4.3 Article

Novel Therapeutic Strategies for Dementia

Journal

CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS
Volume 15, Issue 2, Pages 141-241

Publisher

BENTHAM SCIENCE PUBL
DOI: 10.2174/1871527315666160202121548

Keywords

Alzheimer disease; anti-A beta treatments; anti-tau treatments; cholinesterase inhibitors; dementia; epigenetic drugs; immunotherapy; natural products; pharmacogenomics; therapeutic strategies

Funding

  1. EuroEspes Biomedical Research Center. Institute of Medical Science and Genomic Medicine, Corunna, Spain
  2. Genomic Medicine. Camilo Jose Cela University, Madrid, Spain
  3. GALLY International Biomedical Research Consulting LLC, San Antonio, Texas, USA
  4. Russian Science Foundation (RSCF) [14-23-00160]

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Dementia represents a major problem of health and disability, with a relevant economic impact on our society. Despite important advances in pathogenesis, diagnosis and treatment, its primary causes still remain elusive, accurate biomarkers are not well characterized, and the available pharmacological treatments are not cost-effective. Alzheimer disease (AD), the most prevalent form of dementia, is a polygenic/multifactorial/complex disorder in which hundreds of defective genes distributed across the human genome may contribute to its pathogenesis. Diverse environmental factors, cerebrovascular dysfunction, and epigenetic phenomena, together with structural and functional genomic dysfunctions lead to amyloid deposition, neurofibrillary tangle formation and premature neuronal death, the major neuropathological hallmarks of AD. For the past 20 years, over 1,000 different compounds have been studied as potential candidate drugs for the treatment of AD. About 50% of these substances are novel molecules obtained from natural sources. The candidate compounds can be classified according to their pharmacological properties and/or the AD-related pathogenic cascade to which they are addressed to halt disease progression. In addition to the Food and Drug Administration (FDA)-approved drugs since 1993 (tacrine, donepezil, rivastigmine, galantamine, memantine), most candidate strategies fall into 6 major categories: (i) novel cholinesterase inhibitors and neurotransmitter regulators, (ii) anti-amyloid beta (A beta) treatments (amyloid-beta protein precursor (APP) regulators, A beta breakers, active and passive immunotherapy with vaccines and antibodies, beta- and gamma-secretase inhibitors or modulators), (iii) anti-tau treatments, (iv) pleiotropic products (most of them of natural origin), (v) epigenetic intervention, and (vi) combination therapies. The implementation of pharmacogenomic strategies will contribute to optimize drug development and therapeutics in AD and related disorders.

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