Abstract

Alzheimer’s disease (AD) is the most common form of dementia. It’s a chronic and untreatable neurodegenerative disease with irreversible progression and has important social and economic implications in terms of direct medical and social care costs. Despite prolonged and expensive efforts employed by the scientific community over the last few decades, no effective treatments are still available for patients, and the development of disease-modifying drugs is now a really urgent need. The recent failure of clinical trials based on the immunotherapeutic approach against amyloid-β(Aβ) protein questioned the validity of the “amyloid cascade hypothesis” as the molecular machinery causing the disease. Indeed, most attempts to design effective treatments for AD have been based until now on molecular targets suggested to be implicated in AD pathogenesis by the amyloid cascade hypothesis. However, mounting evidence from scientific literature supports the view of AD as a multifactorial disease that results from the concomitant action of multiple molecular players. This view, together with the lack of success of the disease-modifying single-target approaches, strongly suggests that AD drug design needs to be shifted towards multi-targeted compounds or drug combinations acting synergistically on the main core features of disease pathogenesis. The discovery of drug candidates targeting multiple factors involved in AD would greatly improve drug development. So, it is reasonable that upcoming strategies for the design of preventive and/or therapeutic agents for AD point to a multi-pronged approach including more than one druggable target to definitely defeat the disease.

Highlights

  • Alzheimer’s disease (AD) is a multifactorial neurodegenerative disorder characterized by progressive loss of neurons which may induce a decline in learning ability, loss of memory and impairment of other cognitive functions (Lane et al, 2018)

  • We summarize the reasons for the ineffectiveness of the main experimental strategies targeting the molecular pathways suggested to be crucial for the disease, and highlight the urgent need for a radical change in the therapeutic approaches to AD

  • These approaches, in our opinion, should definitely point to a synergic strategy based on the concomitant use of multiple drugs or of a single multi-target compound to tackle the most relevant events in the molecular machinery that causes the onset of AD and its progression

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Summary

INTRODUCTION

Alzheimer’s disease (AD) is a multifactorial neurodegenerative disorder characterized by progressive loss of neurons which may induce a decline in learning ability, loss of memory and impairment of other cognitive functions (Lane et al, 2018). No new drugs have been approved for AD during the past 16 years and the available medications have very low impact on the disease course (Cacabelos, 2018), and even increase the costs for the care of AD patients by prolonging the length of a person’s ‘‘stay’’ in the Mild, Moderate, or Severe stage of disease (Cimler et al, 2019) For these reasons, AD is recognized by the World Health Organization as a global public health priority. We summarize the reasons for the ineffectiveness of the main experimental strategies targeting the molecular pathways suggested to be crucial for the disease, and highlight the urgent need for a radical change in the therapeutic approaches to AD These approaches, in our opinion, should definitely point to a synergic strategy based on the concomitant use of multiple drugs or of a single multi-target compound to tackle the most relevant events in the molecular machinery that causes the onset of AD and its progression

ON THE SIDE OF AMYLOID CASCADE HYPOTHESIS OR BEYOND IT?
Immunotherapy Against Aβ
Other Therapeutic Strategies Targeting Aβ
Other Approaches Based on Amyloid Cascade Targets
Alternative Pathogenic Hypotheses and Therapeutic Targets
Findings
CONCLUDING REMARKS

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