» Articles » PMID: 38169888

Current Biomarkers and Treatment Strategies in Alzheimer Disease: An Overview and Future Perspectives

Overview
Specialty Neurology
Date 2024 Jan 3
PMID 38169888
Authors
Affiliations
Soon will be listed here.
Abstract

Alzheimer's disease (AD), a progressive degenerative disorder first identified by Alois Alzheimer in 1907, poses a significant public health challenge. Despite its prevalence and impact, there is currently no definitive ante mortem diagnosis for AD pathogenesis. By 2050, the United States may face a staggering 13.8 million AD patients. This review provides a concise summary of current AD biomarkers, available treatments, and potential future therapeutic approaches. The review begins by outlining existing drug targets and mechanisms in AD, along with a discussion of current treatment options. We explore various approaches targeting Amyloid β (Aβ), Tau Protein aggregation, Tau Kinases, Glycogen Synthase kinase-3β, CDK-5 inhibitors, Heat Shock Proteins (HSP), oxidative stress, inflammation, metals, Apolipoprotein E (ApoE) modulators, and Notch signaling. Additionally, we examine the historical use of Estradiol (E2) as an AD therapy, as well as the outcomes of Randomized Controlled Trials (RCTs) that evaluated antioxidants (e.g., vitamin E) and omega-3 polyunsaturated fatty acids as alternative treatment options. Notably, positive effects of docosahexaenoic acid nutriment in older adults with cognitive impairment or AD are highlighted. Furthermore, this review offers insights into ongoing clinical trials and potential therapies, shedding light on the dynamic research landscape in AD treatment.

Citing Articles

Trends and Disparities in Alzheimer's Disease Mortality in the United States: The Impact of COVID-19.

Chaddha J, Blaney E, Al-Salahat A, Noor A, Billion T, Chen Y NeuroSci. 2025; 6(1).

PMID: 39982268 PMC: 11843863. DOI: 10.3390/neurosci6010016.


Identifying Hub Genes and miRNAs Associated with Alzheimer's Disease: A Bioinformatics Pathway to Novel Therapeutic Strategies.

Gascon E, Calvo A, Molina N, Zaragoza P, Osta R Biomolecules. 2025; 14(12.

PMID: 39766348 PMC: 11726968. DOI: 10.3390/biom14121641.


Glutamate: Molecular Mechanisms and Signaling Pathway in Alzheimer's Disease, a Potential Therapeutic Target.

Puranik N, Song M Molecules. 2024; 29(23).

PMID: 39683904 PMC: 11643865. DOI: 10.3390/molecules29235744.


Integrating Machine Learning with Multi-Omics Technologies in Geroscience: Towards Personalized Medicine.

Theodorakis N, Feretzakis G, Tzelves L, Paxinou E, Hitas C, Vamvakou G J Pers Med. 2024; 14(9).

PMID: 39338186 PMC: 11433587. DOI: 10.3390/jpm14090931.


Investigation of the Circular Transcriptome in Alzheimer's Disease Brain.

Gao Y, Xu S, Cheng Y, Takenaka K, Lindner G, Janitz M J Mol Neurosci. 2024; 74(3):64.

PMID: 38981928 PMC: 11233389. DOI: 10.1007/s12031-024-02236-0.


References
1.
Greco S, Sarkar S, Johnston J, Tezapsidis N . Leptin regulates tau phosphorylation and amyloid through AMPK in neuronal cells. Biochem Biophys Res Commun. 2009; 380(1):98-104. PMC: 2657956. DOI: 10.1016/j.bbrc.2009.01.041. View

2.
Kontush A . Amyloid-beta: an antioxidant that becomes a pro-oxidant and critically contributes to Alzheimer's disease. Free Radic Biol Med. 2001; 31(9):1120-31. DOI: 10.1016/s0891-5849(01)00688-8. View

3.
Schneider L, DeKosky S, Farlow M, Tariot P, Hoerr R, Kieser M . A randomized, double-blind, placebo-controlled trial of two doses of Ginkgo biloba extract in dementia of the Alzheimer's type. Curr Alzheimer Res. 2005; 2(5):541-51. DOI: 10.2174/156720505774932287. View

4.
Palmer C, Cotton L, Henley J . The molecular pharmacology and cell biology of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors. Pharmacol Rev. 2005; 57(2):253-77. PMC: 3314513. DOI: 10.1124/pr.57.2.7. View

5.
Mehler M . Epigenetic principles and mechanisms underlying nervous system functions in health and disease. Prog Neurobiol. 2008; 86(4):305-41. PMC: 2636693. DOI: 10.1016/j.pneurobio.2008.10.001. View