Ballard_2016_Lancet.Neurol_15_622

Reference

Title : Dementia in Down's syndrome - Ballard_2016_Lancet.Neurol_15_622
Author(s) : Ballard C , Mobley W , Hardy J , Williams G , Corbett A
Ref : Lancet Neurol , 15 :622 , 2016
Abstract :

Down's syndrome is the most common genetic cause of learning difficulties, and individuals with this condition represent the largest group of people with dementia under the age of 50 years. Genetic drivers result in a high frequency of Alzheimer's pathology in these individuals, evident from neuroimaging, biomarker, and neuropathological findings, and a high incidence of cognitive decline and dementia. However, cognitive assessment is challenging, and diagnostic methods have not been fully validated for use in these patients; hence, early diagnosis remains difficult. Evidence regarding the benefits of cholinesterase inhibitors and other therapeutic options to treat or delay progressive cognitive decline or dementia is very scarce. Despite close similarities with late-onset Alzheimer's disease, individuals with Down's syndrome respond differently to treatment, and a targeted approach to drug development is thus necessary. Genetic and preclinical studies offer opportunities for treatment development, and potential therapies have been identified using these approaches.

PubMedSearch : Ballard_2016_Lancet.Neurol_15_622
PubMedID: 27302127

Related information

Citations formats

Ballard C, Mobley W, Hardy J, Williams G, Corbett A (2016)
Dementia in Down's syndrome
Lancet Neurol 15 :622

Ballard C, Mobley W, Hardy J, Williams G, Corbett A (2016)
Lancet Neurol 15 :622