early detection, clinical trials treatment. Earlier approved drugs mainly ameliorated the symptoms AD, until recent years when two targeting amyloid-beta (Aβ) protein were slow down progression disease. This review article encompasses history drug development in treating AD that failed succeeded. Clinicaltrials.org website was systematically searched screened randomized controlled with results posted past 10 years. Among 3,388 trials, 211 interventional studies registered under met eligibility. includes targets discovery such as Aβ, tau, neurotransmitter receptors, neuroinflammation, multi-target studies, repurposing pharmacological agents, non-pharmacological interventions, therapy neuropsychiatric dementia. Current are ongoing no available yet. With vast choices investigated, this aims present some insights into future design contribute our find cure.

Язык: Английский

Процитировано

4

Therapeutic Potential of Fingolimod on Psychological Symptoms and Cognitive Function in Neuropsychiatric and Neurological Disorders DOI

Fatemeh Rahmati‐Dehkordi,

Hadi Khanifar,

Nazanin Najari

и другие.

Neurochemical Research, Год журнала: 2024, Номер 49(10), С. 2668 - 2681

Опубликована: Июнь 26, 2024

Язык: Английский

Процитировано

3

Muscarinic Receptors and Alzheimer’s Disease: New Perspectives and Mechanisms DOI Creative Commons
Martina Monaco, Hanna Trebesova, Massimo Grilli

и другие.

Current Issues in Molecular Biology, Год журнала: 2024, Номер 46(7), С. 6820 - 6835

Опубликована: Июль 2, 2024

Alzheimer's disease (AD) is one of the most prevalent neurodegenerative diseases on a global scale. Historically, this pathology has been linked to cholinergic transmission, and despite scarcity effective therapies, numerous alternative processes targets have proposed as potential avenues for comprehending complex illness. Nevertheless, fundamental pathophysiological mechanisms underpinning AD remain largely enigmatic, with growing body evidence advocating significance muscarinic receptors in modulating brain's capacity adapt generate new memories. This review summarizes current state art field receptors' involvement AD. A specific key factor was relationship between comorbidity emergence mechanisms.

Язык: Английский

Процитировано

3

Anticorpos anti-amiloide no tratamento da Doença de Alzheimer: uma revisão narrativa DOI Creative Commons

Bruno Souza Fonseca,

Matheus Henrique de Lima Cordeiro,

P. Abreu

и другие.

Revista Sociedade Científica, Год журнала: 2025, Номер 8(1), С. 197 - 203

Опубликована: Янв. 7, 2025

A Doença de Alzheimer (DA) é uma condição neurodegenerativa caracterizada pela formação placas β-amiloide (Aβ) e emaranhados neurofibrilares no cérebro, resultando em um declínio cognitivo progressivo. Esta revisão examina as imunoterapias mais recentes direcionadas ao Aβ, com ênfase na eficácia anticorpos monoclonais, como Aducanumab, Lecanemab Donanemab. Uma busca através do PubMed, utilizando os operadores booleanos "((anti-amyloid antibody)) and ((Alzheimer))", inicialmente identificou 418 artigos. Após a aplicação critérios inclusão que exigiam revisões sistemáticas textos completos gratuitos, publicados entre 2020 2024, foram examinados 6 artigos atenderam aos metodológicos rigorosos necessários para descrever efeitos dos monoclonais tratamento da DA. Embora ensaios clínicos tenham mostrado melhorias nas escalas cognitivas, o ADAS-Cog MMSE, não atingiram nível relevância clínica significativa. As terapias anti-Aβ representam avanço crucial, espera-se combinações futuras tratamentos biomarcadores aprimorem forma eficaz manejo DA melhorem desfechos pacientes.

Процитировано

0

Plasma p‐tau217 and neurofilament/p‐tau217 ratio in differentiating Alzheimer's disease from syndromes associated with frontotemporal lobar degeneration DOI Creative Commons
Alberto Benussi,

Hanna Huber,

Kübra Tan

и другие.

Alzheimer s & Dementia, Год журнала: 2025, Номер unknown

Опубликована: Янв. 8, 2025

Abstract INTRODUCTION Plasma‐based biomarkers have shown promise for clinical implementation, but their accuracy in differentiating Alzheimer's disease (AD) from syndromes associated with frontotemporal lobar degeneration (FTLD) has yet to be fully investigated. This study assessed the potential of plasma differential diagnosis. METHODS cohort included 374 participants (96 AD, 278 FTLD). Plasma phosphorylated tau (p‐tau) 217 , neurofilament light chain (NfL), brain‐derived tau, glial fibrillary acidic protein, and amyloid beta 1‐42 / 1‐40 ratio were measured. Receiver operating characteristic curve analyses diagnostic accuracy, a three‐range threshold approach was used stratify patients based on most accurate biomarker. RESULTS p‐tau effectively distinguished AD FTLD, NfL/p‐tau showing superior accuracy. The identified thresholds 95% 97.5% sensitivity specificity, reducing need cerebrospinal fluid testing by 75% 54%, respectively. DISCUSSION are promising non‐invasive suggesting use as alternative traditional methods. Highlights distinguishes high chain/p‐tau showed highest FTLD. A reduces invasive or positron emission tomography imaging.

Язык: Английский

Процитировано

0

Differenzialdiagnostik der Varianten der Alzheimerkrankheit DOI
Hannes Gramespacher, Gereon R. Fink, Oezguer A. Onur

и другие.

InFo Neurologie + Psychiatrie, Год журнала: 2025, Номер 27(1), С. 26 - 35

Опубликована: Янв. 1, 2025

Процитировано

0