Alzheimer's disease (AD) is the commonest sort of dementia. Pathologically, AD is characterized by amyloid plaques and neurofibrillary tangles within the brain, with associated loss of synapses and neurons, leading to cognitive deficits and eventually dementia. Amyloid-¿ (A¿) peptide and tau protein are the first components of the plaques and tangles, respectively. Within the decades since A¿ and tau were identified, the event of therapies for AD has primarily focused on A¿, but tau has received more attention in recent years, partially due to the failure of varied A¿-targeting treatments in clinical trials. During this article, we review the present status of tau-targeting therapies for AD. Given that tau pathology correlates better with cognitive impairments than do A¿ lesions, targeting of tau is expected to give more effective than A¿ clearance once the clinical symptoms are evident. With future improvements in diagnostics, these two hallmarks of the disease might be targeted prophylactically.

El Dr. Dileep Kumar es profesor asistente en la Facultad de Farmacia de Poona, Pune. Se licenció en Farmacia por la Universidad de Manipal. El Dr. D. Kumar completó su doctorado en el IIT (BHU) de Varanasi. Ha publicado muchos artículos internacionales y capítulos de libros.Umesh Chaudhary se licenció en Farmacia en la Facultad de Farmacia de Poona, Pune.