4.5 Review

Translation of Pre-Clinical Studies into Successful Clinical Trials for Alzheimer's Disease: What are the Roadblocks and How Can They Be Overcome?

期刊

JOURNAL OF ALZHEIMERS DISEASE
卷 47, 期 4, 页码 815-843

出版社

IOS PRESS
DOI: 10.3233/JAD-150136

关键词

Alzheimer's disease; animal model; dementia; memory disorder; pre-clinical; treatment

资金

  1. Alzheimer's Association (USA)
  2. Alzheimer's Research (UK)
  3. International Brain Research Organisation
  4. European Federation of Neurological Sciences
  5. World Federation of Neurology
  6. Medical Research Council [G0502157, G0400074, G0500247, G1100540, G0900652] Funding Source: researchfish
  7. Grants-in-Aid for Scientific Research [15H04271] Funding Source: KAKEN
  8. MRC [G0900652, G0500247, G1100540, G0400074, G0502157] Funding Source: UKRI

向作者/读者索取更多资源

Preclinical studies are essential for translation to disease treatments and effective use in clinical practice. An undue emphasis on single approaches to Alzheimer's disease (AD) appears to have retarded the pace of translation in the field, and there is much frustration in the public about the lack of an effective treatment. We critically reviewed past literature (1990-2014), analyzed numerous data, and discussed key issues at a consensus conference on Brain Ageing and Dementia to identify and overcome roadblocks in studies intended for translation. We highlight various factors that influence the translation of preclinical research and highlight specific preclinical strategies that have failed to demonstrate efficacy in clinical trials. The field has been hindered by the domination of the amyloid hypothesis in AD pathogenesis while the causative pathways in disease pathology are widely considered to be multifactorial. Understanding the causative events and mechanisms in the pathogenesis are equally important for translation. Greater efforts are necessary to fill in the gaps and overcome a variety of confounds in the generation, study design, testing, and evaluation of animal models and the application to future novel anti-dementia drug trials. A greater variety of potential disease mechanisms must be entertained to enhance progress.

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