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progressive degenerative disease of brain
accounts for majority of dementia in UK
''Genetics''
most cases are sporadic
5% inherited as autosomal dominant trait - / related to mutations in amyloid precursor protein (chromosome 21), presenilin 1 (chromosome 14) and presenilin 2 (chromosome 1)
apoprotein E allele E4 - encodes a cholesterol transport protein
''Pathological changes''
macroscopic = widespread cerebral atrophy, particularly involving the cortex and hippocampus
microscopic = intraneuronal neurofibrillary tangles, neuronal plaques, deficiency of neurons
biochemical = deposition of type A-Beta-amyloid protein in cortex, deficit of Ach from damage to an ascending forebrain projection
''Neurofibrillary tangles''
paired helical filaments are partly made from a protein called tau
in AD tau proteins are excessively phosphorylated
''Management''
NICE - acetylcholinesterase inhibitors (donepezil, galantamine and rivastigmine) for mild to moderate Alzheimer's disease
memantine (a NMDA receptor antagonist) is reserved for patients with moderate - severe Alzheimer's